NP-MRD: Showing NP-Card for (3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione (NP0219232)

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Record Information

Version

2.0

Created at

2022-09-05 20:09:39 UTC

Updated at

2022-09-05 20:09:39 UTC

NP-MRD ID

NP0219232

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione

Description

(3R,4aR,9aR)-4a,7-dihydroxy-3-[(2S)-1-hydroxypropan-2-yl]-2,3,4,4a,9,9a-hexahydro-1H-xanthene-4,9-dione 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. (3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione is found in Ganoderma applanatum. Based on a literature review very few articles have been published on (3R,4aR,9aR)-4a,7-dihydroxy-3-[(2S)-1-hydroxypropan-2-yl]-2,3,4,4a,9,9a-hexahydro-1H-xanthene-4,9-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
   -3.7522   -0.5893    1.5702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3829    0.4444    0.5585 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5452    0.7138   -0.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9125   -0.4655   -0.9975 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1432    0.0269   -0.1753 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7128    1.0263   -1.2142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4481    0.4582   -1.8741 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6271    0.4853   -0.8467 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9627    0.1310   -1.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2574   -0.0269   -2.5517 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0246   -0.0506   -0.3608 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3658   -0.0854   -0.6881 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3482   -0.2589    0.2658 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6745   -0.2846   -0.1286 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9985   -0.4036    1.5916 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6607   -0.3701    1.9280 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6623   -0.1943    0.9623 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3178   -0.1615    1.3074 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3250   -0.4281    0.3319 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3706   -1.7491   -0.0410 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0250   -0.1067    0.8227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2167    0.0435    1.9989 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7858   -0.2025    2.6087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7234   -1.0882    1.2909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9997   -1.4025    1.5602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1630    1.3918    1.1320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4082    0.9972    0.2989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3799    1.5461   -1.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8203   -0.3453   -1.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2749   -0.9566   -0.6584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3477    1.9339   -0.6544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4831    1.2618   -1.9468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1639    1.0946   -2.7122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6601   -0.5963   -2.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6938    1.5297   -0.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6034    0.0326   -1.7472 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4439   -0.4074    0.5132 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7485   -0.5432    2.3773 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3664   -0.4843    2.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8974   -1.9162   -0.8594 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
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  6
 19 21  1  0
 21 22  2  0
 21  5  1  0
 19  8  1  0
 17 11  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  1
  3 27  1  0
  3 28  1  0
  4 29  1  0
  5 30  1  6
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  1
 12 36  1  0
 14 37  1  0
 15 38  1  0
 16 39  1  0
 20 40  1  0
M  END


  Mrv1652309052222092D          

 22 24  0  0  1  0            999 V2000
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  1  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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    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
    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 O   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
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    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
    2.1434   -3.7125    0.0000 O   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
  5  2  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  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  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0219232

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CO)[C@H]1CC[C@@H]2C(=O)C3=CC(O)=CC=C3O[C@@]2(O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H18O6/c1-8(7-17)10-3-4-12-14(19)11-6-9(18)2-5-13(11)22-16(12,21)15(10)20/h2,5-6,8,10,12,17-18,21H,3-4,7H2,1H3/t8-,10-,12-,16-/m1/s1

> <INCHI_KEY>
YNHPWMXJGUOPOK-ISTPORRPSA-N

> <FORMULA>
C16H18O6

> <MOLECULAR_WEIGHT>
306.314

> <EXACT_MASS>
306.1103383

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
31.083460587439635

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,4aR,9aR)-4a,7-dihydroxy-3-[(2S)-1-hydroxypropan-2-yl]-2,3,4,4a,9,9a-hexahydro-1H-xanthene-4,9-dione

> <JCHEM_LOGP>
1.6857141766666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.864843127341855

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.093832913948757

> <JCHEM_PKA_STRONGEST_BASIC>
-2.599777391798173

> <JCHEM_POLAR_SURFACE_AREA>
104.06

> <JCHEM_REFRACTIVITY>
76.94359999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4aR,9aR)-4a,7-dihydroxy-3-[(2S)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.000  -7.700   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      12.003  -2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.335  -6.160   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    5                                                  
CONECT    3    2    4                                                       
CONECT    4    3                                                            
CONECT    5    2    6   21                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    8   20   21                                             
CONECT   20   19                                                            
CONECT   21   19    5   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₈O₆

Average Mass

306.3140 Da

Monoisotopic Mass

306.11034 Da

IUPAC Name

(3R,4aR,9aR)-4a,7-dihydroxy-3-[(2S)-1-hydroxypropan-2-yl]-2,3,4,4a,9,9a-hexahydro-1H-xanthene-4,9-dione

Traditional Name

(3R,4aR,9aR)-4a,7-dihydroxy-3-[(2S)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione

CAS Registry Number

Not Available

SMILES

C[C@H](CO)[C@H]1CC[C@@H]2C(=O)C3=CC(O)=CC=C3O[C@@]2(O)C1=O

InChI Identifier

InChI=1S/C16H18O6/c1-8(7-17)10-3-4-12-14(19)11-6-9(18)2-5-13(11)22-16(12,21)15(10)20/h2,5-6,8,10,12,17-18,21H,3-4,7H2,1H3/t8-,10-,12-,16-/m1/s1

InChI Key

YNHPWMXJGUOPOK-ISTPORRPSA-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
Ganoderma applanatum	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
Aryl ketone
Aryl alkyl ketone
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Cyclic alcohol
Ketone
Hemiacetal
Oxacycle
Hydrocarbon derivative
Organic oxide
Primary alcohol
Organooxygen compound
Alcohol
Organic oxygen compound
Carbonyl group
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	1.69	ChemAxon
pKa (Strongest Acidic)	9.09	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	76.94 m³·mol⁻¹	ChemAxon
Polarizability	31.08 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

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FoodDB ID

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KNApSAcK ID

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Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

162981031

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for (3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione (NP0219232)

MOL for NP0219232 ((3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione)

3D MOL for NP0219232 ((3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione)

3D SDF for NP0219232 ((3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione)

3D-SDF for NP0219232 ((3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione)

PDB for NP0219232 ((3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione)

3D PDB for NP0219232 ((3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione)

SMILES for NP0219232 ((3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione)

INCHI for NP0219232 ((3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione)

Structure for NP0219232 ((3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione)

3D Structure for NP0219232 ((3r,4ar,9ar)-4a,7-dihydroxy-3-[(2s)-1-hydroxypropan-2-yl]-1,2,3,9a-tetrahydroxanthene-4,9-dione)