NP-MRD: Showing NP-Card for methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate (NP0144095)

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Record Information

Version

2.0

Created at

2022-09-01 22:58:42 UTC

Updated at

2022-09-01 22:58:42 UTC

NP-MRD ID

NP0144095

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate

Description

CHEMBL401640 belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. Based on a literature review very few articles have been published on CHEMBL401640.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022200582D          

 28 28  0  0  1  0            999 V2000
    1.1266    2.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1647    1.5342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9521    1.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3972    0.5934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7904    0.0345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6848   -0.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2437   -1.3905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8607   -0.8218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2049   -0.3212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0242    0.4837    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7940    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2945   -0.0665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1128    0.0391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6133   -0.6167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4315   -0.5111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2497   -0.4055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3259    0.3071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5371   -1.3293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1117    1.3507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9299    1.4563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2475    2.2177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7470    2.8735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0657    2.3233    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4033    1.2165    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1556    1.8233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9606    1.6427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0904    2.6108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4685    3.2176    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
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 10 24  1  0  0  0  0
  2 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 62 62  0  0  0  0  0  0  0  0999 V2000
   -4.1135   -1.2658   -0.6970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2025   -0.3283   -0.9328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7826    1.0436   -1.1476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5308    1.3553    0.1180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9832    2.4623    0.9243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7380    2.7565    1.1894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5237    3.9992    2.0763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4927    2.0695    0.7618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4168    0.6592    1.1786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9528   -0.3664    0.2096 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4961   -0.2805   -0.0869 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3075    0.5691    0.5253 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7151    0.7546    0.3320 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3778    1.6756    1.0485 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8470    1.8749    0.8522 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2091    1.8947   -0.6131 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5783    0.7467    1.5381 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2054    3.0842    1.4045 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1597   -1.1358   -1.1267 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0636   -2.5032   -0.8376 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6423   -3.3868   -1.7316 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6134   -4.8517   -1.5468 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2319   -2.9508   -2.7667 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7528   -0.6334   -0.9928 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6985   -2.1146   -1.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5739   -2.6461   -2.3593 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8046   -2.9248   -0.1331 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7726   -4.3393   -0.2294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8524   -2.2835   -0.5395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1730   -0.9349   -0.6727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5463    0.9121   -1.9952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1115    1.7832   -1.5293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6949    0.4283    0.7549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6057    1.5942   -0.1785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7762    3.1398    1.3685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4279    4.2153    2.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3001    4.8616    1.4156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6802    3.8225    2.7433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6318    2.6742    1.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2915    2.2761   -0.3104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4553    0.3272    1.5355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8207    0.5403    2.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0191   -1.3529    0.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8359    1.1720    1.2939 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2872    0.1960   -0.3529 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8054    2.2468    1.7532 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3743    0.8578   -0.9984 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4848    2.4118   -1.2451 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1859    2.4422   -0.6996 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5912    1.0958    1.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0609    0.4853    2.4865 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5993   -0.1227    0.8496 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3211    3.8117    0.7633 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1600   -0.8084   -1.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5062   -0.9859   -2.0468 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6596   -5.2421   -1.5630 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1066   -5.1609   -0.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0606   -5.2779   -2.4146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2973   -0.1822   -1.9224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8349   -4.6721   -0.2866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3430   -4.8173    0.6742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2852   -4.6713   -1.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
 28 27  1  0
 27 25  1  0
 25 26  2  0
 25 24  1  0
 24 10  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  1  0
  6  5  2  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
 10 11  1  0
 11 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 15 18  1  0
  2 24  1  0
 28 60  1  0
 28 61  1  0
 28 62  1  0
 24 59  1  6
 10 43  1  1
  9 41  1  0
  9 42  1  0
  8 39  1  0
  8 40  1  0
  7 36  1  0
  7 37  1  0
  7 38  1  0
  5 35  1  0
  4 33  1  0
  4 34  1  0
  3 31  1  0
  3 32  1  0
  1 29  1  0
  1 30  1  0
 19 54  1  0
 19 55  1  0
 22 56  1  0
 22 57  1  0
 22 58  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 16 47  1  0
 16 48  1  0
 16 49  1  0
 17 50  1  0
 17 51  1  0
 17 52  1  0
 18 53  1  0
M  END


  Mrv1652309022200582D          

 28 28  0  0  1  0            999 V2000
    1.1266    2.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1647    1.5342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9521    1.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3972    0.5934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7904    0.0345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6848   -0.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2437   -1.3905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8607   -0.8218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2049   -0.3212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0242    0.4837    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7940    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2945   -0.0665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1128    0.0391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6133   -0.6167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4315   -0.5111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2497   -0.4055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3259    0.3071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5371   -1.3293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1117    1.3507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9299    1.4563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2475    2.2177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7470    2.8735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0657    2.3233    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4033    1.2165    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1556    1.8233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9606    1.6427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0904    2.6108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4685    3.2176    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
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 10 24  1  0  0  0  0
  2 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0144095

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H]1[C@H](CC\C(C)=C\CCC1=C)C(\COC(C)=O)=C\C=C\C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C23H34O5/c1-16-9-7-10-17(2)21(22(25)27-6)20(13-12-16)19(15-28-18(3)24)11-8-14-23(4,5)26/h8-9,11,14,20-21,26H,2,7,10,12-13,15H2,1,3-6H3/b14-8+,16-9+,19-11+/t20-,21+/m1/s1

> <INCHI_KEY>
QAAVINGBTKKGMU-MQQLYBRISA-N

> <FORMULA>
C23H34O5

> <MOLECULAR_WEIGHT>
390.52

> <EXACT_MASS>
390.240624195

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
43.86732741855384

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,2S,5E)-2-[(2Z,4E)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate

> <ALOGPS_LOGP>
4.47

> <JCHEM_LOGP>
3.352115959333333

> <ALOGPS_LOGS>
-4.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.911535249783608

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5252919370245266

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
113.36839999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.92e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,2S,5E)-2-[(2Z,4E)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       2.103   4.402   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.174   2.864   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.644   2.404   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.475   1.108   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.342   0.064   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.145  -1.463   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.188  -2.596   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.607  -1.534   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.382  -0.600   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.045   0.903   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.482   1.100   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.416  -0.124   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.944   0.073   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.878  -1.151   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -6.406  -0.954   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -7.933  -0.757   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.208   0.573   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -6.603  -2.481   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.075   2.521   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.602   2.718   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -4.195   4.140   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.261   5.364   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -5.723   4.337   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.753   2.271   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.290   3.404   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.793   3.066   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       0.169   4.873   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -0.874   6.006   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   24                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   24                                                  
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15                                                            
CONECT   19   11   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   10    2   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₄O₅

Average Mass

390.5200 Da

Monoisotopic Mass

390.24062 Da

IUPAC Name

methyl (1R,2S,5E)-2-[(2Z,4E)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate

Traditional Name

methyl (1R,2S,5E)-2-[(2Z,4E)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H]1[C@H](CC\C(C)=C\CCC1=C)C(\COC(C)=O)=C\C=C\C(C)(C)O

InChI Identifier

InChI=1S/C23H34O5/c1-16-9-7-10-17(2)21(22(25)27-6)20(13-12-16)19(15-28-18(3)24)11-8-14-23(4,5)26/h8-9,11,14,20-21,26H,2,7,10,12-13,15H2,1,3-6H3/b14-8+,16-9+,19-11+/t20-,21+/m1/s1

InChI Key

QAAVINGBTKKGMU-MQQLYBRISA-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 dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Dicarboxylic acids and derivatives

Direct Parent

Dicarboxylic acids and derivatives

Alternative Parents

Substituents

Dicarboxylic acid or derivatives
Methyl ester
Tertiary alcohol
Carboxylic acid ester
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic 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	4.47	ALOGPS
logP	3.35	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	17.91	ChemAxon
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	113.37 m³·mol⁻¹	ChemAxon
Polarizability	43.87 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

23076589

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23655344

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate (NP0144095)

MOL for NP0144095 (methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate)

3D MOL for NP0144095 (methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate)

3D SDF for NP0144095 (methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate)

3D-SDF for NP0144095 (methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate)

PDB for NP0144095 (methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate)

3D PDB for NP0144095 (methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate)

SMILES for NP0144095 (methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate)

INCHI for NP0144095 (methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate)

Structure for NP0144095 (methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate)

3D Structure for NP0144095 (methyl (1r,2s,5e)-2-[(2z,4e)-1-(acetyloxy)-6-hydroxy-6-methylhepta-2,4-dien-2-yl]-5-methyl-9-methylidenecyclonon-5-ene-1-carboxylate)