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                  Page - 1 of 1                  Record - 1 of 5   [TOP]
Compound ID2306
Compound Structure
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Plant SourcePelargonium reniforme     Common Name:
Source FamilyGeraniaceae
OriginAfrica
Plant Part UsedTuber
ExtractN - hexane
Target BacteriaMycobacterium aurum
Assay / Test Done
Positive Control Used (conc.)NR
Inhibition [%]
Activity [MIC] µg/ml2 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedLinoleic Acid
PubChem ID   5280450
Ethnomedicinal InformationTuberculosis, coughs
PubMed ID [Source Literature]15194133
Extract PreparationN/A
Chemical Classification [Active Compound]Aliphatic, Alkene, Fatty acid
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight280.240
Molecular FormulaC18H32O2
SMILESOC(=O)CCCCCCC/C=CC/C=CCCCCC
XLogP7.865
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count14
No. of Rings0
No. of N0
No. of O2
No. of S0
Reference(s)1) Seidel V, Taylor PW. In vitro activity of extracts and constituents of Pelagonium against rapidly growing mycobacteria. Int J Antimicrob Agents. 2004, Jun;23(6):613-9

Curator

                  Record - 2 of 5   [TOP]
Compound ID3607
Compound Structure
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Plant SourceHumulus lupulus     Common Name:
Source FamilyCannabaceae
Origin
Plant Part UsedWhole plant
ExtractHexane
Target BacteriaMycobacterium aurum (Pasteur Institute 104482)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (1 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml8 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedLinoleic acid
PubChem ID   5280450
Ethnomedicinal Information
PubMed ID [Source Literature]15478197
Extract Preparation
Chemical Classification [Active Compound]Aliphatic, Alkene, Fatty acid
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight280.240
Molecular FormulaC18H32O2
SMILESOC(=O)CCCCCCC/C=CC/C=CCCCCC
XLogP7.865
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count14
No. of Rings0
No. of N0
No. of O2
No. of S0
Reference(s)1) Stavri M, Schneider R, O'Donnell G, Lechner D, Bucar F, Gibbons S.The antimycobacterial components of hops (Humulus lupulus) and their dereplication.Phytother Res. 2004 Sep;18(9):774-6

CuratorGppreetha, vikramjitmandal

                  Record - 3 of 5   [TOP]
Compound ID3608
Compound Structure
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Plant SourceHumulus lupulus     Common Name:
Source FamilyCannabaceae
Origin
Plant Part UsedWhole plant
ExtractHexane
Target BacteriaMycobacterium fortuitum (ATCC 6841)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (4 µg/ml), Isoniazid (0.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml4 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedLinoleic acid
PubChem ID   5280450
Ethnomedicinal Information
PubMed ID [Source Literature]15478197
Extract Preparation
Chemical Classification [Active Compound]Aliphatic, Alkene, Fatty acid
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight280.240
Molecular FormulaC18H32O2
SMILESOC(=O)CCCCCCC/C=CC/C=CCCCCC
XLogP7.865
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count14
No. of Rings0
No. of N0
No. of O2
No. of S0
Reference(s)1) Stavri M, Schneider R, O'Donnell G, Lechner D, Bucar F, Gibbons S.The antimycobacterial components of hops (Humulus lupulus) and their dereplication.Phytother Res. 2004 Sep;18(9):774-6

CuratorGppreetha, vikramjitmandal

                  Record - 4 of 5   [TOP]
Compound ID3609
Compound Structure
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Plant SourceHumulus lupulus     Common Name:
Source FamilyCannabaceae
Origin
Plant Part UsedWhole plant
ExtractHexane
Target BacteriaMycobacterium phlei (ATCC 11758)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (2 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml8 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedLinoleic acid
PubChem ID   5280450
Ethnomedicinal Information
PubMed ID [Source Literature]15478197
Extract Preparation
Chemical Classification [Active Compound]Aliphatic, Alkene, Fatty acid
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight280.240
Molecular FormulaC18H32O2
SMILESOC(=O)CCCCCCC/C=CC/C=CCCCCC
XLogP7.865
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count14
No. of Rings0
No. of N0
No. of O2
No. of S0
Reference(s)1) Stavri M, Schneider R, O'Donnell G, Lechner D, Bucar F, Gibbons S.The antimycobacterial components of hops (Humulus lupulus) and their dereplication.Phytother Res. 2004 Sep;18(9):774-6

CuratorGppreetha, vikramjitmandal

                  Record - 5 of 5   [TOP]
Compound ID3610
Compound Structure
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Plant SourceHumulus lupulus     Common Name:
Source FamilyCannabaceae
Origin
Plant Part UsedWhole plant
ExtractHexane
Target BacteriaMycobacterium smegmatis (ATCC 14468)
Assay / Test Done
Positive Control Used (conc.)Ethambutol (0.5 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml8 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedLinoleic acid
PubChem ID   5280450
Ethnomedicinal Information
PubMed ID [Source Literature]15478197
Extract Preparation
Chemical Classification [Active Compound]Aliphatic, Alkene, Fatty acid
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight280.240
Molecular FormulaC18H32O2
SMILESOC(=O)CCCCCCC/C=CC/C=CCCCCC
XLogP7.865
PSA37.300
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count14
No. of Rings0
No. of N0
No. of O2
No. of S0
Reference(s)1) Stavri M, Schneider R, O'Donnell G, Lechner D, Bucar F, Gibbons S.The antimycobacterial components of hops (Humulus lupulus) and their dereplication.Phytother Res. 2004 Sep;18(9):774-6

CuratorGppreetha, vikramjitmandal


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