NP-MRD: Showing NP-Card for 6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol (NP0179085)

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Record Information

Version

2.0

Created at

2022-09-03 17:12:28 UTC

Updated at

2022-09-03 17:12:28 UTC

NP-MRD ID

NP0179085

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol

Description

6-(4,5-Dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]Nonadecane-3,15-diol belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol is found in Varronia multispicata. 6-(4,5-Dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]Nonadecane-3,15-diol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171513152D          

 37 41  0  0  0  0            999 V2000
   10.3210    2.8641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.9996    0.7714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7914    1.5343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.3509    0.8368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 31 37  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004171513152D          

 37 41  0  0  0  0            999 V2000
   10.3210    2.8641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4967    2.8968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.7571   -1.1218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0595   -0.6814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9408   -1.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2628    0.1182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6721    0.6941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8780    0.4704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2872    1.0463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6746   -0.3292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2654   -0.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6331   -1.6436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0196   -1.7192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1791   -1.8468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5714   -1.2482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7113   -1.5887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1485   -2.2883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1022   -2.1450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9630   -1.0209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1779   -1.2744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2355   -0.1309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0747    0.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8130   -0.3542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0550   -0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6690   -0.9445    0.0000 O   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
  3  5  1  0  0  0  0
  3  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
 10  8  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 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
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 22 35  1  0  0  0  0
 27 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 31 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0179085

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(C)(C)C(O)C(O)C=C(C)C1CCC2(C)C1CC(O)C1C2(C)CCC2C(C)(C)C3(O)CCC12CO3

> <INCHI_IDENTIFIER>
InChI=1S/C31H52O6/c1-18(15-22(33)25(34)27(4,5)36-8)19-9-11-28(6)20(19)16-21(32)24-29(28,7)12-10-23-26(2,3)31(35)14-13-30(23,24)17-37-31/h15,19-25,32-35H,9-14,16-17H2,1-8H3

> <INCHI_KEY>
ANFJBMXRWPPYJK-UHFFFAOYSA-N

> <FORMULA>
C31H52O6

> <MOLECULAR_WEIGHT>
520.751

> <EXACT_MASS>
520.376389394

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
59.295819413087045

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol

> <ALOGPS_LOGP>
3.29

> <JCHEM_LOGP>
3.487804002666665

> <ALOGPS_LOGS>
-4.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.963260355250547

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.661538077790839

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8425696106124185

> <JCHEM_POLAR_SURFACE_AREA>
99.38000000000001

> <JCHEM_REFRACTIVITY>
144.55239999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.91e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol

> <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      19.266   5.346   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      17.727   5.407   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      16.905   4.105   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.603   4.927   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.207   3.283   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.083   2.803   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      16.799   1.440   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      14.544   2.864   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      13.827   4.227   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      13.722   1.562   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.183   1.623   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.466   2.986   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.361   0.321   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.931  -1.110   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.747  -2.094   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.444  -1.272   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.223  -2.796   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.824   0.221   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.721   1.296   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.239   0.878   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.136   1.953   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.859  -0.614   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.962  -1.689   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.648  -3.068   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.503  -3.209   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.934  -3.447   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.800  -2.330   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.194  -2.965   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.011  -4.271   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.057  -4.004   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.798  -1.906   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       0.332  -2.379   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       2.306  -0.244   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.873   0.472   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.251  -0.661   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.836  -0.619   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       3.115  -1.763   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5    6                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    3    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   23                                             
CONECT   17   16                                                            
CONECT   18   16   13   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   35                                                  
CONECT   23   22   16   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   35                                                  
CONECT   28   27   29   30   31                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   28   32   33   37                                             
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   22   27   36                                             
CONECT   36   35   37                                                       
CONECT   37   36   31                                                       
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₅₂O₆

Average Mass

520.7510 Da

Monoisotopic Mass

520.37639 Da

IUPAC Name

6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol

Traditional Name

6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol

CAS Registry Number

Not Available

SMILES

COC(C)(C)C(O)C(O)C=C(C)C1CCC2(C)C1CC(O)C1C2(C)CCC2C(C)(C)C3(O)CCC12CO3

InChI Identifier

InChI=1S/C31H52O6/c1-18(15-22(33)25(34)27(4,5)36-8)19-9-11-28(6)20(19)16-21(32)24-29(28,7)12-10-23-26(2,3)31(35)14-13-30(23,24)17-37-31/h15,19-25,32-35H,9-14,16-17H2,1-8H3

InChI Key

ANFJBMXRWPPYJK-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
Varronia multispicata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Naphthopyran
Naphthalene
Pyran
Oxane
Cyclic alcohol
Hemiacetal
Secondary alcohol
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxygen compound
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	3.29	ALOGPS
logP	3.49	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	11.66	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	99.38 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	144.55 m³·mol⁻¹	ChemAxon
Polarizability	59.3 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

72959209

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol (NP0179085)

MOL for NP0179085 (6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol)

3D MOL for NP0179085 (6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol)

3D SDF for NP0179085 (6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol)

3D-SDF for NP0179085 (6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol)

PDB for NP0179085 (6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol)

3D PDB for NP0179085 (6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol)

SMILES for NP0179085 (6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol)

INCHI for NP0179085 (6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol)

Structure for NP0179085 (6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol)

3D Structure for NP0179085 (6-(4,5-dihydroxy-6-methoxy-6-methylhept-2-en-2-yl)-9,10,14,14-tetramethyl-16-oxapentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecane-3,15-diol)