NP-MRD: Showing NP-Card for (1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid (NP0320374)

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Record Information

Version

2.0

Created at

2022-09-11 21:59:10 UTC

Updated at

2022-09-11 21:59:11 UTC

NP-MRD ID

NP0320374

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid

Description

Subergorgic acid, also known as subergorgate, belongs to the class of organic compounds known as angular triquinanes. These are triquinane with a structure based on a [6.3.0.0^1,5] Undecane carbon skeleton. (1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid is found in Isis hippuris and Subergorgia suberosa. (1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid was first documented in 2005 (PMID: 16124781). Based on a literature review a small amount of articles have been published on Subergorgic acid (PMID: 34788028) (PMID: 30736380) (PMID: 18075899).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
   -3.3527    0.6691   -0.1186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2875   -0.2778    0.4467 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6679    0.4384    1.6009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3301    0.8605    1.1153 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3078    1.7584    1.6176 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0411    0.0276   -0.0199 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2409   -0.5279   -0.5824 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9509   -1.9680   -0.8481 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5697   -2.1193   -0.7595 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9037   -1.1665    0.3320 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5988   -1.7402    1.6726 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2546   -0.5572    0.2406 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2553    0.4946   -0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4205    1.3329   -0.8736 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5174    1.0570   -0.3597 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3285    2.4148   -1.7220 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8860    0.6572   -1.0624 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5262    2.0827   -1.3712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6847    0.3605   -1.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8637    1.6812   -0.1090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1586    0.6970    0.6462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8066   -1.2125    0.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6120   -0.1687    2.5237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2222    1.3718    1.8980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5144   -0.0023   -1.5310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4352   -2.6385   -0.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3076   -2.2807   -1.8590 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7662   -3.1806   -0.4274 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0664   -1.9455   -1.7161 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3794   -2.4945    1.9038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3553   -2.2768    1.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6399   -0.9966    2.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1047   -0.9549    0.7772 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1369    3.3462   -1.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8142    0.0564   -1.9951 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8508    2.7468   -0.5571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9962    2.3478   -2.3300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5739    2.1076   -1.5321 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  6  4  1  1
  6 17  1  0
 17 18  1  0
 17 13  1  0
 13 12  2  0
 12 10  1  0
 10 11  1  1
 10  9  1  0
  9  8  1  0
  8  7  1  0
 13 14  1  0
 14 16  1  0
 14 15  2  0
  7  2  1  0
 10  6  1  0
  7  6  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  1
  3 23  1  0
  3 24  1  0
 17 35  1  6
 18 36  1  0
 18 37  1  0
 18 38  1  0
 12 33  1  0
 11 30  1  0
 11 31  1  0
 11 32  1  0
  9 28  1  0
  9 29  1  0
  8 26  1  0
  8 27  1  0
  7 25  1  6
 16 34  1  0
M  END


  Mrv1652309112223592D          

 18 20  0  0  1  0            999 V2000
   -1.2352   -0.1956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4506   -0.4506    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1956   -1.2352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6294   -1.2352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1143   -1.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8843   -0.4506    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2169    0.0343    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4718    0.8190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2968    0.8190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5517    0.0343    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2192    0.5193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2192   -0.4506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9642   -1.2352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -1.9026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2696   -1.8164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1136   -2.6563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1392   -1.2352    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3942   -2.0198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  4  1  6  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 13 17  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0320374

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC(=O)[C@@]23[C@@H](C)C(=C[C@]2(C)CC[C@@H]13)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O3/c1-8-6-12(16)15-9(2)10(13(17)18)7-14(15,3)5-4-11(8)15/h7-9,11H,4-6H2,1-3H3,(H,17,18)/t8-,9+,11+,14+,15+/m1/s1

> <INCHI_KEY>
LFKSRWRSZVCLFJ-VDHTUSMASA-N

> <FORMULA>
C15H20O3

> <MOLECULAR_WEIGHT>
248.322

> <EXACT_MASS>
248.141244504

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
26.88664200194788

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,5S,8S,9R)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0^{1,5}]undec-3-ene-3-carboxylic acid

> <JCHEM_LOGP>
2.625567424

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.656996451339909

> <JCHEM_PKA_STRONGEST_BASIC>
-7.512800098939316

> <JCHEM_POLAR_SURFACE_AREA>
54.370000000000005

> <JCHEM_REFRACTIVITY>
68.10480000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5S,8S,9R)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0^{1,5}]undec-3-ene-3-carboxylic acid

> <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      -2.306  -0.365   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.841  -0.841   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.365  -2.306   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.175  -2.306   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.080  -3.552   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.651  -0.841   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.405   0.064   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.881   1.529   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.421   1.529   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.897   0.064   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.142   0.969   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.142  -0.841   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.667  -2.306   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.572  -3.552   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.103  -3.391   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       3.945  -4.958   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.127  -2.306   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.602  -3.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   10   17                                             
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6   11   12                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   13    6   18                                                  
CONECT   18   17                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

View in JSmol

Synonyms

Value	Source
Subergorgate	Generator

Chemical Formula

C₁₅H₂₀O₃

Average Mass

248.3220 Da

Monoisotopic Mass

248.14124 Da

IUPAC Name

(1S,2R,5S,8S,9R)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0^{1,5}]undec-3-ene-3-carboxylic acid

Traditional Name

(1S,2R,5S,8S,9R)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0^{1,5}]undec-3-ene-3-carboxylic acid

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC(=O)[C@@]23[C@@H](C)C(=C[C@]2(C)CC[C@@H]13)C(O)=O

InChI Identifier

InChI=1S/C15H20O3/c1-8-6-12(16)15-9(2)10(13(17)18)7-14(15,3)5-4-11(8)15/h7-9,11H,4-6H2,1-3H3,(H,17,18)/t8-,9+,11+,14+,15+/m1/s1

InChI Key

LFKSRWRSZVCLFJ-VDHTUSMASA-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
Isis hippuris	LOTUS Database	35616633
Subergorgia suberosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as angular triquinanes. These are triquinane with a structure based on a [6.3.0.0^1,5] Undecane carbon skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Angular triquinanes

Alternative Parents

Substituents

Angular triquinane sesquiterpenoid
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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	2.63	ChemAxon
pKa (Strongest Acidic)	4.66	ChemAxon
pKa (Strongest Basic)	-7.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.37 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	68.1 m³·mol⁻¹	ChemAxon
Polarizability	26.89 Å³	ChemAxon
Number of Rings	3	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

C00021817

Chemspider ID

9229161

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11054000

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Qi SH, Zhang S, Li X, Li QX: A cytotoxic sesquiterpene alkaloid from the South China Sea gorgonian Subergorgia suberosa. J Nat Prod. 2005 Aug;68(8):1288-9. doi: 10.1021/np050105l. [PubMed:16124781 ]
Kotha S, Keesari RR: A Modular Approach to Angularly Fused Polyquinanes via Ring-Rearrangement Metathesis: Synthetic Access to Cameroonanol Analogues and the Basic Core of Subergorgic Acid and Crinipellin. J Org Chem. 2021 Dec 3;86(23):17129-17155. doi: 10.1021/acs.joc.1c02258. Epub 2021 Nov 17. [PubMed:34788028 ]
Zhang J, Ling W, Yang Z, Liang Y, Zhang L, Guo C, Wang K, Zhong B, Xu S, Xu Y: Isolation and Structure-Activity Relationship of Subergorgic Acid and Synthesis of Its Derivatives as Antifouling Agent. Mar Drugs. 2019 Feb 6;17(2). pii: md17020101. doi: 10.3390/md17020101. [PubMed:30736380 ]
Qi SH, Zhang S, Yang LH, Qian PY: Antifouling and antibacterial compounds from the gorgonians Subergorgia suberosa and Scripearia gracillis. Nat Prod Res. 2008 Jan 20;22(2):154-66. doi: 10.1080/14786410701642441. [PubMed:18075899 ]
LOTUS database [Link]

Showing NP-Card for (1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid (NP0320374)

MOL for NP0320374 ((1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid)

3D MOL for NP0320374 ((1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid)

3D SDF for NP0320374 ((1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid)

3D-SDF for NP0320374 ((1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid)

PDB for NP0320374 ((1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid)

3D PDB for NP0320374 ((1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid)

SMILES for NP0320374 ((1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid)

INCHI for NP0320374 ((1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid)

Structure for NP0320374 ((1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid)

3D Structure for NP0320374 ((1s,2r,5s,8s,9r)-2,5,9-trimethyl-11-oxotricyclo[6.3.0.0¹,⁵]undec-3-ene-3-carboxylic acid)