NP-MRD: Showing NP-Card for (3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate (NP0151175)

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Record Information

Version

2.0

Created at

2022-09-02 07:27:22 UTC

Updated at

2022-09-02 07:27:22 UTC

NP-MRD ID

NP0151175

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate

Description

(3,5,6-Trihydroxy-4-{7-methyl-1-oxo-1H,3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-1H,3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carboxylate belongs to the class of organic compounds known as saccharolipids. Saccharolipids are compounds in which fatty acids are linked directly to a sugar backbone, forming structures that are compatible with membrane bilayers. In the saccharolipids, a sugar substitutes for the glycerol backbone that is present in glycerolipids and glycerophospholipids. The most familiar saccharolipids contain an acylated glucosamine. (3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate is found in Linaria japonica. In contrast to others glycolipids, the fatty acid is not glycosidically linked to the sugar moiety (3,5,6-trihydroxy-4-{7-methyl-1-oxo-1H,3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-1H,3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171515382D          

 38 42  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004171515382D          

 38 42  0  0  0  0            999 V2000
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    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1355    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  2  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 26 36  1  0  0  0  0
 31 36  1  0  0  0  0
 22 37  1  0  0  0  0
 16 37  1  0  0  0  0
 37 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0151175

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C2C(CC1)C(COC2=O)C(=O)OCC1OC(O)C(O)C(OC(=O)C2COC(=O)C3=C(C)CCC23)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C26H32O12/c1-10-3-5-12-14(7-34-24(31)17(10)12)22(29)36-9-16-19(27)21(20(28)26(33)37-16)38-23(30)15-8-35-25(32)18-11(2)4-6-13(15)18/h12-16,19-21,26-28,33H,3-9H2,1-2H3

> <INCHI_KEY>
HGDABMUUBCWUFX-UHFFFAOYSA-N

> <FORMULA>
C26H32O12

> <MOLECULAR_WEIGHT>
536.53

> <EXACT_MASS>
536.18937647

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
54.11005226124488

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3,5,6-trihydroxy-4-{7-methyl-1-oxo-1H,3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-1H,3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carboxylate

> <ALOGPS_LOGP>
0.08

> <JCHEM_LOGP>
0.6178078046666671

> <ALOGPS_LOGS>
-2.31

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.841938807023517

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.302192724408192

> <JCHEM_PKA_STRONGEST_BASIC>
-3.663875243726469

> <JCHEM_POLAR_SURFACE_AREA>
175.12

> <JCHEM_REFRACTIVITY>
125.08859999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.65e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3,5,6-trihydroxy-4-{7-methyl-1-oxo-3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       4.060  17.341   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.584  15.876   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.120  15.400   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.120  13.860   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.584  13.384   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.489  14.630   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.786  13.090   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.548  13.860   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.548  15.400   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.786  16.170   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.786  17.710   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.786  11.550   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.548  10.780   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       2.120  10.780   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.120   9.240   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.453   8.470   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.787   9.240   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.121   8.470   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.454   9.240   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.121   6.930   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.454   6.160   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.787   6.160   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.787   4.620   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       7.454   4.620   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.454   0.000   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.121  -2.310   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.846  -1.941   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.453   6.930   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       2.120   6.160   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4   10                                                  
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    2                                                       
CONECT    7    4    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    3   11                                                  
CONECT   11   10                                                            
CONECT   12    7   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   37                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   37                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   36                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   36                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   26   31                                                  
CONECT   37   22   16   38                                                  
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   84    0
END

View in JSmol

Synonyms

Value	Source
(3,5,6-Trihydroxy-4-{7-methyl-1-oxo-1H,3H,4H,4ah,5H,6H-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-1H,3H,4H,4ah,5H,6H-cyclopenta[c]pyran-4-carboxylic acid	Generator

Chemical Formula

C₂₆H₃₂O₁₂

Average Mass

536.5300 Da

Monoisotopic Mass

536.18938 Da

IUPAC Name

(3,5,6-trihydroxy-4-{7-methyl-1-oxo-1H,3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-1H,3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carboxylate

Traditional Name

(3,5,6-trihydroxy-4-{7-methyl-1-oxo-3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3H,4H,4aH,5H,6H-cyclopenta[c]pyran-4-carboxylate

CAS Registry Number

Not Available

SMILES

CC1=C2C(CC1)C(COC2=O)C(=O)OCC1OC(O)C(O)C(OC(=O)C2COC(=O)C3=C(C)CCC23)C1O

InChI Identifier

InChI=1S/C26H32O12/c1-10-3-5-12-14(7-34-24(31)17(10)12)22(29)36-9-16-19(27)21(20(28)26(33)37-16)38-23(30)15-8-35-25(32)18-11(2)4-6-13(15)18/h12-16,19-21,26-28,33H,3-9H2,1-2H3

InChI Key

HGDABMUUBCWUFX-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
Linaria japonica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as saccharolipids. Saccharolipids are compounds in which fatty acids are linked directly to a sugar backbone, forming structures that are compatible with membrane bilayers. In the saccharolipids, a sugar substitutes for the glycerol backbone that is present in glycerolipids and glycerophospholipids. The most familiar saccharolipids contain an acylated glucosamine. In contrast to others glycolipids, the fatty acid is not glycosidically linked to the sugar moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Saccharolipids

Sub Class

Not Available

Direct Parent

Saccharolipids

Alternative Parents

Substituents

Saccharolipid
Tetracarboxylic acid or derivatives
Delta valerolactone
Delta_valerolactone
Monosaccharide
Oxane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Hemiacetal
Lactone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Polyol
Carboxylic acid derivative
Organooxygen compound
Alcohol
Carbonyl group
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
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	0.08	ALOGPS
logP	0.62	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	11.3	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	175.12 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	125.09 m³·mol⁻¹	ChemAxon
Polarizability	54.11 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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 (3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate (NP0151175)

MOL for NP0151175 ((3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate)

3D MOL for NP0151175 ((3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate)

3D SDF for NP0151175 ((3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate)

3D-SDF for NP0151175 ((3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate)

PDB for NP0151175 ((3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate)

3D PDB for NP0151175 ((3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate)

SMILES for NP0151175 ((3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate)

INCHI for NP0151175 ((3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate)

Structure for NP0151175 ((3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate)

3D Structure for NP0151175 ((3,5,6-trihydroxy-4-{7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carbonyloxy}oxan-2-yl)methyl 7-methyl-1-oxo-3h,4h,4ah,5h,6h-cyclopenta[c]pyran-4-carboxylate)