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                  Page - 1 of 1                  Record - 1 of 3   [TOP]
Compound ID3680
Compound Structure
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Plant SourceEvodia rutaecarpa (Juss.) Benth.     Common Name:
Source FamilyRutaceae
Origin
Plant Part UsedUnripe Fruit
ExtractN - hexane
Target BacteriaMycobacterium fortuitum (ATCC 6841)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (16 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml2 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1 - Methyl - 4 - Methylidene - 2 - [(8E) - Tridec - 8 - En - 1 - Yl] - 1, 4 - Dihydroquinoline
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]16051468
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Quinolone, Alkene, Alkaloid
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight339.256
Molecular FormulaC23H33NO
SMILESCCCC/C=C/CCCCCCCc1cc(=O)c2c(cccc2)n1C
XLogP8.152
PSA17.070
H-bond Donor0
H-bond Acceptor1
No. of Rotatable Bond Count11
No. of Rings2
No. of N1
No. of O1
No. of S0
Reference(s)1) Adams M, Wube AA, Bucar F, Bauer R, Kunert O, Haslinger E.Quinolone alkaloids from Evodia rutaecarpa: a potent new group of antimycobacterial compounds.Int J Antimicrob Agents. 2005 Sep;26(3):262-4

CuratorVsheeba, vikramjitmandal

                  Record - 2 of 3   [TOP]
Compound ID3685
Compound Structure
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Plant SourceEvodia rutaecarpa (Juss.) Benth.     Common Name:
Source FamilyRutaceae
Origin
Plant Part UsedUnripe Fruit
ExtractN - hexane
Target BacteriaMycobacterium smegmatis (ATCC 19429)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (1 µg/ml), Isoniazid (4 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml2 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1 - Methyl - 4 - Methylidene - 2 - [(8E) - Tridec - 8 - En - 1 - Yl] - 1, 4 - Dihydroquinoline
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]16051468
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Quinolone, Alkene, Alkaloid
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight339.256
Molecular FormulaC23H33NO
SMILESCCCC/C=C/CCCCCCCc1cc(=O)c2c(cccc2)n1C
XLogP8.152
PSA17.070
H-bond Donor0
H-bond Acceptor1
No. of Rotatable Bond Count11
No. of Rings2
No. of N1
No. of O1
No. of S0
Reference(s)1) Adams M, Wube AA, Bucar F, Bauer R, Kunert O, Haslinger E.Quinolone alkaloids from Evodia rutaecarpa: a potent new group of antimycobacterial compounds.Int J Antimicrob Agents. 2005 Sep;26(3):262-4

CuratorVsheeba, vikramjitmandal

                  Record - 3 of 3   [TOP]
Compound ID3690
Compound Structure
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Plant SourceEvodia rutaecarpa (Juss.) Benth.     Common Name:
Source FamilyRutaceae
Origin
Plant Part UsedUnripe Fruit
ExtractN - hexane
Target BacteriaMycobacterium phlei (ATCC 19249)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (2 µg/ml), Isoniazid (4 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml2 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified1 - Methyl - 4 - Methylidene - 2 - [(8E) - Tridec - 8 - En - 1 - Yl] - 1, 4 - Dihydroquinoline
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]16051468
Extract Preparation
Chemical Classification [Active Compound]Aromatic, Quinolone, Alkene, Alkaloid
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight339.256
Molecular FormulaC23H33NO
SMILESCCCC/C=C/CCCCCCCc1cc(=O)c2c(cccc2)n1C
XLogP8.152
PSA17.070
H-bond Donor0
H-bond Acceptor1
No. of Rotatable Bond Count11
No. of Rings2
No. of N1
No. of O1
No. of S0
Reference(s)1) Adams M, Wube AA, Bucar F, Bauer R, Kunert O, Haslinger E.Quinolone alkaloids from Evodia rutaecarpa: a potent new group of antimycobacterial compounds.Int J Antimicrob Agents. 2005 Sep;26(3):262-4

CuratorVsheeba, vikramjitmandal


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