NP-MRD: Showing NP-Card for Morellic acid (NP0071509)

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Record Information

Version

2.0

Created at

2022-04-28 16:53:03 UTC

Updated at

2022-04-28 16:53:03 UTC

NP-MRD ID

NP0071509

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Morellic acid

Description

Morellic acid, also known as morellate, belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system. Morellic acid is found in Garcinia dulcis , Garcinia gaudichaudii, Garcinia hanburyi , Garcinia lateriflora, Garcinia morella and Garcinia tetralata. Morellic acid was first documented in 2007 (PMID: 17396587). Based on a literature review a significant number of articles have been published on Morellic acid (PMID: 31377565) (PMID: 26608681) (PMID: 27216998) (PMID: 26071609) (PMID: 24335612) (PMID: 21067206).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282218532D          

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M  END

     RDKit          3D

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M  END


  Mrv1652304282218532D          

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    2.7061    1.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0084    1.4703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6735    2.7350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1339    1.9671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3522    1.0669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7096    1.8630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2268    2.5319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5647    3.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4060    2.4482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8873    1.1313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5771    0.3723    0.0000 C   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  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  1  0  0  0
  8 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
 19 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
 22 27  1  1  0  0  0
 16 27  1  0  0  0  0
 19 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 30 34  1  0  0  0  0
  7 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
  1 40  1  0  0  0  0
  1 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0071509

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=C2O[C@@]34[C@H]5C[C@@H](C=C3C(=O)C2=C(O)C2=C1OC(C)(C)C=C2)C(=O)[C@]4(C\C=C(\C)C(O)=O)OC5(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C33H36O8/c1-16(2)8-9-20-26-19(11-12-30(4,5)39-26)24(34)23-25(35)21-14-18-15-22-31(6,7)41-32(28(18)36,13-10-17(3)29(37)38)33(21,22)40-27(20)23/h8,10-12,14,18,22,34H,9,13,15H2,1-7H3,(H,37,38)/b17-10-/t18-,22+,32+,33-/m1/s1

> <INCHI_KEY>
COVMVPHACFXMAX-OYNOKLRGSA-N

> <FORMULA>
C33H36O8

> <MOLECULAR_WEIGHT>
560.643

> <EXACT_MASS>
560.241018119

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
59.08629090074061

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2Z)-4-[(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-en-1-yl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.0^{2,15}.0^{2,19}.0^{4,13}.0^{6,11}]docosa-4,6(11),9,12,15-pentaen-19-yl]-2-methylbut-2-enoic acid

> <ALOGPS_LOGP>
4.62

> <JCHEM_LOGP>
6.046089143666666

> <ALOGPS_LOGS>
-5.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.582151616184376

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.756892258520436

> <JCHEM_PKA_STRONGEST_BASIC>
-4.135570183967039

> <JCHEM_POLAR_SURFACE_AREA>
119.36

> <JCHEM_REFRACTIVITY>
155.43600000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.47e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2Z)-4-[(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-en-1-yl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.0^{2,15}.0^{2,19}.0^{4,13}.0^{6,11}]docosa-4,6(11),9,12,15-pentaen-19-yl]-2-methylbut-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      14.310   0.448   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.687  -1.045   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.583  -2.119   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.101  -1.699   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.724  -0.206   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      12.828   0.867   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      10.242   0.214   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.138  -0.860   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.515  -2.353   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.997  -2.772   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      11.488  -4.335   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.479  -3.559   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.910  -5.145   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.011  -2.956   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.200  -4.322   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.784  -3.677   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.499  -2.800   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.971  -3.410   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.373  -1.440   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.235  -1.477   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.587  -0.547   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.202  -0.435   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.090   0.700   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.075  -0.476   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.821   2.461   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.654   1.659   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.245  -2.167   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.071   0.424   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.475   1.311   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.414   2.850   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.051   3.567   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.749   2.745   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       4.991   5.105   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       7.717   3.672   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.991   1.992   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.658   3.478   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       9.757   4.726   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      10.387   6.131   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.225   4.570   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      14.723   2.112   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      16.011   0.695   0.000  0.00  0.00           C+0
CONECT    1    2    6   40   41                                             
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   35                                                  
CONECT    8    7    9   21                                                  
CONECT    9    8   10   12                                                  
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    9   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   27                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   24   28                                             
CONECT   20   19   14   21   22                                             
CONECT   21   20    8                                                       
CONECT   22   20   23   27                                                  
CONECT   23   22   24   25   26                                             
CONECT   24   23   19                                                       
CONECT   25   23                                                            
CONECT   26   23                                                            
CONECT   27   22   16                                                       
CONECT   28   19   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   34                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   30                                                            
CONECT   35    7   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40    1                                                            
CONECT   41    1                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   92    0
END

View in JSmol

Synonyms

Value	Source
Morellate	Generator

Chemical Formula

C₃₃H₃₆O₈

Average Mass

560.6430 Da

Monoisotopic Mass

560.24102 Da

IUPAC Name

(2Z)-4-[(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-en-1-yl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.0^{2,15}.0^{2,19}.0^{4,13}.0^{6,11}]docosa-4,6(11),9,12,15-pentaen-19-yl]-2-methylbut-2-enoic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C2O[C@@]34[C@H]5C[C@@H](C=C3C(=O)C2=C(O)C2=C1OC(C)(C)C=C2)C(=O)[C@]4(C\C=C(\C)C(O)=O)OC5(C)C

InChI Identifier

InChI=1S/C33H36O8/c1-16(2)8-9-20-26-19(11-12-30(4,5)39-26)24(34)23-25(35)21-14-18-15-22-31(6,7)41-32(28(18)36,13-10-17(3)29(37)38)33(21,22)40-27(20)23/h8,10-12,14,18,22,34H,9,13,15H2,1-7H3,(H,37,38)/b17-10-/t18-,22+,32+,33-/m1/s1

InChI Key

COVMVPHACFXMAX-OYNOKLRGSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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 dulcis	Plant	KNApSAcK
Garcinia gaudichaudii	Plant	KNApSAcK
Garcinia hanburyi	Plant	KNApSAcK
Garcinia lateriflora	LOTUS Database	35616633
Garcinia morella	Plant	KNApSAcK
Garcinia tetralata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Pyranoxanthones

Alternative Parents

Substituents

Pyranoxanthone
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
Aromatic monoterpenoid
Monoterpenoid
Aryl ketone
Alkyl aryl ether
Cyclohexenone
Oxepane
Phenol
Benzenoid
Oxolane
Vinylogous acid
Ketone
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid
Carboxylic acid derivative
Oxacycle
Carbonyl group
Organic oxygen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
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	4.62	ALOGPS
logP	6.05	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	3.76	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	155.44 m³·mol⁻¹	ChemAxon
Polarizability	59.09 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

C00030538

Chemspider ID

26347021

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54580250

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Pan LY, Wang YS, Liu XH, Wang N, Xu W, Xiu YF: Pharmacokinetic comparison of five xanthones in rat plasma after oral administration of crude and processed Garcinia hanburyi extracts. J Chromatogr B Analyt Technol Biomed Life Sci. 2019 Sep 15;1126-1127:121737. doi: 10.1016/j.jchromb.2019.121737. Epub 2019 Jul 26. [PubMed:31377565 ]
Xu M, Fu W, Zhang B, Tan H, Xiu Y, Xu H: Combinative application of pH-zone-refining and conventional high-speed counter-current chromatography for preparative separation of caged polyprenylated xanthones from gamboge. J Sep Sci. 2016 Feb;39(3):559-65. doi: 10.1002/jssc.201500996. Epub 2015 Dec 21. [PubMed:26608681 ]
Chaiyakunvat P, Anantachoke N, Reutrakul V, Jiarpinitnun C: Caged xanthones: Potent inhibitors of global predominant MRSA USA300. Bioorg Med Chem Lett. 2016 Jul 1;26(13):2980-2983. doi: 10.1016/j.bmcl.2016.05.030. Epub 2016 May 11. [PubMed:27216998 ]
Li Y, Zhang Q, Jiang D: Validation of an HPLC-MS-MS assay for determination of morellic acid in rat plasma: application to pharmacokinetic studies. J Chromatogr Sci. 2015 Nov-Dec;53(10):1695-700. doi: 10.1093/chromsci/bmv073. Epub 2015 Jun 12. [PubMed:26071609 ]
Yang J, He S, Li S, Zhang R, Peng A, Chen L: In vitro and in vivo antiangiogenic activity of caged polyprenylated xanthones isolated from Garcinia hanburyi Hook. f. Molecules. 2013 Dec 11;18(12):15305-13. doi: 10.3390/molecules181215305. [PubMed:24335612 ]
Ren Y, Yuan C, Chai HB, Ding Y, Li XC, Ferreira D, Kinghorn AD: Absolute configuration of (-)-gambogic acid, an antitumor agent. J Nat Prod. 2011 Mar 25;74(3):460-3. doi: 10.1021/np100422z. Epub 2010 Nov 10. [PubMed:21067206 ]
Ren Y, Lantvit DD, Carcache de Blanco EJ, Kardono LB, Riswan S, Chai H, Cottrell CE, Farnsworth NR, Swanson SM, Ding Y, Li XC, Marais JP, Ferreira D, Kinghorn AD: Proteasome-inhibitory and cytotoxic constituents of Garcinia lateriflora: absolute configuration of caged xanthones. Tetrahedron. 2010 Jul 17;66(29):5311-5320. doi: 10.1016/j.tet.2010.05.010. [PubMed:20730041 ]
Li SL, Song JZ, Han QB, Qiao CF, Xu HX: Improved high-performance liquid chromatographic method for simultaneous determination of 12 cytotoxic caged xanthones in gamboges, a potential anticancer resin from Garcinia hanburyi. Biomed Chromatogr. 2008 Jun;22(6):637-44. doi: 10.1002/bmc.981. [PubMed:18254140 ]
Song JZ, Yip YK, Han QB, Qiao CF, Xu HX: Rapid determination of polyprenylated xanthones in gamboge resin of Garcinia hanburyi by HPLC. J Sep Sci. 2007 Feb;30(3):304-9. doi: 10.1002/jssc.200600294. [PubMed:17396587 ]
Reutrakul V, Anantachoke N, Pohmakotr M, Jaipetch T, Sophasan S, Yoosook C, Kasisit J, Napaswat C, Santisuk T, Tuchinda P: Cytotoxic and anti-HIV-1 caged xanthones from the resin and fruits of Garcinia hanburyi. Planta Med. 2007 Jan;73(1):33-40. doi: 10.1055/s-2006-951748. Epub 2006 Nov 21. [PubMed:17117343 ]

Showing NP-Card for Morellic acid (NP0071509)

MOL for NP0071509 (Morellic acid)

3D MOL for NP0071509 (Morellic acid)

3D SDF for NP0071509 (Morellic acid)

3D-SDF for NP0071509 (Morellic acid)

PDB for NP0071509 (Morellic acid)

3D PDB for NP0071509 (Morellic acid)

SMILES for NP0071509 (Morellic acid)

INCHI for NP0071509 (Morellic acid)

Structure for NP0071509 (Morellic acid)

3D Structure for NP0071509 (Morellic acid)