Citation 89480

DAI,JQ: LIU,ZL: YANG,L:. (2002). NON-GLYCOSIDIC IRIDOIDS FROM CYMBARIA MONGOLICA.. 59(5)

Citation Details

Title	NON-GLYCOSIDIC IRIDOIDS FROM CYMBARIA MONGOLICA.
Authors	DAI,JQ: LIU,ZL: YANG,L:
Year	2002
Volume	59
Issue	5

Summary

Year: 2002

Journal: Unknown

Organisms and Their Experiments (1)

Cymbaria mongolica (SCROPHULARIACEAE)

Experiment #	Pharmacology Type	Worktypes	Compound	Results
1	Not specified	VOUCHER SPECIMEN REPORTED FOR	None	None
2	Not specified	MASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4S-4AS-7S-7AS):	None
3	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4S-4AS-7S-7AS):	INACTIVE
4	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4S-4AS-7S-7AS):	INACTIVE
5	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4S-4AS-7S-7AS):	INACTIVE
6	ANTIBACTERIAL ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4S-4AS-7S-7AS):PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1S-4R-4AS-7S-7AS):PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4R-4AS-7S-7AS):PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-HYDROXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4S-4AS-7AS):REHMAGLUTIN DALYXIALACTONE,4-EPI:BOONEIN,ISO:GARDENDIOLMUSSAENIN A	ACTIVE
7	ANTIBACTERIAL ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4S-4AS-7S-7AS):PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1S-4R-4AS-7S-7AS):PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4R-4AS-7S-7AS):PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-HYDROXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4S-4AS-7AS):REHMAGLUTIN DALYXIALACTONE,4-EPI:BOONEIN,ISO:GARDENDIOLMUSSAENIN A	ACTIVE
8	ANTIBACTERIAL ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4S-4AS-7S-7AS):PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1S-4R-4AS-7S-7AS):PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4R-4AS-7S-7AS):PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-HYDROXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4S-4AS-7AS):REHMAGLUTIN DALYXIALACTONE,4-EPI:BOONEIN,ISO:GARDENDIOLMUSSAENIN A	ACTIVE
9	Not specified	MASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1S-4R-4AS-7S-7AS):	None
10	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1S-4R-4AS-7S-7AS):	INACTIVE
11	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1S-4R-4AS-7S-7AS):	INACTIVE
12	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1S-4R-4AS-7S-7AS):	INACTIVE
13	Not specified	MASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4R-4AS-7S-7AS):	None
14	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4R-4AS-7S-7AS):	INACTIVE
15	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4R-4AS-7S-7AS):	INACTIVE
16	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,7-HYDROXY-4-HYDROXY-METHYL-7-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA[E]: (1R-4R-4AS-7S-7AS):	INACTIVE
17	Not specified	MASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):	None
18	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):	INACTIVE
19	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):	INACTIVE
20	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):	INACTIVE
21	Not specified	MASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-HYDROXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):	None
22	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-HYDROXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):	INACTIVE
23	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-HYDROXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):	EQUIVOCAL
24	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-HYDROXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4R-4AS-7AS):	INACTIVE
25	Not specified	MASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4S-4AS-7AS):	None
26	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4S-4AS-7AS):	INACTIVE
27	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4S-4AS-7AS):	INACTIVE
28	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	PYRAN-3-ONE,4-7-DIHYDROXY-METHYL-1-METHOXY-1-METHOXY-1-4-4(A)-7(A)-TETRAHYDRO-CYCLOPENTA-6-ENE[E]: (1R-4S-4AS-7AS):	INACTIVE
29	Not specified	ISOLATION AND IDENTIFICATION OFQUANTITATIVE DATA	MUSSAENIN A	None
30	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	MUSSAENIN A	INACTIVE
31	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	MUSSAENIN A	INACTIVE
32	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	MUSSAENIN A	INACTIVE
33	Not specified	ISOLATION AND IDENTIFICATION OFQUANTITATIVE DATA	GARDENDIOL	None
34	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	GARDENDIOL	INACTIVE
35	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	GARDENDIOL	INACTIVE
36	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	GARDENDIOL	INACTIVE
37	Not specified	ISOLATION AND IDENTIFICATION OFQUANTITATIVE DATA	BOONEIN,ISO:	None
38	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	BOONEIN,ISO:	INACTIVE
39	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	BOONEIN,ISO:	INACTIVE
40	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	BOONEIN,ISO:	INACTIVE
41	Not specified	ISOLATION AND IDENTIFICATION OFQUANTITATIVE DATA	ALYXIALACTONE,4-EPI:	None
42	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	ALYXIALACTONE,4-EPI:	INACTIVE
43	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	ALYXIALACTONE,4-EPI:	INACTIVE
44	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	ALYXIALACTONE,4-EPI:	INACTIVE
45	Not specified	ISOLATION AND IDENTIFICATION OFQUANTITATIVE DATA	REHMAGLUTIN D	None
46	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	REHMAGLUTIN D	EQUIVOCAL
47	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	REHMAGLUTIN D	INACTIVE
48	CYTOTOXIC ACTIVITY	PHARMACOLOGY OF COMPOUND - IN VITRO	REHMAGLUTIN D	INACTIVE

Citation 89480

Citation Details

Summary

Organisms and Their Experiments (1)

Cymbaria mongolica (SCROPHULARIACEAE)

Show SPARQL Queries (1)

Query 1