NP-MRD: Showing NP-Card for methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate (NP0152744)

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Record Information

Version

2.0

Created at

2022-09-02 09:16:42 UTC

Updated at

2022-09-02 09:16:42 UTC

NP-MRD ID

NP0152744

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate

Description

Methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]Nonadec-2-ene-9-carboxylate belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group. methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate is found in Penicillium citreonigrum. Methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]Nonadec-2-ene-9-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161519482D          

 37 41  0  0  0  0            999 V2000
    3.3816    3.8944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6127    3.1025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0424    2.5063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3407    2.9402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2735    1.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9030    2.2476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0988    3.0491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6047    1.8138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3813    1.5352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9629    2.5570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4089    1.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9422    0.3829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5862    0.9509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9769    0.2243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0813    0.2984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3940   -0.4650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2638    0.4094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9512    1.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4560    1.8254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5425    2.6458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2607    2.6269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5122    2.9739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7742    2.6051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1990    1.6028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3309    1.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7589    1.8845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4875    2.2716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7298    1.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3686    2.3723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1836    2.9852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8763    3.0226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0972    1.9852    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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 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
 18 26  1  0  0  0  0
 26 27  1  0  0  0  0
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 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
 22 37  1  0  0  0  0
 26 37  1  0  0  0  0
M  END

     RDKit          3D

 71 75  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004161519482D          

 37 41  0  0  0  0            999 V2000
    3.3816    3.8944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0988    3.0491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  5 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 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
 18 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
 22 37  1  0  0  0  0
 26 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0152744

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C12C(=O)C(C)(O)C(=O)C1(C)C(=C)C=C1C34CCC(OC(C)=O)C(C)(C)C3C(CC21C)OC4=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H34O9/c1-13-11-16-24(5,28(22(33)35-8)20(31)26(7,34)19(30)25(13,28)6)12-15-18-23(3,4)17(36-14(2)29)9-10-27(16,18)21(32)37-15/h11,15,17-18,34H,1,9-10,12H2,2-8H3

> <INCHI_KEY>
PJBZWVDHHJBMHH-UHFFFAOYSA-N

> <FORMULA>
C28H34O9

> <MOLECULAR_WEIGHT>
514.571

> <EXACT_MASS>
514.220282675

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
52.589009660207225

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate

> <ALOGPS_LOGP>
2.60

> <JCHEM_LOGP>
2.532515677

> <ALOGPS_LOGS>
-4.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.487392804522422

> <JCHEM_PKA_STRONGEST_BASIC>
-4.335214387301892

> <JCHEM_POLAR_SURFACE_AREA>
133.27000000000004

> <JCHEM_REFRACTIVITY>
129.05669999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.33e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       6.312   7.270   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.744   5.791   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.679   4.679   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.369   5.488   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.111   3.200   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.286   4.196   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.651   5.692   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.595   3.386   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.045   2.866   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.264   4.773   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.230   1.890   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       9.225   0.715   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.694   1.775   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.424   0.419   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.752   0.557   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.335  -0.868   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.226   0.764   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.642   2.189   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.585   3.407   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.746   4.939   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.220   4.904   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.823   5.551   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.445   4.863   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.125   3.357   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.372   2.992   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.102   2.167   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.797   1.350   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.563   2.073   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.618   3.612   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -1.978   4.334   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -3.283   3.518   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -4.643   4.240   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -3.229   1.979   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.688   4.428   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -0.343   5.572   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.636   5.642   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.048   3.706   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   13   19                                             
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    5   14   15                                             
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18    5   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   37                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   18   27   37                                             
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   29   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   34   22   26                                                  
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

View in JSmol

Synonyms

Value	Source
Methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0,.0,.0,]nonadec-2-ene-9-carboxylic acid	Generator
Methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylic acid	Generator

Chemical Formula

C₂₈H₃₄O₉

Average Mass

514.5710 Da

Monoisotopic Mass

514.22028 Da

IUPAC Name

methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate

Traditional Name

methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C12C(=O)C(C)(O)C(=O)C1(C)C(=C)C=C1C34CCC(OC(C)=O)C(C)(C)C3C(CC21C)OC4=O

InChI Identifier

InChI=1S/C28H34O9/c1-13-11-16-24(5,28(22(33)35-8)20(31)26(7,34)19(30)25(13,28)6)12-15-18-23(3,4)17(36-14(2)29)9-10-27(16,18)21(32)37-15/h11,15,17-18,34H,1,9-10,12H2,2-8H3

InChI Key

PJBZWVDHHJBMHH-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

Species Name	Source	Reference
Penicillium citreonigrum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid esters

Direct Parent

Steroid esters

Alternative Parents

Substituents

Steroid ester
Tricarboxylic acid or derivatives
Caprolactone
Oxepane
Acyloin
Gamma butyrolactone
Cyclic alcohol
Methyl ester
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Ketone
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic oxide
Alcohol
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	2.6	ALOGPS
logP	2.53	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	11.49	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	133.27 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	129.06 m³·mol⁻¹	ChemAxon
Polarizability	52.59 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	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

73821860

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate (NP0152744)

MOL for NP0152744 (methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate)

3D MOL for NP0152744 (methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate)

3D SDF for NP0152744 (methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate)

3D-SDF for NP0152744 (methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate)

PDB for NP0152744 (methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate)

3D PDB for NP0152744 (methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate)

SMILES for NP0152744 (methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate)

INCHI for NP0152744 (methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate)

Structure for NP0152744 (methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate)

3D Structure for NP0152744 (methyl 15-(acetyloxy)-7-hydroxy-5,7,10,14,14-pentamethyl-4-methylidene-6,8,18-trioxo-19-oxapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadec-2-ene-9-carboxylate)