NP-MRD: Showing NP-Card for (2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid (NP0317223)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 16:57:56 UTC

Updated at

2022-09-11 16:57:57 UTC

NP-MRD ID

NP0317223

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid

Description

Trans-Cinnamic acid (1R,2S,3S,5E,7Z)-1-[(S)-1-methylbutyl]-2-methyl-3-hydroxy-9-amino-9-oxo-5,7-nonadienyl ester belongs to the class of organic compounds known as cinnamic acid esters. These are compound containing an ester derivative of cinnamic acid. Based on a literature review very few articles have been published on trans-Cinnamic acid (1R,2S,3S,5E,7Z)-1-[(S)-1-methylbutyl]-2-methyl-3-hydroxy-9-amino-9-oxo-5,7-nonadienyl ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112218572D          

 29 29  0  0  1  0            999 V2000
   -0.8101   -3.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401   -3.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3502   -3.6573    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6203   -4.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8903   -3.0336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6203   -2.2541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101   -2.0982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700   -2.7218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401   -1.3186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700   -1.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401   -0.3832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3502   -0.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6203    0.5523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0802    1.1760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700    1.0200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.2405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7004   -3.1895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2405   -2.5659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9705   -3.9691    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4304   -4.5927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7806   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0507   -4.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8608   -5.0605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1308   -5.8400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9410   -5.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4811   -5.3723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2110   -4.5927    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.2912   -5.5282    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 62 62  0  0  0  0  0  0  0  0999 V2000
    6.5607   -6.7030    1.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5943   -6.8532    0.8350 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8601   -5.7899    0.6127 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5845   -6.0072    0.1839 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4373   -4.5081    0.8298 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8107   -3.3925    0.6373 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4608   -3.2740    0.1829 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8629   -2.0776   -0.0003 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5217   -1.9113   -0.4519 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4403   -1.2647    0.3015 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6706   -1.1968   -0.6408 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7972    0.1892    0.6351 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8649    0.1585    1.7056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4317    0.8840    1.1755 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4488    0.8981    0.1546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6672    0.2838    0.3328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8895   -0.3089    1.4315 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7282    0.2671   -0.6635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6058    0.8610   -1.8353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6450    0.8684   -2.8631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4011    1.5591   -4.0459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3648    1.5823   -5.0421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5604    0.9231   -4.8607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8212    0.2346   -3.7000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8439    0.2175   -2.7033 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2751    2.3048    1.5914 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0762    2.5415    3.0030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1715    3.2640    0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6047    3.5337    0.3645 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3201    4.1333    1.5553 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2692   -6.3590   -0.6862 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4946   -4.4709    1.1877 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3860   -2.4670    0.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8379   -4.0836   -0.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5141   -1.2397    0.1981 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5555   -1.4726   -1.5140 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1306   -2.9640   -0.7060 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0275   -1.7153    1.1761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3205   -1.1216   -1.5440 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2144    0.6185   -0.2680 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4959    0.5418    2.7008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1271   -0.9082    1.9798 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8140    0.6382    1.4171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8361    0.2995    2.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6487   -0.2476   -0.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6472    1.3634   -1.9937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4693    2.0893   -4.2208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1914    2.1210   -5.9824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3034    0.9498   -5.6445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7688   -0.2786   -3.5755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0808   -0.3307   -1.8116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4532    2.6036    1.6422 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1075    2.6821    3.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5472    3.3933    3.4629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3176    1.6615    3.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2705    2.9366   -0.4363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3243    4.2793    0.6870 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6646    4.3546   -0.4257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2073    2.7245   -0.1020 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9735    3.3782    2.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0796    4.9094    1.2016 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6649    4.6979    2.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
 30 29  1  0
 29 28  1  0
 28 26  1  0
 26 27  1  0
 26 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 14 12  1  0
 12 13  1  0
 12 10  1  0
 10 11  1  0
 10  9  1  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  2  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
 25 20  1  0
 30 60  1  0
 30 61  1  0
 30 62  1  0
 29 58  1  0
 29 59  1  0
 28 56  1  0
 28 57  1  0
 26 52  1  1
 27 53  1  0
 27 54  1  0
 27 55  1  0
 14 44  1  1
 18 45  1  0
 19 46  1  0
 21 47  1  0
 22 48  1  0
 23 49  1  0
 24 50  1  0
 25 51  1  0
 12 40  1  6
 13 41  1  0
 13 42  1  0
 13 43  1  0
 10 38  1  1
 11 39  1  0
  9 36  1  0
  9 37  1  0
  8 35  1  0
  7 34  1  0
  6 33  1  0
  5 32  1  0
  4 31  1  0
  2  1  1  0
M  END


  Mrv1652309112218572D          

 29 29  0  0  1  0            999 V2000
   -0.8101   -3.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401   -3.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3502   -3.6573    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6203   -4.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8903   -3.0336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6203   -2.2541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101   -2.0982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700   -2.7218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401   -1.3186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700   -1.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401   -0.3832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3502   -0.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6203    0.5523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0802    1.1760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700    1.0200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.2405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7004   -3.1895    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2405   -2.5659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9705   -3.9691    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4304   -4.5927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7806   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0507   -4.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8608   -5.0605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1308   -5.8400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9410   -5.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4811   -5.3723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2110   -4.5927    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.2912   -5.5282    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0317223

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C24H33NO4/c1-4-11-18(2)24(19(3)21(26)14-9-6-10-15-22(25)27)29-23(28)17-16-20-12-7-5-8-13-20/h5-10,12-13,15-19,21,24,26H,4,11,14H2,1-3H3,(H2,25,27)/b9-6+,15-10-,17-16+/t18-,19-,21-,24+/m0/s1

> <INCHI_KEY>
OJAGQZQYWOJBHT-SWPMXRTOSA-N

> <FORMULA>
C24H33NO4

> <MOLECULAR_WEIGHT>
399.531

> <EXACT_MASS>
399.240958547

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
46.18481665781658

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2Z,4E,7S,8S,9R,10S)-7-hydroxy-8,10-dimethyl-9-{[(2E)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid

> <JCHEM_LOGP>
2.9586406492013633

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.819003335834118

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2150591884416286

> <JCHEM_PKA_STRONGEST_BASIC>
12.48344775695069

> <JCHEM_POLAR_SURFACE_AREA>
90.61

> <JCHEM_REFRACTIVITY>
130.00040000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2Z,4E,7S,8S,9R,10S)-7-hydroxy-8,10-dimethyl-9-{[(2E)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.512  -7.409   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.008  -6.536   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.520  -6.827   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.024  -8.282   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.529  -5.663   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.024  -4.208   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.512  -3.917   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.504  -5.081   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.008  -2.461   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.504  -2.170   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.008  -0.715   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.520  -0.424   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.024   1.031   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.016   2.195   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.504   1.904   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   0.449   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.041  -5.954   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.049  -4.790   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.545  -7.409   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.537  -8.573   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.057  -7.700   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.561  -9.155   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.073  -9.446   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.578 -10.901   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.090 -11.192   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.098 -10.028   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0      11.594  -8.573   0.000  0.00  0.00           N+0
HETATM   29  O   UNK     0      13.610 -10.319   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   18                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18    6   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END

View in JSmol

Synonyms

Value	Source
trans-Cinnamate (1R,2S,3S,5E,7Z)-1-[(S)-1-methylbutyl]-2-methyl-3-hydroxy-9-amino-9-oxo-5,7-nonadienyl ester	Generator

Chemical Formula

C₂₄H₃₃NO₄

Average Mass

399.5310 Da

Monoisotopic Mass

399.24096 Da

IUPAC Name

(2Z,4E,7S,8S,9R,10S)-7-hydroxy-8,10-dimethyl-9-{[(2E)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid

Traditional Name

(2Z,4E,7S,8S,9R,10S)-7-hydroxy-8,10-dimethyl-9-{[(2E)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C24H33NO4/c1-4-11-18(2)24(19(3)21(26)14-9-6-10-15-22(25)27)29-23(28)17-16-20-12-7-5-8-13-20/h5-10,12-13,15-19,21,24,26H,4,11,14H2,1-3H3,(H2,25,27)/b9-6+,15-10-,17-16+/t18-,19-,21-,24+/m0/s1

InChI Key

OJAGQZQYWOJBHT-SWPMXRTOSA-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 cinnamic acid esters. These are compound containing an ester derivative of cinnamic acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Cinnamic acid esters

Direct Parent

Cinnamic acid esters

Alternative Parents

Substituents

Cinnamic acid ester
Styrene
Fatty acid ester
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxamide group
Carboxylic acid ester
Primary carboxylic acid amide
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Alcohol
Organic nitrogen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
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	2.96	ChemAxon
pKa (Strongest Acidic)	1.22	ChemAxon
pKa (Strongest Basic)	12.48	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	90.61 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	130 m³·mol⁻¹	ChemAxon
Polarizability	46.18 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

8041370

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9865679

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid (NP0317223)

MOL for NP0317223 ((2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid)

3D MOL for NP0317223 ((2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid)

3D SDF for NP0317223 ((2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid)

3D-SDF for NP0317223 ((2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid)

PDB for NP0317223 ((2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid)

3D PDB for NP0317223 ((2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid)

SMILES for NP0317223 ((2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid)

INCHI for NP0317223 ((2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid)

Structure for NP0317223 ((2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid)

3D Structure for NP0317223 ((2z,4e,7s,8s,9r,10s)-7-hydroxy-8,10-dimethyl-9-{[(2e)-3-phenylprop-2-enoyl]oxy}trideca-2,4-dienimidic acid)