NP-MRD: Showing NP-Card for (2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one (NP0255316)

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Record Information

Version

2.0

Created at

2022-09-07 19:46:11 UTC

Updated at

2022-09-07 19:46:11 UTC

NP-MRD ID

NP0255316

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one

Description

(2S)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1H,2H,6H-furo[2,3-c]xanthen-6-one belongs to the class of organic compounds known as 8-prenylated xanthones. These are organic compounds containing a C5-isoprenoid group linked to a xanthone moiety at the 8-position. Xanthone is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring that carries a ketone group. (2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one is found in Garcinia xanthochymus. Based on a literature review very few articles have been published on (2S)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1H,2H,6H-furo[2,3-c]xanthen-6-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072221462D          

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 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 11 22  1  0  0  0  0
 22 23  2  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 15 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 32 35  1  0  0  0  0
 31 36  1  0  0  0  0
 14 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0255316

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=C(O)C(O)=C2OC3=C4C[C@H](OC4=CC(O)=C3C(=O)C2=C1CCC(C)(C)O)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C28H34O8/c1-13(2)7-8-15-14(9-10-27(3,4)33)20-23(31)21-17(29)12-18-16(11-19(35-18)28(5,6)34)25(21)36-26(20)24(32)22(15)30/h7,12,19,29-30,32-34H,8-11H2,1-6H3/t19-/m0/s1

> <INCHI_KEY>
JGHVJKITVFRFAO-IBGZPJMESA-N

> <FORMULA>
C28H34O8

> <MOLECULAR_WEIGHT>
498.572

> <EXACT_MASS>
498.225368055

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
54.980915301890334

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1H,2H,6H-furo[2,3-c]xanthen-6-one

> <JCHEM_LOGP>
5.0395770419999995

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.687117674758277

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.5001157573676664

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6303688379261327

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
137.023

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1H,2H-furo[2,3-c]xanthen-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.443  -7.777   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.977  -6.309   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.015  -5.172   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.527  -5.979   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.993  -4.511   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.497  -4.180   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.963  -2.713   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.924  -1.575   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.467  -2.382   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.933  -0.914   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.505  -3.520   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.009  -3.189   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.048  -4.326   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.552  -3.996   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.590  -5.133   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.124  -6.601   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.620  -6.932   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.154  -8.399   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.582  -5.794   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.078  -6.125   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.612  -7.593   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.039  -4.987   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.535  -5.318   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.069  -6.786   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.565  -7.116   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.099  -8.584   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.368  -8.118   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.567  -9.050   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       0.634 -10.052   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      11.992  -4.497   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      11.821  -2.967   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.958  -1.929   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.096  -0.890   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.997  -3.066   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      11.920  -0.791   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      10.313  -2.657   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   22                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15   36                                                  
CONECT   15   14   16   30                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   13   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   11   23                                                  
CONECT   23   22    6   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26                                                            
CONECT   30   15   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33   34   35                                             
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   32                                                            
CONECT   36   31   14                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₄O₈

Average Mass

498.5720 Da

Monoisotopic Mass

498.22537 Da

IUPAC Name

(2S)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1H,2H,6H-furo[2,3-c]xanthen-6-one

Traditional Name

(2S)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1H,2H-furo[2,3-c]xanthen-6-one

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C(O)C(O)=C2OC3=C4C[C@H](OC4=CC(O)=C3C(=O)C2=C1CCC(C)(C)O)C(C)(C)O

InChI Identifier

InChI=1S/C28H34O8/c1-13(2)7-8-15-14(9-10-27(3,4)33)20-23(31)21-17(29)12-18-16(11-19(35-18)28(5,6)34)25(21)36-26(20)24(32)22(15)30/h7,12,19,29-30,32-34H,8-11H2,1-6H3/t19-/m0/s1

InChI Key

JGHVJKITVFRFAO-IBGZPJMESA-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
Garcinia xanthochymus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 8-prenylated xanthones. These are organic compounds containing a C5-isoprenoid group linked to a xanthone moiety at the 8-position. Xanthone is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring that carries a ketone group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

8-prenylated xanthones

Alternative Parents

Substituents

2-prenylated xanthone
8-prenylated xanthone
Chromone
Coumaran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Pyran
Benzenoid
Heteroaromatic compound
Tertiary alcohol
Vinylogous acid
Polyol
Ether
Oxacycle
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
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	5.04	ChemAxon
pKa (Strongest Acidic)	7.5	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	137.02 m³·mol⁻¹	ChemAxon
Polarizability	54.98 Å³	ChemAxon
Number of Rings	4	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

162984817

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one (NP0255316)

MOL for NP0255316 ((2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one)

3D MOL for NP0255316 ((2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one)

3D SDF for NP0255316 ((2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one)

3D-SDF for NP0255316 ((2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one)

PDB for NP0255316 ((2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one)

3D PDB for NP0255316 ((2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one)

SMILES for NP0255316 ((2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one)

INCHI for NP0255316 ((2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one)

Structure for NP0255316 ((2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one)

3D Structure for NP0255316 ((2s)-5,9,10-trihydroxy-7-(3-hydroxy-3-methylbutyl)-2-(2-hydroxypropan-2-yl)-8-(3-methylbut-2-en-1-yl)-1h,2h-furo[2,3-c]xanthen-6-one)