NP-MRD: Showing NP-Card for (2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol (NP0276863)

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Record Information

Version

2.0

Created at

2022-09-09 01:11:35 UTC

Updated at

2022-09-09 01:11:35 UTC

NP-MRD ID

NP0276863

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol

Description

(2R,5S,7R,9S,10R,12R,15R,16R)-2,16-dimethyl-15-[(2R,5R)-5-[(1R,2R)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]Octadec-1(11)-ene-5,10-diol belongs to the class of organic compounds known as cholestane steroids. These are steroids with a structure containing the 27-carbon cholestane skeleton. Based on a literature review very few articles have been published on (2R,5S,7R,9S,10R,12R,15R,16R)-2,16-dimethyl-15-[(2R,5R)-5-[(1R,2R)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]Octadec-1(11)-ene-5,10-diol.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309092203112D          

 32 37  0  0  1  0            999 V2000
    3.6467   -1.8479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4640   -1.7351    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7749   -0.9709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2685   -0.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5794    0.4446    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3966    0.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0730    1.0959    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3024    1.8884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6195    2.3514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682    1.8451    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1561    1.9903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242    1.3596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9045    0.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7167    0.4384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2485    1.0691    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6083    0.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8121    1.5048    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0924    0.7289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2803    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318    1.0193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121    1.7952    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6242    1.9404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2803    2.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318    2.2807    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2515    3.0566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0636    2.9114    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8758    2.7662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4076    3.3969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9703   -2.3864    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7345   -2.6973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0832   -3.2036    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7723   -3.9678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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  1  6  0  0  0
  7  5  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  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
 10 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  6  0  0  0
 12 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  1  0  0  0
 26 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  6  0  0  0
 29  2  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  1  0  0  0
M  END


  Mrv1652309092203112D          

 32 37  0  0  1  0            999 V2000
    3.6467   -1.8479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4640   -1.7351    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7749   -0.9709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2685   -0.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5794    0.4446    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3966    0.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0730    1.0959    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3024    1.8884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6195    2.3514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682    1.8451    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1561    1.9903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242    1.3596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9045    0.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7167    0.4384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2485    1.0691    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6083    0.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8121    1.5048    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0924    0.7289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2803    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318    1.0193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121    1.7952    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6242    1.9404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2803    2.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318    2.2807    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2515    3.0566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0636    2.9114    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8758    2.7662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4076    3.3969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9703   -2.3864    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7345   -2.6973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0832   -3.2036    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7723   -3.9678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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  1  6  0  0  0
  7  5  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  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
 10 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  6  0  0  0
 12 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  1  0  0  0
 26 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  6  0  0  0
 29  2  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0276863

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CC[C@@H](C)[C@H]1CC[C@H]2C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)C[C@@]11O[C@H]1[C@@H]3O)[C@@H]1C[C@H]1C

> <INCHI_IDENTIFIER>
InChI=1S/C29H46O3/c1-16(20-14-18(20)3)6-7-17(2)21-8-9-22-24-23(11-12-27(21,22)4)28(5)13-10-19(30)15-29(28)26(32-29)25(24)31/h16-22,25-26,30-31H,6-15H2,1-5H3/t16-,17-,18-,19+,20+,21-,22+,25-,26+,27-,28-,29+/m1/s1

> <INCHI_KEY>
JHWWAUUSEPEHFV-QSYBCBNESA-N

> <FORMULA>
C29H46O3

> <MOLECULAR_WEIGHT>
442.684

> <EXACT_MASS>
442.344695341

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
54.1773145081111

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,5S,7R,9S,10R,12R,15R,16R)-2,16-dimethyl-15-[(2R,5R)-5-[(1R,2R)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-1(11)-ene-5,10-diol

> <JCHEM_LOGP>
5.115253543333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.169529724720107

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.48822144542022

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7288287417726877

> <JCHEM_POLAR_SURFACE_AREA>
52.989999999999995

> <JCHEM_REFRACTIVITY>
128.18829999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,5S,7R,9S,10R,12R,15R,16R)-2,16-dimethyl-15-[(2R,5R)-5-[(1R,2R)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-1(11)-ene-5,10-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       6.807  -3.449   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.333  -3.239   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.913  -1.812   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.968  -0.597   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.548   0.830   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.074   1.041   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.603   2.046   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.031   3.525   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.756   4.389   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.541   3.444   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.025   3.715   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.032   2.538   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.555   1.089   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.071   0.818   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.064   1.996   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.736   0.610   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.516   2.809   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.039   1.361   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.523   1.632   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.993   1.903   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.516   3.351   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -3.032   3.622   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.523   4.528   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.993   4.257   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.470   5.706   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.985   5.435   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.501   5.164   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.494   6.341   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.278  -4.455   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.704  -5.035   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.489  -5.980   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.908  -7.407   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   15                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12   27                                                  
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10    7   16                                             
CONECT   16   15                                                            
CONECT   17   12   18   19   24                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   17   25   26                                             
CONECT   25   24   26                                                       
CONECT   26   25   24   27                                                  
CONECT   27   26   11   28                                                  
CONECT   28   27                                                            
CONECT   29    2   30   31                                                  
CONECT   30   29   31                                                       
CONECT   31   30   29   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₆O₃

Average Mass

442.6840 Da

Monoisotopic Mass

442.34470 Da

IUPAC Name

(2R,5S,7R,9S,10R,12R,15R,16R)-2,16-dimethyl-15-[(2R,5R)-5-[(1R,2R)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-1(11)-ene-5,10-diol

Traditional Name

(2R,5S,7R,9S,10R,12R,15R,16R)-2,16-dimethyl-15-[(2R,5R)-5-[(1R,2R)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-1(11)-ene-5,10-diol

CAS Registry Number

Not Available

SMILES

C[C@H](CC[C@@H](C)[C@H]1CC[C@H]2C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)C[C@@]11O[C@H]1[C@@H]3O)[C@@H]1C[C@H]1C

InChI Identifier

InChI=1S/C29H46O3/c1-16(20-14-18(20)3)6-7-17(2)21-8-9-22-24-23(11-12-27(21,22)4)28(5)13-10-19(30)15-29(28)26(32-29)25(24)31/h16-22,25-26,30-31H,6-15H2,1-5H3/t16-,17-,18-,19+,20+,21-,22+,25-,26+,27-,28-,29+/m1/s1

InChI Key

JHWWAUUSEPEHFV-QSYBCBNESA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cholestane steroids. These are steroids with a structure containing the 27-carbon cholestane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cholestane steroids

Direct Parent

Cholestane steroids

Alternative Parents

Substituents

Cholestane-skeleton
5,6-epoxysteroid
Cyclic alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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	5.12	ChemAxon
pKa (Strongest Acidic)	13.49	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	52.99 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	128.19 m³·mol⁻¹	ChemAxon
Polarizability	54.18 Å³	ChemAxon
Number of Rings	6	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

17257397

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16099488

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol (NP0276863)

MOL for NP0276863 ((2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol)

3D MOL for NP0276863 ((2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol)

3D SDF for NP0276863 ((2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol)

3D-SDF for NP0276863 ((2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol)

PDB for NP0276863 ((2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol)

3D PDB for NP0276863 ((2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol)

SMILES for NP0276863 ((2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol)

INCHI for NP0276863 ((2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol)

Structure for NP0276863 ((2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol)

3D Structure for NP0276863 ((2r,5s,7r,9s,10r,12r,15r,16r)-2,16-dimethyl-15-[(2r,5r)-5-[(1r,2r)-2-methylcyclopropyl]hexan-2-yl]-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-1(11)-ene-5,10-diol)