Citation 90565

SHEN,YC: WANG,CH: CHENG,YB: WANG,LT: GUH,JH: CHIEN,CT: KHALIL,AT:. (2004). NEW CYTOTOXIC CLERODANE DITERPENOIDS FROM THE LEAVES AND TWIGS OF CASEARIA MEMBRANACEA.. 67(3)

Citation Details

TitleNEW CYTOTOXIC CLERODANE DITERPENOIDS FROM THE LEAVES AND TWIGS OF CASEARIA MEMBRANACEA.
AuthorsSHEN,YC: WANG,CH: CHENG,YB: WANG,LT: GUH,JH: CHIEN,CT: KHALIL,AT:
Year2004
Volume67
Issue3

Summary

Year: 2004

Journal: Unknown

Organisms and Their Experiments (2)

Unknown organism

Experiment #Pharmacology TypeWorktypesCompoundResults
1
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CLERODA-3-13(16)-14-TRIENE,18-19-EPOXY-18-19-DIACETOXY-2-HYDROXY-2-(2-METHYL-BUTANOYL-OXY): 6-O-NICOTINYL ESTER*
WEAK ACTIVITY
2
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CLERODA-3-13(16)-14-TRIENE,18-19-EPOXY-18-19-DIACETOXY-2-HYDROXY-2-(2-METHYL-BUTANOYL-OXY): 6-O-NICOTINYL ESTER*
WEAK ACTIVITY
3
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN D-6-O-ACETYL ESTER*
WEAK ACTIVITY
4
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN D-6-O-ACETYL ESTER*
WEAK ACTIVITY

Casearia membranacea (FLACOURTIACEAE)

Experiment #Pharmacology TypeWorktypesCompoundResults
1Not specified
VOUCHER SPECIMEN REPORTED FOR
NoneNone
2
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF EXTRACT - IN VITRO
None
ACTIVE
3Not specified
UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE
CASEAMEMBRIN A
None
4
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN A
ACTIVE
5
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN A
ACTIVE
6Not specified
UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE
CASEAMEMBRIN B
None
7
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN B
WEAK ACTIVITY
8
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN B
WEAK ACTIVITY
9Not specified
UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE
CASEAMEMBRIN C
None
10
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN C
ACTIVE
11
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN C
ACTIVE
12Not specified
UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE
CASEAMEMBRIN C
None
13
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN C
ACTIVE
14
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN C
ACTIVE
15Not specified
UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE
CASEAMEMBRIN E
None
16
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN E
ACTIVE
17
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN E
ACTIVE
18Not specified
UV SPECTRUM GIVEN FORMASS-SPECTRAL FRAGMENTATION REPORTEDPMR SPECTRUM REPORTEDCMR SPECTRUM REPORTEDINFRARED SPECTRUM REPORTED FORQUANTITATIVE DATAISOLATION OF A COMPOUND WITH NOVEL STRUCTURE
CASEAMEMBRIN F
None
19
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN F
ACTIVE
20
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CASEAMEMBRIN F
WEAK ACTIVITY
21Not specified
ISOLATION AND IDENTIFICATION OFQUANTITATIVE DATA
CLERODA-3-13(16)-14-TRIENE,18-19-EPOXY-18-19-DIACETOXY-6-HYDROXY-2-(2-METHYL-BUTANOYL-OXY): (2S-5R-8S-9S-10R-18S-19R):
None
22
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CLERODA-3-13(16)-14-TRIENE,18-19-EPOXY-18-19-DIACETOXY-6-HYDROXY-2-(2-METHYL-BUTANOYL-OXY): (2S-5R-8S-9S-10R-18S-19R):
ACTIVE
23
CYTOTOXIC ACTIVITY
PHARMACOLOGY OF COMPOUND - IN VITRO
CLERODA-3-13(16)-14-TRIENE,18-19-EPOXY-18-19-DIACETOXY-6-HYDROXY-2-(2-METHYL-BUTANOYL-OXY): (2S-5R-8S-9S-10R-18S-19R):
ACTIVE
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