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Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2021-09-14 15:46:18 UTC

HMDB ID

HMDB0001045

Secondary Accession Numbers

HMDB01045

Metabolite Identification

Common Name

Enkephalin L

Description

Enkephalin L is an opioid peptide. Opioid peptides are a group of neuropeptides which include enkephalins, endorphins and dynorphins. In addition to their central and peripheral antinociceptive function, opioids can modulate immune activity and cell proliferation. Enkephalins typically have a turnover rate measured in seconds to minutes, both in vivo and in vitro, and this stability is related to the age of the cell system under study. It is noteworthy that the residues most essential to enkephalin function are also either neurotransmitters themselves (glycine) or immediate precursors of L-Dopa, dopamine and norepinephrine (tyrosine and phenylalanine). The variable fifth amino acid leucine (leu5) or methionine (met5) has not yet been assigned any neurotransmitter candidacy. Again, this suggests that enkephalin is polyfunctional in that, in its intact state it elicits binding to the same sites in the brain as morphine and other opiates, and its degradation products have a potential for follow-up accessory functions by reacting as signaling entities themselves, or as the immediate precursors to inhibitory or metabotropic neurotransmitters. Enkephalins are present in macrophages infiltrating the dermal papillae in involved psoriatic skin and that the amount of enkephalin is significantly increased in involved psoriatic skin. Major enkephalin pathways in the brain involve the extrapyramidal system, including motor pathways controlled by the basal ganglia, the limbic system that governs emotional and behavioral control, and the hypothalamic-neuroendocrine axis. The apparent overlap of localization within the central nervous system of dopaminergic, glycinergic, and enkephalinergic pathways is speculated to be of neurophysiological significance, especially in light of the relatively short half-life of the enkephalins and the immediate precursor-product relationship between tyrosine and dopamine, and glycinergic signaling. Enkephalins are released into the bloodstream of mammals by the adrenal medulla. Once they are in the blood, these peptides undergo a fairly rapid hydrolysis by several plasma-contained enzymes. However, a fraction of the enkephalins present in the plasma are bound to the serum albumin, and the bound peptides are almost completely intact even after a long incubation in the presence of serum enzymes. (PMID: 9450624 , 16802191 , 4069309 ).

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

  Mrv0541 02231218532D          

 40 41  0  0  1  0            999 V2000
   18.6139   -5.0971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.4717   -5.9221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7572   -7.1596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4704   -7.1596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3270  -10.8721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1848  -10.0471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3270  -15.8221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.3283   -6.3346    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.8994   -7.1596    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   16.4704   -8.8096    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.7559  -10.8721    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.7559  -12.5221    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   20.0427   -5.0971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7572   -4.6846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0427   -5.9221    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   16.4704   -4.6846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1 19  2  0  0  0  0
  2 21  1  0  0  0  0
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  4 23  2  0  0  0  0
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 15  8  1  1  0  0  0
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 16  9  1  1  0  0  0
  9 23  1  0  0  0  0
 10 26  1  0  0  0  0
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 11 32  1  0  0  0  0
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 27 12  1  1  0  0  0
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 34 35  1  0  0  0  0
 36 38  1  0  0  0  0
 37 39  2  0  0  0  0
 38 40  2  0  0  0  0
 39 40  1  0  0  0  0
M  END

HMDB0001045
     RDKit          3D
Enkephalin L
 77 78  0  0  0  0  0  0  0  0999 V2000
   -7.4199    2.3758    1.9391 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7110   -0.1472    0.9592 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9991   -0.1189   -0.3597 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7084    0.4306   -0.3830 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4181   -1.7124   -2.5973 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2153    1.6220   -2.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0033    0.1683    0.9144 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5280   -0.8454    1.8057 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2410   -0.2011    0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4041   -0.5225    1.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2118    0.4803    1.5239 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3076    0.2106    2.3232 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6323   -1.0932    2.6738 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.7246   -1.8310    1.3968 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2085    0.8360   -1.1635 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3956    4.4286   -1.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0955    2.6499    0.2248 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8006    2.1399   -3.0696 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8794    0.6608   -2.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1353    1.6964   -1.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1300    1.1222    1.4891 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2356   -1.2066    2.4616 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9025   -1.5421    1.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6019    0.6002   -0.5043 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0247   -1.0951   -0.4750 H   0  0  0  0  0  0  0  0  0  0  0  0
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 40 77  1  0
M  END

  Mrv0541 02231218532D          

 40 41  0  0  1  0            999 V2000
   18.6139   -5.0971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.4717   -5.9221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7572   -7.1596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4704   -7.1596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3270  -10.8721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1848  -10.0471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3270  -15.8221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.3283   -6.3346    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.8994   -7.1596    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   16.4704   -8.8096    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.7559  -10.8721    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.7559  -12.5221    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   20.0427   -5.0971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   20.0427   -5.9221    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   17.1848   -8.3971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0415  -12.1096    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.3270  -12.5221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4704   -3.8596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8994   -3.8596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3270  -13.3471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0415  -11.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1848   -3.4471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7559  -10.0471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4704   -9.6346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0415  -13.7596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6124  -13.7596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0415  -14.5846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6124  -14.5846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3270  -14.9971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 19  2  0  0  0  0
  2 21  1  0  0  0  0
  3 21  2  0  0  0  0
  4 23  2  0  0  0  0
  5 32  2  0  0  0  0
  6 35  2  0  0  0  0
  7 40  1  0  0  0  0
 15  8  1  1  0  0  0
  8 19  1  0  0  0  0
 16  9  1  1  0  0  0
  9 23  1  0  0  0  0
 10 26  1  0  0  0  0
 10 35  1  0  0  0  0
 11 32  1  0  0  0  0
 11 34  1  0  0  0  0
 27 12  1  1  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 14 17  1  0  0  0  0
 14 18  1  0  0  0  0
 15 21  1  0  0  0  0
 16 19  1  0  0  0  0
 16 20  1  0  0  0  0
 20 22  1  0  0  0  0
 22 24  2  0  0  0  0
 22 25  1  0  0  0  0
 23 26  1  0  0  0  0
 24 29  1  0  0  0  0
 25 30  2  0  0  0  0
 27 28  1  0  0  0  0
 27 32  1  0  0  0  0
 28 31  1  0  0  0  0
 29 33  2  0  0  0  0
 30 33  1  0  0  0  0
 31 36  2  0  0  0  0
 31 37  1  0  0  0  0
 34 35  1  0  0  0  0
 36 38  1  0  0  0  0
 37 39  2  0  0  0  0
 38 40  2  0  0  0  0
 39 40  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0001045

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H37N5O7/c1-17(2)12-23(28(39)40)33-27(38)22(14-18-6-4-3-5-7-18)32-25(36)16-30-24(35)15-31-26(37)21(29)13-19-8-10-20(34)11-9-19/h3-11,17,21-23,34H,12-16,29H2,1-2H3,(H,30,35)(H,31,37)(H,32,36)(H,33,38)(H,39,40)/t21-,22-,23-/m0/s1

> <INCHI_KEY>
URLZCHNOLZSCCA-VABKMULXSA-N

> <FORMULA>
C28H37N5O7

> <MOLECULAR_WEIGHT>
555.6227

> <EXACT_MASS>
555.269298563

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_AVERAGE_POLARIZABILITY>
57.94392046214587

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-[(2S)-2-(2-{2-[(2S)-2-amino-3-(4-hydroxyphenyl)propanamido]acetamido}acetamido)-3-phenylpropanamido]-4-methylpentanoic acid

> <ALOGPS_LOGP>
-1.05

> <JCHEM_LOGP>
-1.8638327128310346

> <ALOGPS_LOGS>
-4.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.509926614598232

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.7021072404559847

> <JCHEM_PKA_STRONGEST_BASIC>
7.727305934916092

> <JCHEM_POLAR_SURFACE_AREA>
199.95

> <JCHEM_REFRACTIVITY>
145.59159999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.46e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S)-2-(2-{2-[(2S)-2-amino-3-(4-hydroxyphenyl)propanamido]acetamido}acetamido)-3-phenylpropanamido]-4-methylpentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0001045
     RDKit          3D
Enkephalin L
 77 78  0  0  0  0  0  0  0  0999 V2000
   -7.4199    2.3758    1.9391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5545    1.0858    2.1481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5515   -0.0692    2.1988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7053    0.9516    0.9387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7110   -0.1472    0.9592 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9991   -0.1189   -0.3597 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7084    0.4306   -0.3830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2406    0.8564    0.7330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8774    0.5440   -1.6279 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4184   -0.7321   -2.1774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4181   -1.7124   -2.5973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9247   -1.6552   -3.8859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8597   -2.6365   -4.2729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2781   -3.6281   -3.4319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7602   -3.6566   -2.1619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8334   -2.7003   -1.7519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6938    1.3267   -1.2201 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8423    2.7088   -0.9206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9856    3.2304   -0.9847 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3013    3.5328   -0.5350 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5704    2.8013   -0.6486 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0041    2.3456   -1.9115 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1936    2.6283   -2.8938 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2153    1.6220   -2.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1370    1.2892   -1.2210 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9240    0.4538   -0.0882 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7646   -0.0579    0.0442 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0033    0.1683    0.9144 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5280   -0.8454    1.8057 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2410   -0.2011    0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4041   -0.5225    1.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2118    0.4803    1.5239 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3076    0.2106    2.3232 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6323   -1.0932    2.6738 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7528   -1.3274    3.4851 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8219   -2.0909    2.1960 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7246   -1.8310    1.3968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1294   -1.4905    1.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3081   -2.3955    0.3924 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3652   -1.9254    2.5847 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8174    3.2154    2.3863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5621    2.4865    0.8548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3409    2.1845    2.5096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0154    1.2268    3.0811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5690    0.3882    2.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4215   -0.8044    1.3956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5360   -0.5562    3.1740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1371    1.9116    0.7517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3772    0.8602    0.0148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9417    0.1596    1.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5252   -0.5008   -1.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4331    1.1875   -2.3372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7024   -0.5311   -3.0155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7539   -1.2413   -1.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6017   -0.8949   -4.5474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2541   -2.6006   -5.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9899   -4.3674   -3.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0593   -4.4240   -1.4437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4222   -2.7138   -0.7627 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085    0.8360   -1.1635 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3956    4.4286   -1.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1286    3.9081    0.4878 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0955    2.6499    0.2248 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8006    2.1399   -3.0696 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8794    0.6608   -2.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1353    1.6964   -1.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1300    1.1222    1.4891 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2356   -1.2066    2.4616 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9025   -1.5421    1.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6019    0.6002   -0.5043 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0247   -1.0951   -0.4750 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9821    1.5267    1.2663 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9699    0.9902    2.7182 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6810   -1.4818    3.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0612   -3.1288    2.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0796   -2.6004    1.0080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0048   -2.6950    2.8045 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  9 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  2  0
 32 33  1  0
 33 34  2  0
 34 35  1  0
 34 36  1  0
 36 37  2  0
  5 38  1  0
 38 39  2  0
 38 40  1  0
 16 11  1  0
 37 31  1  0
  1 41  1  0
  1 42  1  0
  1 43  1  0
  2 44  1  0
  3 45  1  0
  3 46  1  0
  3 47  1  0
  4 48  1  0
  4 49  1  0
  5 50  1  1
  6 51  1  0
  9 52  1  6
 10 53  1  0
 10 54  1  0
 12 55  1  0
 13 56  1  0
 14 57  1  0
 15 58  1  0
 16 59  1  0
 17 60  1  0
 20 61  1  0
 20 62  1  0
 21 63  1  0
 24 64  1  0
 24 65  1  0
 25 66  1  0
 28 67  1  1
 29 68  1  0
 29 69  1  0
 30 70  1  0
 30 71  1  0
 32 72  1  0
 33 73  1  0
 35 74  1  0
 36 75  1  0
 37 76  1  0
 40 77  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0      34.746  -9.514   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      40.080 -11.054   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      38.747 -13.365   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      30.745 -13.365   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      26.744 -20.294   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      32.078 -18.754   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      26.744 -29.534   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0      36.079 -11.825   0.000  0.00  0.00           N+0
HETATM    9  N   UNK     0      33.412 -13.365   0.000  0.00  0.00           N+0
HETATM   10  N   UNK     0      30.745 -16.445   0.000  0.00  0.00           N+0
HETATM   11  N   UNK     0      29.411 -20.294   0.000  0.00  0.00           N+0
HETATM   12  N   UNK     0      29.411 -23.374   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      37.413  -9.514   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      38.747  -8.745   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      37.413 -11.054   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      33.412 -11.825   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      38.747  -7.205   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      40.080  -9.514   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      34.746 -11.054   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      32.078 -11.054   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      38.747 -11.825   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      32.078  -9.514   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      32.078 -14.134   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      30.745  -8.745   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      33.412  -8.745   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      32.078 -15.674   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      28.077 -22.605   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      26.744 -23.374   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      30.745  -7.205   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      33.412  -7.205   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      26.744 -24.914   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      28.077 -21.065   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      32.078  -6.434   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      29.411 -18.754   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      30.745 -17.985   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      28.077 -25.685   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      25.410 -25.685   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      28.077 -27.225   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      25.410 -27.225   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      26.744 -27.994   0.000  0.00  0.00           C+0
CONECT    1   19                                                            
CONECT    2   21                                                            
CONECT    3   21                                                            
CONECT    4   23                                                            
CONECT    5   32                                                            
CONECT    6   35                                                            
CONECT    7   40                                                            
CONECT    8   15   19                                                       
CONECT    9   16   23                                                       
CONECT   10   26   35                                                       
CONECT   11   32   34                                                       
CONECT   12   27                                                            
CONECT   13   14   15                                                       
CONECT   14   13   17   18                                                  
CONECT   15    8   13   21                                                  
CONECT   16    9   19   20                                                  
CONECT   17   14                                                            
CONECT   18   14                                                            
CONECT   19    1    8   16                                                  
CONECT   20   16   22                                                       
CONECT   21    2    3   15                                                  
CONECT   22   20   24   25                                                  
CONECT   23    4    9   26                                                  
CONECT   24   22   29                                                       
CONECT   25   22   30                                                       
CONECT   26   10   23                                                       
CONECT   27   12   28   32                                                  
CONECT   28   27   31                                                       
CONECT   29   24   33                                                       
CONECT   30   25   33                                                       
CONECT   31   28   36   37                                                  
CONECT   32    5   11   27                                                  
CONECT   33   29   30                                                       
CONECT   34   11   35                                                       
CONECT   35    6   10   34                                                  
CONECT   36   31   38                                                       
CONECT   37   31   39                                                       
CONECT   38   36   40                                                       
CONECT   39   37   40                                                       
CONECT   40    7   38   39                                                  
MASTER        0    0    0    0    0    0    0    0   40    0   82    0
END

COMPND    HMDB0001045
HETATM    1  C1  UNL     1      -7.420   2.376   1.939  1.00  0.00           C  
HETATM    2  C2  UNL     1      -6.554   1.086   2.148  1.00  0.00           C  
HETATM    3  C3  UNL     1      -7.551  -0.069   2.199  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.705   0.952   0.939  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.711  -0.147   0.959  1.00  0.00           C  
HETATM    6  N1  UNL     1      -3.999  -0.119  -0.360  1.00  0.00           N  
HETATM    7  C6  UNL     1      -2.708   0.431  -0.383  1.00  0.00           C  
HETATM    8  O1  UNL     1      -2.241   0.856   0.733  1.00  0.00           O  
HETATM    9  C7  UNL     1      -1.877   0.544  -1.628  1.00  0.00           C  
HETATM   10  C8  UNL     1      -1.418  -0.732  -2.177  1.00  0.00           C  
HETATM   11  C9  UNL     1      -2.418  -1.712  -2.597  1.00  0.00           C  
HETATM   12  C10 UNL     1      -2.925  -1.655  -3.886  1.00  0.00           C  
HETATM   13  C11 UNL     1      -3.860  -2.637  -4.273  1.00  0.00           C  
HETATM   14  C12 UNL     1      -4.278  -3.628  -3.432  1.00  0.00           C  
HETATM   15  C13 UNL     1      -3.760  -3.657  -2.162  1.00  0.00           C  
HETATM   16  C14 UNL     1      -2.833  -2.700  -1.752  1.00  0.00           C  
HETATM   17  N2  UNL     1      -0.694   1.327  -1.220  1.00  0.00           N  
HETATM   18  C15 UNL     1      -0.842   2.709  -0.921  1.00  0.00           C  
HETATM   19  O2  UNL     1      -1.986   3.230  -0.985  1.00  0.00           O  
HETATM   20  C16 UNL     1       0.301   3.533  -0.535  1.00  0.00           C  
HETATM   21  N3  UNL     1       1.570   2.801  -0.649  1.00  0.00           N  
HETATM   22  C17 UNL     1       2.004   2.346  -1.911  1.00  0.00           C  
HETATM   23  O3  UNL     1       1.194   2.628  -2.894  1.00  0.00           O  
HETATM   24  C18 UNL     1       3.215   1.622  -2.240  1.00  0.00           C  
HETATM   25  N4  UNL     1       4.137   1.289  -1.221  1.00  0.00           N  
HETATM   26  C19 UNL     1       3.924   0.454  -0.088  1.00  0.00           C  
HETATM   27  O4  UNL     1       2.765  -0.058   0.044  1.00  0.00           O  
HETATM   28  C20 UNL     1       5.003   0.168   0.914  1.00  0.00           C  
HETATM   29  N5  UNL     1       4.528  -0.845   1.806  1.00  0.00           N  
HETATM   30  C21 UNL     1       6.241  -0.201   0.164  1.00  0.00           C  
HETATM   31  C22 UNL     1       7.404  -0.522   1.047  1.00  0.00           C  
HETATM   32  C23 UNL     1       8.212   0.480   1.524  1.00  0.00           C  
HETATM   33  C24 UNL     1       9.308   0.211   2.323  1.00  0.00           C  
HETATM   34  C25 UNL     1       9.632  -1.093   2.674  1.00  0.00           C  
HETATM   35  O5  UNL     1      10.753  -1.327   3.485  1.00  0.00           O  
HETATM   36  C26 UNL     1       8.822  -2.091   2.196  1.00  0.00           C  
HETATM   37  C27 UNL     1       7.725  -1.831   1.397  1.00  0.00           C  
HETATM   38  C28 UNL     1      -5.129  -1.490   1.297  1.00  0.00           C  
HETATM   39  O6  UNL     1      -5.308  -2.396   0.392  1.00  0.00           O  
HETATM   40  O7  UNL     1      -5.365  -1.925   2.585  1.00  0.00           O  
HETATM   41  H1  UNL     1      -6.817   3.215   2.386  1.00  0.00           H  
HETATM   42  H2  UNL     1      -7.562   2.487   0.855  1.00  0.00           H  
HETATM   43  H3  UNL     1      -8.341   2.184   2.510  1.00  0.00           H  
HETATM   44  H4  UNL     1      -6.015   1.227   3.081  1.00  0.00           H  
HETATM   45  H5  UNL     1      -8.569   0.388   2.005  1.00  0.00           H  
HETATM   46  H6  UNL     1      -7.422  -0.804   1.396  1.00  0.00           H  
HETATM   47  H7  UNL     1      -7.536  -0.556   3.174  1.00  0.00           H  
HETATM   48  H8  UNL     1      -5.137   1.912   0.752  1.00  0.00           H  
HETATM   49  H9  UNL     1      -6.377   0.860   0.015  1.00  0.00           H  
HETATM   50  H10 UNL     1      -3.942   0.160   1.746  1.00  0.00           H  
HETATM   51  H11 UNL     1      -4.525  -0.501  -1.140  1.00  0.00           H  
HETATM   52  H12 UNL     1      -2.433   1.188  -2.337  1.00  0.00           H  
HETATM   53  H13 UNL     1      -0.702  -0.531  -3.015  1.00  0.00           H  
HETATM   54  H14 UNL     1      -0.754  -1.241  -1.390  1.00  0.00           H  
HETATM   55  H15 UNL     1      -2.602  -0.895  -4.547  1.00  0.00           H  
HETATM   56  H16 UNL     1      -4.254  -2.601  -5.260  1.00  0.00           H  
HETATM   57  H17 UNL     1      -4.990  -4.367  -3.744  1.00  0.00           H  
HETATM   58  H18 UNL     1      -4.059  -4.424  -1.444  1.00  0.00           H  
HETATM   59  H19 UNL     1      -2.422  -2.714  -0.763  1.00  0.00           H  
HETATM   60  H20 UNL     1       0.208   0.836  -1.164  1.00  0.00           H  
HETATM   61  H21 UNL     1       0.396   4.429  -1.203  1.00  0.00           H  
HETATM   62  H22 UNL     1       0.129   3.908   0.488  1.00  0.00           H  
HETATM   63  H23 UNL     1       2.096   2.650   0.225  1.00  0.00           H  
HETATM   64  H24 UNL     1       3.801   2.140  -3.070  1.00  0.00           H  
HETATM   65  H25 UNL     1       2.879   0.661  -2.792  1.00  0.00           H  
HETATM   66  H26 UNL     1       5.135   1.696  -1.256  1.00  0.00           H  
HETATM   67  H27 UNL     1       5.130   1.122   1.489  1.00  0.00           H  
HETATM   68  H28 UNL     1       5.236  -1.207   2.462  1.00  0.00           H  
HETATM   69  H29 UNL     1       3.902  -1.542   1.402  1.00  0.00           H  
HETATM   70  H30 UNL     1       6.602   0.600  -0.504  1.00  0.00           H  
HETATM   71  H31 UNL     1       6.025  -1.095  -0.475  1.00  0.00           H  
HETATM   72  H32 UNL     1       7.982   1.527   1.266  1.00  0.00           H  
HETATM   73  H33 UNL     1       9.970   0.990   2.718  1.00  0.00           H  
HETATM   74  H34 UNL     1      11.681  -1.482   3.129  1.00  0.00           H  
HETATM   75  H35 UNL     1       9.061  -3.129   2.464  1.00  0.00           H  
HETATM   76  H36 UNL     1       7.080  -2.600   1.008  1.00  0.00           H  
HETATM   77  H37 UNL     1      -6.005  -2.695   2.805  1.00  0.00           H  
CONECT    1    2   41   42   43
CONECT    2    3    4   44
CONECT    3   45   46   47
CONECT    4    5   48   49
CONECT    5    6   38   50
CONECT    6    7   51
CONECT    7    8    8    9
CONECT    9   10   17   52
CONECT   10   11   53   54
CONECT   11   12   12   16
CONECT   12   13   55
CONECT   13   14   14   56
CONECT   14   15   57
CONECT   15   16   16   58
CONECT   16   59
CONECT   17   18   60
CONECT   18   19   19   20
CONECT   20   21   61   62
CONECT   21   22   63
CONECT   22   23   23   24
CONECT   24   25   64   65
CONECT   25   26   66
CONECT   26   27   27   28
CONECT   28   29   30   67
CONECT   29   68   69
CONECT   30   31   70   71
CONECT   31   32   32   37
CONECT   32   33   72
CONECT   33   34   34   73
CONECT   34   35   36
CONECT   35   74
CONECT   36   37   37   75
CONECT   37   76
CONECT   38   39   39   40
CONECT   40   77
END

HMDB0001045
     RDKit          3D
Enkephalin L
 77 78  0  0  0  0  0  0  0  0999 V2000
   -7.4199    2.3758    1.9391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5545    1.0858    2.1481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5515   -0.0692    2.1988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7053    0.9516    0.9387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7110   -0.1472    0.9592 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9991   -0.1189   -0.3597 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7084    0.4306   -0.3830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2406    0.8564    0.7330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8774    0.5440   -1.6279 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4184   -0.7321   -2.1774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4181   -1.7124   -2.5973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9247   -1.6552   -3.8859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8597   -2.6365   -4.2729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2781   -3.6281   -3.4319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7602   -3.6566   -2.1619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8334   -2.7003   -1.7519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6938    1.3267   -1.2201 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8423    2.7088   -0.9206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9856    3.2304   -0.9847 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3013    3.5328   -0.5350 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5704    2.8013   -0.6486 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0041    2.3456   -1.9115 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1936    2.6283   -2.8938 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2153    1.6220   -2.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1370    1.2892   -1.2210 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9240    0.4538   -0.0882 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7646   -0.0579    0.0442 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0033    0.1683    0.9144 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5280   -0.8454    1.8057 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2410   -0.2011    0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4041   -0.5225    1.0472 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2118    0.4803    1.5239 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3076    0.2106    2.3232 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6323   -1.0932    2.6738 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7528   -1.3274    3.4851 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8219   -2.0909    2.1960 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7246   -1.8310    1.3968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1294   -1.4905    1.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3081   -2.3955    0.3924 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3652   -1.9254    2.5847 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8174    3.2154    2.3863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5621    2.4865    0.8548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3409    2.1845    2.5096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0154    1.2268    3.0811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5690    0.3882    2.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4215   -0.8044    1.3956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5360   -0.5562    3.1740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1371    1.9116    0.7517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3772    0.8602    0.0148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9417    0.1596    1.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5252   -0.5008   -1.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4331    1.1875   -2.3372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7024   -0.5311   -3.0155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7539   -1.2413   -1.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6017   -0.8949   -4.5474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2541   -2.6006   -5.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9899   -4.3674   -3.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0593   -4.4240   -1.4437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4222   -2.7138   -0.7627 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085    0.8360   -1.1635 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3956    4.4286   -1.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1286    3.9081    0.4878 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0955    2.6499    0.2248 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8006    2.1399   -3.0696 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8794    0.6608   -2.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1353    1.6964   -1.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1300    1.1222    1.4891 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2356   -1.2066    2.4616 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9025   -1.5421    1.4022 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6019    0.6002   -0.5043 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0247   -1.0951   -0.4750 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9821    1.5267    1.2663 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9699    0.9902    2.7182 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6810   -1.4818    3.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0612   -3.1288    2.4639 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0796   -2.6004    1.0080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0048   -2.6950    2.8045 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  9 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  2  0
 32 33  1  0
 33 34  2  0
 34 35  1  0
 34 36  1  0
 36 37  2  0
  5 38  1  0
 38 39  2  0
 38 40  1  0
 16 11  1  0
 37 31  1  0
  1 41  1  0
  1 42  1  0
  1 43  1  0
  2 44  1  0
  3 45  1  0
  3 46  1  0
  3 47  1  0
  4 48  1  0
  4 49  1  0
  5 50  1  1
  6 51  1  0
  9 52  1  6
 10 53  1  0
 10 54  1  0
 12 55  1  0
 13 56  1  0
 14 57  1  0
 15 58  1  0
 16 59  1  0
 17 60  1  0
 20 61  1  0
 20 62  1  0
 21 63  1  0
 24 64  1  0
 24 65  1  0
 25 66  1  0
 28 67  1  1
 29 68  1  0
 29 69  1  0
 30 70  1  0
 30 71  1  0
 32 72  1  0
 33 73  1  0
 35 74  1  0
 36 75  1  0
 37 76  1  0
 40 77  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
(2S)-2-[(2S)-2-(2-{2-[(2S)-2-amino-3-(4-hydroxyphenyl)propanamido]acetamido}acetamido)-3-phenylpropanamido]-4-methylpentanoic acid	ChEBI
[5-Leucine]enkephalin	ChEBI
[Leu(5)]-enkephalin	ChEBI
[Leu(5)]enkephalin	ChEBI
[Leu]enkephalin	ChEBI
Enkephalin, leucine	ChEBI
H-Tyr-gly-gly-phe-leu-OH	ChEBI
L-ENK	ChEBI
L-Tyr-gly-gly-L-phe-L-leu	ChEBI
Leu-enk	ChEBI
Leucine enkephalin	ChEBI
Leucine-enkephalin	ChEBI
Leucyl-enkephalin	ChEBI
LeuENK	ChEBI
N-(N-(N-(N-L-Tyrosylglycyl)glycyl)-L-phenylalanyl)-L-leucine	ChEBI
Tyr-gly-gly-phe-leu	ChEBI
Tyr-gly-gly-phe-leu-OH	ChEBI
Y-g-g-F-L	ChEBI
YGGFL	ChEBI
(2S)-2-[(2S)-2-(2-{2-[(2S)-2-amino-3-(4-hydroxyphenyl)propanamido]acetamido}acetamido)-3-phenylpropanamido]-4-methylpentanoate	Generator
Leucine- enkephalin	ChEMBL, HMDB
Leu-enkephalin	ChEMBL, HMDB, MeSH
[Leu 5]enkephalin	HMDB
[Leu5]-enkephalin	HMDB
Enkephalin, 5-leucine	MeSH, HMDB
Leu enkephalin	MeSH, HMDB
5 Leucine enkephalin	MeSH, HMDB
Leu(5)-enkephalin	MeSH, HMDB
5-Leucine enkephalin	MeSH, HMDB
(2S)-2-{[(2S)-2-({2-[(2-{[(2S)-2-amino-1-hydroxy-3-(4-hydroxyphenyl)propylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyethylidene}amino)-1-hydroxy-3-phenylpropylidene]amino}-4-methylpentanoate	Generator, HMDB

Chemical Formula

C₂₈H₃₇N₅O₇

Average Molecular Weight

555.6227

Monoisotopic Molecular Weight

555.269298563

IUPAC Name

(2S)-2-[(2S)-2-(2-{2-[(2S)-2-amino-3-(4-hydroxyphenyl)propanamido]acetamido}acetamido)-3-phenylpropanamido]-4-methylpentanoic acid

Traditional Name

(2S)-2-[(2S)-2-(2-{2-[(2S)-2-amino-3-(4-hydroxyphenyl)propanamido]acetamido}acetamido)-3-phenylpropanamido]-4-methylpentanoic acid

CAS Registry Number

14-18-6

SMILES

CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)C(O)=O

InChI Identifier

InChI=1S/C28H37N5O7/c1-17(2)12-23(28(39)40)33-27(38)22(14-18-6-4-3-5-7-18)32-25(36)16-30-24(35)15-31-26(37)21(29)13-19-8-10-20(34)11-9-19/h3-11,17,21-23,34H,12-16,29H2,1-2H3,(H,30,35)(H,31,37)(H,32,36)(H,33,38)(H,39,40)/t21-,22-,23-/m0/s1

InChI Key

URLZCHNOLZSCCA-VABKMULXSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Tyrosine or derivatives
Phenylalanine or derivatives
Leucine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
N-acyl-l-alpha-amino acid
Alpha-amino acid amide
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
Amphetamine or derivatives
1-hydroxy-2-unsubstituted benzenoid
Phenol
Aralkylamine
Benzenoid
Fatty acyl
Monocyclic benzene moiety
Fatty amide
Secondary carboxylic acid amide
Amino acid or derivatives
Carboxamide group
Amino acid
Carboxylic acid
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Primary aliphatic amine
Organic oxide
Organonitrogen compound
Carbonyl group
Organooxygen compound
Organopnictogen compound
Organic nitrogen compound
Amine
Organic oxygen compound
Primary amine
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Health effect

Digestive system disorder

Hepatobiliary disorder

Hepatic disorder

Cirrhosis (HMDB: HMDB0001045)
Liver disease (HMDB: HMDB0001045)

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 2583565)

Source

Endogenous

Endogenous (HMDB: HMDB0001045)

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Process

Not Available

Role

Industrial application

Pharmaceutical industry

Biomarker

Acute liver disease (MarkerDB: MDB00000296)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.015 g/L	ALOGPS
logP	-1	ALOGPS
logP	-1.9	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	3.7	ChemAxon
pKa (Strongest Basic)	7.73	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	199.95 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	145.59 m³·mol⁻¹	ChemAxon
Polarizability	57.94 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	225.673	31661259
DarkChem	[M-H]-	221.212	31661259
AllCCS	[M+H]+	231.129	32859911
AllCCS	[M-H]-	217.545	32859911
DeepCCS	[M+H]+	222.152	30932474
DeepCCS	[M-H]-	220.327	30932474
DeepCCS	[M-2H]-	253.57	30932474
DeepCCS	[M+Na]+	227.827	30932474
AllCCS	[M+H]+	231.1	32859911
AllCCS	[M+H-H2O]+	229.9	32859911
AllCCS	[M+NH4]+	232.3	32859911
AllCCS	[M+Na]+	232.6	32859911
AllCCS	[M-H]-	217.5	32859911
AllCCS	[M+Na-2H]-	220.0	32859911
AllCCS	[M+HCOO]-	222.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Enkephalin L	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)C(O)=O	5477.6	Standard polar	33892256
Enkephalin L	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)C(O)=O	3121.9	Standard non polar	33892256
Enkephalin L	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)C(O)=O	5031.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Enkephalin L,1TMS,isomer #1	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O	4740.6	Semi standard non polar	33892256
Enkephalin L,1TMS,isomer #2	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C	4643.1	Semi standard non polar	33892256
Enkephalin L,1TMS,isomer #3	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)C(=O)O	4806.7	Semi standard non polar	33892256
Enkephalin L,1TMS,isomer #4	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C	4613.7	Semi standard non polar	33892256
Enkephalin L,1TMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)C(=O)O	4636.9	Semi standard non polar	33892256
Enkephalin L,1TMS,isomer #6	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)C(=O)O	4663.3	Semi standard non polar	33892256
Enkephalin L,1TMS,isomer #7	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)C(=O)O	4639.2	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #1	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	4578.5	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #10	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4468.7	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #11	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4441.4	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #12	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C	4585.6	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #13	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4596.0	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #14	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4619.6	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #15	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4608.9	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #16	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	4740.1	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #17	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	4410.5	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #18	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	4414.2	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #19	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	4407.6	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #2	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O	4715.5	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #20	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4442.6	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #21	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4421.1	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #22	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4426.7	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #3	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C	4537.5	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #4	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O	4550.9	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O	4577.6	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #6	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O	4551.2	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #7	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	4623.9	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #8	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C	4455.3	Semi standard non polar	33892256
Enkephalin L,2TMS,isomer #9	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4439.8	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #1	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	4593.4	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #1	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	3978.4	Standard non polar	33892256
Enkephalin L,3TMS,isomer #1	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	6073.7	Standard polar	33892256
Enkephalin L,3TMS,isomer #10	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	4665.6	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #10	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	4096.9	Standard non polar	33892256
Enkephalin L,3TMS,isomer #10	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	6204.7	Standard polar	33892256
Enkephalin L,3TMS,isomer #11	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	4417.7	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #11	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	3989.3	Standard non polar	33892256
Enkephalin L,3TMS,isomer #11	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	6558.4	Standard polar	33892256
Enkephalin L,3TMS,isomer #12	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	4411.3	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #12	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	4013.2	Standard non polar	33892256
Enkephalin L,3TMS,isomer #12	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	6558.1	Standard polar	33892256
Enkephalin L,3TMS,isomer #13	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	4403.0	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #13	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	4000.4	Standard non polar	33892256
Enkephalin L,3TMS,isomer #13	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	6411.3	Standard polar	33892256
Enkephalin L,3TMS,isomer #14	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4445.5	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #14	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4026.8	Standard non polar	33892256
Enkephalin L,3TMS,isomer #14	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6612.8	Standard polar	33892256
Enkephalin L,3TMS,isomer #15	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4400.2	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #15	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4024.8	Standard non polar	33892256
Enkephalin L,3TMS,isomer #15	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6444.4	Standard polar	33892256
Enkephalin L,3TMS,isomer #16	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4428.1	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #16	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4045.9	Standard non polar	33892256
Enkephalin L,3TMS,isomer #16	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6466.8	Standard polar	33892256
Enkephalin L,3TMS,isomer #17	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C	4483.5	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #17	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C	4017.6	Standard non polar	33892256
Enkephalin L,3TMS,isomer #17	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C	6171.6	Standard polar	33892256
Enkephalin L,3TMS,isomer #18	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4473.5	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #18	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4048.5	Standard non polar	33892256
Enkephalin L,3TMS,isomer #18	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6172.0	Standard polar	33892256
Enkephalin L,3TMS,isomer #19	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4497.4	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #19	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4073.0	Standard non polar	33892256
Enkephalin L,3TMS,isomer #19	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6186.7	Standard polar	33892256
Enkephalin L,3TMS,isomer #2	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C	4438.4	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #2	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C	3913.8	Standard non polar	33892256
Enkephalin L,3TMS,isomer #2	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C	6546.7	Standard polar	33892256
Enkephalin L,3TMS,isomer #20	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4476.4	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #20	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4072.6	Standard non polar	33892256
Enkephalin L,3TMS,isomer #20	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6161.5	Standard polar	33892256
Enkephalin L,3TMS,isomer #21	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4600.3	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #21	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4098.3	Standard non polar	33892256
Enkephalin L,3TMS,isomer #21	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6248.8	Standard polar	33892256
Enkephalin L,3TMS,isomer #22	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	4322.2	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #22	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	4000.7	Standard non polar	33892256
Enkephalin L,3TMS,isomer #22	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	6719.3	Standard polar	33892256
Enkephalin L,3TMS,isomer #23	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	4308.0	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #23	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	4020.8	Standard non polar	33892256
Enkephalin L,3TMS,isomer #23	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	6727.3	Standard polar	33892256
Enkephalin L,3TMS,isomer #24	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	4299.5	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #24	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	4006.6	Standard non polar	33892256
Enkephalin L,3TMS,isomer #24	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C	6566.8	Standard polar	33892256
Enkephalin L,3TMS,isomer #25	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4321.7	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #25	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4030.8	Standard non polar	33892256
Enkephalin L,3TMS,isomer #25	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6743.9	Standard polar	33892256
Enkephalin L,3TMS,isomer #26	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4290.8	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #26	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4029.2	Standard non polar	33892256
Enkephalin L,3TMS,isomer #26	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6560.4	Standard polar	33892256
Enkephalin L,3TMS,isomer #27	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4328.4	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #27	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4045.5	Standard non polar	33892256
Enkephalin L,3TMS,isomer #27	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6596.5	Standard polar	33892256
Enkephalin L,3TMS,isomer #28	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4449.9	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #28	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4088.0	Standard non polar	33892256
Enkephalin L,3TMS,isomer #28	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6241.8	Standard polar	33892256
Enkephalin L,3TMS,isomer #29	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4450.8	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #29	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4122.8	Standard non polar	33892256
Enkephalin L,3TMS,isomer #29	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6234.2	Standard polar	33892256
Enkephalin L,3TMS,isomer #3	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4437.0	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #3	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3931.1	Standard non polar	33892256
Enkephalin L,3TMS,isomer #3	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6551.3	Standard polar	33892256
Enkephalin L,3TMS,isomer #30	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4435.4	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #30	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4119.0	Standard non polar	33892256
Enkephalin L,3TMS,isomer #30	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6209.7	Standard polar	33892256
Enkephalin L,3TMS,isomer #31	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4581.9	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #31	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4139.9	Standard non polar	33892256
Enkephalin L,3TMS,isomer #31	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6300.3	Standard polar	33892256
Enkephalin L,3TMS,isomer #32	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4472.5	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #32	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4134.3	Standard non polar	33892256
Enkephalin L,3TMS,isomer #32	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6284.2	Standard polar	33892256
Enkephalin L,3TMS,isomer #33	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4440.1	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #33	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4146.8	Standard non polar	33892256
Enkephalin L,3TMS,isomer #33	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6240.3	Standard polar	33892256
Enkephalin L,3TMS,isomer #34	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4584.8	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #34	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4159.7	Standard non polar	33892256
Enkephalin L,3TMS,isomer #34	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6341.4	Standard polar	33892256
Enkephalin L,3TMS,isomer #35	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4467.7	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #35	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4166.3	Standard non polar	33892256
Enkephalin L,3TMS,isomer #35	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6249.4	Standard polar	33892256
Enkephalin L,3TMS,isomer #36	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4608.4	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #36	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4196.0	Standard non polar	33892256
Enkephalin L,3TMS,isomer #36	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6335.8	Standard polar	33892256
Enkephalin L,3TMS,isomer #37	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4601.8	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #37	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4177.5	Standard non polar	33892256
Enkephalin L,3TMS,isomer #37	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6314.4	Standard polar	33892256
Enkephalin L,3TMS,isomer #38	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4329.0	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #38	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4092.6	Standard non polar	33892256
Enkephalin L,3TMS,isomer #38	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6742.9	Standard polar	33892256
Enkephalin L,3TMS,isomer #39	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4306.4	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #39	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4090.1	Standard non polar	33892256
Enkephalin L,3TMS,isomer #39	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6575.3	Standard polar	33892256
Enkephalin L,3TMS,isomer #4	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4452.5	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #4	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3951.7	Standard non polar	33892256
Enkephalin L,3TMS,isomer #4	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6571.1	Standard polar	33892256
Enkephalin L,3TMS,isomer #40	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4310.6	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #40	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4111.1	Standard non polar	33892256
Enkephalin L,3TMS,isomer #40	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6589.4	Standard polar	33892256
Enkephalin L,3TMS,isomer #41	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4325.1	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #41	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4125.5	Standard non polar	33892256
Enkephalin L,3TMS,isomer #41	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6640.1	Standard polar	33892256
Enkephalin L,3TMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4418.7	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3944.0	Standard non polar	33892256
Enkephalin L,3TMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6408.9	Standard polar	33892256
Enkephalin L,3TMS,isomer #6	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C	4559.0	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #6	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C	4019.8	Standard non polar	33892256
Enkephalin L,3TMS,isomer #6	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C	6118.7	Standard polar	33892256
Enkephalin L,3TMS,isomer #7	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4568.9	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #7	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4038.9	Standard non polar	33892256
Enkephalin L,3TMS,isomer #7	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6150.7	Standard polar	33892256
Enkephalin L,3TMS,isomer #8	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4593.6	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #8	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4069.6	Standard non polar	33892256
Enkephalin L,3TMS,isomer #8	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6155.8	Standard polar	33892256
Enkephalin L,3TMS,isomer #9	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4576.5	Semi standard non polar	33892256
Enkephalin L,3TMS,isomer #9	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4073.1	Standard non polar	33892256
Enkephalin L,3TMS,isomer #9	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6129.5	Standard polar	33892256
Enkephalin L,4TMS,isomer #1	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C	4474.6	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #1	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C	3989.8	Standard non polar	33892256
Enkephalin L,4TMS,isomer #1	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C	5715.6	Standard polar	33892256
Enkephalin L,4TMS,isomer #10	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4316.2	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #10	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3988.3	Standard non polar	33892256
Enkephalin L,4TMS,isomer #10	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6121.3	Standard polar	33892256
Enkephalin L,4TMS,isomer #11	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4348.1	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #11	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4001.6	Standard non polar	33892256
Enkephalin L,4TMS,isomer #11	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6157.2	Standard polar	33892256
Enkephalin L,4TMS,isomer #12	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4464.5	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #12	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4060.9	Standard non polar	33892256
Enkephalin L,4TMS,isomer #12	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5792.9	Standard polar	33892256
Enkephalin L,4TMS,isomer #13	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4462.8	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #13	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4082.7	Standard non polar	33892256
Enkephalin L,4TMS,isomer #13	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5791.6	Standard polar	33892256
Enkephalin L,4TMS,isomer #14	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4442.8	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #14	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4081.0	Standard non polar	33892256
Enkephalin L,4TMS,isomer #14	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5770.9	Standard polar	33892256
Enkephalin L,4TMS,isomer #15	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4574.9	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #15	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4109.5	Standard non polar	33892256
Enkephalin L,4TMS,isomer #15	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5838.4	Standard polar	33892256
Enkephalin L,4TMS,isomer #16	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4486.6	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #16	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4095.5	Standard non polar	33892256
Enkephalin L,4TMS,isomer #16	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	5830.4	Standard polar	33892256
Enkephalin L,4TMS,isomer #17	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4449.2	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #17	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4103.7	Standard non polar	33892256
Enkephalin L,4TMS,isomer #17	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	5792.7	Standard polar	33892256
Enkephalin L,4TMS,isomer #18	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4571.0	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #18	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4123.9	Standard non polar	33892256
Enkephalin L,4TMS,isomer #18	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	5866.4	Standard polar	33892256
Enkephalin L,4TMS,isomer #19	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4479.4	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #19	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4124.3	Standard non polar	33892256
Enkephalin L,4TMS,isomer #19	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	5809.0	Standard polar	33892256
Enkephalin L,4TMS,isomer #2	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4474.5	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #2	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4008.1	Standard non polar	33892256
Enkephalin L,4TMS,isomer #2	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	5719.1	Standard polar	33892256
Enkephalin L,4TMS,isomer #20	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4600.8	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #20	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4151.5	Standard non polar	33892256
Enkephalin L,4TMS,isomer #20	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	5869.5	Standard polar	33892256
Enkephalin L,4TMS,isomer #21	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4608.9	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #21	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4145.3	Standard non polar	33892256
Enkephalin L,4TMS,isomer #21	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	5854.5	Standard polar	33892256
Enkephalin L,4TMS,isomer #22	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4369.9	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #22	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4065.0	Standard non polar	33892256
Enkephalin L,4TMS,isomer #22	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6284.2	Standard polar	33892256
Enkephalin L,4TMS,isomer #23	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4335.1	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #23	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4059.0	Standard non polar	33892256
Enkephalin L,4TMS,isomer #23	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6147.3	Standard polar	33892256
Enkephalin L,4TMS,isomer #24	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4340.3	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #24	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4073.9	Standard non polar	33892256
Enkephalin L,4TMS,isomer #24	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6164.2	Standard polar	33892256
Enkephalin L,4TMS,isomer #25	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4363.6	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #25	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4085.8	Standard non polar	33892256
Enkephalin L,4TMS,isomer #25	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	6204.6	Standard polar	33892256
Enkephalin L,4TMS,isomer #26	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4380.6	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #26	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4070.3	Standard non polar	33892256
Enkephalin L,4TMS,isomer #26	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5813.2	Standard polar	33892256
Enkephalin L,4TMS,isomer #27	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4368.9	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #27	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4091.9	Standard non polar	33892256
Enkephalin L,4TMS,isomer #27	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5818.2	Standard polar	33892256
Enkephalin L,4TMS,isomer #28	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4353.5	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #28	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4089.5	Standard non polar	33892256
Enkephalin L,4TMS,isomer #28	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5798.2	Standard polar	33892256
Enkephalin L,4TMS,isomer #29	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4508.1	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #29	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4123.8	Standard non polar	33892256
Enkephalin L,4TMS,isomer #29	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5874.1	Standard polar	33892256
Enkephalin L,4TMS,isomer #3	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4492.7	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #3	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4027.4	Standard non polar	33892256
Enkephalin L,4TMS,isomer #3	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	5738.9	Standard polar	33892256
Enkephalin L,4TMS,isomer #30	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4382.8	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #30	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4105.9	Standard non polar	33892256
Enkephalin L,4TMS,isomer #30	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	5833.5	Standard polar	33892256
Enkephalin L,4TMS,isomer #31	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4355.4	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #31	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4112.5	Standard non polar	33892256
Enkephalin L,4TMS,isomer #31	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	5794.5	Standard polar	33892256
Enkephalin L,4TMS,isomer #32	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4505.2	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #32	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4137.2	Standard non polar	33892256
Enkephalin L,4TMS,isomer #32	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	5878.3	Standard polar	33892256
Enkephalin L,4TMS,isomer #33	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4388.0	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #33	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4127.4	Standard non polar	33892256
Enkephalin L,4TMS,isomer #33	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	5823.7	Standard polar	33892256
Enkephalin L,4TMS,isomer #34	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4541.5	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #34	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4158.9	Standard non polar	33892256
Enkephalin L,4TMS,isomer #34	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	5892.6	Standard polar	33892256
Enkephalin L,4TMS,isomer #35	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4563.2	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #35	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4152.5	Standard non polar	33892256
Enkephalin L,4TMS,isomer #35	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	5878.0	Standard polar	33892256
Enkephalin L,4TMS,isomer #36	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4273.8	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #36	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4071.5	Standard non polar	33892256
Enkephalin L,4TMS,isomer #36	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6407.9	Standard polar	33892256
Enkephalin L,4TMS,isomer #37	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4249.4	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #37	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4061.6	Standard non polar	33892256
Enkephalin L,4TMS,isomer #37	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6261.1	Standard polar	33892256
Enkephalin L,4TMS,isomer #38	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4250.5	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #38	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4076.3	Standard non polar	33892256
Enkephalin L,4TMS,isomer #38	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6286.9	Standard polar	33892256
Enkephalin L,4TMS,isomer #39	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4267.6	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #39	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4088.5	Standard non polar	33892256
Enkephalin L,4TMS,isomer #39	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6292.9	Standard polar	33892256
Enkephalin L,4TMS,isomer #4	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4472.8	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #4	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4028.9	Standard non polar	33892256
Enkephalin L,4TMS,isomer #4	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	5716.4	Standard polar	33892256
Enkephalin L,4TMS,isomer #40	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4385.5	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #40	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4162.0	Standard non polar	33892256
Enkephalin L,4TMS,isomer #40	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5913.3	Standard polar	33892256
Enkephalin L,4TMS,isomer #41	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4366.4	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #41	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4172.7	Standard non polar	33892256
Enkephalin L,4TMS,isomer #41	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5874.9	Standard polar	33892256
Enkephalin L,4TMS,isomer #42	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4527.4	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #42	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4193.7	Standard non polar	33892256
Enkephalin L,4TMS,isomer #42	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5961.6	Standard polar	33892256
Enkephalin L,4TMS,isomer #43	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4371.7	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #43	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4191.2	Standard non polar	33892256
Enkephalin L,4TMS,isomer #43	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5878.7	Standard polar	33892256
Enkephalin L,4TMS,isomer #44	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4534.2	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #44	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4219.1	Standard non polar	33892256
Enkephalin L,4TMS,isomer #44	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5951.6	Standard polar	33892256
Enkephalin L,4TMS,isomer #45	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4557.1	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #45	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4206.5	Standard non polar	33892256
Enkephalin L,4TMS,isomer #45	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	5939.3	Standard polar	33892256
Enkephalin L,4TMS,isomer #46	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4380.4	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #46	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4206.1	Standard non polar	33892256
Enkephalin L,4TMS,isomer #46	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	5919.7	Standard polar	33892256
Enkephalin L,4TMS,isomer #47	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4545.3	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #47	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4229.8	Standard non polar	33892256
Enkephalin L,4TMS,isomer #47	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	5994.5	Standard polar	33892256
Enkephalin L,4TMS,isomer #48	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4541.4	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #48	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4228.1	Standard non polar	33892256
Enkephalin L,4TMS,isomer #48	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	5964.9	Standard polar	33892256
Enkephalin L,4TMS,isomer #49	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4571.8	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #49	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	4249.3	Standard non polar	33892256
Enkephalin L,4TMS,isomer #49	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	5973.6	Standard polar	33892256
Enkephalin L,4TMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4590.9	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4060.8	Standard non polar	33892256
Enkephalin L,4TMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	5787.3	Standard polar	33892256
Enkephalin L,4TMS,isomer #50	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4276.8	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #50	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	4154.9	Standard non polar	33892256
Enkephalin L,4TMS,isomer #50	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	6301.5	Standard polar	33892256
Enkephalin L,4TMS,isomer #6	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	4347.9	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #6	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	3972.5	Standard non polar	33892256
Enkephalin L,4TMS,isomer #6	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	6250.8	Standard polar	33892256
Enkephalin L,4TMS,isomer #7	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	4334.7	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #7	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	3987.5	Standard non polar	33892256
Enkephalin L,4TMS,isomer #7	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	6261.8	Standard polar	33892256
Enkephalin L,4TMS,isomer #8	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	4318.1	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #8	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	3969.3	Standard non polar	33892256
Enkephalin L,4TMS,isomer #8	CC(C)C[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C	6127.2	Standard polar	33892256
Enkephalin L,4TMS,isomer #9	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4357.7	Semi standard non polar	33892256
Enkephalin L,4TMS,isomer #9	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3999.6	Standard non polar	33892256
Enkephalin L,4TMS,isomer #9	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	6276.0	Standard polar	33892256
Enkephalin L,1TBDMS,isomer #1	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	4986.0	Semi standard non polar	33892256
Enkephalin L,1TBDMS,isomer #2	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	4895.3	Semi standard non polar	33892256
Enkephalin L,1TBDMS,isomer #3	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O	4966.9	Semi standard non polar	33892256
Enkephalin L,1TBDMS,isomer #4	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C	4822.3	Semi standard non polar	33892256
Enkephalin L,1TBDMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O	4856.1	Semi standard non polar	33892256
Enkephalin L,1TBDMS,isomer #6	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O	4896.6	Semi standard non polar	33892256
Enkephalin L,1TBDMS,isomer #7	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O	4866.2	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #1	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	5019.1	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #10	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4943.5	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #11	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4909.3	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #12	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4924.7	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #13	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4960.3	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #14	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5014.0	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #15	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5000.6	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #16	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5119.2	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #17	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4846.9	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #18	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4894.5	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #19	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4870.5	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #2	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O	5095.0	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #20	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4897.8	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #21	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4891.7	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #22	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4906.6	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #3	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	4948.0	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #4	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O	4985.2	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O	5038.1	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #6	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O	4998.7	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #7	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4999.2	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #8	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C	4874.3	Semi standard non polar	33892256
Enkephalin L,2TBDMS,isomer #9	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4899.6	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #1	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5176.0	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #1	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4457.6	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #1	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	6034.1	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #10	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5298.3	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #10	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4508.9	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #10	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6096.1	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #11	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5055.7	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #11	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4447.4	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #11	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6429.0	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #12	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5107.7	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #12	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4457.1	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #12	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6442.5	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #13	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5078.1	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #13	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4442.0	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #13	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6354.0	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #14	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5128.6	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #14	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4466.3	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #14	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6476.7	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #15	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5113.0	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #15	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4455.0	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #15	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6369.5	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #16	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5117.6	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #16	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4470.7	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #16	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6403.2	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #17	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5027.4	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #17	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4493.9	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #17	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6083.8	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #18	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5053.6	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #18	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4508.0	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #18	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	6078.0	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #19	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5081.7	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #19	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4523.8	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #19	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	6103.8	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #2	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	5074.0	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #2	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	4395.3	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #2	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	6420.5	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #20	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5065.5	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #20	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4524.8	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #20	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	6093.7	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #21	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5208.9	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #21	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4524.8	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #21	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	6115.9	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #22	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4988.7	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #22	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4466.1	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #22	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6521.8	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #23	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5034.8	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #23	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4475.8	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #23	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6539.8	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #24	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5011.7	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #24	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4460.1	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #24	CC(C)C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6446.4	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #25	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5035.2	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #25	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4479.3	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #25	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	6548.1	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #26	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5031.9	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #26	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4468.7	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #26	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	6434.7	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #27	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5036.3	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #27	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4477.4	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #27	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	6481.4	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #28	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5007.3	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #28	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4540.8	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #28	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6139.0	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #29	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5056.7	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #29	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4562.2	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #29	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6141.5	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #3	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5101.8	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #3	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4394.7	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #3	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	6416.2	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #30	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5052.7	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #30	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4558.0	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #30	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6134.6	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #31	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5185.7	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #31	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4561.0	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #31	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6153.8	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #32	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5064.9	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #32	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4568.4	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #32	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6175.5	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #33	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5079.3	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #33	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4574.6	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #33	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6146.6	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #34	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5214.8	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #34	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4570.2	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #34	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6173.6	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #35	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5081.3	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #35	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4586.7	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #35	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6175.2	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #36	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5243.2	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #36	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4592.0	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #36	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6182.0	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #37	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5221.9	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #37	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4587.2	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #37	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6183.4	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #38	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5007.1	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #38	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4530.1	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #38	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6547.8	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #39	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5000.9	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #39	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4519.1	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #39	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6448.7	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #4	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5135.6	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #4	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4404.1	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #4	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	6449.9	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #40	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5017.3	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #40	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4529.7	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #40	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6472.9	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #41	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5026.4	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #41	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4540.7	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #41	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CN(C(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6504.5	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5100.8	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4396.0	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #5	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	6348.5	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #6	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5103.1	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #6	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4487.5	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #6	CC(C)C[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	6064.2	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #7	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5145.3	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #7	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4493.1	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #7	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N(C(=O)CNC(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6081.0	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #8	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5184.7	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #8	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4511.3	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #8	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CN(C(=O)CNC(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6096.0	Standard polar	33892256
Enkephalin L,3TBDMS,isomer #9	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5165.9	Semi standard non polar	33892256
Enkephalin L,3TBDMS,isomer #9	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4514.6	Standard non polar	33892256
Enkephalin L,3TBDMS,isomer #9	CC(C)C[C@H](NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CN(C(=O)[C@H](CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	6084.6	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (Non-derivatized) - 70eV, Positive	splash10-01pc-2913210000-2030f7d4362602946613	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (2 TMS) - 70eV, Positive	splash10-05nf-4193224000-961c021df7886c910304	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS ("Enkephalin L,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Enkephalin L GC-MS (TMS_2_16) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 10V, Positive-QTOF	splash10-0f76-0940020000-01b1154dc17e8249a8c8	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 20V, Positive-QTOF	splash10-000i-2921000000-331e8269299530ed1230	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 40V, Positive-QTOF	splash10-000i-2900000000-f5b115db9b594e70d85a	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 10V, Negative-QTOF	splash10-0udi-0222190000-7ff6ef9ac638217877c1	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 20V, Negative-QTOF	splash10-0043-2985460000-6237cdca7e8b9de1b20d	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 40V, Negative-QTOF	splash10-003u-4952000000-fa381454fd5b34e40546	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 10V, Negative-QTOF	splash10-0udi-0000090000-efdd42b91eacfd26a6f6	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 20V, Negative-QTOF	splash10-01ox-4954270000-35d9c71cc6409d67df92	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 40V, Negative-QTOF	splash10-004l-5930000000-c9b69a3ab0d5f58d2de1	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 10V, Positive-QTOF	splash10-0a4i-0211190000-0f087cdf9e8587268ad9	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 20V, Positive-QTOF	splash10-01qd-3528920000-f5a527ab02d072443d7d	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Enkephalin L 40V, Positive-QTOF	splash10-007d-4910000000-994574c817d228a4f09f	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected and Quantified	0.00030 (0.00018-0.00056) uM	Adult (>18 years old)	Both	Normal	2583565	details

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected and Quantified	0.00096 (0.00047-0.00290) uM	Adult (>18 years old)	Both	Cirrhosis	2583565	details
Blood	Detected and Quantified	0.0014 (0.0008-0.0024) uM	Adult (>18 years old)	Both	Acute liver disease	2583565	details

Associated Disorders and Diseases

Disease References

Acute liver disease
Thornton JR, Losowsky MS: Plasma leucine enkephalin is increased in liver disease. Gut. 1989 Oct;30(10):1392-5. [PubMed:2583565 ]
Cirrhosis
Thornton JR, Losowsky MS: Plasma leucine enkephalin is increased in liver disease. Gut. 1989 Oct;30(10):1392-5. [PubMed:2583565 ]

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022389

KNApSAcK ID

Not Available

Chemspider ID

406229

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Leu-enkephalin

METLIN ID

Not Available

PubChem Compound

461776

PDB ID

Not Available

ChEBI ID

89656

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

MDB00000296

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Nissen JB, Kragballe K: Enkephalins modulate differentiation of normal human keratinocytes in vitro. Exp Dermatol. 1997 Oct;6(5):222-9. [PubMed:9450624 ]
Lukiw WJ: Endogenous signaling complexity in neuropeptides- leucine- and methionine-enkephalin. Cell Mol Neurobiol. 2006 Jul-Aug;26(4-6):1003-10. Epub 2006 Jun 27. [PubMed:16802191 ]
De Marco V, Possenti R, Vita F, Rapposelli B, D'Alagni M, Roda LG: Enkephalin binding systems in human plasma. II: Leu-enkephalin serum albumin interaction. Neurochem Res. 1985 Oct;10(10):1355-69. [PubMed:4069309 ]

Showing metabocard for Enkephalin L (HMDB0001045)

MOL for HMDB0001045 (Enkephalin L)

3D MOL for HMDB0001045 (Enkephalin L)

3D SDF for HMDB0001045 (Enkephalin L)

3D-SDF for HMDB0001045 (Enkephalin L)

PDB for HMDB0001045 (Enkephalin L)

3D PDB for HMDB0001045 (Enkephalin L)

SMILES for HMDB0001045 (Enkephalin L)

INCHI for HMDB0001045 (Enkephalin L)

Structure for HMDB0001045 (Enkephalin L)

3D Structure for HMDB0001045 (Enkephalin L)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra