NP-MRD: Showing NP-Card for 7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid (NP0211542)

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Record Information

Version

2.0

Created at

2022-09-05 09:52:03 UTC

Updated at

2022-09-05 09:52:03 UTC

NP-MRD ID

NP0211542

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid

Description

4-Chloro-3-dihydroxy-1b,5,5-tetramethyl-octahydro-H-naphtho[1,8a-b]oxirene--carboxylic acid belongs to the class of organic compounds known as abscisic acids and derivatives. These are terpene compounds containing the abscisic acid moiety, which is characterized by a 3-methylpenta-2,4-dienoic acid attached to the C1 carbon of a 4-oxocyclohex-2-ene moiety. 4-Chloro-3-dihydroxy-1b,5,5-tetramethyl-octahydro-H-naphtho[1,8a-b]oxirene--carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 46  0  0  0  0  0  0  0  0999 V2000
   -2.9582   -1.1304   -0.9344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9513   -0.5899    0.0726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1977   -1.4132    1.3483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3771    0.8169    0.4165 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8696    0.6511    1.4146 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -1.3883    1.5560    1.2448 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7584    2.9137    1.2313 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470    1.3307    0.8944 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2609    0.5308   -0.3640 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2928    1.4050   -1.5044 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7032    0.3154   -0.6196 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4374    1.5380   -0.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9032    2.3754   -1.0307 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6741    1.8656    1.1375 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3185   -0.9377   -0.1180 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1331   -0.7268    1.1719 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3088   -1.3651   -1.0407 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4146   -2.0734    0.1297 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0523   -1.9816   -0.4404 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2879   -1.4213   -1.6221 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5451   -0.7242   -0.3576 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9721   -0.8191   -0.5961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7617   -0.8197   -1.9571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9367   -2.2522   -0.8751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6092   -1.0244    2.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9894   -2.4746    1.2114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2961   -1.3549    1.6063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7009    1.4042   -0.4666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5286    1.2433    2.3220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3344    3.1154    0.4355 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6214    0.9395    1.7408 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4591    2.3581    0.6589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6303    2.3858   -1.1613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0488    0.8519   -2.1106 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5245    1.6304   -2.2556 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8196    0.2888   -1.7494 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6720    2.7908    1.4977 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9856   -0.0619    1.0112 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5047   -0.5115    2.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5828   -1.7467    1.3686 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4450   -0.6729   -1.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8613   -3.0468   -0.2370 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2799   -2.2712    1.2379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5744   -2.8874   -0.1869 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 17  1  6
 15 18  1  0
 18 19  1  0
 19 20  1  0
 21 20  1  6
 21  2  1  0
  2  1  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  1  0
 12 14  1  0
 12 13  2  0
 11 15  1  0
 21 19  1  0
  9 21  1  0
 16 38  1  0
 16 39  1  0
 16 40  1  0
 17 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  1
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  6
  6 29  1  1
  7 30  1  0
  8 31  1  0
  8 32  1  0
 10 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  6
 14 37  1  0
M  END


  Mrv1533004161513042D          

 21 23  0  0  0  0            999 V2000
   -0.8125    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822   -0.7752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6131    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6737    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  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
  8 10  1  0  0  0  0
  8 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
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
  2 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0211542

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(O)CC2OC22C(C)(C)C(Cl)C(O)CC2(C)C1C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H23ClO5/c1-12(2)10(16)7(17)5-13(3)9(11(18)19)14(4,20)6-8-15(12,13)21-8/h7-10,17,20H,5-6H2,1-4H3,(H,18,19)

> <INCHI_KEY>
QUHIFZVMNSLMAB-UHFFFAOYSA-N

> <FORMULA>
C15H23ClO5

> <MOLECULAR_WEIGHT>
318.79

> <EXACT_MASS>
318.1234015

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
31.8892037705017

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-chloro-3-dihydroxy-1b,5,5-tetramethyl-octahydro-H-naphtho[1,8a-b]oxirene--carboxylic acid

> <ALOGPS_LOGP>
1.32

> <JCHEM_LOGP>
0.8859758973333329

> <ALOGPS_LOGS>
-2.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.982769686949386

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.381293217848923

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0540988710981303

> <JCHEM_POLAR_SURFACE_AREA>
90.29

> <JCHEM_REFRACTIVITY>
75.1053

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.99e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-chloro-3-dihydroxy-1b,5,5-tetramethyl-hexahydronaphtho[1,8a-b]oxirene--carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -1.517   0.267   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.527  -1.447   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.667   3.080   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.011   3.490   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.991   3.490   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   12 Cl   UNK     0       6.668   2.310   0.000  0.00  0.00          Cl+0
HETATM   13  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667  -1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   18                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5    7                                                       
CONECT    7    6    5    8   16                                             
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15    7   17   18                                             
CONECT   17   16                                                            
CONECT   18   16    2   19                                                  
CONECT   19   18   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
4-Chloro-3-dihydroxy-1b,5,5-tetramethyl-octahydro-H-naphtho[1,8a-b]oxirene--carboxylate	Generator

Chemical Formula

C₁₅H₂₃ClO₅

Average Mass

318.7900 Da

Monoisotopic Mass

318.12340 Da

IUPAC Name

4-chloro-3-dihydroxy-1b,5,5-tetramethyl-octahydro-H-naphtho[1,8a-b]oxirene--carboxylic acid

Traditional Name

4-chloro-3-dihydroxy-1b,5,5-tetramethyl-hexahydronaphtho[1,8a-b]oxirene--carboxylic acid

CAS Registry Number

Not Available

SMILES

CC1(O)CC2OC22C(C)(C)C(Cl)C(O)CC2(C)C1C(O)=O

InChI Identifier

InChI=1S/C15H23ClO5/c1-12(2)10(16)7(17)5-13(3)9(11(18)19)14(4,20)6-8-15(12,13)21-8/h7-10,17,20H,5-6H2,1-4H3,(H,18,19)

InChI Key

QUHIFZVMNSLMAB-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as abscisic acids and derivatives. These are terpene compounds containing the abscisic acid moiety, which is characterized by a 3-methylpenta-2,4-dienoic acid attached to the C1 carbon of a 4-oxocyclohex-2-ene moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Abscisic acids and derivatives

Alternative Parents

Substituents

Abscisic acid
Oxepane
Cyclic alcohol
Tertiary alcohol
Chlorohydrin
Halohydrin
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Dialkyl ether
Ether
Oxirane
Hydrocarbon derivative
Alcohol
Organic oxide
Organic oxygen compound
Organohalogen compound
Organochloride
Carbonyl group
Alkyl halide
Alkyl chloride
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	1.32	ALOGPS
logP	0.89	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	4.38	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	90.29 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	75.11 m³·mol⁻¹	ChemAxon
Polarizability	31.89 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

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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

73062602

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid (NP0211542)

MOL for NP0211542 (7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid)

3D MOL for NP0211542 (7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid)

3D SDF for NP0211542 (7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid)

3D-SDF for NP0211542 (7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid)

PDB for NP0211542 (7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid)

3D PDB for NP0211542 (7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid)

SMILES for NP0211542 (7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid)

INCHI for NP0211542 (7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid)

Structure for NP0211542 (7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid)

3D Structure for NP0211542 (7-chloro-3,6-dihydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid)