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Record Information

Version

5.0

Status

Predicted

Creation Date

2021-08-23 16:13:18 UTC

Update Date

2021-09-16 22:46:40 UTC

HMDB ID

HMDB0242044

Secondary Accession Numbers

None

Metabolite Identification

Common Name

N-Lauroyl Valine

Description

N-lauroyl valine 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 Lauric acid amide of Valine. 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-Lauroyl Valine 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-Lauroyl Valine 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

HMDB0242044
     RDKit          3D
N-Lauroyl Valine
 54 53  0  0  0  0  0  0  0  0999 V2000
    7.4516    0.5339   -0.1522 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5941   -0.6771    0.0507 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4829   -0.3262    1.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6206    0.8058    0.5313 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9532    0.4622   -0.7826 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0725   -0.7332   -0.6865 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9412   -0.6182    0.2936 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9916    0.4803    0.0313 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2862    0.4279   -1.2875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5381   -0.7714   -1.5246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6446   -1.0013   -0.5527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6564    0.0718   -0.4885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5853    1.0747   -1.2163 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7227   -0.0717    0.4341 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7665    0.9361    0.5670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7518    1.3728    1.9897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9555    0.9070    2.8463 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6442    2.3396    2.4357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0790    0.2228    0.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2788   -0.9143    1.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9492   -0.3202   -1.1765 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3669    0.2033   -0.7190 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7880    0.8934    0.8397 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9227    1.3424   -0.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2055   -1.0710   -0.8864 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2348   -1.4736    0.5061 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8120   -1.2061    1.1756 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9066   -0.0539    2.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8259    0.9557    1.2952 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2562    1.7227    0.4294 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7655    0.2128   -1.5074 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4490    1.3453   -1.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6707   -0.9247   -1.7271 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7084   -1.6194   -0.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3829   -0.4718    1.3017 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4649   -1.6301    0.3391 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2059    0.4562    0.8238 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5170    1.4452    0.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3091    1.3363   -1.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1007    0.4558   -2.0724 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0275   -1.7190   -1.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0325   -0.6530   -2.5356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2023   -1.9354   -0.7961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2910   -1.1532    0.4918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8201   -0.8983    1.0642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6015    1.7743   -0.1230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5004    2.4464    1.9214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8909    0.9518    0.3438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3692   -1.0902    1.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7918   -1.8459    0.8346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8754   -0.6116    2.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6437    0.5106   -1.8309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1845   -1.1259   -1.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9208   -0.7703   -1.4706 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  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 15 19  1  0
 19 20  1  0
 19 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 14 45  1  0
 15 46  1  0
 18 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 21 52  1  0
 21 53  1  0
 21 54  1  0
M  END

  Mrv1652308232118232D          

 21 20  0  0  0  0            999 V2000
    8.8539    3.4618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8539    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1395    4.6993    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7105    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9961    4.2868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7105    5.5243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    3.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1395    3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7105    3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5684    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2829    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9974    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7118    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4263    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1408    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8552    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5697    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2842    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9987    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7131    4.6993    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  2 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
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0242044

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCCCCCCC(=O)NC(C(C)C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H33NO3/c1-4-5-6-7-8-9-10-11-12-13-15(19)18-16(14(2)3)17(20)21/h14,16H,4-13H2,1-3H3,(H,18,19)(H,20,21)

> <INCHI_KEY>
WQHXCNGQDLRDMP-UHFFFAOYSA-N

> <FORMULA>
C17H33NO3

> <MOLECULAR_WEIGHT>
299.455

> <EXACT_MASS>
299.246043927

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
36.58540107268921

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-dodecanamido-3-methylbutanoic acid

> <ALOGPS_LOGP>
4.81

> <JCHEM_LOGP>
4.829284341666668

> <ALOGPS_LOGS>
-4.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.560653422684346

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.205626669086803

> <JCHEM_PKA_STRONGEST_BASIC>
-1.1305964903860874

> <JCHEM_POLAR_SURFACE_AREA>
66.4

> <JCHEM_REFRACTIVITY>
84.97259999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.01e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-dodecanamido-3-methylbutanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0242044
     RDKit          3D
N-Lauroyl Valine
 54 53  0  0  0  0  0  0  0  0999 V2000
    7.4516    0.5339   -0.1522 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5941   -0.6771    0.0507 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4829   -0.3262    1.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6206    0.8058    0.5313 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9532    0.4622   -0.7826 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0725   -0.7332   -0.6865 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9412   -0.6182    0.2936 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9916    0.4803    0.0313 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2862    0.4279   -1.2875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5381   -0.7714   -1.5246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6446   -1.0013   -0.5527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6564    0.0718   -0.4885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5853    1.0747   -1.2163 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7227   -0.0717    0.4341 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7665    0.9361    0.5670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7518    1.3728    1.9897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9555    0.9070    2.8463 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6442    2.3396    2.4357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0790    0.2228    0.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2788   -0.9143    1.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9492   -0.3202   -1.1765 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3669    0.2033   -0.7190 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7880    0.8934    0.8397 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9227    1.3424   -0.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2055   -1.0710   -0.8864 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2348   -1.4736    0.5061 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8120   -1.2061    1.1756 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9066   -0.0539    2.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8259    0.9557    1.2952 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2562    1.7227    0.4294 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7655    0.2128   -1.5074 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4490    1.3453   -1.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6707   -0.9247   -1.7271 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7084   -1.6194   -0.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3829   -0.4718    1.3017 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4649   -1.6301    0.3391 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2059    0.4562    0.8238 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5170    1.4452    0.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3091    1.3363   -1.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1007    0.4558   -2.0724 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0275   -1.7190   -1.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0325   -0.6530   -2.5356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2023   -1.9354   -0.7961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2910   -1.1532    0.4918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8201   -0.8983    1.0642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6015    1.7743   -0.1230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5004    2.4464    1.9214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8909    0.9518    0.3438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3692   -1.0902    1.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7918   -1.8459    0.8346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8754   -0.6116    2.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6437    0.5106   -1.8309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1845   -1.1259   -1.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9208   -0.7703   -1.4706 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  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 15 19  1  0
 19 20  1  0
 19 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 14 45  1  0
 15 46  1  0
 18 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 21 52  1  0
 21 53  1  0
 21 54  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      16.527   6.462   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      16.527   8.002   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      15.194   8.772   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      13.860   8.002   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.526   8.772   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      11.193   8.002   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      12.526  10.312   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      13.860   6.462   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      15.194   5.692   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.526   5.692   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.861   8.772   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      19.195   8.002   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      20.528   8.772   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      21.862   8.002   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      23.196   8.772   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      24.529   8.002   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      25.863   8.772   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      27.197   8.002   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      28.530   8.772   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      29.864   8.002   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      31.198   8.772   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    4    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    2   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   21                                                       
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

COMPND    HMDB0242044
HETATM    1  C1  UNL     1       7.452   0.534  -0.152  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.594  -0.677   0.051  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.483  -0.326   1.038  1.00  0.00           C  
HETATM    4  C4  UNL     1       4.621   0.806   0.531  1.00  0.00           C  
HETATM    5  C5  UNL     1       3.953   0.462  -0.783  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.073  -0.733  -0.687  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.941  -0.618   0.294  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.992   0.480   0.031  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.286   0.428  -1.288  1.00  0.00           C  
HETATM   10  C10 UNL     1      -0.538  -0.771  -1.525  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.645  -1.001  -0.553  1.00  0.00           C  
HETATM   12  C12 UNL     1      -2.656   0.072  -0.488  1.00  0.00           C  
HETATM   13  O1  UNL     1      -2.585   1.075  -1.216  1.00  0.00           O  
HETATM   14  N1  UNL     1      -3.723  -0.072   0.434  1.00  0.00           N  
HETATM   15  C13 UNL     1      -4.766   0.936   0.567  1.00  0.00           C  
HETATM   16  C14 UNL     1      -4.752   1.373   1.990  1.00  0.00           C  
HETATM   17  O2  UNL     1      -3.955   0.907   2.846  1.00  0.00           O  
HETATM   18  O3  UNL     1      -5.644   2.340   2.436  1.00  0.00           O  
HETATM   19  C15 UNL     1      -6.079   0.223   0.240  1.00  0.00           C  
HETATM   20  C16 UNL     1      -6.279  -0.914   1.218  1.00  0.00           C  
HETATM   21  C17 UNL     1      -5.949  -0.320  -1.177  1.00  0.00           C  
HETATM   22  H1  UNL     1       8.367   0.203  -0.719  1.00  0.00           H  
HETATM   23  H2  UNL     1       7.788   0.893   0.840  1.00  0.00           H  
HETATM   24  H3  UNL     1       6.923   1.342  -0.689  1.00  0.00           H  
HETATM   25  H4  UNL     1       6.206  -1.071  -0.886  1.00  0.00           H  
HETATM   26  H5  UNL     1       7.235  -1.474   0.506  1.00  0.00           H  
HETATM   27  H6  UNL     1       4.812  -1.206   1.176  1.00  0.00           H  
HETATM   28  H7  UNL     1       5.907  -0.054   2.025  1.00  0.00           H  
HETATM   29  H8  UNL     1       3.826   0.956   1.295  1.00  0.00           H  
HETATM   30  H9  UNL     1       5.256   1.723   0.429  1.00  0.00           H  
HETATM   31  H10 UNL     1       4.766   0.213  -1.507  1.00  0.00           H  
HETATM   32  H11 UNL     1       3.449   1.345  -1.228  1.00  0.00           H  
HETATM   33  H12 UNL     1       2.671  -0.925  -1.727  1.00  0.00           H  
HETATM   34  H13 UNL     1       3.708  -1.619  -0.482  1.00  0.00           H  
HETATM   35  H14 UNL     1       2.383  -0.472   1.302  1.00  0.00           H  
HETATM   36  H15 UNL     1       1.465  -1.630   0.339  1.00  0.00           H  
HETATM   37  H16 UNL     1       0.206   0.456   0.824  1.00  0.00           H  
HETATM   38  H17 UNL     1       1.517   1.445   0.164  1.00  0.00           H  
HETATM   39  H18 UNL     1      -0.309   1.336  -1.483  1.00  0.00           H  
HETATM   40  H19 UNL     1       1.101   0.456  -2.072  1.00  0.00           H  
HETATM   41  H20 UNL     1       0.027  -1.719  -1.613  1.00  0.00           H  
HETATM   42  H21 UNL     1      -1.032  -0.653  -2.536  1.00  0.00           H  
HETATM   43  H22 UNL     1      -2.202  -1.935  -0.796  1.00  0.00           H  
HETATM   44  H23 UNL     1      -1.291  -1.153   0.492  1.00  0.00           H  
HETATM   45  H24 UNL     1      -3.820  -0.898   1.064  1.00  0.00           H  
HETATM   46  H25 UNL     1      -4.601   1.774  -0.123  1.00  0.00           H  
HETATM   47  H26 UNL     1      -6.500   2.446   1.921  1.00  0.00           H  
HETATM   48  H27 UNL     1      -6.891   0.952   0.344  1.00  0.00           H  
HETATM   49  H28 UNL     1      -7.369  -1.090   1.363  1.00  0.00           H  
HETATM   50  H29 UNL     1      -5.792  -1.846   0.835  1.00  0.00           H  
HETATM   51  H30 UNL     1      -5.875  -0.612   2.201  1.00  0.00           H  
HETATM   52  H31 UNL     1      -5.644   0.511  -1.831  1.00  0.00           H  
HETATM   53  H32 UNL     1      -5.184  -1.126  -1.141  1.00  0.00           H  
HETATM   54  H33 UNL     1      -6.921  -0.770  -1.471  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3   25   26
CONECT    3    4   27   28
CONECT    4    5   29   30
CONECT    5    6   31   32
CONECT    6    7   33   34
CONECT    7    8   35   36
CONECT    8    9   37   38
CONECT    9   10   39   40
CONECT   10   11   41   42
CONECT   11   12   43   44
CONECT   12   13   13   14
CONECT   14   15   45
CONECT   15   16   19   46
CONECT   16   17   17   18
CONECT   18   47
CONECT   19   20   21   48
CONECT   20   49   50   51
CONECT   21   52   53   54
END

HMDB0242044
     RDKit          3D
N-Lauroyl Valine
 54 53  0  0  0  0  0  0  0  0999 V2000
    7.4516    0.5339   -0.1522 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5941   -0.6771    0.0507 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4829   -0.3262    1.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6206    0.8058    0.5313 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9532    0.4622   -0.7826 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0725   -0.7332   -0.6865 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9412   -0.6182    0.2936 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9916    0.4803    0.0313 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2862    0.4279   -1.2875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5381   -0.7714   -1.5246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6446   -1.0013   -0.5527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6564    0.0718   -0.4885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5853    1.0747   -1.2163 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7227   -0.0717    0.4341 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7665    0.9361    0.5670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7518    1.3728    1.9897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9555    0.9070    2.8463 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6442    2.3396    2.4357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0790    0.2228    0.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2788   -0.9143    1.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9492   -0.3202   -1.1765 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3669    0.2033   -0.7190 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7880    0.8934    0.8397 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9227    1.3424   -0.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2055   -1.0710   -0.8864 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2348   -1.4736    0.5061 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8120   -1.2061    1.1756 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9066   -0.0539    2.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8259    0.9557    1.2952 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2562    1.7227    0.4294 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7655    0.2128   -1.5074 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4490    1.3453   -1.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6707   -0.9247   -1.7271 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7084   -1.6194   -0.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3829   -0.4718    1.3017 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4649   -1.6301    0.3391 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2059    0.4562    0.8238 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5170    1.4452    0.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3091    1.3363   -1.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1007    0.4558   -2.0724 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0275   -1.7190   -1.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0325   -0.6530   -2.5356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2023   -1.9354   -0.7961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2910   -1.1532    0.4918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8201   -0.8983    1.0642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6015    1.7743   -0.1230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5004    2.4464    1.9214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8909    0.9518    0.3438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3692   -1.0902    1.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7918   -1.8459    0.8346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8754   -0.6116    2.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6437    0.5106   -1.8309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1845   -1.1259   -1.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9208   -0.7703   -1.4706 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  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 15 19  1  0
 19 20  1  0
 19 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 14 45  1  0
 15 46  1  0
 18 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 21 52  1  0
 21 53  1  0
 21 54  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₇H₃₃NO₃

Average Molecular Weight

299.455

Monoisotopic Molecular Weight

299.246043927

IUPAC Name

2-dodecanamido-3-methylbutanoic acid

Traditional Name

2-dodecanamido-3-methylbutanoic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCC(=O)NC(C(C)C)C(O)=O

InChI Identifier

InChI=1S/C17H33NO3/c1-4-5-6-7-8-9-10-11-12-13-15(19)18-16(14(2)3)17(20)21/h14,16H,4-13H2,1-3H3,(H,18,19)(H,20,21)

InChI Key

WQHXCNGQDLRDMP-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

Valine or derivatives
N-acyl-alpha-amino acid
Branched fatty acid
Methyl-branched fatty acid
Fatty amide
Fatty acyl
Fatty acid
N-acyl-amine
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid
Monocarboxylic acid or derivatives
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
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	4.81	ALOGPS
logP	4.83	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	4.21	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.4 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	84.97 m³·mol⁻¹	ChemAxon
Polarizability	36.59 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]+	180.221	30932474
DeepCCS	[M-H]-	176.769	30932474
DeepCCS	[M-2H]-	212.289	30932474
DeepCCS	[M+Na]+	188.58	30932474
AllCCS	[M+H]+	181.6	32859911
AllCCS	[M+H-H2O]+	178.8	32859911
AllCCS	[M+NH4]+	184.2	32859911
AllCCS	[M+Na]+	184.9	32859911
AllCCS	[M-H]-	180.0	32859911
AllCCS	[M+Na-2H]-	181.2	32859911
AllCCS	[M+HCOO]-	182.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N-Lauroyl Valine	CCCCCCCCCCCC(=O)NC(C(C)C)C(O)=O	3214.4	Standard polar	33892256
N-Lauroyl Valine	CCCCCCCCCCCC(=O)NC(C(C)C)C(O)=O	2101.4	Standard non polar	33892256
N-Lauroyl Valine	CCCCCCCCCCCC(=O)NC(C(C)C)C(O)=O	2233.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
N-Lauroyl Valine,2TMS,isomer #1	CCCCCCCCCCCC(=O)N(C(C(=O)O[Si](C)(C)C)C(C)C)[Si](C)(C)C	2313.3	Semi standard non polar	33892256
N-Lauroyl Valine,2TMS,isomer #1	CCCCCCCCCCCC(=O)N(C(C(=O)O[Si](C)(C)C)C(C)C)[Si](C)(C)C	2289.8	Standard non polar	33892256
N-Lauroyl Valine,2TMS,isomer #1	CCCCCCCCCCCC(=O)N(C(C(=O)O[Si](C)(C)C)C(C)C)[Si](C)(C)C	2366.1	Standard polar	33892256
N-Lauroyl Valine,2TBDMS,isomer #1	CCCCCCCCCCCC(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)C)[Si](C)(C)C(C)(C)C	2799.2	Semi standard non polar	33892256
N-Lauroyl Valine,2TBDMS,isomer #1	CCCCCCCCCCCC(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)C)[Si](C)(C)C(C)(C)C	2640.2	Standard non polar	33892256
N-Lauroyl Valine,2TBDMS,isomer #1	CCCCCCCCCCCC(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)C)[Si](C)(C)C(C)(C)C	2636.1	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - N-Lauroyl Valine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0zfu-9760000000-a1a0e720fc7712407767	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Lauroyl Valine 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-Lauroyl Valine 10V, Negative-QTOF	splash10-001j-0090000000-2a8c7fda7d596d7aea12	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Lauroyl Valine 20V, Negative-QTOF	splash10-014i-1930000000-ed533e1efa5c4c207b32	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Lauroyl Valine 40V, Negative-QTOF	splash10-00nf-6900000000-0427a1cf10fa71981eff	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Lauroyl Valine 10V, Positive-QTOF	splash10-0udi-1489000000-f1da21154948e80d05a9	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Lauroyl Valine 20V, Positive-QTOF	splash10-0ue9-5971000000-38bfe06ef69467029eb0	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Lauroyl Valine 40V, Positive-QTOF	splash10-053v-9200000000-53c89c62e2e495d4a549	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

13714585

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

13313084

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-Lauroyl Valine (HMDB0242044)

MOL for HMDB0242044 (N-Lauroyl Valine)

3D MOL for HMDB0242044 (N-Lauroyl Valine)

3D SDF for HMDB0242044 (N-Lauroyl Valine)

3D-SDF for HMDB0242044 (N-Lauroyl Valine)

PDB for HMDB0242044 (N-Lauroyl Valine)

3D PDB for HMDB0242044 (N-Lauroyl Valine)

SMILES for HMDB0242044 (N-Lauroyl Valine)

INCHI for HMDB0242044 (N-Lauroyl Valine)

Structure for HMDB0242044 (N-Lauroyl Valine)

3D Structure for HMDB0242044 (N-Lauroyl Valine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra