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Compound ID3973
Compound Structure
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Plant SourceRudbeckia laciniata     Common Name:Thimbleweed
Source FamilyAsteraceae (Compositae)
OriginEastern North America
Plant Part Used
Extract
Target BacteriaMycobacterium avium
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/mlNR
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified2,10-bisaboladiene- 1,4-endoperoxide
PubChem ID   10082849
Ethnomedicinal Information
PubMed ID [Source Literature]16243360
Extract Preparation
Chemical Classification [Active Compound]Alicyclic, Terpene, Sesquiterpene, Peroxy, Prenylated
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight236.178
Molecular FormulaC15H24O2
SMILESO1O[C@@H]2C[C@@H](C(CCC=C(C)C)C)[C@@H]1C=C2C
XLogP4.400
PSA18.460
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count4
No. of Rings0
No. of N0
No. of O2
No. of S0
Reference(s)1) Pauli GF, Case RJ, Inui T, Wang Y, Cho S, Fischer NH, Franzblau SG.New perspectives on natural products in TB drug research.Life Sci. 2005 Dec 22;78(5):485-94

Curator

                  Record - 2 of 2   [TOP]
Compound ID3118
Compound Structure
DOWNLOAD:
Plant SourceRudbeckia laciniata     Common Name:Thimbleweed
Source FamilyAsteraceae (Compositae)
OriginEastern North America
Plant Part UsedNR
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)NR
Inhibition [%]NR
Activity [MIC] µg/mlNR
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound Identified2,10-bisaboladiene- 1,4-endoperoxide
PubChem ID   10082849
Ethnomedicinal InformationNR
PubMed ID [Source Literature]16243360
Extract PreparationNR
Chemical Classification [Active Compound]Alicyclic, Terpene, Sesquiterpene, Peroxy, Prenylated
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]NR
Molecular Weight236.178
Molecular FormulaC15H24O2
SMILESO1O[C@@H]2C[C@@H](C(CCC=C(C)C)C)[C@@H]1C=C2C
XLogP4.400
PSA18.460
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count4
No. of Rings0
No. of N0
No. of O2
No. of S0
Reference(s)1) Pauli GF, Case RJ, Inui T, Wang Y, Cho S, Fischer NH, Franzblau SG.New perspectives on natural products in TB drug research.Life Sci. 2005 Dec 22;78(5):485-94

CuratorKeyaMukherjee, reshmi


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