NP-MRD: Showing NP-Card for 10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid (NP0218547)

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Record Information

Version

2.0

Created at

2022-09-05 19:14:44 UTC

Updated at

2022-09-05 19:14:44 UTC

NP-MRD ID

NP0218547

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid

Description

10-Hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]Hexadecane-5-carboxylic acid belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. 10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid is found in Goyazianthus tetrastichus, Oyedaea verbesinoides, Steiractinia sodiroi and Viguiera hypargyrea. 10-Hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]Hexadecane-5-carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004171512482D          

 30 33  0  0  0  0            999 V2000
   -0.5833   -3.5450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4053   -2.7395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3814   -2.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9900   -3.0477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5593   -1.6852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0493   -1.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3460   -1.4366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5239   -0.6310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9271    0.0076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1083   -0.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3468    0.7645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9499    1.3881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7817    1.1890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9702    0.3405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5461    0.9313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7888    0.1804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0316    0.9689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3318    0.8015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1412    0.6418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4076   -0.1390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8646   -0.7601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5667   -1.5294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0552   -0.6004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5166   -1.2331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6973   -1.0762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3575   -0.2939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8864    0.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5705   -1.1870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5538   -2.0118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2932   -0.7891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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
 16 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
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  8 26  1  0  0  0  0
 14 26  1  0  0  0  0
 26 27  1  0  0  0  0
 11 27  1  0  0  0  0
 21 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
M  END


  Mrv1533004171512482D          

 30 33  0  0  0  0            999 V2000
   -0.5833   -3.5450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4053   -2.7395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3814   -2.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9900   -3.0477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5593   -1.6852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0493   -1.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3460   -1.4366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5239   -0.6310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9271    0.0076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1083   -0.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3468    0.7645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9499    1.3881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7817    1.1890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9702    0.3405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5461    0.9313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7888    0.1804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0316    0.9689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3318    0.8015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1412    0.6418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4076   -0.1390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8646   -0.7601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5667   -1.5294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0552   -0.6004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5166   -1.2331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6973   -1.0762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3575   -0.2939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8864    0.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5705   -1.1870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5538   -2.0118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2932   -0.7891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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
 16 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
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  8 26  1  0  0  0  0
 14 26  1  0  0  0  0
 26 27  1  0  0  0  0
 11 27  1  0  0  0  0
 21 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0218547

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(=O)OC1C(=C)C2CC11CCC3C(C)(CCCC3(C)C1(O)CC2)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H36O5/c1-6-15(2)20(26)30-19-16(3)17-8-13-25(29)23(5)11-7-10-22(4,21(27)28)18(23)9-12-24(19,25)14-17/h6,17-19,29H,3,7-14H2,1-2,4-5H3,(H,27,28)

> <INCHI_KEY>
CSECYHNWAWCJBQ-UHFFFAOYSA-N

> <FORMULA>
C25H36O5

> <MOLECULAR_WEIGHT>
416.558

> <EXACT_MASS>
416.256274259

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
45.762203203627294

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid

> <ALOGPS_LOGP>
4.25

> <JCHEM_LOGP>
4.942472086999999

> <ALOGPS_LOGS>
-4.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.941245942832847

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.375140292054424

> <JCHEM_PKA_STRONGEST_BASIC>
-3.262547340468096

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
113.92899999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.92e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid

> <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      -1.089  -6.617   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.757  -5.114   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.712  -4.649   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.848  -5.689   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.044  -3.146   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.092  -2.106   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       2.512  -2.682   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.845  -1.178   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.731   0.014   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.202  -0.174   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.514   1.427   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.640   2.591   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.192   2.219   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.544   0.636   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.619   1.738   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.072   0.337   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.526   1.809   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.086   1.496   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.597   1.198   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.094  -0.259   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.081  -1.419   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.525  -2.855   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.570  -1.121   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.564  -2.302   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.035  -2.009   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.401  -0.549   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.521   0.479   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.398  -2.216   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      10.367  -3.755   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      11.747  -1.473   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   26                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   27                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   26                                             
CONECT   15   14                                                            
CONECT   16   14   17   18   23                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   28                                             
CONECT   22   21                                                            
CONECT   23   21   16   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    8   14   27                                             
CONECT   27   26   11                                                       
CONECT   28   21   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Value	Source
10-Hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0,.0,]hexadecane-5-carboxylate	Generator
10-Hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate	Generator

Chemical Formula

C₂₅H₃₆O₅

Average Mass

416.5580 Da

Monoisotopic Mass

416.25627 Da

IUPAC Name

10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid

Traditional Name

10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC=C(C)C(=O)OC1C(=C)C2CC11CCC3C(C)(CCCC3(C)C1(O)CC2)C(O)=O

InChI Identifier

InChI=1S/C25H36O5/c1-6-15(2)20(26)30-19-16(3)17-8-13-25(29)23(5)11-7-10-22(4,21(27)28)18(23)9-12-24(19,25)14-17/h6,17-19,29H,3,7-14H2,1-2,4-5H3,(H,27,28)

InChI Key

CSECYHNWAWCJBQ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Goyazianthus tetrastichus	LOTUS Database	35616633
Oyedaea verbesinoides	LOTUS Database	35616633
Steiractinia sodiroi	LOTUS Database	35616633
Viguiera hypargyrea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Carboxylic acid
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organooxygen compound
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	4.25	ALOGPS
logP	4.94	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	4.38	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	113.93 m³·mol⁻¹	ChemAxon
Polarizability	45.76 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

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METLIN ID

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PubChem Compound

74146145

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for 10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid (NP0218547)

MOL for NP0218547 (10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

3D MOL for NP0218547 (10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

3D SDF for NP0218547 (10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

3D-SDF for NP0218547 (10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

PDB for NP0218547 (10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

3D PDB for NP0218547 (10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

SMILES for NP0218547 (10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

INCHI for NP0218547 (10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

Structure for NP0218547 (10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

3D Structure for NP0218547 (10-hydroxy-5,9-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)