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                  Page - 1 of 1                  Record - 1 of 6   [TOP]
Compound ID1428
Compound Structure
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Plant SourceChamaedora tepejilote     Common Name:Pacaya Palm
Source FamilyArecaceae (Palmae)
OriginMexico
Plant Part UsedLeaf
ExtractHexane
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneRadiorespirometric BACTEC Assay
Positive Control Used (conc.)
Inhibition [%]99 %
Activity [MIC] µg/ml100 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedUrsolic acid
PubChem ID   64945
Ethnomedicinal InformationCough, Pneumonia
PubMed ID [Source Literature]16041726
Extract PreparationN/A
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, Acid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight456.360
Molecular FormulaC30H48O3
SMILESO[C@@H]1C([C@H]2[C@@]([C@@H]3[C@]([C@]4(C(=CC3)[C@H]3[C@@](CC4)(CC[C@H]([C@@H]3C)C)C(=O)O)C)(CC2)C)(CC1)C)(C)C
XLogP8.954
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count1
No. of Rings5
No. of N0
No. of O3
No. of S0
Reference(s)1) Jiménez A, Meckes M, Alvarez V, Torres J, Parra R. Secondary metabolites from Chamaedora tepejilote (Palmae) are active against Mycobacterium tuberculosis.Phytother Res. 2005 Apr;19(4):320-2

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                  Record - 2 of 6   [TOP]
Compound ID2036
Compound Structure
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Plant SourceLeyssera gnaphaloides L.     Common Name:
Source FamilyAsteraceae (Compositae)
OriginAfrica
Plant Part UsedWhole plant
ExtractHexane
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneDisk Diffusion Assay
Positive Control Used (conc.)Rifampin (2.5 µg/disk)
Inhibition [%]
Activity [MIC] µg/ml5 µg/Disk
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedUrsolic acid
PubChem ID   64945
Ethnomedicinal InformationRespiratory ailments, tuberculosis
PubMed ID [Source Literature]18384988
Extract PreparationN/A
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, Acid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight456.360
Molecular FormulaC30H48O3
SMILESO[C@@H]1C([C@H]2[C@@]([C@@H]3[C@]([C@]4(C(=CC3)[C@H]3[C@@](CC4)(CC[C@H]([C@@H]3C)C)C(=O)O)C)(CC2)C)(CC1)C)(C)C
XLogP8.954
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count1
No. of Rings5
No. of N0
No. of O3
No. of S0
Reference(s)1) Bamuamba K, Gammon DW, Meyers P, Dijoux-Franca MG, Scott G.Anti-mycobacterial activity of five plant species used as traditional medicines in the Western Cape Province (South Africa).J Ethnopharmacol. 2008 May 8;117(2):385-90

Curator

                  Record - 3 of 6   [TOP]
Compound ID2038
Compound Structure
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Plant SourceLeyssera gnaphaloides L.     Common Name:
Source FamilyAsteraceae (Compositae)
OriginAfrica
Plant Part UsedWhole plant
ExtractHexane
Target BacteriaMycobacterium tuberculosis H37Rv, Mycobacterium microti (ATCC 19422)
Assay / Test DoneBioautography on TLC plates
Positive Control Used (conc.)Rifampin (2.5 µg/spot)
Inhibition [%]
Activity [MIC] µg/ml2.5 µg/spot
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedUrsolic acid
PubChem ID   64945
Ethnomedicinal InformationRespiratory ailments, tuberculosis
PubMed ID [Source Literature]18384988
Extract PreparationN/A
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, Acid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight456.360
Molecular FormulaC30H48O3
SMILESO[C@@H]1C([C@H]2[C@@]([C@@H]3[C@]([C@]4(C(=CC3)[C@H]3[C@@](CC4)(CC[C@H]([C@@H]3C)C)C(=O)O)C)(CC2)C)(CC1)C)(C)C
XLogP8.954
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count1
No. of Rings5
No. of N0
No. of O3
No. of S0
Reference(s)1) Bamuamba K, Gammon DW, Meyers P, Dijoux-Franca MG, Scott G.Anti-mycobacterial activity of five plant species used as traditional medicines in the Western Cape Province (South Africa).J Ethnopharmacol. 2008 May 8;117(2):385-90

Curator

                  Record - 4 of 6   [TOP]
Compound ID2039
Compound Structure
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Plant SourceLeyssera gnaphaloides L.     Common Name:
Source FamilyAsteraceae (Compositae)
OriginAfrica
Plant Part UsedWhole plant
ExtractHexane
Target BacteriaMycobacterium avium (ATCC 25291), Mycobacterium scrofulaceum (ATCC 19981)
Assay / Test DoneBioautography on TLC plates
Positive Control Used (conc.)Rifampin (2.5 µg/spot)
Inhibition [%]
Activity [MIC] µg/ml1.25 µg/spot
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedUrsolic acid
PubChem ID   64945
Ethnomedicinal InformationRespiratory ailments, tuberculosis
PubMed ID [Source Literature]18384988
Extract PreparationN/A
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, Acid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight456.360
Molecular FormulaC30H48O3
SMILESO[C@@H]1C([C@H]2[C@@]([C@@H]3[C@]([C@]4(C(=CC3)[C@H]3[C@@](CC4)(CC[C@H]([C@@H]3C)C)C(=O)O)C)(CC2)C)(CC1)C)(C)C
XLogP8.954
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count1
No. of Rings5
No. of N0
No. of O3
No. of S0
Reference(s)1) Bamuamba K, Gammon DW, Meyers P, Dijoux-Franca MG, Scott G.Anti-mycobacterial activity of five plant species used as traditional medicines in the Western Cape Province (South Africa).J Ethnopharmacol. 2008 May 8;117(2):385-90

Curator

                  Record - 5 of 6   [TOP]
Compound ID2959
Compound Structure
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Plant SourceHaloxylon salicornicum Bunge ex Boiss     Common Name:NR
Source FamilyChenopodiaceae
OriginPakistan, Egypt, Jordan, Palestine, Iran, Iraq and Kuwait (in unfertile areas)
Plant Part UsedWhole plant
ExtractNR
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicro Broth Dilution Method
Positive Control Used (conc.)Isoniazid (0.02 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml100 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedUrsolic acid
PubChem ID   64945
Ethnomedicinal InformationNR
PubMed ID [Source Literature]20542692
Extract PreparationMethanol extract further partitioned with water and hexane. The water layer was further extracted with chloroform and subjected to silica gel column chromatography
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, Acid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Molecular Weight456.360
Molecular FormulaC30H48O3
SMILESO[C@@H]1C([C@H]2[C@@]([C@@H]3[C@]([C@]4(C(=CC3)[C@H]3[C@@](CC4)(CC[C@H]([C@@H]3C)C)C(=O)O)C)(CC2)C)(CC1)C)(C)C
XLogP8.954
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count1
No. of Rings5
No. of N0
No. of O3
No. of S0
Reference(s)1) Bibi N, Tanoli SA, Farheen S, Afza N, Siddiqi S, Zhang Y, Kazmi SU, Malik A.In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.Bioorg Med Chem Lett. 2010 Jul 15;20(14):4173-6

CuratorKeyaMukherjee, vsheeba

                  Record - 6 of 6   [TOP]
Compound ID3590
Compound Structure
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Plant SourceCaleolaria pinnifolia Cav.     Common Name:NR
Source FamilyScrophulariaceae
OriginNR
Plant Part UsedAerial
ExtractDichloromethane:Methanol
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 27 294)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.06 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml8 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound Identified3 - Epi - Ursolic Acid
PubChem ID   64945
Ethnomedicinal InformationNR
PubMed ID [Source Literature]12898418
Extract PreparationNR
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, Acid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]NR
Molecular Weight456.360
Molecular FormulaC30H48O3
SMILESO[C@@H]1C([C@H]2[C@@]([C@@H]3[C@]([C@]4(C(=CC3)[C@H]3[C@@](CC4)(CC[C@H]([C@@H]3C)C)C(=O)O)C)(CC2)C)(CC1)C)(C)C
XLogP8.954
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count1
No. of Rings5
No. of N0
No. of O3
No. of S0
Reference(s)1) Woldemichael GM, Franzblau SG, Zhang F, Wang Y, Timmermann BN.Inhibitory effect of sterols from Ruprechtia triflora and diterpenes from Calceolaria pinnifolia on the growth of Mycobacterium tuberculosis.Planta Med. 2003 Jul;69(7):628-31

CuratorReshmi, vikramjitmandal


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