|  Home  |Search   |  Browse  |Similarity   |Data Visualization  |Submission  |Contact Us  |  












   



                  Page - 1 of 3                  Record - 1 of 68   [TOP]
Compound ID2305
Compound Structure
Plant SourcePelargonium reniforme     Common Name:
Source FamilyGeraniaceae
OriginAfrica
Plant Part UsedTuber
ExtractN - hexane
Target BacteriaMycobacterium aurum, Mycobacterium smegmatis, Mycobacterium fortuitum, Mycobacterium abscessus, Mycobacterium phlei
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationTuberculosis, coughs
PubMed ID [Source Literature]15194133
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) 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 68   [TOP]
Compound ID2306
Compound Structure
DOWNLOAD:
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 - 3 of 68   [TOP]
Compound ID2864
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 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 - 4 of 68   [TOP]
Compound ID2865
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/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 - 5 of 68   [TOP]
Compound ID2866
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 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 68   [TOP]
Compound ID2867
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/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 - 7 of 68   [TOP]
Compound ID2868
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 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 68   [TOP]
Compound ID2869
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 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 - 9 of 68   [TOP]
Compound ID2870
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 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 68   [TOP]
Compound ID2871
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/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 68   [TOP]
Compound ID2872
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 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 - 12 of 68   [TOP]
Compound ID2873
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 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 - 13 of 68   [TOP]
Compound ID2874
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 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 68   [TOP]
Compound ID2875
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 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 - 15 of 68   [TOP]
Compound ID2876
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/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 68   [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 - 17 of 68   [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 - 18 of 68   [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 - 19 of 68   [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 - 20 of 68   [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 - 21 of 68   [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 - 22 of 68   [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 - 23 of 68   [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 - 24 of 68   [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 - 25 of 68   [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


Developed by: CSIR- OSDD Unit, Delhi, India and Hosted by: Bioinformatics Centre,   Institute of Microbial Technology, Sec-39A, Chandigarh, India.
The website has been tested on the latest version of Google Chrome (34.0.1847.137 m) and Mozilla Firefox (29.0.1)