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












   



                  Page - 1 of 21                  Record - 1 of 506   [TOP]
Compound ID2852
Compound StructureN/A
Plant SourceCananga odorata     Common Name:Ylang - Ylang Cananga Tree, Macassar - Oil Plant, Perfume Tree
Source FamilyAnnonaceae
OriginColombia
Plant Part UsedFlower
ExtractFlower extract (1.2 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneColorimetric Macrodilution Method, following the protocol described by Abate et al. (1998)
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml300 ± 217 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - assisted hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorReshmi

                  Record - 2 of 506   [TOP]
Compound ID2853
Compound StructureN/A
Plant SourceHyptis mutabilis     Common Name:Tropical Bushmint
Source FamilyLamiaceae
OriginColombia
Plant Part UsedLeaf, stem
ExtractLeaf and stem (0.3 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneColorimetric Macrodilution Method, following the protocol described by Abate et al. (1998)
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml125 ± 0.01 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - assisted hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorReshmi, KeyaMukherjee

                  Record - 3 of 506   [TOP]
Compound ID2854
Compound StructureN/A
Plant SourceLippia alba     Common Name:Bushy Matgrass
Source FamilyVerbenaceae
OriginColombia
Plant Part UsedLeaf, stem
ExtractLeaf and stem (2.5 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneColorimetric Macrodilution Method, following the protocol described by Abate et al. (1998)
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml200 ± 72 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - assisted hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorReshmi

                  Record - 4 of 506   [TOP]
Compound ID2855
Compound StructureN/A
Plant SourceLippia alba     Common Name:Bushy Matgrass
Source FamilyVerbenaceae
OriginColombia
Plant Part UsedLeaf, stem
ExtractLeaf and stem extract (1.6 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneColorimetric Macrodilution Method, following the protocol described by Abate et al. (1998)
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml130 ± 95 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - assisted hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorReshmi

                  Record - 5 of 506   [TOP]
Compound ID2856
Compound StructureN/A
Plant SourceLippia origanoides     Common Name:Wild Marjoram
Source FamilyVerbenaceae
OriginColombia
Plant Part UsedLeaf, stem
ExtractLeaf and stem (3.1 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMTT assay
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml125 ± 0.01 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - Assisted Hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorKeya Mukherjee, reshmi

                  Record - 6 of 506   [TOP]
Compound ID2857
Compound StructureN/A
Plant SourceLippia origanoides     Common Name:Wild Marjoram
Source FamilyVerbenaceae
OriginColombia
Plant Part UsedLeaf, stem
ExtractLeaf and stem (3.1 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMTT assay
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml125 ± 0.01 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - Assisted Hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorKeya Mukherjee, reshmi

                  Record - 7 of 506   [TOP]
Compound ID2858
Compound StructureN/A
Plant SourceLippia origanoides     Common Name:Wild Marjoram
Source FamilyVerbenaceae
OriginColombia
Plant Part UsedLeaf, stem
ExtractLeaf and stem (1.5 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneColorimetric Macrodilution Method, following the protocol described by Abate et al. (1998)
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml400 ± 220 µg.ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - Assisted Hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorReshmi

                  Record - 8 of 506   [TOP]
Compound ID2859
Compound StructureN/A
Plant SourcePiper auritum     Common Name:Mexican Pepper Leaves
Source FamilyPiperaceae
OriginColombia
Plant Part UsedLeaf
ExtractLeaf (2.3 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneColorimetric Macrodilution Method, following the protocol described by Abate et al. (1998)
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml400 ± 220 µg.ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - Assisted Hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorReshmi

                  Record - 9 of 506   [TOP]
Compound ID2860
Compound StructureN/A
Plant SourcePiper bogotense     Common Name:NR
Source FamilyPiperaceae
OriginColombia
Plant Part UsedLeaf
ExtractLeaf (0.2 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneColorimetric Macrodilution Method, following the protocol described by Abate et al. (1998)
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml130 ± 95 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - Assisted Hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorReshmi

                  Record - 10 of 506   [TOP]
Compound ID2861
Compound StructureN/A
Plant SourceSwinglea glutinosa     Common Name:Tabog, Glutinous Swinglea
Source FamilyRutaceae
OriginColombia
Plant Part UsedFruit peel
ExtractFruit peel (0.7 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneColorimetric Macrodilution Method, following the protocol described by Abate et al. (1998)
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml100 ± 36 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - Assisted Hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorVikramjitmandal, reshmi

                  Record - 11 of 506   [TOP]
Compound ID2862
Compound Structure
DOWNLOAD:
Plant SourceHelichrysum aureonitens     Common Name:Golden Everlasting
Source FamilyAsteraceae (Compositae)
OriginAfrica
Plant Part UsedCallus tissue from young leaf
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 27264)
Assay / Test DoneRadiorespirometric BACTEC Assay
Positive Control Used (conc.)Isoniazid (0.2 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml1000 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound Identified4 - Chloro - 2 - (Hepta - 1, 3, 5 - Triyn - 1 - yl) - Phenol
PubChem IDNR
Ethnomedicinal InformationAnticancer activity, inhibition on DNA topoisomerase I
PubMed ID [Source Literature]19881282
Extract PreparationCell suspension culture
Chemical Classification [Active Compound]Aromatic, Alkyl, Alkyne, Phenol, Haloginated
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]Against Vero and Human prostate epithelial carcinoma DU 145 cell lines
Molecular Weight214.019
Molecular FormulaC13H7ClO
SMILESC1(cc(c(cc1)O)C#CC#CC#CC)Cl
XLogP3.971
PSA20.230
H-bond Donor1
H-bond Acceptor2
No. of Rotatable Bond Count0
No. of Rings1
No. of N0
No. of O1
No. of S0
Reference(s)1) Ziaratnia SM, Ohyama K, Hussein AA, Muranaka T, Lall N, Kunert KJ, Meyer JJ.Isolation and identification of a novel chlorophenol from a cell suspension culture of Helichrysum aureonitens.Chem Pharm Bull (Tokyo). 2009 Nov;57(11):1282-3

CuratorGppreetha, keyamukherjee, reshmi

                  Record - 12 of 506   [TOP]
Compound ID2863
Compound Structure
DOWNLOAD:
Plant SourceCurcuma longa     Common Name:Turmeric
Source FamilyZingiberaceae
OriginSoutheast Asian countries
Plant Part UsedDried rhizome
Extract
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneNR
Positive Control Used (conc.)NR
Inhibition [%]NR
Activity [MIC] µg/ml1961 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedDemethoxycurcumin
PubChem ID   5324476
Ethnomedicinal InformationFolk medicine, Antioxidant, anti - HIV, antimutagenic, antiangiogenic, antimalarial, antitubercular, antiandrogenic, COX inhibitory activities
PubMed ID [Source Literature]20027668
Extract PreparationNR
Chemical Classification [Active Compound]Aromatic, Alkene, Curcuminoid, Ether, Phenol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]NR
Molecular Weight338.115
Molecular FormulaC20H18O5
SMILESO(c1cc(ccc1O)/C=C/C(=C/C(=O)/C=C/c1ccc(O)cc1)/O)C
XLogP3.610
PSA86.990
H-bond Donor3
H-bond Acceptor5
No. of Rotatable Bond Count6
No. of Rings2
No. of N0
No. of O5
No. of S0
Reference(s)1) Agrawal DK, Mishra PK.Curcumin and its analogues: potential anticancer agents.Med Res Rev. 2010 Sep;30(5):818-60

CuratorReshmi

                  Record - 13 of 506   [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 - 14 of 506   [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 - 15 of 506   [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 - 16 of 506   [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 - 17 of 506   [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 - 18 of 506   [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 - 19 of 506   [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 - 20 of 506   [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 - 21 of 506   [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 - 22 of 506   [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 - 23 of 506   [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 - 24 of 506   [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 - 25 of 506   [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


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)