NP-MRD: Showing NP-Card for ({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid (NP0326074)

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Record Information

Version

2.0

Created at

2022-09-12 07:19:15 UTC

Updated at

2022-09-12 07:19:16 UTC

NP-MRD ID

NP0326074

Secondary Accession Numbers

None

Natural Product Identification

Common Name

({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid

Description

2-({1-Hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid 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. 2-({1-Hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533005021511372D          

 39 38  0  0  0  0            999 V2000
    3.3000    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0125    7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4875    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000   10.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250   10.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    8.5737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375    7.8592    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375    6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625    6.4302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250    5.7158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375   10.7171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3750   10.0026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3750   11.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2000   11.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6125   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4375   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8500   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6750   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0875   13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9125   13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3250   14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1500   14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5625   15.0039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3875   15.0039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8000   15.7184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8000   14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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  1  0  0  0  0
  7  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  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 28 27  1  4  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
M  END

     RDKit          3D

100 99  0  0  0  0  0  0  0  0999 V2000
    8.6594   -4.9562    1.7265 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.0882   -1.8595    1.3793 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5981   -1.2400    0.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5359   -0.4916   -1.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1550    0.8373   -1.3474 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9280    1.8016   -0.2624 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3498    2.9498   -0.3950 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7898    3.5758   -1.5888 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3530    3.9586   -1.3607 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5370    2.7750   -1.0543 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9926    1.6322   -1.0583 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2200    2.9723   -0.7531 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7124    1.8876   -0.4247 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0114    1.9115    0.9839 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.1662    1.3817    1.1951 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.9624   -5.2355    0.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.5394    2.9162   -1.8229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5053    3.9570   -1.1422 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4621    2.7608   -2.9206 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3834    3.7730   -3.3328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3701    4.1805   -2.3291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4193    3.6882   -1.1928 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2900    5.1593   -2.6617 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6118   -4.5125    2.0701 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8282   -4.8090    2.4471 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8228   -6.0368    1.6062 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1781   -4.1975    0.3870 H   0  0  0  0  0  0  0  0  0  0  0  0
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   10.0751   -3.1893    0.3494 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.1255   -0.2508    0.0042 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9159   -0.3821    1.0699 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8044    2.9016   -2.4947 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3800    4.4900   -1.9025 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2676    4.7159   -0.5262 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0233    0.9799   -0.5590 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0478    2.0019    1.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
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  3 44  1  0
  3 45  1  0
  3 46  1  0
M  END


  Mrv1533005021511372D          

 39 38  0  0  0  0            999 V2000
    3.3000    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9500    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4250    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4875    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000   10.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250   10.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250    8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    8.5737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375    7.8592    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250    7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375    6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625    6.4302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250    5.7158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375   10.7171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3750   10.0026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3750   11.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2000   11.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6125   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4375   12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8500   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6750   12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0875   13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9125   13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3250   14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1500   14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5625   15.0039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3875   15.0039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8000   15.7184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8000   14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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  1  0  0  0  0
  7  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  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 28 27  1  4  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0326074

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCCCCCCCCCC(CC(=O)NCC(O)=O)OC(=O)CCC=CCCCCCCCC(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C33H61NO5/c1-28(2)22-18-14-10-6-5-7-13-17-21-25-33(38)39-30(26-31(35)34-27-32(36)37)24-20-16-12-9-8-11-15-19-23-29(3)4/h13,17,28-30H,5-12,14-16,18-27H2,1-4H3,(H,34,35)(H,36,37)

> <INCHI_KEY>
HFBDKDXMZGXWHQ-UHFFFAOYSA-N

> <FORMULA>
C33H61NO5

> <MOLECULAR_WEIGHT>
551.853

> <EXACT_MASS>
551.454974068

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
70.1772215225636

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecanamido}acetic acid

> <ALOGPS_LOGP>
8.49

> <JCHEM_LOGP>
9.719952914333337

> <ALOGPS_LOGS>
-7.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
15.681259794116247

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6531182191464917

> <JCHEM_PKA_STRONGEST_BASIC>
-2.3917460916669513

> <JCHEM_POLAR_SURFACE_AREA>
92.70000000000002

> <JCHEM_REFRACTIVITY>
161.4048

> <JCHEM_ROTATABLE_BOND_COUNT>
28

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.85e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecanamido}acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-MAY-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-MAY-15         0                                  
HETATM    1  C   UNK     0       6.160  10.669   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.930  12.003   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.160  13.337   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.470  12.003   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.240  13.337   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.780  13.337   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.550  14.670   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.090  14.670   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.860  16.004   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.400  16.004   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.170  17.338   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.710  17.338   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      18.480  18.672   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      20.020  18.672   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      20.790  17.338   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      20.020  16.004   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      18.480  16.004   0.000  0.00  0.00           O+0
HETATM   18  N   UNK     0      20.790  14.670   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      20.020  13.337   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      20.790  12.003   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      22.330  12.003   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      20.020  10.669   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      20.790  20.005   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      22.330  20.005   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      23.100  18.672   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      23.100  21.339   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      24.640  21.339   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      25.410  22.673   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      26.950  22.673   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      27.720  24.006   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      29.260  24.006   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      30.030  25.340   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      31.570  25.340   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      32.340  26.674   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      33.880  26.674   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      34.650  28.007   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      36.190  28.007   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      36.960  29.341   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      36.960  26.674   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    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   23                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   14   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   76    0
END

View in JSmol

Synonyms

Value	Source
2-({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetate	Generator

Chemical Formula

C₃₃H₆₁NO₅

Average Mass

551.8530 Da

Monoisotopic Mass

551.45497 Da

IUPAC Name

2-{14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecanamido}acetic acid

Traditional Name

{14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecanamido}acetic acid

CAS Registry Number

Not Available

SMILES

CC(C)CCCCCCCCCCC(CC(=O)NCC(O)=O)OC(=O)CCC=CCCCCCCCC(C)C

InChI Identifier

InChI=1S/C33H61NO5/c1-28(2)22-18-14-10-6-5-7-13-17-21-25-33(38)39-30(26-31(35)34-27-32(36)37)24-20-16-12-9-8-11-15-19-23-29(3)4/h13,17,28-30H,5-12,14-16,18-27H2,1-4H3,(H,34,35)(H,36,37)

InChI Key

HFBDKDXMZGXWHQ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

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 acid ester
Dicarboxylic acid or derivatives
Fatty amide
N-acyl-amine
Fatty acyl
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid ester
Carboxylic acid
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	8.49	ALOGPS
logP	9.72	ChemAxon
logS	-7.3	ALOGPS
pKa (Strongest Acidic)	3.65	ChemAxon
pKa (Strongest Basic)	-2.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	92.7 Å²	ChemAxon
Rotatable Bond Count	28	ChemAxon
Refractivity	161.4 m³·mol⁻¹	ChemAxon
Polarizability	70.18 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

85071130

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for ({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid (NP0326074)

MOL for NP0326074 (({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid)

3D MOL for NP0326074 (({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid)

3D SDF for NP0326074 (({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid)

3D-SDF for NP0326074 (({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid)

PDB for NP0326074 (({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid)

3D PDB for NP0326074 (({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid)

SMILES for NP0326074 (({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid)

INCHI for NP0326074 (({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid)

Structure for NP0326074 (({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid)

3D Structure for NP0326074 (({1-hydroxy-14-methyl-3-[(13-methyltetradec-4-enoyl)oxy]pentadecylidene}amino)acetic acid)