NP-MRD: Showing NP-Card for (2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid (NP0327010)

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Record Information

Version

1.0

Created at

2022-09-12 09:10:17 UTC

Updated at

2022-09-12 09:10:18 UTC

NP-MRD ID

NP0327010

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid

Description

(2R)-2-[(3R,3aR,6S,7S,9bR)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1H,2H,3H,3aH,4H,6H,7H,8H,9bH-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. It was first documented in 2022 (PMID: 36130844). Based on a literature review a significant number of articles have been published on (2R)-2-[(3R,3aR,6S,7S,9bR)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1H,2H,3H,3aH,4H,6H,7H,8H,9bH-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid (PMID: 36130843) (PMID: 36130842) (PMID: 36130841) (PMID: 36130840).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122211102D          

 34 36  0  0  1  0            999 V2000
   11.1144    7.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9429    6.3341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.5890    5.5693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2021    5.0173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0306    4.2103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309122211102D          

 34 36  0  0  1  0            999 V2000
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  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 12 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  6 26  1  0  0  0  0
 10 26  1  0  0  0  0
 26 27  1  6  0  0  0
  7 28  1  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0327010

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C30H44O4/c1-8-21-10-12-25-24(28(21,5)16-15-26(31)32)14-18-29(6)23(13-17-30(25,29)7)22(27(33)34)11-9-20(4)19(2)3/h8,12,14,19,21-23H,1,4,9-11,13,15-18H2,2-3,5-7H3,(H,31,32)(H,33,34)/t21-,22-,23-,28+,29-,30+/m1/s1

> <INCHI_KEY>
IDLSIHOLGUQNMM-MQQZDLKESA-N

> <FORMULA>
C30H44O4

> <MOLECULAR_WEIGHT>
468.678

> <EXACT_MASS>
468.323959897

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
55.58190572193304

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-2-[(3R,3aR,6S,7S,9bR)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1H,2H,3H,3aH,4H,6H,7H,8H,9bH-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid

> <JCHEM_LOGP>
6.553238714999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.178162755412575

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.576099883049955

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
138.40220000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-[(3R,3aR,6S,7S,9bR)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1H,2H,3H,4H,7H,8H-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      20.747  13.330   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.427  11.824   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.962  11.348   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.818  12.378   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.353  11.902   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.033  10.396   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      17.177   9.366   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.857   7.859   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      15.392   7.383   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.248   8.414   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.772   6.949   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.716   8.253   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.946   6.919   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.406   6.919   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.636   5.586   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.096   5.586   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.326   6.919   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.326   4.252   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.786   4.252   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.096   2.918   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.716   5.586   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      14.256   5.586   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      11.946   4.252   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      12.090   9.660   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.235  10.690   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.568   9.920   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.729  11.452   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      18.642   9.841   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      19.169   8.394   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      20.136   9.469   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      21.206  10.577   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      22.700  10.204   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      23.770  11.312   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      23.125   8.724   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   26                                                  
CONECT    7    6    8   28                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   26                                             
CONECT   11   10                                                            
CONECT   12   10   13   24                                                  
CONECT   13   12   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   13   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   12   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    6   10   27                                             
CONECT   27   26                                                            
CONECT   28    7    3   29   30                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

View in JSmol

Synonyms

Value	Source
(2R)-2-[(3R,3AR,6S,7S,9BR)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1H,2H,3H,3ah,4H,6H,7H,8H,9BH-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoate	Generator

Chemical Formula

C₃₀H₄₄O₄

Average Mass

468.6780 Da

Monoisotopic Mass

468.32396 Da

IUPAC Name

(2R)-2-[(3R,3aR,6S,7S,9bR)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1H,2H,3H,3aH,4H,6H,7H,8H,9bH-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid

Traditional Name

(2R)-2-[(3R,3aR,6S,7S,9bR)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1H,2H,3H,4H,7H,8H-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C30H44O4/c1-8-21-10-12-25-24(28(21,5)16-15-26(31)32)14-18-29(6)23(13-17-30(25,29)7)22(27(33)34)11-9-20(4)19(2)3/h8,12,14,19,21-23H,1,4,9-11,13,15-18H2,2-3,5-7H3,(H,31,32)(H,33,34)/t21-,22-,23-,28+,29-,30+/m1/s1

InChI Key

IDLSIHOLGUQNMM-MQQZDLKESA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Medium-chain fatty acid
Branched fatty acid
Methyl-branched fatty acid
Dicarboxylic acid or derivatives
Unsaturated fatty acid
Fatty acyl
Fatty acid
Carboxylic acid
Carboxylic acid derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
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	6.55	ChemAxon
pKa (Strongest Acidic)	4.58	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	138.4 m³·mol⁻¹	ChemAxon
Polarizability	55.58 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	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

162953200

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Cani I, Righini M, Cenni P, Foschi M: Teaching NeuroImage: Partially Reversible Widespread Leukoencephalopathy Associated With Atypical Hemolytic Uremic Syndrome. Neurology. 2022 Sep 21. pii: WNL.0000000000201378. doi: 10.1212/WNL.0000000000201378. [PubMed:36130844 ]
Sasaki R, Morimoto S, Ozawa F, Okano H, Yoshida M, Ishiura H, Tsuji S, Kuzuhara S, Kokubo Y: APOE Alleles With Tau and Abeta Pathology In Patients With Amyotrophic Lateral Sclerosis and Parkinsonism-Dementia Complex in the Kii Peninsula. Neurology. 2022 Sep 21. pii: WNL.0000000000201156. doi: 10.1212/WNL.0000000000201156. [PubMed:36130843 ]
Zhang Z, Wang M, Gill D, Liu X: Genetically Predicted Smoking and Alcohol Consumption and Functional Outcome After Ischemic Stroke. Neurology. 2022 Sep 21. pii: WNL.0000000000201291. doi: 10.1212/WNL.0000000000201291. [PubMed:36130842 ]
Khamis S, Mitakidou MR, Champion M, Goyal S, Jones RL, Siddiqui A, Sabanathan S, Hedderly T, Lin JP, Jungbluth H, Papandreou A: Clinical Reasoning: A Teenage Girl With Progressive Hyperkinetic Movements, Seizures, and Encephalopathy. Neurology. 2022 Sep 21. pii: WNL.0000000000201385. doi: 10.1212/WNL.0000000000201385. [PubMed:36130841 ]
Rosenberg A, Ohlund-Wistbacka U, Hall A, Bonnard A, Hagman G, Ryden M, Thunborg C, Wiggenraad F, Sandebring-Matton A, Solomon A, Kivipelto M: beta-Amyloid, Tau, Neurodegeneration Classification and Eligibility for Anti-amyloid Treatment in a Memory Clinic Population. Neurology. 2022 Sep 21. pii: WNL.0000000000201043. doi: 10.1212/WNL.0000000000201043. [PubMed:36130840 ]
LOTUS database [Link]

Showing NP-Card for (2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid (NP0327010)

MOL for NP0327010 ((2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid)

3D MOL for NP0327010 ((2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid)

3D SDF for NP0327010 ((2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid)

3D-SDF for NP0327010 ((2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid)

PDB for NP0327010 ((2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid)

3D PDB for NP0327010 ((2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid)

SMILES for NP0327010 ((2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid)

INCHI for NP0327010 ((2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid)

Structure for NP0327010 ((2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid)

3D Structure for NP0327010 ((2r)-2-[(3r,3ar,6s,7s,9br)-6-(2-carboxyethyl)-7-ethenyl-3a,6,9b-trimethyl-1h,2h,3h,4h,7h,8h-cyclopenta[a]naphthalen-3-yl]-6-methyl-5-methylideneheptanoic acid)