NP-MRD: Showing NP-Card for (2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid (NP0322537)

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Record Information

Version

2.0

Created at

2022-09-12 01:21:39 UTC

Updated at

2022-09-12 01:21:39 UTC

NP-MRD ID

NP0322537

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid

Description

(2E,4E,6S,7R,9S,10R)-12-(4-aminophenyl)-10-hydroxy-6-[(1S)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms. (2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid is found in Streptomyces griseus. Based on a literature review very few articles have been published on (2E,4E,6S,7R,9S,10R)-12-(4-aminophenyl)-10-hydroxy-6-[(1S)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122203212D          

 28 28  0  0  1  0            999 V2000
   -4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    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  6  0  0  0
  2  4  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 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
 22 23  2  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
 27 28  2  0  0  0  0
 22 28  1  0  0  0  0
M  END

     RDKit          3D

 59 59  0  0  0  0  0  0  0  0999 V2000
    1.6374    2.6516   -2.9041 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3447    2.3401   -1.5932 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7210    2.1905   -1.8438 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7701    1.1526   -0.8813 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5130    1.0349    0.4454 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4454    1.8537    0.8539 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0993    1.6330    2.1668 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0419    2.4230    2.6247 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7052    2.2405    3.9024 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3935    1.2930    4.6424 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6942    3.1156    4.3196 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0184   -0.1568   -1.5844 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4955   -0.2652   -2.9933 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6507   -1.3834   -0.8157 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2778   -1.6676   -0.3920 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7632   -1.7949   -1.4283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1776   -1.2119    0.9480 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6041   -1.8085    1.9767 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6063   -1.3932    1.3254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6010   -0.6366    0.5552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2979    0.3143   -0.1880 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0356   -0.9766    0.6287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9713   -0.2783   -0.0876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3180   -0.5743   -0.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7641   -1.6078    0.7558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1557   -1.9402    0.8303 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8478   -2.3189    1.4799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4889   -2.0085    1.4201 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5540    2.5197   -2.7235 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7165    3.7865   -3.0793 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9930    2.1120   -3.7663 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2380    3.2302   -0.9661 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8114    1.9675   -2.7992 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7441    1.3147   -0.6353 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2722    0.2050    1.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7255    2.6927    0.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7877    0.7979    2.7599 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3286    3.2569    1.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6684    4.0509    3.9300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1293   -0.2162   -1.6955 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6050    0.2702   -3.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2223   -1.3678   -3.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3125   -0.1765   -3.7733 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0283   -2.2365   -1.4862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3313   -1.4633    0.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4055   -2.8518   -0.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4939   -2.6788   -2.1390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0190   -0.9355   -2.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6873   -2.1956   -0.9714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0382   -0.0764    1.0588 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5977   -1.1559    2.7186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7518   -1.2727    2.4316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8336   -2.4932    1.1239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6272    0.5436   -0.7200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0669   -0.0155   -0.6114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4833   -2.6664    1.4856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8523   -1.4550    0.2266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2145   -3.1287    2.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7884   -2.5824    1.9983 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 11  1  0
  9 10  2  0
  4 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  2  0
 28 22  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  1
  3 33  1  0
  4 34  1  1
  5 35  1  0
  6 36  1  0
  7 37  1  0
  8 38  1  0
 11 39  1  0
 12 40  1  6
 13 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  1
 16 47  1  0
 16 48  1  0
 16 49  1  0
 17 50  1  6
 18 51  1  0
 19 52  1  0
 19 53  1  0
 23 54  1  0
 24 55  1  0
 26 56  1  0
 26 57  1  0
 27 58  1  0
 28 59  1  0
M  END


  Mrv1652309122203212D          

 28 28  0  0  1  0            999 V2000
   -4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    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  6  0  0  0
  2  4  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 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
 22 23  2  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
 27 28  2  0  0  0  0
 22 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322537

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](O)[C@H](\C=C\C=C\C(O)=O)[C@H](C)C[C@H](C)[C@H](O)CC(=O)C1=CC=C(N)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H31NO5/c1-14(19(16(3)24)6-4-5-7-22(27)28)12-15(2)20(25)13-21(26)17-8-10-18(23)11-9-17/h4-11,14-16,19-20,24-25H,12-13,23H2,1-3H3,(H,27,28)/b6-4+,7-5+/t14-,15+,16+,19-,20-/m1/s1

> <INCHI_KEY>
KCSUEQGOSJTUAZ-PCLKYAQSSA-N

> <FORMULA>
C22H31NO5

> <MOLECULAR_WEIGHT>
389.492

> <EXACT_MASS>
389.220223102

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
43.49967002869137

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,4E,6S,7R,9S,10R)-12-(4-aminophenyl)-10-hydroxy-6-[(1S)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid

> <JCHEM_LOGP>
2.3735895887094927

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.696013038977728

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.747223609949463

> <JCHEM_PKA_STRONGEST_BASIC>
2.972462663648846

> <JCHEM_POLAR_SURFACE_AREA>
120.85000000000001

> <JCHEM_REFRACTIVITY>
112.4272

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2E,4E,6S,7R,9S,10R)-12-(4-aminophenyl)-10-hydroxy-6-[(1S)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.002  -0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -5.335  -0.000   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -12.003  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -13.337  -3.080   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0     -14.670  -2.310   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0     -13.337  -4.620   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       1.334   3.850   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   12                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    4   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   22                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   56    0
END

View in JSmol

Synonyms

Value	Source
(2E,4E,6S,7R,9S,10R)-12-(4-Aminophenyl)-10-hydroxy-6-[(1S)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoate	Generator

Chemical Formula

C₂₂H₃₁NO₅

Average Mass

389.4920 Da

Monoisotopic Mass

389.22022 Da

IUPAC Name

(2E,4E,6S,7R,9S,10R)-12-(4-aminophenyl)-10-hydroxy-6-[(1S)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid

Traditional Name

(2E,4E,6S,7R,9S,10R)-12-(4-aminophenyl)-10-hydroxy-6-[(1S)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid

CAS Registry Number

Not Available

SMILES

C[C@H](O)[C@H](\C=C\C=C\C(O)=O)[C@H](C)C[C@H](C)[C@H](O)CC(=O)C1=CC=C(N)C=C1

InChI Identifier

InChI=1S/C22H31NO5/c1-14(19(16(3)24)6-4-5-7-22(27)28)12-15(2)20(25)13-21(26)17-8-10-18(23)11-9-17/h4-11,14-16,19-20,24-25H,12-13,23H2,1-3H3,(H,27,28)/b6-4+,7-5+/t14-,15+,16+,19-,20-/m1/s1

InChI Key

KCSUEQGOSJTUAZ-PCLKYAQSSA-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

Species Name	Source	Reference
Streptomyces griseus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Long-chain fatty acids

Alternative Parents

Substituents

Long-chain fatty acid
Alkyl-phenylketone
Butyrophenone
Phenylketone
Benzoyl
Aryl ketone
Aryl alkyl ketone
Aniline or substituted anilines
Amino fatty acid
Branched fatty acid
Hydroxy fatty acid
Keto fatty acid
Unsaturated fatty acid
Benzenoid
Monocyclic benzene moiety
Beta-hydroxy ketone
Secondary alcohol
Amino acid
Amino acid or derivatives
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Carboxylic acid
Primary amine
Carbonyl group
Organic oxygen compound
Amine
Hydrocarbon derivative
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Organic oxide
Organopnictogen compound
Alcohol
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	2.37	ChemAxon
pKa (Strongest Acidic)	4.75	ChemAxon
pKa (Strongest Basic)	2.97	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	120.85 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	112.43 m³·mol⁻¹	ChemAxon
Polarizability	43.5 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

162981424

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid (NP0322537)

MOL for NP0322537 ((2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid)

3D MOL for NP0322537 ((2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid)

3D SDF for NP0322537 ((2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid)

3D-SDF for NP0322537 ((2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid)

PDB for NP0322537 ((2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid)

3D PDB for NP0322537 ((2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid)

SMILES for NP0322537 ((2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid)

INCHI for NP0322537 ((2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid)

Structure for NP0322537 ((2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid)

3D Structure for NP0322537 ((2e,4e,6s,7r,9s,10r)-12-(4-aminophenyl)-10-hydroxy-6-[(1s)-1-hydroxyethyl]-7,9-dimethyl-12-oxododeca-2,4-dienoic acid)