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                  Page - 1 of 1                  Record - 1 of 22   [TOP]
Compound ID1006
Compound Structure
Plant SourceAbuta grandifolia (Mart.) Sandwith     Common Name:
Source FamilyMenispermaceae
OriginPeru
Plant Part UsedLeaf
ExtractDichloromethane
Target BacteriaMycobacterium tuberculosis (ATCC 27294)
Assay / Test DoneBACTEC 460 (Becton Dickinson Diagnostic Instrument Systems, Sparks MD) Radiometric Assay
Positive Control Used (conc.)Rifampin (2 µg/ml), Ethambutol (7.5 µg/ml)
Inhibition [%]57 %
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedN/A
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

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                  Record - 2 of 22   [TOP]
Compound ID1007
Compound Structure
Plant SourceAbuta grandifolia (Mart.) Sandwith     Common Name:
Source FamilyMenispermaceae
OriginPeru
Plant Part UsedRoot, stem
ExtractDichloromethane
Target BacteriaMycobacterium tuberculosis (ATCC 27294)
Assay / Test DoneBACTEC 460 (Becton Dickinson Diagnostic Instrument Systems, Sparks MD) Radiometric Assay
Positive Control Used (conc.)Rifampin (2 µg/ml), Ethambutol (7.5 µg/ml)
Inhibition [%]< 50 %
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedN/A
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

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                  Record - 3 of 22   [TOP]
Compound ID1439
Compound Structure
Plant SourceChondrodendron tomentosum R. & P.     Common Name:
Source FamilyMenispermaceae
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.)Rifampin (2 µg/ml), Ethambutol (7.5 µg/ml)
Inhibition [%]< 50 %
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 - 4 of 22   [TOP]
Compound ID1456
Compound Structure
Plant SourceCissampelos pareira L.     Common Name:Velvet - Leaf Pareira, Pareira Brava (English)
Source FamilyMenispermaceae
OriginIndia, Puerto Rico
Plant Part UsedLeaf
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMiddlebrook 7H9 Broth using BACTEC 460 System
Positive Control Used (conc.)Rifampin
Inhibition [%]60 %
Activity [MIC] µg/ml100 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationFor menstrual problems, heart problems, asthma, stomach cramps, muscle pain/strains, irritable bowel syndrome, kidney stones, kidney/urinary infections and pain
PubMed ID [Source Literature]11746852
Extract PreparationThe plants were dried, at a temperature not exceeding 30°C, in an air - circulating oven. The material was powdered and extracted with 95% ethanol. The organic solvent was removed by distillation under reduced pressure
Chemical Classification [Active Compound]N/A
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Reference(s)1) Antoun MD, Ramos Z, Vazques J, Oquendo I, Proctor GR, Gerena L, Franzblau SG.Evaluation of the flora of Puerto Rico for in vitro antiplasmodial and antimycobacterial activities.Phytother Res. 2001 Nov;15(7):638-42

2) http://rainforest-database.com/plants/abuta.htm

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                  Record - 5 of 22   [TOP]
Compound ID1457
Compound Structure
Plant SourceCissampelos pareira L.     Common Name:Velvet - Leaf pareira, Pareira Brava (English)
Source FamilyMenispermaceae
OriginIndia, Puerto Rico
Plant Part UsedStem
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMiddlebrook 7H9 Broth using BACTEC 460 System
Positive Control Used (conc.)Rifampin
Inhibition [%]52 %
Activity [MIC] µg/ml100 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationFor menstrual problems, for heart problems, asthma, stomach cramps, muscle pain/strains, irritable bowel syndrome, kidney stones, kidney/urinary infections and pain
PubMed ID [Source Literature]11746852
Extract PreparationThe plants were dried, at a temperature not exceeding 30°C, in an air - circulating oven. The material was powdered and extracted with 95% ethanol. The organic solvent was removed by distillation under reduced pressure
Chemical Classification [Active Compound]N/A
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Reference(s)1) Antoun MD, Ramos Z, Vazques J, Oquendo I, Proctor GR, Gerena L, Franzblau SG.Evaluation of the flora of Puerto Rico for in vitro antiplasmodial and antimycobacterial activities.Phytother Res. 2001 Nov;15(7):638-42

2) http://rainforest-database.com/plants/abuta.htm

Curator

                  Record - 6 of 22   [TOP]
Compound ID1501
Compound Structure
Plant SourceCocculus indicus     Common Name: Indian Cockle (English)
Source FamilyMenispermaceae
OriginIndia
Plant Part UsedMother tinture
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Rv (human)
Assay / Test DoneTube Dilution Test
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml
Activity (In terms of dilution)1:40 dilution
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationThe allied species C. hirsutus Diels for tubercular glands and cough, random screening
PubMed ID [Source Literature]2118130
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) Grange JM, Davey RW.Detection of antituberculous activity in plant extracts.J Appl Bacteriol. 1990 Jun;68(6):587-91

2) Kirtikar, K.R., Basu, B.D., 1935. Indian Medicinal Plants, vols. 1–4. Lalit Mohan Basu, Allahabad, India

Curator

                  Record - 7 of 22   [TOP]
Compound ID1574
Compound Structure
Plant SourceCurarea sp.     Common Name:
Source FamilyMenispermaceae
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.)Rifampin (2 µg/ml), Ethambutol (7.5 µg/ml)
Inhibition [%]< 50 %
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 - 8 of 22   [TOP]
Compound ID2278
Compound Structure
Plant SourceOrthomene schomburgkii (Miers) Krukoff & Barneby     Common Name:
Source FamilyMenispermaceae
OriginPeru
Plant Part UsedRoot, stem
ExtractDichloromethane
Target BacteriaMycobacterium tuberculosis (ATCC 27294)
Assay / Test DoneBACTEC 460 (Becton Dickinson Diagnostic Instrument Systems, Sparks MD) Radiometric Assay
Positive Control Used (conc.)Rifampin (2 µg/ml), Ethambutol (7.5 µg/ml)
Inhibition [%]< 50 %
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 - 9 of 22   [TOP]
Compound ID2635
Compound Structure
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Plant SourceStephania dinklagei     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Isoniazid (0.06 µg/ml), Ethambutol (2 µg/ml), Rifampin (0.06 µg/ml), Streptomycin (0.50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml3.125 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedLiriodenin
PubChem ID   10144
Ethnomedicinal InformationCough, stomach troubles, diarrhoea, dysentery
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Isoquinoline, Alkaloid, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight275.058
Molecular FormulaC17H9NO3
SMILESO1c2c3c4c(cc2OC1)ccnc4C(=O)c1c3cccc1
XLogP3.275
PSA48.420
H-bond Donor0
H-bond Acceptor3
No. of Rotatable Bond Count0
No. of Rings5
No. of N1
No. of O3
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_241

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                  Record - 10 of 22   [TOP]
Compound ID2636
Compound Structure
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Plant SourceStephania dinklagei     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Isoniazid (0.06 µg/ml), Ethambutol (2 µg/ml), Rifampin (0.06 µg/ml), Streptomycin (0.50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedDicentrinone
PubChem ID   177744
Ethnomedicinal InformationCough, stomach troubles, diarrhoea, dysentery
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Alkaloid, Quinoline, Ketone, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight335.079
Molecular FormulaC19H13NO5
SMILESO1c2c3c4c(cc2OC1)ccnc4C(=O)c1c3cc(OC)c(OC)c1
XLogP1.754
PSA66.880
H-bond Donor0
H-bond Acceptor5
No. of Rotatable Bond Count2
No. of Rings5
No. of N1
No. of O5
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_241

Curator

                  Record - 11 of 22   [TOP]
Compound ID2637
Compound Structure
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Plant SourceStephania dinklagei     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis (345)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (3.125 µg/ml), Isoniazid (< 50 µg/ml), Ethambutol (12.50 µg/ml), Rifampin (< 50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml> 200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedLiriodenin
PubChem ID   10144
Ethnomedicinal InformationCough, stomach troubles, diarrhoea, dysentery
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Isoquinoline, Alkaloid, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight275.058
Molecular FormulaC17H9NO3
SMILESO1c2c3c4c(cc2OC1)ccnc4C(=O)c1c3cccc1
XLogP3.275
PSA48.420
H-bond Donor0
H-bond Acceptor3
No. of Rotatable Bond Count0
No. of Rings5
No. of N1
No. of O3
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_241

Curator

                  Record - 12 of 22   [TOP]
Compound ID2638
Compound Structure
DOWNLOAD:
Plant SourceStephania dinklagei     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis (345)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (3.125 µg/ml), Isoniazid (< 50 µg/ml), Ethambutol (12.50 µg/ml), Rifampin (< 50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml> 200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedDicentrinone
PubChem ID   177744
Ethnomedicinal InformationCough, stomach troubles, diarrhoea, dysentery
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Alkaloid, Quinoline, Ketone, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight335.079
Molecular FormulaC19H13NO5
SMILESO1c2c3c4c(cc2OC1)ccnc4C(=O)c1c3cc(OC)c(OC)c1
XLogP1.754
PSA66.880
H-bond Donor0
H-bond Acceptor5
No. of Rotatable Bond Count2
No. of Rings5
No. of N1
No. of O5
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_241

Curator

                  Record - 13 of 22   [TOP]
Compound ID2639
Compound Structure
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Plant SourceStephania dinklagei     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis (M12)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (12.50 µg/ml), Isoniazid (< 50 µg/ml), Ethambutol (12.50 µg/ml), Rifampin (< 50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml> 200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedLiriodenin
PubChem ID   10144
Ethnomedicinal InformationCough, stomach troubles, diarrhoea, dysentery
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Isoquinoline, Alkaloid, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight275.058
Molecular FormulaC17H9NO3
SMILESO1c2c3c4c(cc2OC1)ccnc4C(=O)c1c3cccc1
XLogP3.275
PSA48.420
H-bond Donor0
H-bond Acceptor3
No. of Rotatable Bond Count0
No. of Rings5
No. of N1
No. of O3
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_241

Curator

                  Record - 14 of 22   [TOP]
Compound ID2640
Compound Structure
DOWNLOAD:
Plant SourceStephania dinklagei     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis (M12)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (12.50 µg/ml), Isoniazid (< 50 µg/ml), Ethambutol (12.50 µg/ml), Rifampin (< 50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml> 200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedDicentrinone
PubChem ID   177744
Ethnomedicinal InformationCough, stomach troubles, diarrhoea, dysentery
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Alkaloid, Quinoline, Ketone, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight335.079
Molecular FormulaC19H13NO5
SMILESO1c2c3c4c(cc2OC1)ccnc4C(=O)c1c3cc(OC)c(OC)c1
XLogP1.754
PSA66.880
H-bond Donor0
H-bond Acceptor5
No. of Rotatable Bond Count2
No. of Rings5
No. of N1
No. of O5
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_241

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                  Record - 15 of 22   [TOP]
Compound ID2641
Compound Structure
DOWNLOAD:
Plant SourceStephania dinklagei     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis (M20)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (25 µg/ml), Isoniazid (< 50 µg/ml), Ethambutol (12.50 µg/ml), Rifampin (< 50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml100 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedLiriodenin
PubChem ID   10144
Ethnomedicinal InformationCough, stomach troubles, diarrhoea, dysentery
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Isoquinoline, Alkaloid, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight275.058
Molecular FormulaC17H9NO3
SMILESO1c2c3c4c(cc2OC1)ccnc4C(=O)c1c3cccc1
XLogP3.275
PSA48.420
H-bond Donor0
H-bond Acceptor3
No. of Rotatable Bond Count0
No. of Rings5
No. of N1
No. of O3
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_241

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                  Record - 16 of 22   [TOP]
Compound ID2642
Compound Structure
DOWNLOAD:
Plant SourceStephania dinklagei     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis (M20)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (25 µg/ml), Isoniazid (< 50 µg/ml), Ethambutol (12.50 µg/ml), Rifampin (< 50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml> 200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedDicentrinone
PubChem ID   177744
Ethnomedicinal InformationCough,stomach troubles, diarrhoea, dysentery
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Alkaloid, Quinoline, Ketone, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight335.079
Molecular FormulaC19H13NO5
SMILESO1c2c3c4c(cc2OC1)ccnc4C(=O)c1c3cc(OC)c(OC)c1
XLogP1.754
PSA66.880
H-bond Donor0
H-bond Acceptor5
No. of Rotatable Bond Count2
No. of Rings5
No. of N1
No. of O5
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_241

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                  Record - 17 of 22   [TOP]
Compound ID2728
Compound Structure
Plant SourceTinospora cordifolia (Willd.) Miers ex Hook. f. & Thomb.     Common Name:Guduuchi, Guduuchikaa, Guluuchi, Amrita (Sanskrit)
Source FamilyMenispermaceae
OriginIndia
Plant Part UsedLeaf
ExtractVolatile oil
Target BacteriaMycobacterium tuberculosis MTH52 (human)
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml
Activity (In terms of dilution)1:50000 dilution
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationExpectorant, cough, pulmonary tuberculosis, asthma, cough, leprosy
PubMed ID [Source Literature]
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) Gupta, K.C., Viswanathan, R., 1956. Antitubercular substances from plants. A preliminary study. Antibiotics and Chemotherapy 6, 194–195

2) Kirtikar, K.R., Basu, B.D., 1935. Indian Medicinal Plants, vols. 1–4. Lalit Mohan Basu, Allahabad, India

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                  Record - 18 of 22   [TOP]
Compound ID2729
Compound Structure
Plant SourceTinospora crispa (L.) Miers ex Hook. f. & Thoms.     Common Name:
Source FamilyMenispermaceae
OriginMalaysia
Plant Part UsedStem
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneColorimetric Tetrazolium Microplate Assay (TEMA)
Positive Control Used (conc.)Isoniazid (0.078 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]21094237
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) Mohamad S, Zin NM, Wahab HA, Ibrahim P, Sulaiman SF, Zahariluddin AS, Noor SS.Antituberculosis potential of some ethnobotanically selected Malaysian plants.J Ethnopharmacol. 2011 Feb 16;133(3):1021-6

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                  Record - 19 of 22   [TOP]
Compound ID2747
Compound Structure
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Plant SourceTriclisia patens     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Isoniazid (0.06 µg/ml), Ethambutol (2 µg/ml), Rifampin (0.06 µg/ml), Streptomycin (0.50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedPhaeanthine
PubChem ID   73664
Ethnomedicinal InformationDropsy, swellings, oedema, gout, leprosy, malnutrition, debility, pain - killers, paralysis, epilepsy, convulsions, spasm, pulmonary troubles, sedatives
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Polycyclic, Quinoline, Alkaloid, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight622.304
Molecular FormulaC38H42N2O6
SMILESO1c2c3[C@H](N(CCc3cc(OC)c2OC)C)Cc2cc(Oc3ccc(C[C@H]4N(CCc5c4cc1c(OC)c5)C)cc3)c(OC)cc2
XLogP6.098
PSA61.860
H-bond Donor0
H-bond Acceptor8
No. of Rotatable Bond Count4
No. of Rings6
No. of N2
No. of O6
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_253

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                  Record - 20 of 22   [TOP]
Compound ID2748
Compound Structure
DOWNLOAD:
Plant SourceTriclisia patens     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis (345)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (3.125 µg/ml), Isoniazid (< 50 µg/ml), Ethambutol (12.50 µg/ml), Rifampin (< 50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedPhaeanthine
PubChem ID   73664
Ethnomedicinal InformationDropsy, swellings, oedema, gout, leprosy, malnutrition, debility, pain - killers, paralysis, epilepsy, convulsions, spasm, pulmonary troubles, sedatives
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Polycyclic, Quinoline, Alkaloid, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight622.304
Molecular FormulaC38H42N2O6
SMILESO1c2c3[C@H](N(CCc3cc(OC)c2OC)C)Cc2cc(Oc3ccc(C[C@H]4N(CCc5c4cc1c(OC)c5)C)cc3)c(OC)cc2
XLogP6.098
PSA61.860
H-bond Donor0
H-bond Acceptor8
No. of Rotatable Bond Count4
No. of Rings6
No. of N2
No. of O6
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_253

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                  Record - 21 of 22   [TOP]
Compound ID2749
Compound Structure
DOWNLOAD:
Plant SourceTriclisia patens     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis (M12)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (12.50 µg/ml), Isoniazid (< 50 µg/ml), Ethambutol (12.50 µg/ml), Rifampin (< 50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedPhaeanthine
PubChem ID   73664
Ethnomedicinal InformationDropsy, swellings, oedema, gout, leprosy, malnutrition, debility, pain - killers, paralysis, epilepsy, convulsions, spasm, pulmonary troubles, sedatives
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Polycyclic, Quinoline, Alkaloid, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight622.304
Molecular FormulaC38H42N2O6
SMILESO1c2c3[C@H](N(CCc3cc(OC)c2OC)C)Cc2cc(Oc3ccc(C[C@H]4N(CCc5c4cc1c(OC)c5)C)cc3)c(OC)cc2
XLogP6.098
PSA61.860
H-bond Donor0
H-bond Acceptor8
No. of Rotatable Bond Count4
No. of Rings6
No. of N2
No. of O6
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_253

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                  Record - 22 of 22   [TOP]
Compound ID2750
Compound Structure
DOWNLOAD:
Plant SourceTriclisia patens     Common Name:
Source FamilyMenispermaceae
OriginMexico
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis (M20)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Streptomycin (25 µg/ml), Isoniazid (< 50 µg/ml), Ethambutol (12.50 µg/ml), Rifampin (< 50 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml100 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedPhaeanthine
PubChem ID   73664
Ethnomedicinal InformationDropsy, swellings, oedema, gout, leprosy, malnutrition, debility, pain - killers, paralysis, epilepsy, convulsions, spasm, pulmonary troubles, sedatives
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Polycyclic, Quinoline, Alkaloid, Ether
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight622.304
Molecular FormulaC38H42N2O6
SMILESO1c2c3[C@H](N(CCc3cc(OC)c2OC)C)Cc2cc(Oc3ccc(C[C@H]4N(CCc5c4cc1c(OC)c5)C)cc3)c(OC)cc2
XLogP6.098
PSA61.860
H-bond Donor0
H-bond Acceptor8
No. of Rotatable Bond Count4
No. of Rings6
No. of N2
No. of O6
No. of S0
Reference(s)1) María del Rayo Camacho-Corona, Juan Manuel de Jesús Favela-Hernández, Omar González-Santiago, Elvira Garza-González, Gloria María Molina-Salinas, Salvador Said-Fernández, Guillermo Delgado, Julieta Luna-Herrerae.Evaluation of Some Plant-derived Secondary Metabolites Against Sensitive and Multidrug-resistant Mycobacterium tuberculosis.J. Mex. Chem. Soc. 2009, 53(2), 71-75

2) http://plants.jstor.org/upwta/4_253

Curator


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