NP-MRD: Showing NP-Card for 12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid (NP0255959)

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Record Information

Version

2.0

Created at

2022-09-07 20:38:35 UTC

Updated at

2022-09-07 20:38:35 UTC

NP-MRD ID

NP0255959

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid

Description

12-(Chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]Dodeca-2,6-diene-7-carboxylic acid belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. 12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid is found in Streptomyces filipinensis. 12-(Chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]Dodeca-2,6-diene-7-carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
    3.3860    0.4085    1.6523 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0443    0.2216    0.9701 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1648   -0.7235    1.1887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0448   -0.5961    0.3318 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0272    0.3258    0.9841 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2021   -0.3665    1.6004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9135   -1.7326    1.8827 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4719   -2.5051    0.8433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9133   -3.7033    0.6655 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4713   -1.9267   -0.0731 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6432   -2.8209   -0.0006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9987   -2.0691   -1.4737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5438   -1.2401   -1.7411 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.4937    1.1923   -0.1128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7313    1.9685   -0.0771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5228    1.9672    0.8929 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0344    2.7559   -1.2008 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6298    1.1576   -1.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4770    0.2927   -0.7611 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5320    1.1222   -0.0770 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6120    1.5453   -1.0533 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4787    1.4737    1.9293 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4042   -0.2567    2.5365 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2088    0.1442    0.9620 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3268   -1.5198    1.9353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5135    0.9964    1.7256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1301   -0.2691    1.0084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4005    0.1044    2.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3647   -2.5197   -0.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3038   -1.7640   -2.2542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2020   -3.1638   -1.6416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9965    3.0837   -1.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7338    1.7106   -2.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9359   -0.2516   -1.5977 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0904    2.0503    0.3851 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2113    1.4959   -2.1056 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9515    2.5723   -0.8014 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4472    0.8396   -0.9305 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 14  2  0
 14  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  6
 10 12  1  0
 12 13  1  0
 10  4  1  0
  4  3  1  1
  3  2  2  0
  2  1  1  0
 14 15  1  0
 15 17  1  0
 15 16  2  0
  2 20  1  0
  4 19  1  0
  4  5  1  0
 21 36  1  0
 21 37  1  0
 21 38  1  0
 20 35  1  1
 19 34  1  6
 18 33  1  0
  5 26  1  1
  6 27  1  0
  6 28  1  0
 11 29  1  0
 12 30  1  0
 12 31  1  0
  3 25  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
 17 32  1  0
M  END


  Mrv1533004201501032D          

 21 23  0  0  0  0            999 V2000
    0.0001    0.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8032   -0.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4280    0.4444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6167    1.2475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4389    1.3162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7582    0.5555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5372    0.2839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6915   -0.5266    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0667   -1.0654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2209   -1.8759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2877   -0.7937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4628   -0.8049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1554   -1.6081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3841   -1.9007    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.1335    0.0167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9447   -0.7864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1226   -0.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6949   -1.5605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8666    2.0217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6914    2.0040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4694    2.7448    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
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  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
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 11 15  1  0  0  0  0
  3 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0255959

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C=C(C3COC(=O)C(O)(CCl)C23C=C1C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H17ClO5/c1-7-4-14-10(8(7)2)3-9(12(17)18)11(14)5-21-13(19)15(14,20)6-16/h3-4,8,10-11,20H,5-6H2,1-2H3,(H,17,18)

> <INCHI_KEY>
JIBVJJZCSYJNBC-UHFFFAOYSA-N

> <FORMULA>
C15H17ClO5

> <MOLECULAR_WEIGHT>
312.75

> <EXACT_MASS>
312.0764513

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
30.092742080429204

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid

> <ALOGPS_LOGP>
1.42

> <JCHEM_LOGP>
1.0617438743333338

> <ALOGPS_LOGS>
-2.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.238033029722954

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.364000325931734

> <JCHEM_PKA_STRONGEST_BASIC>
-4.444980954089197

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
76.2598

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.54e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0       0.000   0.176   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.499  -0.176   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.666   0.830   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.018   2.329   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.553   2.457   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.149   1.037   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.603   0.530   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.891  -0.983   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.725  -1.989   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.012  -3.502   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.270  -1.482   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.731  -1.502   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.023  -3.002   0.000  0.00  0.00           C+0
HETATM   14 Cl   UNK     0       2.584  -3.548   0.000  0.00  0.00          Cl+0
HETATM   15  C   UNK     0       3.982   0.031   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.630  -1.468   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.096  -1.596   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.297  -2.913   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.351   3.774   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.891   3.741   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       4.610   5.124   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   17                                                  
CONECT    3    2    4   15                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   19                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13   15                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13                                                            
CONECT   15   11    3    6   16                                             
CONECT   16   15   17                                                       
CONECT   17   16    2   18                                                  
CONECT   18   17                                                            
CONECT   19    5   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Value	Source
12-(Chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0,]dodeca-2,6-diene-7-carboxylate	Generator
12-(Chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylate	Generator

Chemical Formula

C₁₅H₁₇ClO₅

Average Mass

312.7500 Da

Monoisotopic Mass

312.07645 Da

IUPAC Name

12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid

Traditional Name

12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC1C2C=C(C3COC(=O)C(O)(CCl)C23C=C1C)C(O)=O

InChI Identifier

InChI=1S/C15H17ClO5/c1-7-4-14-10(8(7)2)3-9(12(17)18)11(14)5-21-13(19)15(14,20)6-16/h3-4,8,10-11,20H,5-6H2,1-2H3,(H,17,18)

InChI Key

JIBVJJZCSYJNBC-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
Streptomyces filipinensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Iridoid-skeleton
Monoterpenoid
Delta valerolactone
Delta_valerolactone
Dicarboxylic acid or derivatives
Oxane
Tertiary alcohol
Carboxylic acid ester
Chlorohydrin
Halohydrin
Lactone
Organoheterocyclic compound
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Alcohol
Organic oxygen compound
Organochloride
Alkyl chloride
Organooxygen compound
Carbonyl group
Organohalogen compound
Organic oxide
Hydrocarbon derivative
Alkyl halide
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	1.42	ALOGPS
logP	1.06	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	4.36	ChemAxon
pKa (Strongest Basic)	-4.4	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	2	ChemAxon
Refractivity	76.26 m³·mol⁻¹	ChemAxon
Polarizability	30.09 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid (NP0255959)

MOL for NP0255959 (12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid)

3D MOL for NP0255959 (12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid)

3D SDF for NP0255959 (12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid)

3D-SDF for NP0255959 (12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid)

PDB for NP0255959 (12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid)

3D PDB for NP0255959 (12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid)

SMILES for NP0255959 (12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid)

INCHI for NP0255959 (12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid)

Structure for NP0255959 (12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid)

3D Structure for NP0255959 (12-(chloromethyl)-12-hydroxy-3,4-dimethyl-11-oxo-10-oxatricyclo[6.4.0.0¹,⁵]dodeca-2,6-diene-7-carboxylic acid)