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                  Page - 1 of 1                  Record - 1 of 17   [TOP]
Compound ID2899
Compound Structure
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Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 27 294)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 2 of 17   [TOP]
Compound ID2900
Compound Structure
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Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 35822) (Isoniazid resistant)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml3.12 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 3 of 17   [TOP]
Compound ID2901
Compound Structure
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Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 35838) (Rifampin resistant)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml6.25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 4 of 17   [TOP]
Compound ID2902
Compound Structure
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Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 35820) (Streptomycin resistant)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml3.12 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 5 of 17   [TOP]
Compound ID2903
Compound Structure
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Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 35837) (Ethambutol resistant)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml6.25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 6 of 17   [TOP]
Compound ID2904
Compound Structure
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Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (Clinical isolate MMDO)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml3.12 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 7 of 17   [TOP]
Compound ID2905
Compound Structure
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Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (clinical isolate MTY650)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml6.25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 8 of 17   [TOP]
Compound ID2906
Compound Structure
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Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (clinical isolate MTY663)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 9 of 17   [TOP]
Compound ID2907
Compound Structure
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Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (clinical isolate MTY675)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 10 of 17   [TOP]
Compound ID2908
Compound Structure
DOWNLOAD:
Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (clinical isolate MTY282)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 11 of 17   [TOP]
Compound ID2909
Compound Structure
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Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (Clinical isolate HG8)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml3.12 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 12 of 17   [TOP]
Compound ID2910
Compound Structure
DOWNLOAD:
Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (Clinical isolate SIN3)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml6.25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 13 of 17   [TOP]
Compound ID2911
Compound Structure
DOWNLOAD:
Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (clinical isolate MTY234)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 14 of 17   [TOP]
Compound ID2912
Compound Structure
DOWNLOAD:
Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (clinical isolate MTY112)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 15 of 17   [TOP]
Compound ID2913
Compound Structure
DOWNLOAD:
Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (clinical isolate MTY559)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal

                  Record - 16 of 17   [TOP]
Compound ID2914
Compound Structure
DOWNLOAD:
Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (Clinical isolate SIN4)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml3.12 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal, farzana-shamsudeen-shamsudeen

                  Record - 17 of 17   [TOP]
Compound ID2915
Compound Structure
DOWNLOAD:
Plant SourceAristolochia taliscana Hook.     Common Name:Dutchman's Pipes
Source FamilyAristolochiaceae
OriginMexico
Plant Part UsedRoot
ExtractN - hexane
Target BacteriaMycobacterium tuberculosis (clinical isolate MTY172)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin A
PubChem ID   6442393
Ethnomedicinal InformationCough and snake bites
PubMed ID [Source Literature]20209328
Extract PreparationPowdered air - dried roots (1.5 kg) were macerated (3 × 48 h) with 12 l of n - Hexane. The extract was filtered and evaporated in vacuo to yield 33 g of the crude extract
Chemical Classification [Active Compound]Aromatic, Tricyclic, Furanoid, Alkene, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]J774A.1 murine macrophage cell line (ATCC HB - 197) using the trypan blue exclusion test
Molecular Weight326.152
Molecular FormulaC20H22O4
SMILESO1[C@H]([C@@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc(OC)c(O)cc1
XLogP4.363
PSA47.920
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count4
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) León-Díaz R, Meckes M, Said-Fernández S, Molina-Salinas GM, Vargas-Villarreal J, Torres J, Luna-Herrera J, Jiménez-Arellanes A.Antimycobacterial neolignans isolated from Aristolochia taliscana.Mem Inst Oswaldo Cruz. 2010 Feb;105(1):45-51

CuratorVikramjitmandal, farzana-shamsudeen-shamsudeen


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