NP-MRD: Showing NP-Card for methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate (NP0171269)

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Record Information

Version

1.0

Created at

2022-09-03 07:42:55 UTC

Updated at

2022-09-03 07:42:55 UTC

NP-MRD ID

NP0171269

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate

Description

Methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate is found in Pseudopestalotiopsis theae and Rhizophora apiculata. Methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
   -2.9998    3.6374   -0.4041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1939    2.4758   -0.4115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6067    1.2431   -0.0555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8668    1.2248    0.3097 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9739   -0.0417    0.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7507   -1.2085   -0.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1694   -2.4468   -0.1035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9380   -3.6078   -0.1952 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3589   -3.5410   -0.2768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8117   -2.6248   -0.0299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0434   -4.1974   -0.0481 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.0364   -1.4913    0.0623 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2623   -1.6423    0.1381 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0763   -0.6235    0.2346 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4450   -0.8524    0.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3402    0.1964    0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7958   -0.0477    0.4950 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8492    1.4719    0.4394 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4704    1.7712    0.3656 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0833    3.0611    0.3982 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6169    0.6763    0.2631 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2434    0.8280    0.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1585    2.0099    0.2138 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6280   -0.2344    0.0771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0281    3.4352   -0.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5875    4.4083    0.2920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0082    4.1324   -1.4111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8199   -1.0960   -0.1483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6624   -3.1989   -1.2890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7147   -2.8143    0.4849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8270   -4.5130   -0.0934 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8505   -1.8613    0.2917 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1142   -0.4334   -0.5099 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9713   -0.7985    1.2933 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3194    0.8916    0.7396 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5074    2.3197    0.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2385    3.4920    0.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  2  0
 10 11  1  0
 10 12  1  0
 12 24  2  0
 24 22  1  0
 22 23  2  0
 22 21  1  0
 21 19  2  0
 19 20  1  0
 19 18  1  0
 18 16  2  0
 16 17  1  0
 16 15  1  0
 15 14  2  0
 14 13  1  0
 24  5  1  0
 14 21  1  0
 13 12  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  6 28  1  0
  9 29  1  0
  9 30  1  0
  9 31  1  0
 20 37  1  0
 18 36  1  0
 17 33  1  0
 17 34  1  0
 17 35  1  0
 15 32  1  0
M  END


  Mrv1533004231522032D          

 24 26  0  0  0  0            999 V2000
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  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
  7 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  5 24  1  0  0  0  0
 12 24  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0171269

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CC(OC)=C(Cl)C2=C1C(=O)C1=C(O)C=C(C)C=C1O2

> <INCHI_IDENTIFIER>
InChI=1S/C17H13ClO6/c1-7-4-9(19)13-10(5-7)24-16-12(15(13)20)8(17(21)23-3)6-11(22-2)14(16)18/h4-6,19H,1-3H3

> <INCHI_KEY>
LXCYTVFSERMJQS-UHFFFAOYSA-N

> <FORMULA>
C17H13ClO6

> <MOLECULAR_WEIGHT>
348.74

> <EXACT_MASS>
348.0400658

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
34.14163126168283

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate

> <ALOGPS_LOGP>
3.61

> <JCHEM_LOGP>
4.269346662666666

> <ALOGPS_LOGS>
-4.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.491410299804636

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7746901244077455

> <JCHEM_POLAR_SURFACE_AREA>
82.06

> <JCHEM_REFRACTIVITY>
87.13169999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.49e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.335  -7.700   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   11 Cl   UNK     0       4.001  -0.770   0.000  0.00  0.00          Cl+0
HETATM   12  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.336  -6.930   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   24                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   24                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   14   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    5   12                                                  
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
Methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxo-9H-xanthene-1-carboxylic acid	Generator
Chloroisosulochrin dehydric acid	Generator

Chemical Formula

C₁₇H₁₃ClO₆

Average Mass

348.7400 Da

Monoisotopic Mass

348.04007 Da

IUPAC Name

methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate

Traditional Name

methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CC(OC)=C(Cl)C2=C1C(=O)C1=C(O)C=C(C)C=C1O2

InChI Identifier

InChI=1S/C17H13ClO6/c1-7-4-9(19)13-10(5-7)24-16-12(15(13)20)8(17(21)23-3)6-11(22-2)14(16)18/h4-6,19H,1-3H3

InChI Key

LXCYTVFSERMJQS-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
Pseudopestalotiopsis theae	LOTUS Database	35616633
Rhizophora apiculata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthones

Alternative Parents

Substituents

Xanthone
Chromone
M-methoxybenzoic acid or derivatives
4-halobenzoic acid or derivatives
Halobenzoic acid or derivatives
Anisole
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Pyran
Aryl chloride
Benzenoid
Aryl halide
Heteroaromatic compound
Vinylogous acid
Methyl ester
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Ether
Hydrocarbon derivative
Organic oxygen compound
Organohalogen compound
Organochloride
Organooxygen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.61	ALOGPS
logP	4.27	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	8.49	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	82.06 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	87.13 m³·mol⁻¹	ChemAxon
Polarizability	34.14 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

11824253

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate (NP0171269)

MOL for NP0171269 (methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate)

3D MOL for NP0171269 (methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate)

3D SDF for NP0171269 (methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate)

3D-SDF for NP0171269 (methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate)

PDB for NP0171269 (methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate)

3D PDB for NP0171269 (methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate)

SMILES for NP0171269 (methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate)

INCHI for NP0171269 (methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate)

Structure for NP0171269 (methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate)

3D Structure for NP0171269 (methyl 4-chloro-8-hydroxy-3-methoxy-6-methyl-9-oxoxanthene-1-carboxylate)