Citation 88636

MOREL,C: HAY,AE: LITAUDON,M: SEVENET,T: SERAPHIN,D: BRUNETON,J: RICHOMME,P:. (2002). THIRTEEN NEW XANTHONE DERIVATIVES FROM CALOPHYLLUM CALEDONICUM (CLUSIACEAE).. 7(1)

Citation Details

Title	THIRTEEN NEW XANTHONE DERIVATIVES FROM CALOPHYLLUM CALEDONICUM (CLUSIACEAE).
Authors	MOREL,C: HAY,AE: LITAUDON,M: SEVENET,T: SERAPHIN,D: BRUNETON,J: RICHOMME,P:
Year	2002
Volume	7
Issue	1

Summary

Year: 2002

Journal: Unknown

Organisms and Their Experiments (1)

Calophyllum caledonicum (CLUSIACEAE)

Experiment #	Pharmacology Type	Worktypes	Compound	Results
1	Not specified	VOUCHER SPECIMEN REPORTED FORUV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	XANTHONE,5-HYDROXY-8-METHOXY:	None
2	DIURETIC ACTIVITY	MEDICINAL FOLKLORE REPORTED FOR	None	None
3	ANTIYEAST ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	XANTHONE,5-HYDROXY-8-METHOXY:XANTHONE,3-5-DIHYDROXY-1-2-JDIMETHOXY:XANTHONE,1-8-DIHYDROXY-6-7-DIMETHOXY:XANTHONE,5-7-DIHYDROXY-2-6-DIMETHOXY:XANTHONE,6-8-DIHYDROXY-3-7-DIMETHOXY:XANTHONE,2-5-6-7-8-PENTAHYDROXY:XANTHONE,1-3-TRIHYDROXY-5-7-DIMETHOXY:CALEDONIXANTHONE GCALEDONIXANTHONE HCALEDONIXANTHONE ICALEDONIXANTHONE JCALEDONIXANTHONE KCALEDONIXANTHONE L	INACTIVE
4	ANTIFUNGAL ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	XANTHONE,5-HYDROXY-8-METHOXY:XANTHONE,3-5-DIHYDROXY-1-2-JDIMETHOXY:XANTHONE,1-8-DIHYDROXY-6-7-DIMETHOXY:XANTHONE,5-7-DIHYDROXY-2-6-DIMETHOXY:XANTHONE,6-8-DIHYDROXY-3-7-DIMETHOXY:XANTHONE,2-5-6-7-8-PENTAHYDROXY:XANTHONE,1-3-TRIHYDROXY-5-7-DIMETHOXY:CALEDONIXANTHONE GCALEDONIXANTHONE HCALEDONIXANTHONE ICALEDONIXANTHONE JCALEDONIXANTHONE KCALEDONIXANTHONE L	INACTIVE
5	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	XANTHONE,3-5-DIHYDROXY-1-2-JDIMETHOXY:	None
6	Not specified	QUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	XANTHONE,1-8-DIHYDROXY-6-7-DIMETHOXY:	None
7	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	XANTHONE,5-7-DIHYDROXY-2-6-DIMETHOXY:	None
8	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	XANTHONE,6-8-DIHYDROXY-3-7-DIMETHOXY:	None
9	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	XANTHONE,2-5-6-7-8-PENTAHYDROXY:	None
10	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	XANTHONE,1-3-TRIHYDROXY-5-7-DIMETHOXY:	None
11	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURECD SPECTRUM REPORTED FOR	CALEDONIXANTHONE G	None
12	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	CALEDONIXANTHONE H	None
13	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	CALEDONIXANTHONE I	None
14	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	CALEDONIXANTHONE J	None
15	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	CALEDONIXANTHONE K	None
16	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	CALEDONIXANTHONE L	None

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