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                  Page - 1 of 3                  Record - 1 of 52   [TOP]
Compound ID1207
Compound Structure
Plant SourceAristolochia cauliflora Ule     Common Name:
Source FamilyAristolochiaceae
OriginPeru
Plant Part UsedStem
ExtractDichloromethane
Target BacteriaMycobacterium tuberculosis (ATCC 27294)
Assay / Test DoneBACTEC 460 (Becton Dickinson Diagnostic Instrument Systems, Sparks MD) Radiometric Assay
Positive Control Used (conc.)Ethambutol (2 µg/ml) and Ethambutol (7.5 µg/ml)
Inhibition [%]81 %
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]13678239
Extract PreparationN/A
Chemical Classification [Active Compound]N/A
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Reference(s)1) Graham JG, Pendland SL, Prause JL, Danzinger LH, Schunke Vigo J, Cabieses F, Farnsworth NR.Antimycobacterial evaluation of Peruvian plants.Phytomedicine. 2003;10(6-7):528-35

Curator

                  Record - 2 of 52   [TOP]
Compound ID2864
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/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedEupomatenoid 7
PubChem IDNR
Ethnomedicinal InformationNR
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 Weight324.136
Molecular FormulaC20H20O4
SMILESC1c(cc(c2c1c(c(o2)c1cc(c(cc1)O)OC)C)OC)/C=C/C
XLogP4.461
PSA51.830
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 52   [TOP]
Compound ID2865
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/ml50 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2866
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/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2867
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/ml50 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2868
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/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2869
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/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2870
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/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2871
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/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2872
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 B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2873
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 B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2874
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 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 B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2875
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/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2876
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 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/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2877
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/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 52   [TOP]
Compound ID2878
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/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 - 17 of 52   [TOP]
Compound ID2879
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/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 - 18 of 52   [TOP]
Compound ID2880
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/ml50 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal InformationNR
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, Tetracyclic, Benzofuranoid, Ether
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 Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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 - 19 of 52   [TOP]
Compound ID2881
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 Done
Positive Control Used (conc.)Streptomycin (0.5 µg/ml), Isoniazid (0.06 µg/ml), Rifampin (0.1 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedLicarin B
PubChem ID   5384942
Ethnomedicinal Information
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, Tetracyclic, Benzofuranoid, Ether
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight324.136
Molecular FormulaC20H20O4
SMILESO1C([C@H](c2c1c(OC)cc(c2)/C=C/C)C)c1cc2OCOc2cc1
XLogP4.809
PSA36.920
H-bond Donor0
H-bond Acceptor4
No. of Rotatable Bond Count3
No. of Rings4
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

Curator

                  Record - 20 of 52   [TOP]
Compound ID2883
Compound Structure
DOWNLOAD:
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 IdentifiedEupomatenoid 7
PubChem IDNR
Ethnomedicinal InformationNR
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 Weight324.136
Molecular FormulaC20H20O4
SMILESC1c(cc(c2c1c(c(o2)c1cc(c(cc1)O)OC)C)OC)/C=C/C
XLogP4.461
PSA51.830
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 - 21 of 52   [TOP]
Compound ID2884
Compound Structure
DOWNLOAD:
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/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedEupomatenoid 7
PubChem IDNR
Ethnomedicinal InformationNR
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 Weight324.136
Molecular FormulaC20H20O4
SMILESC1c(cc(c2c1c(c(o2)c1cc(c(cc1)O)OC)C)OC)/C=C/C
XLogP4.461
PSA51.830
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 - 22 of 52   [TOP]
Compound ID2885
Compound Structure
DOWNLOAD:
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/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedEupomatenoid 7
PubChem IDNR
Ethnomedicinal InformationNR
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 Weight324.136
Molecular FormulaC20H20O4
SMILESC1c(cc(c2c1c(c(o2)c1cc(c(cc1)O)OC)C)OC)/C=C/C
XLogP4.461
PSA51.830
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 - 23 of 52   [TOP]
Compound ID2886
Compound Structure
DOWNLOAD:
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/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedEupomatenoid 7
PubChem IDNR
Ethnomedicinal InformationNR
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 Weight324.136
Molecular FormulaC20H20O4
SMILESC1c(cc(c2c1c(c(o2)c1cc(c(cc1)O)OC)C)OC)/C=C/C
XLogP4.461
PSA51.830
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 - 24 of 52   [TOP]
Compound ID2887
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 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/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedEupomatenoid 7
PubChem IDNR
Ethnomedicinal InformationNR
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 Weight324.136
Molecular FormulaC20H20O4
SMILESC1c(cc(c2c1c(c(o2)c1cc(c(cc1)O)OC)C)OC)/C=C/C
XLogP4.461
PSA51.830
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 - 25 of 52   [TOP]
Compound ID2888
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 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/ml50 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedEupomatenoid 7
PubChem IDNR
Ethnomedicinal InformationNR
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 Weight324.136
Molecular FormulaC20H20O4
SMILESC1c(cc(c2c1c(c(o2)c1cc(c(cc1)O)OC)C)OC)/C=C/C
XLogP4.461
PSA51.830
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


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