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Record Information

Version

5.0

Status

Predicted

Creation Date

2021-08-23 16:21:46 UTC

Update Date

2021-09-16 22:46:40 UTC

HMDB ID

HMDB0242046

Secondary Accession Numbers

None

Metabolite Identification

Common Name

N-Myristoyl Arginine

Description

N-myristoyl arginine belongs to the class of compounds known as N-acylamides. These are molecules characterized by a fatty acyl group linked to a primary amine by an amide bond. More specifically, it is a Myristic acid amide of Arginine. It is believed that there are more than 800 types of N-acylamides in the human body. N-acylamides fall into several categories: amino acid conjugates (e.g., those acyl amides conjugated with amino acids), neurotransmitter conjugates (e.g., those acylamides conjugated with neurotransmitters), ethanolamine conjugates (e.g., those acylamides conjugated to ethanolamine), and taurine conjugates (e.g., those acyamides conjugated to taurine). N-Myristoyl Arginine is an amino acid conjugate. N-acylamides can be classified into 9 different categories depending on the size of their acyl-group: 1) short-chain N-acylamides; 2) medium-chain N-acylamides; 3) long-chain N-acylamides; and 4) very long-chain N-acylamides; 5) hydroxy N-acylamides; 6) branched chain N-acylamides; 7) unsaturated N-acylamides; 8) dicarboxylic N-acylamides and 9) miscellaneous N-acylamides. N-Myristoyl Arginine is therefore classified as a long chain N-acylamide. N-acyl amides have a variety of signaling functions in physiology, including in cardiovascular activity, metabolic homeostasis, memory, cognition, pain, motor control and others (PMID: 15655504 ). N-acyl amides have also been shown to play a role in cell migration, inflammation and certain pathological conditions such as diabetes, cancer, neurodegenerative disease, and obesity (PMID: 23144998 ; PMID: 25136293 ; PMID: 28854168 ).N-acyl amides can be synthesized both endogenously and by gut microbiota (PMID: 28854168 ). N-acylamides can be biosynthesized via different routes, depending on the parent amine group. N-acyl ethanolamines (NAEs) are formed via the hydrolysis of an unusual phospholipid precursor, N-acyl-phosphatidylethanolamine (NAPE), by a specific phospholipase D. N-acyl amino acids are synthesized via a circulating peptidase M20 domain containing 1 (PM20D1), which can catalyze the bidirectional the condensation and hydrolysis of a variety of N-acyl amino acids. The degradation of N-acylamides is largely mediated by an enzyme called fatty acid amide hydrolase (FAAH), which catalyzes the hydrolysis of N-acylamides into fatty acids and the biogenic amines. Many N-acylamides are involved in lipid signaling system through interactions with transient receptor potential channels (TRP). TRP channel proteins interact with N-acyl amides such as N-arachidonoyl ethanolamide (Anandamide), N-arachidonoyl dopamine and others in an opportunistic fashion (PMID: 23178153 ). This signaling system has been shown to play a role in the physiological processes involved in inflammation (PMID: 25136293 ). Other N-acyl amides, including N-oleoyl-glutamine, have also been characterized as TRP channel antagonists (PMID: 29967167 ). N-acylamides have also been shown to have G-protein-coupled receptors (GPCRs) binding activity (PMID: 28854168 ). The study of N-acylamides is an active area of research and it is likely that many novel N-acylamides will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered for these molecules.

Structure

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


  Mrv1652308232118312D          

 27 26  0  0  0  0            999 V2000
   19.9026    7.3658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.1881    6.9533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4737    7.3658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.1881    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4737    5.7158    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.7592    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7592    6.9533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.0447    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3302    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6158    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9013    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1868    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4724    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7579    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0434    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3289    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6145    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1855    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4711    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9026    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6171    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3315    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0460    6.1283    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   22.7605    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4749    6.1283    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   22.7605    4.8908    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END

HMDB0242046
     RDKit          3D
N-Myristoyl Arginine
 67 66  0  0  0  0  0  0  0  0999 V2000
   -8.3561   -0.2967    2.1696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2210    0.5116    2.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4542    1.3193    1.7482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6856    0.6237    0.6719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4201   -0.2145   -0.2728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6535   -0.8505   -1.3851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6112   -1.8217   -1.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3589   -1.6882   -0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2815   -0.7529   -0.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5460    0.6912   -0.8788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5512    1.6462   -1.3909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1985    1.8046   -0.8491 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7048    0.6542   -1.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0906    0.9733   -0.4790 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2901    2.0982    0.0228 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0575   -0.0326   -0.5790 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4665    0.2305   -0.0461 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3522    0.0716   -1.2300 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7841    0.2589   -1.2464 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6881   -0.6052   -0.4524 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5664   -0.5518    0.9544 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5251   -0.2897    1.7713 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8150   -0.0305    1.2398 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.3308   -0.2536    3.1774 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5844   -0.8582    0.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2647   -2.0414    0.6726 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0480   -0.5822    2.2091 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1880   -1.3850    2.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2284   -0.1810    2.8851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6375    0.0860    1.1771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6069    1.1282    3.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5191   -0.2360    3.2146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6927    1.9206    2.3280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0766    2.1141    1.2563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2050    1.4622    0.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8422    0.0541    1.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9090   -1.1195    0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2612    0.3452   -0.7584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4565   -1.4128   -2.0548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3836   -0.0220   -2.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1625   -2.7053   -0.5832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4478   -2.4232   -2.1482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5019   -1.6002    0.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8840   -2.7767   -0.5133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4785   -0.9129   -0.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7698   -1.1399   -1.7796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5041    0.9456   -1.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8732    0.9882    0.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952    1.4358   -2.5349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0227    2.7050   -1.4467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2223    2.0095    0.2822 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2879    2.7763   -1.2113 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8317    0.3771   -2.1070 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4048   -0.2108   -0.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -0.9434   -1.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4793    1.2363    0.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1758   -0.9954   -1.6783 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9086    0.6780   -2.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1779    0.2004   -2.3381 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0851    1.3376   -0.9558 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5277   -1.7057   -0.7320 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7683   -0.3570   -0.7037 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6139   -0.7152    1.3466 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0451    0.8504    0.7143 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6844    0.3947    3.6657 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8719   -0.9229    3.7707 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4369   -1.2941    2.8133 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  3
 22 23  1  0
 22 24  1  0
 17 25  1  0
 25 26  2  0
 25 27  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  0
 12 52  1  0
 13 53  1  0
 13 54  1  0
 16 55  1  0
 17 56  1  0
 18 57  1  0
 18 58  1  0
 19 59  1  0
 19 60  1  0
 20 61  1  0
 20 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 27 67  1  0
M  END


  Mrv1652308232118312D          

 27 26  0  0  0  0            999 V2000
   19.9026    7.3658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.1881    6.9533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4737    7.3658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.1881    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4737    5.7158    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.7592    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7592    6.9533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.0447    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3302    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6158    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9013    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1868    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4724    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7579    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0434    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3289    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6145    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1855    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4711    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9026    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6171    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3315    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0460    6.1283    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   22.7605    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4749    6.1283    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   22.7605    4.8908    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0242046

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H40N4O3/c1-2-3-4-5-6-7-8-9-10-11-12-15-18(25)24-17(19(26)27)14-13-16-23-20(21)22/h17H,2-16H2,1H3,(H,24,25)(H,26,27)(H4,21,22,23)

> <INCHI_KEY>
ANKFOZDLPDQNEO-UHFFFAOYSA-N

> <FORMULA>
C20H40N4O3

> <MOLECULAR_WEIGHT>
384.565

> <EXACT_MASS>
384.310041164

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
47.002356305702506

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-[(diaminomethylidene)amino]-2-tetradecanamidopentanoic acid

> <ALOGPS_LOGP>
3.63

> <JCHEM_LOGP>
2.221625544896722

> <ALOGPS_LOGS>
-4.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.59480280769715

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.785811962216696

> <JCHEM_PKA_STRONGEST_BASIC>
11.377735690043915

> <JCHEM_POLAR_SURFACE_AREA>
130.8

> <JCHEM_REFRACTIVITY>
108.31199999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.94e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[(diaminomethylidene)amino]-2-tetradecanamidopentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0242046
     RDKit          3D
N-Myristoyl Arginine
 67 66  0  0  0  0  0  0  0  0999 V2000
   -8.3561   -0.2967    2.1696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2210    0.5116    2.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4542    1.3193    1.7482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6856    0.6237    0.6719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4201   -0.2145   -0.2728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6535   -0.8505   -1.3851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6112   -1.8217   -1.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3589   -1.6882   -0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2815   -0.7529   -0.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5460    0.6912   -0.8788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5512    1.6462   -1.3909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1985    1.8046   -0.8491 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7048    0.6542   -1.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0906    0.9733   -0.4790 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2901    2.0982    0.0228 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0575   -0.0326   -0.5790 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4665    0.2305   -0.0461 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3522    0.0716   -1.2300 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7841    0.2589   -1.2464 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6881   -0.6052   -0.4524 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5664   -0.5518    0.9544 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5251   -0.2897    1.7713 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8150   -0.0305    1.2398 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.3308   -0.2536    3.1774 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5844   -0.8582    0.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2647   -2.0414    0.6726 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0480   -0.5822    2.2091 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1880   -1.3850    2.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2284   -0.1810    2.8851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6375    0.0860    1.1771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6069    1.1282    3.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5191   -0.2360    3.2146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6927    1.9206    2.3280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0766    2.1141    1.2563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2050    1.4622    0.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8422    0.0541    1.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9090   -1.1195    0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2612    0.3452   -0.7584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4565   -1.4128   -2.0548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3836   -0.0220   -2.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1625   -2.7053   -0.5832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4478   -2.4232   -2.1482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5019   -1.6002    0.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8840   -2.7767   -0.5133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4785   -0.9129   -0.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7698   -1.1399   -1.7796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5041    0.9456   -1.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8732    0.9882    0.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952    1.4358   -2.5349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0227    2.7050   -1.4467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2223    2.0095    0.2822 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2879    2.7763   -1.2113 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8317    0.3771   -2.1070 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4048   -0.2108   -0.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -0.9434   -1.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4793    1.2363    0.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1758   -0.9954   -1.6783 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9086    0.6780   -2.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1779    0.2004   -2.3381 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0851    1.3376   -0.9558 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5277   -1.7057   -0.7320 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7683   -0.3570   -0.7037 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6139   -0.7152    1.3466 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0451    0.8504    0.7143 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6844    0.3947    3.6657 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8719   -0.9229    3.7707 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4369   -1.2941    2.8133 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  3
 22 23  1  0
 22 24  1  0
 17 25  1  0
 25 26  2  0
 25 27  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  0
 12 52  1  0
 13 53  1  0
 13 54  1  0
 16 55  1  0
 17 56  1  0
 18 57  1  0
 18 58  1  0
 19 59  1  0
 19 60  1  0
 20 61  1  0
 20 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 27 67  1  0
M  END

HEADER    PROTEIN                                 23-AUG-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-AUG-21         0                                  
HETATM    1  O   UNK     0      37.152  13.749   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      35.818  12.979   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      34.484  13.749   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      35.818  11.439   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      34.484  10.669   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      33.150  11.439   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      33.150  12.979   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      31.817  10.669   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      30.483  11.439   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      29.149  10.669   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      27.816  11.439   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      26.482  10.669   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      25.148  11.439   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      23.815  10.669   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      22.481  11.439   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.147  10.669   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      19.814  11.439   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      18.480  10.669   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.146  11.439   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.813  10.669   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      37.152  10.669   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      38.485  11.439   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      39.819  10.669   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0      41.153  11.439   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0      42.486  10.669   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0      43.820  11.439   0.000  0.00  0.00           N+0
HETATM   27  N   UNK     0      42.486   9.129   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   21                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21    4   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   52    0
END

COMPND    HMDB0242046
HETATM    1  C1  UNL     1      -8.356  -0.297   2.170  1.00  0.00           C  
HETATM    2  C2  UNL     1      -7.221   0.512   2.712  1.00  0.00           C  
HETATM    3  C3  UNL     1      -6.454   1.319   1.748  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.686   0.624   0.672  1.00  0.00           C  
HETATM    5  C5  UNL     1      -6.420  -0.215  -0.273  1.00  0.00           C  
HETATM    6  C6  UNL     1      -5.653  -0.851  -1.385  1.00  0.00           C  
HETATM    7  C7  UNL     1      -4.611  -1.822  -1.145  1.00  0.00           C  
HETATM    8  C8  UNL     1      -3.359  -1.688  -0.444  1.00  0.00           C  
HETATM    9  C9  UNL     1      -2.281  -0.753  -0.873  1.00  0.00           C  
HETATM   10  C10 UNL     1      -2.546   0.691  -0.879  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.551   1.646  -1.391  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.198   1.805  -0.849  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.705   0.654  -1.026  1.00  0.00           C  
HETATM   14  C14 UNL     1       2.091   0.973  -0.479  1.00  0.00           C  
HETATM   15  O1  UNL     1       2.290   2.098   0.023  1.00  0.00           O  
HETATM   16  N1  UNL     1       3.058  -0.033  -0.579  1.00  0.00           N  
HETATM   17  C15 UNL     1       4.466   0.230  -0.046  1.00  0.00           C  
HETATM   18  C16 UNL     1       5.352   0.072  -1.230  1.00  0.00           C  
HETATM   19  C17 UNL     1       6.784   0.259  -1.246  1.00  0.00           C  
HETATM   20  C18 UNL     1       7.688  -0.605  -0.452  1.00  0.00           C  
HETATM   21  N2  UNL     1       7.566  -0.552   0.954  1.00  0.00           N  
HETATM   22  C19 UNL     1       8.525  -0.290   1.771  1.00  0.00           C  
HETATM   23  N3  UNL     1       9.815  -0.031   1.240  1.00  0.00           N  
HETATM   24  N4  UNL     1       8.331  -0.254   3.177  1.00  0.00           N  
HETATM   25  C20 UNL     1       4.584  -0.858   0.940  1.00  0.00           C  
HETATM   26  O2  UNL     1       4.265  -2.041   0.673  1.00  0.00           O  
HETATM   27  O3  UNL     1       5.048  -0.582   2.209  1.00  0.00           O  
HETATM   28  H1  UNL     1      -8.188  -1.385   2.134  1.00  0.00           H  
HETATM   29  H2  UNL     1      -9.228  -0.181   2.885  1.00  0.00           H  
HETATM   30  H3  UNL     1      -8.637   0.086   1.177  1.00  0.00           H  
HETATM   31  H4  UNL     1      -7.607   1.128   3.567  1.00  0.00           H  
HETATM   32  H5  UNL     1      -6.519  -0.236   3.215  1.00  0.00           H  
HETATM   33  H6  UNL     1      -5.693   1.921   2.328  1.00  0.00           H  
HETATM   34  H7  UNL     1      -7.077   2.114   1.256  1.00  0.00           H  
HETATM   35  H8  UNL     1      -5.205   1.462   0.069  1.00  0.00           H  
HETATM   36  H9  UNL     1      -4.842   0.054   1.126  1.00  0.00           H  
HETATM   37  H10 UNL     1      -6.909  -1.120   0.251  1.00  0.00           H  
HETATM   38  H11 UNL     1      -7.261   0.345  -0.758  1.00  0.00           H  
HETATM   39  H12 UNL     1      -6.457  -1.413  -2.055  1.00  0.00           H  
HETATM   40  H13 UNL     1      -5.384  -0.022  -2.095  1.00  0.00           H  
HETATM   41  H14 UNL     1      -5.163  -2.705  -0.583  1.00  0.00           H  
HETATM   42  H15 UNL     1      -4.448  -2.423  -2.148  1.00  0.00           H  
HETATM   43  H16 UNL     1      -3.502  -1.600   0.667  1.00  0.00           H  
HETATM   44  H17 UNL     1      -2.884  -2.777  -0.513  1.00  0.00           H  
HETATM   45  H18 UNL     1      -1.479  -0.913  -0.051  1.00  0.00           H  
HETATM   46  H19 UNL     1      -1.770  -1.140  -1.780  1.00  0.00           H  
HETATM   47  H20 UNL     1      -3.504   0.946  -1.450  1.00  0.00           H  
HETATM   48  H21 UNL     1      -2.873   0.988   0.188  1.00  0.00           H  
HETATM   49  H22 UNL     1      -1.495   1.436  -2.535  1.00  0.00           H  
HETATM   50  H23 UNL     1      -2.023   2.705  -1.447  1.00  0.00           H  
HETATM   51  H24 UNL     1      -0.222   2.010   0.282  1.00  0.00           H  
HETATM   52  H25 UNL     1       0.288   2.776  -1.211  1.00  0.00           H  
HETATM   53  H26 UNL     1       0.832   0.377  -2.107  1.00  0.00           H  
HETATM   54  H27 UNL     1       0.405  -0.211  -0.439  1.00  0.00           H  
HETATM   55  H28 UNL     1       2.839  -0.943  -1.003  1.00  0.00           H  
HETATM   56  H29 UNL     1       4.479   1.236   0.360  1.00  0.00           H  
HETATM   57  H30 UNL     1       5.176  -0.995  -1.678  1.00  0.00           H  
HETATM   58  H31 UNL     1       4.909   0.678  -2.111  1.00  0.00           H  
HETATM   59  H32 UNL     1       7.178   0.200  -2.338  1.00  0.00           H  
HETATM   60  H33 UNL     1       7.085   1.338  -0.956  1.00  0.00           H  
HETATM   61  H34 UNL     1       7.528  -1.706  -0.732  1.00  0.00           H  
HETATM   62  H35 UNL     1       8.768  -0.357  -0.704  1.00  0.00           H  
HETATM   63  H36 UNL     1      10.614  -0.715   1.347  1.00  0.00           H  
HETATM   64  H37 UNL     1      10.045   0.850   0.714  1.00  0.00           H  
HETATM   65  H38 UNL     1       7.684   0.395   3.666  1.00  0.00           H  
HETATM   66  H39 UNL     1       8.872  -0.923   3.771  1.00  0.00           H  
HETATM   67  H40 UNL     1       5.437  -1.294   2.813  1.00  0.00           H  
CONECT    1    2   28   29   30
CONECT    2    3   31   32
CONECT    3    4   33   34
CONECT    4    5   35   36
CONECT    5    6   37   38
CONECT    6    7   39   40
CONECT    7    8   41   42
CONECT    8    9   43   44
CONECT    9   10   45   46
CONECT   10   11   47   48
CONECT   11   12   49   50
CONECT   12   13   51   52
CONECT   13   14   53   54
CONECT   14   15   15   16
CONECT   16   17   55
CONECT   17   18   25   56
CONECT   18   19   57   58
CONECT   19   20   59   60
CONECT   20   21   61   62
CONECT   21   22   22
CONECT   22   23   24
CONECT   23   63   64
CONECT   24   65   66
CONECT   25   26   26   27
CONECT   27   67
END

HMDB0242046
     RDKit          3D
N-Myristoyl Arginine
 67 66  0  0  0  0  0  0  0  0999 V2000
   -8.3561   -0.2967    2.1696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2210    0.5116    2.7116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4542    1.3193    1.7482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6856    0.6237    0.6719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4201   -0.2145   -0.2728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6535   -0.8505   -1.3851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6112   -1.8217   -1.1446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3589   -1.6882   -0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2815   -0.7529   -0.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5460    0.6912   -0.8788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5512    1.6462   -1.3909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1985    1.8046   -0.8491 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7048    0.6542   -1.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0906    0.9733   -0.4790 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2901    2.0982    0.0228 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0575   -0.0326   -0.5790 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4665    0.2305   -0.0461 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3522    0.0716   -1.2300 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7841    0.2589   -1.2464 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6881   -0.6052   -0.4524 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5664   -0.5518    0.9544 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5251   -0.2897    1.7713 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8150   -0.0305    1.2398 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.3308   -0.2536    3.1774 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5844   -0.8582    0.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2647   -2.0414    0.6726 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0480   -0.5822    2.2091 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1880   -1.3850    2.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2284   -0.1810    2.8851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6375    0.0860    1.1771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6069    1.1282    3.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5191   -0.2360    3.2146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6927    1.9206    2.3280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0766    2.1141    1.2563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2050    1.4622    0.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8422    0.0541    1.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9090   -1.1195    0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2612    0.3452   -0.7584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4565   -1.4128   -2.0548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3836   -0.0220   -2.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1625   -2.7053   -0.5832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4478   -2.4232   -2.1482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5019   -1.6002    0.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8840   -2.7767   -0.5133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4785   -0.9129   -0.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7698   -1.1399   -1.7796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5041    0.9456   -1.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8732    0.9882    0.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4952    1.4358   -2.5349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0227    2.7050   -1.4467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2223    2.0095    0.2822 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2879    2.7763   -1.2113 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8317    0.3771   -2.1070 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4048   -0.2108   -0.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -0.9434   -1.0033 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4793    1.2363    0.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1758   -0.9954   -1.6783 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9086    0.6780   -2.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1779    0.2004   -2.3381 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0851    1.3376   -0.9558 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5277   -1.7057   -0.7320 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7683   -0.3570   -0.7037 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6139   -0.7152    1.3466 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0451    0.8504    0.7143 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6844    0.3947    3.6657 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8719   -0.9229    3.7707 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4369   -1.2941    2.8133 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  3
 22 23  1  0
 22 24  1  0
 17 25  1  0
 25 26  2  0
 25 27  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  0
 12 52  1  0
 13 53  1  0
 13 54  1  0
 16 55  1  0
 17 56  1  0
 18 57  1  0
 18 58  1  0
 19 59  1  0
 19 60  1  0
 20 61  1  0
 20 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 27 67  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₀H₄₀N₄O₃

Average Molecular Weight

384.565

Monoisotopic Molecular Weight

384.310041164

IUPAC Name

5-[(diaminomethylidene)amino]-2-tetradecanamidopentanoic acid

Traditional Name

5-[(diaminomethylidene)amino]-2-tetradecanamidopentanoic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N)C(O)=O

InChI Identifier

InChI=1S/C20H40N4O3/c1-2-3-4-5-6-7-8-9-10-11-12-15-18(25)24-17(19(26)27)14-13-16-23-20(21)22/h17H,2-16H2,1H3,(H,24,25)(H,26,27)(H4,21,22,23)

InChI Key

ANKFOZDLPDQNEO-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-alpha amino acids

Alternative Parents

Substituents

N-acyl-alpha-amino acid
Fatty amide
N-acyl-amine
Fatty acid
Fatty acyl
Carboxamide group
Guanidine
Secondary carboxylic acid amide
Carboximidamide
Monocarboxylic acid or derivatives
Carboxylic acid
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

State

Not Available

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
logP	3.63	ALOGPS
logP	2.22	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	3.79	ChemAxon
pKa (Strongest Basic)	11.38	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	130.8 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	108.31 m³·mol⁻¹	ChemAxon
Polarizability	47 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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
DeepCCS	[M+H]+	200.295	30932474
DeepCCS	[M-H]-	197.863	30932474
DeepCCS	[M-2H]-	230.948	30932474
DeepCCS	[M+Na]+	206.638	30932474
AllCCS	[M+H]+	202.2	32859911
AllCCS	[M+H-H2O]+	200.1	32859911
AllCCS	[M+NH4]+	204.2	32859911
AllCCS	[M+Na]+	204.8	32859911
AllCCS	[M-H]-	200.2	32859911
AllCCS	[M+Na-2H]-	201.5	32859911
AllCCS	[M+HCOO]-	203.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N-Myristoyl Arginine	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N)C(O)=O	3937.3	Standard polar	33892256
N-Myristoyl Arginine	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N)C(O)=O	2868.7	Standard non polar	33892256
N-Myristoyl Arginine	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N)C(O)=O	3404.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
N-Myristoyl Arginine,2TMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	3314.3	Semi standard non polar	33892256
N-Myristoyl Arginine,2TMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2980.3	Standard non polar	33892256
N-Myristoyl Arginine,2TMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	5334.5	Standard polar	33892256
N-Myristoyl Arginine,2TMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3167.7	Semi standard non polar	33892256
N-Myristoyl Arginine,2TMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2960.8	Standard non polar	33892256
N-Myristoyl Arginine,2TMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N)C(=O)O[Si](C)(C)C)[Si](C)(C)C	5494.2	Standard polar	33892256
N-Myristoyl Arginine,2TMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O	3497.4	Semi standard non polar	33892256
N-Myristoyl Arginine,2TMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O	3011.6	Standard non polar	33892256
N-Myristoyl Arginine,2TMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O	5093.3	Standard polar	33892256
N-Myristoyl Arginine,2TMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3301.7	Semi standard non polar	33892256
N-Myristoyl Arginine,2TMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3017.3	Standard non polar	33892256
N-Myristoyl Arginine,2TMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C	5343.1	Standard polar	33892256
N-Myristoyl Arginine,2TMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	3399.0	Semi standard non polar	33892256
N-Myristoyl Arginine,2TMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	3116.4	Standard non polar	33892256
N-Myristoyl Arginine,2TMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	5253.1	Standard polar	33892256
N-Myristoyl Arginine,3TMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	3468.9	Semi standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2928.4	Standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	4694.9	Standard polar	33892256
N-Myristoyl Arginine,3TMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3297.1	Semi standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2984.5	Standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	5147.3	Standard polar	33892256
N-Myristoyl Arginine,3TMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3369.7	Semi standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3031.0	Standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	5040.6	Standard polar	33892256
N-Myristoyl Arginine,3TMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3456.2	Semi standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2972.5	Standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C	4721.2	Standard polar	33892256
N-Myristoyl Arginine,3TMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	3531.8	Semi standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	3114.4	Standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	4474.4	Standard polar	33892256
N-Myristoyl Arginine,3TMS,isomer #6	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3386.9	Semi standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #6	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3099.5	Standard non polar	33892256
N-Myristoyl Arginine,3TMS,isomer #6	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	5061.1	Standard polar	33892256
N-Myristoyl Arginine,4TMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3450.8	Semi standard non polar	33892256
N-Myristoyl Arginine,4TMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2909.3	Standard non polar	33892256
N-Myristoyl Arginine,4TMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	4372.3	Standard polar	33892256
N-Myristoyl Arginine,4TMS,isomer #2	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3483.6	Semi standard non polar	33892256
N-Myristoyl Arginine,4TMS,isomer #2	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3002.5	Standard non polar	33892256
N-Myristoyl Arginine,4TMS,isomer #2	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	4084.6	Standard polar	33892256
N-Myristoyl Arginine,4TMS,isomer #3	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3383.2	Semi standard non polar	33892256
N-Myristoyl Arginine,4TMS,isomer #3	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3033.6	Standard non polar	33892256
N-Myristoyl Arginine,4TMS,isomer #3	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	4908.2	Standard polar	33892256
N-Myristoyl Arginine,4TMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3470.0	Semi standard non polar	33892256
N-Myristoyl Arginine,4TMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3045.6	Standard non polar	33892256
N-Myristoyl Arginine,4TMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	4176.8	Standard polar	33892256
N-Myristoyl Arginine,4TMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	3599.7	Semi standard non polar	33892256
N-Myristoyl Arginine,4TMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	3213.2	Standard non polar	33892256
N-Myristoyl Arginine,4TMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	3963.4	Standard polar	33892256
N-Myristoyl Arginine,5TMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3448.1	Semi standard non polar	33892256
N-Myristoyl Arginine,5TMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2997.7	Standard non polar	33892256
N-Myristoyl Arginine,5TMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3847.2	Standard polar	33892256
N-Myristoyl Arginine,5TMS,isomer #2	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3531.6	Semi standard non polar	33892256
N-Myristoyl Arginine,5TMS,isomer #2	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3148.2	Standard non polar	33892256
N-Myristoyl Arginine,5TMS,isomer #2	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3597.2	Standard polar	33892256
N-Myristoyl Arginine,5TMS,isomer #3	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3538.0	Semi standard non polar	33892256
N-Myristoyl Arginine,5TMS,isomer #3	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3185.4	Standard non polar	33892256
N-Myristoyl Arginine,5TMS,isomer #3	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3729.4	Standard polar	33892256
N-Myristoyl Arginine,6TMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3508.5	Semi standard non polar	33892256
N-Myristoyl Arginine,6TMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3167.7	Standard non polar	33892256
N-Myristoyl Arginine,6TMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3425.4	Standard polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3796.4	Semi standard non polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3291.3	Standard non polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	5232.9	Standard polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3627.4	Semi standard non polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3313.0	Standard non polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5412.4	Standard polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O	3948.5	Semi standard non polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O	3283.7	Standard non polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O	4809.7	Standard polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3759.7	Semi standard non polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3301.1	Standard non polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	5242.7	Standard polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3828.4	Semi standard non polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3399.9	Standard non polar	33892256
N-Myristoyl Arginine,2TBDMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	5150.0	Standard polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4147.6	Semi standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3400.9	Standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4471.8	Standard polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3959.7	Semi standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3451.5	Standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	5081.2	Standard polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)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	4021.0	Semi standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)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	3528.6	Standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N)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	5003.4	Standard polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	4088.1	Semi standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3392.6	Standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	4532.0	Standard polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4157.7	Semi standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3561.9	Standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4351.1	Standard polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #6	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)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	4004.8	Semi standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #6	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)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	3539.7	Standard non polar	33892256
N-Myristoyl Arginine,3TBDMS,isomer #6	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)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	5028.7	Standard polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4269.2	Semi standard non polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3537.8	Standard non polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #1	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4298.9	Standard polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)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	4307.5	Semi standard non polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)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	3670.0	Standard non polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #2	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N[Si](C)(C)C(C)(C)C)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	4124.6	Standard polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)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)[Si](C)(C)C(C)(C)C	4190.6	Semi standard non polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)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)[Si](C)(C)C(C)(C)C	3679.8	Standard non polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #3	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N)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)[Si](C)(C)C(C)(C)C	4889.3	Standard polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C(C)(C)C)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	4284.1	Semi standard non polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C(C)(C)C)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	3667.9	Standard non polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #4	CCCCCCCCCCCCCC(=O)N(C(CCCN=C(N[Si](C)(C)C(C)(C)C)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	4207.4	Standard polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4360.1	Semi standard non polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3813.0	Standard non polar	33892256
N-Myristoyl Arginine,4TBDMS,isomer #5	CCCCCCCCCCCCCC(=O)NC(CCCN=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4047.4	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - N-Myristoyl Arginine GC-MS (Non-derivatized) - 70eV, Positive	splash10-01r6-9673000000-04c1b6d3a09b9f74cf04	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Myristoyl Arginine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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 - N-Myristoyl Arginine 10V, Positive-QTOF	splash10-000i-0009000000-0d8efe0f791f5c695a89	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Myristoyl Arginine 20V, Positive-QTOF	splash10-0409-1902000000-d4ecbbd07e1da202dfa6	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Myristoyl Arginine 40V, Positive-QTOF	splash10-01t9-9800000000-9059bbaccd9c7fa86186	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Myristoyl Arginine 10V, Negative-QTOF	splash10-001i-0009000000-1ebe285733c0ef7a0d5d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Myristoyl Arginine 20V, Negative-QTOF	splash10-00lu-2009000000-a79ae99516d3c9ddeff0	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Myristoyl Arginine 40V, Negative-QTOF	splash10-0006-9410000000-5a3b825a059304644f91	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

11291378

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

22266947

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Bradshaw HB, Walker JM: The expanding field of cannabimimetic and related lipid mediators. Br J Pharmacol. 2005 Feb;144(4):459-65. doi: 10.1038/sj.bjp.0706093. [PubMed:15655504 ]
Grapov D, Adams SH, Pedersen TL, Garvey WT, Newman JW: Type 2 diabetes associated changes in the plasma non-esterified fatty acids, oxylipins and endocannabinoids. PLoS One. 2012;7(11):e48852. doi: 10.1371/journal.pone.0048852. Epub 2012 Nov 8. [PubMed:23144998 ]
Raboune S, Stuart JM, Leishman E, Takacs SM, Rhodes B, Basnet A, Jameyfield E, McHugh D, Widlanski T, Bradshaw HB: Novel endogenous N-acyl amides activate TRPV1-4 receptors, BV-2 microglia, and are regulated in brain in an acute model of inflammation. Front Cell Neurosci. 2014 Aug 1;8:195. doi: 10.3389/fncel.2014.00195. eCollection 2014. [PubMed:25136293 ]
Cohen LJ, Esterhazy D, Kim SH, Lemetre C, Aguilar RR, Gordon EA, Pickard AJ, Cross JR, Emiliano AB, Han SM, Chu J, Vila-Farres X, Kaplitt J, Rogoz A, Calle PY, Hunter C, Bitok JK, Brady SF: Commensal bacteria make GPCR ligands that mimic human signalling molecules. Nature. 2017 Sep 7;549(7670):48-53. doi: 10.1038/nature23874. Epub 2017 Aug 30. [PubMed:28854168 ]
Bradshaw HB, Raboune S, Hollis JL: Opportunistic activation of TRP receptors by endogenous lipids: exploiting lipidomics to understand TRP receptor cellular communication. Life Sci. 2013 Mar 19;92(8-9):404-9. doi: 10.1016/j.lfs.2012.11.008. Epub 2012 Nov 20. [PubMed:23178153 ]
Long JZ, Roche AM, Berdan CA, Louie SM, Roberts AJ, Svensson KJ, Dou FY, Bateman LA, Mina AI, Deng Z, Jedrychowski MP, Lin H, Kamenecka TM, Asara JM, Griffin PR, Banks AS, Nomura DK, Spiegelman BM: Ablation of PM20D1 reveals N-acyl amino acid control of metabolism and nociception. Proc Natl Acad Sci U S A. 2018 Jul 17;115(29):E6937-E6945. doi: 10.1073/pnas.1803389115. Epub 2018 Jul 2. [PubMed:29967167 ]

Showing metabocard for N-Myristoyl Arginine (HMDB0242046)

MOL for HMDB0242046 (N-Myristoyl Arginine)

3D MOL for HMDB0242046 (N-Myristoyl Arginine)

3D SDF for HMDB0242046 (N-Myristoyl Arginine)

3D-SDF for HMDB0242046 (N-Myristoyl Arginine)

PDB for HMDB0242046 (N-Myristoyl Arginine)

3D PDB for HMDB0242046 (N-Myristoyl Arginine)

SMILES for HMDB0242046 (N-Myristoyl Arginine)

INCHI for HMDB0242046 (N-Myristoyl Arginine)

Structure for HMDB0242046 (N-Myristoyl Arginine)

3D Structure for HMDB0242046 (N-Myristoyl Arginine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra