NP-MRD: Showing NP-Card for (2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one (NP0305964)

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Record Information

Version

2.0

Created at

2022-09-10 22:09:26 UTC

Updated at

2022-09-10 22:09:26 UTC

NP-MRD ID

NP0305964

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one

Description

20-O-Methylcyclocitrinol belongs to the class of organic compounds known as secondary alcohols. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl). (2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one is found in Penicillium citrinum. (2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one was first documented in 2008 (PMID: 18656987). Based on a literature review very few articles have been published on 20-O-Methylcyclocitrinol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112200092D          

 30 33  0  0  1  0            999 V2000
   -2.2942    2.0818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1345    1.2724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7557    0.7295    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3769    0.1865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2987    1.3506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1081    1.1910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6510    1.8122    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4604    1.6525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3845    2.5929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2128    0.1083    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3962   -0.6961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6878   -1.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0667   -0.5761    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2476   -0.6744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0025   -1.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8030   -1.7542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8639   -2.5770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5826   -1.3468    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3562   -0.6213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1378    0.1065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9069    0.5137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7106    0.2282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9541   -0.5673    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7673   -0.7062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4479   -1.2537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0773    0.7444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8964    0.8427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3911    0.1824    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7930    0.9029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  1  0  0  0
 10  3  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
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 18 16  1  6  0  0  0
 18 19  1  0  0  0  0
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 18 25  1  0  0  0  0
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 26 14  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 10 29  1  0  0  0  0
 13 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END

     RDKit          3D

 68 71  0  0  0  0  0  0  0  0999 V2000
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    3.0494    2.2973    0.3112 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3306    1.7926   -0.4545 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1999    2.1157   -1.5135 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8605    0.3726   -0.6103 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8840    1.0438   -0.3572 C   0  0  0  0  0  0  0  0  0  0  0  0
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 30 68  1  0
M  END


  Mrv1652309112200092D          

 30 33  0  0  1  0            999 V2000
   -2.2942    2.0818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1345    1.2724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 10  3  1  6  0  0  0
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 29 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0305964

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@](C)(\C=C\[C@@H](C)O)[C@H]1CC[C@H]2C3=CC(=O)[C@H]4C[C@@H](O)CC=C(C4)[C@H]3CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C26H38O4/c1-16(27)9-12-26(3,30-4)24-8-7-22-21-15-23(29)18-13-17(5-6-19(28)14-18)20(21)10-11-25(22,24)2/h5,9,12,15-16,18-20,22,24,27-28H,6-8,10-11,13-14H2,1-4H3/b12-9+/t16-,18-,19+,20-,22+,24+,25+,26+/m1/s1

> <INCHI_KEY>
JLTZJSMHAJUVNI-SGSHSNTCSA-N

> <FORMULA>
C26H38O4

> <MOLECULAR_WEIGHT>
414.586

> <EXACT_MASS>
414.277009704

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
47.1993175663291

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,5S,6S,9R,13R,15S)-15-hydroxy-6-[(2S,3E,5R)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0^{2,10}.0^{5,9}]octadeca-1(17),10-dien-12-one

> <JCHEM_LOGP>
3.3698782210000013

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.544658741401594

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.934365324361032

> <JCHEM_PKA_STRONGEST_BASIC>
-2.667803565244843

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
122.07519999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,5S,6S,9R,13R,15S)-15-hydroxy-6-[(2S,3E,5R)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0^{2,10}.0^{5,9}]octadeca-1(17),10-dien-12-one

> <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      -4.282   3.886   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.984   2.375   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.144   1.362   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.303   0.348   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.157   2.521   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.668   2.223   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.682   3.383   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -10.193   3.085   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -8.184   4.840   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -4.130   0.202   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.473  -1.299   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.151  -2.089   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.991  -1.075   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.462  -1.259   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.005  -2.753   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.499  -3.275   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.613  -4.810   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.954  -2.514   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.532  -1.160   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.124   0.199   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.560   0.959   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.060   0.426   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.514  -1.059   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       7.032  -1.318   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.569  -2.340   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.461  -0.026   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.144   1.389   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.673   1.573   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.597   0.341   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.347   1.685   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   10                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    3   11   29                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   29                                                  
CONECT   14   13   15   26                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   25                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   18                                                       
CONECT   26   20   14   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   10   13   30                                             
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₈O₄

Average Mass

414.5860 Da

Monoisotopic Mass

414.27701 Da

IUPAC Name

(2R,5S,6S,9R,13R,15S)-15-hydroxy-6-[(2S,3E,5R)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0^{2,10}.0^{5,9}]octadeca-1(17),10-dien-12-one

Traditional Name

(2R,5S,6S,9R,13R,15S)-15-hydroxy-6-[(2S,3E,5R)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0^{2,10}.0^{5,9}]octadeca-1(17),10-dien-12-one

CAS Registry Number

Not Available

SMILES

CO[C@@](C)(\C=C\[C@@H](C)O)[C@H]1CC[C@H]2C3=CC(=O)[C@H]4C[C@@H](O)CC=C(C4)[C@H]3CC[C@]12C

InChI Identifier

InChI=1S/C26H38O4/c1-16(27)9-12-26(3,30-4)24-8-7-22-21-15-23(29)18-13-17(5-6-19(28)14-18)20(21)10-11-25(22,24)2/h5,9,12,15-16,18-20,22,24,27-28H,6-8,10-11,13-14H2,1-4H3/b12-9+/t16-,18-,19+,20-,22+,24+,25+,26+/m1/s1

InChI Key

JLTZJSMHAJUVNI-SGSHSNTCSA-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 citrinum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as secondary alcohols. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Secondary alcohols

Alternative Parents

Substituents

Secondary alcohol
Ketone
Ether
Dialkyl ether
Organic oxide
Hydrocarbon derivative
Carbonyl group
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	3.37	ChemAxon
pKa (Strongest Acidic)	14.93	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	122.08 m³·mol⁻¹	ChemAxon
Polarizability	47.2 Å³	ChemAxon
Number of Rings	4	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

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

102476202

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Du L, Zhu T, Fang Y, Gu Q, Zhu W: Unusual C25 steroid isomers with bicyclo[4.4.1]A/B rings from a volcano ash-derived fungus Penicillium citrinum. J Nat Prod. 2008 Aug;71(8):1343-51. doi: 10.1021/np8000442. Epub 2008 Jul 26. [PubMed:18656987 ]
LOTUS database [Link]

Showing NP-Card for (2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one (NP0305964)

MOL for NP0305964 ((2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one)

3D MOL for NP0305964 ((2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one)

3D SDF for NP0305964 ((2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one)

3D-SDF for NP0305964 ((2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one)

PDB for NP0305964 ((2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one)

3D PDB for NP0305964 ((2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one)

SMILES for NP0305964 ((2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one)

INCHI for NP0305964 ((2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one)

Structure for NP0305964 ((2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one)

3D Structure for NP0305964 ((2r,5s,6s,9r,13r,15s)-15-hydroxy-6-[(2s,3e,5r)-5-hydroxy-2-methoxyhex-3-en-2-yl]-5-methyltetracyclo[11.4.1.0²,¹⁰.0⁵,⁹]octadeca-1(17),10-dien-12-one)