NP-MRD: Showing NP-Card for ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate (NP0194837)

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Record Information

Version

2.0

Created at

2022-09-04 12:35:09 UTC

Updated at

2022-09-04 12:35:10 UTC

NP-MRD ID

NP0194837

Secondary Accession Numbers

None

Natural Product Identification

Common Name

ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate

Description

Ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]Hexadec-6-ene-4-carboxylate belongs to the class of organic compounds known as androstane steroids. These are steroids with a structure based on the 19-carbon androstane skeleton. ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate is found in Acanthella cavernosa. Ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]Hexadec-6-ene-4-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004171515552D          

 36 39  0  0  0  0            999 V2000
    3.9254    6.6037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4404    7.2711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6200    7.1849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1350    7.8523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4706    8.6060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3145    7.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3145    8.5911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4861    6.9591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7716    6.5466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4390    6.0617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6001    5.7397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2132    5.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416    4.3807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2570    4.1257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8091    3.5126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0785    3.3720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8990    3.4583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0705    4.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3561    4.6777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1845    5.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7976    6.0367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5823    5.7818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6261    6.8437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1585    7.0987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4941    7.8523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0816    8.5668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3340    2.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0785    1.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1590    2.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5715    1.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3965    1.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8090    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6340    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8090    2.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3965    3.3720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6340    2.6576    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  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
  9 24  1  0  0  0  0
 24 25  1  0  0  0  0
  6 25  1  0  0  0  0
 25 26  2  0  0  0  0
 16 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
M  END


  Mrv1533004171515552D          

 36 39  0  0  0  0            999 V2000
    3.9254    6.6037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4404    7.2711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6200    7.1849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1350    7.8523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4706    8.6060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3145    7.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3145    8.5911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4861    6.9591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7716    6.5466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4390    6.0617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6001    5.7397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2132    5.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416    4.3807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2570    4.1257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8091    3.5126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0785    3.3720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8990    3.4583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0705    4.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3561    4.6777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1845    5.4847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7976    6.0367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5823    5.7818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6261    6.8437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1585    7.0987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4941    7.8523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0816    8.5668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3340    2.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0785    1.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1590    2.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5715    1.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3965    1.9431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8090    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6340    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8090    2.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3965    3.3720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6340    2.6576    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  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
  9 24  1  0  0  0  0
 24 25  1  0  0  0  0
  6 25  1  0  0  0  0
 25 26  2  0  0  0  0
 16 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0194837

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCOC(=O)C1(O)CC2(C)C3CCC4(C)C(CCC4C3C(=O)C=C2C1=O)C(C)CCC(CC)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C31H48O5/c1-8-20(18(3)4)11-10-19(5)21-12-13-22-26-23(14-15-29(21,22)6)30(7)17-31(35,28(34)36-9-2)27(33)24(30)16-25(26)32/h16,18-23,26,35H,8-15,17H2,1-7H3

> <INCHI_KEY>
SRPUNIPEAXRVPW-UHFFFAOYSA-N

> <FORMULA>
C31H48O5

> <MOLECULAR_WEIGHT>
500.72

> <EXACT_MASS>
500.350174646

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
59.82827929786333

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate

> <ALOGPS_LOGP>
6.18

> <JCHEM_LOGP>
7.045793660666668

> <ALOGPS_LOGS>
-6.61

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.645319993802925

> <JCHEM_PKA_STRONGEST_BASIC>
-4.7035370347106005

> <JCHEM_POLAR_SURFACE_AREA>
80.67

> <JCHEM_REFRACTIVITY>
142.04219999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.23e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       7.327  12.327   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.422  13.573   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.891  13.412   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.985  14.658   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.612  16.065   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.454  14.497   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.454  16.037   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.774  12.990   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.440  12.220   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.686  11.315   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.120  10.714   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.265   9.684   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.944   8.177   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.480   7.701   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.510   6.557   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.147   6.294   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.678   6.455   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.998   7.962   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.665   8.732   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.344  10.238   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.489  11.269   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.954  10.793   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.169  12.775   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.296  13.251   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.922  14.658   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.152  15.991   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.623   4.961   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.147   3.627   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.163   4.961   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.933   3.627   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.473   3.627   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.243   2.293   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.783   2.293   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.243   4.961   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.473   6.294   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.783   4.961   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8   25                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11   24                                             
CONECT   10    9                                                            
CONECT   11    9   12   20                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   19                                             
CONECT   15   14                                                            
CONECT   16   14   17   27                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14   20                                                  
CONECT   20   19   11   21                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23    9   25                                                  
CONECT   25   24    6   26                                                  
CONECT   26   25                                                            
CONECT   27   16   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   31   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Value	Source
Ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0,.0,]hexadec-6-ene-4-carboxylic acid	Generator
Ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylic acid	Generator

Chemical Formula

C₃₁H₄₈O₅

Average Mass

500.7200 Da

Monoisotopic Mass

500.35017 Da

IUPAC Name

ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate

Traditional Name

ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate

CAS Registry Number

Not Available

SMILES

CCOC(=O)C1(O)CC2(C)C3CCC4(C)C(CCC4C3C(=O)C=C2C1=O)C(C)CCC(CC)C(C)C

InChI Identifier

InChI=1S/C31H48O5/c1-8-20(18(3)4)11-10-19(5)21-12-13-22-26-23(14-15-29(21,22)6)30(7)17-31(35,28(34)36-9-2)27(33)24(30)16-25(26)32/h16,18-23,26,35H,8-15,17H2,1-7H3

InChI Key

SRPUNIPEAXRVPW-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Acanthella cavernosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as androstane steroids. These are steroids with a structure based on the 19-carbon androstane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Androstane steroids

Direct Parent

Androstane steroids

Alternative Parents

Substituents

Androstane-skeleton
Cyclohexenone
Acyloin
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	6.18	ALOGPS
logP	7.05	ChemAxon
logS	-6.6	ALOGPS
pKa (Strongest Acidic)	10.65	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	80.67 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	142.04 m³·mol⁻¹	ChemAxon
Polarizability	59.83 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

74400231

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate (NP0194837)

MOL for NP0194837 (ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate)

3D MOL for NP0194837 (ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate)

3D SDF for NP0194837 (ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate)

3D-SDF for NP0194837 (ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate)

PDB for NP0194837 (ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate)

3D PDB for NP0194837 (ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate)

SMILES for NP0194837 (ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate)

INCHI for NP0194837 (ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate)

Structure for NP0194837 (ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate)

3D Structure for NP0194837 (ethyl 13-(5-ethyl-6-methylheptan-2-yl)-4-hydroxy-2,14-dimethyl-5,8-dioxotetracyclo[7.7.0.0²,⁶.0¹⁰,¹⁴]hexadec-6-ene-4-carboxylate)