Citation 88660

YOKOSUKA,A: MIMAKI,Y: SAKAGAMI,H: SASHIDA,Y:. (2002). NEW DIARYLHEPTANOIDS AND DIARYLHEPTANOID GLUCOSIDES FROM THE RHIZOMES OF TACCA CHANTRIERI AND THEIR CYTOTOXIC ACTIVITY.. 65(3)

Citation Details

Title	NEW DIARYLHEPTANOIDS AND DIARYLHEPTANOID GLUCOSIDES FROM THE RHIZOMES OF TACCA CHANTRIERI AND THEIR CYTOTOXIC ACTIVITY.
Authors	YOKOSUKA,A: MIMAKI,Y: SAKAGAMI,H: SASHIDA,Y:
Year	2002
Volume	65
Issue	3

Summary

Year: 2002

Journal: Unknown

Organisms and Their Experiments (1)

Tacca chantrieri (TACCACEAE)

Experiment #	Pharmacology Type	Worktypes	Compound	Results
1	Not specified	VOUCHER SPECIMEN REPORTED FOR	None	None
2	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL):	None
3	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL):	ACTIVE
4	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL):	INACTIVE
5	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL):	INACTIVE
6	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS-(3-4-DIHYDROXY-PHENYL):	None
7	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS-(3-4-DIHYDROXY-PHENYL):	ACTIVE
8	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS-(3-4-DIHYDROXY-PHENYL):	INACTIVE
9	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS-(3-4-DIHYDROXY-PHENYL):	INACTIVE
10	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL): 3-O-BETA-GLUCOPYRANOSIDE	None
11	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL): 3-O-BETA-GLUCOPYRANOSIDE	WEAK ACTIVITY
12	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL): 3-O-BETA-GLUCOPYRANOSIDE	INACTIVE
13	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL): 3-O-BETA-GLUCOPYRANOSIDE	INACTIVE
14	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL): 5-O-BETA-D-GLUCOPYRANOSIDE	None
15	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL): 5-O-BETA-D-GLUCOPYRANOSIDE	WEAK ACTIVITY
16	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL): 5-O-BETA-D-GLUCOPYRANOSIDE	WEAK ACTIVITY
17	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(3-4-DIHYDROXY-PHENYL)-7-(4-HYDROXY-PHENYL): 5-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
18	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(4-HYDROXY-3-METHOXY-PHENYL)-7-(4-HYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	None
19	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(4-HYDROXY-3-METHOXY-PHENYL)-7-(4-HYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
20	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(4-HYDROXY-3-METHOXY-PHENYL)-7-(4-HYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
21	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(4-HYDROXY-3-METHOXY-PHENYL)-7-(4-HYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
22	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(3-4-DIHYDROXY-PHENYL: 3-O-BETA-D-GLUCOPYRANOSIDE	None
23	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(3-4-DIHYDROXY-PHENYL: 3-O-BETA-D-GLUCOPYRANOSIDE	ACTIVE
24	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(3-4-DIHYDROXY-PHENYL: 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
25	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(3-4-DIHYDROXY-PHENYL: 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
26	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(4-HYDROXY-3-METHOXY-PHENYL)-7-(3-4-DIHYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	None
27	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(4-HYDROXY-3-METHOXY-PHENYL)-7-(3-4-DIHYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	ACTIVE
28	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(4-HYDROXY-3-METHOXY-PHENYL)-7-(3-4-DIHYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
29	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-(4-HYDROXY-3-METHOXY-PHENYL)-7-(3-4-DIHYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
30	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(4-HYDROXY-3-METHOXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	None
31	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(4-HYDROXY-3-METHOXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
32	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(4-HYDROXY-3-METHOXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
33	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(4-HYDROXY-3-METHOXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
34	Not specified	UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(4-HYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	None
35	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(4-HYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
36	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(4-HYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE
37	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	HEPTANE,3(R)-5(R)-DIHYDROXY-1-7-BIS(4-HYDROXY-PHENYL): 3-O-BETA-D-GLUCOPYRANOSIDE	INACTIVE

Citation 88660

Citation Details

Summary

Organisms and Their Experiments (1)

Tacca chantrieri (TACCACEAE)

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