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                  Page - 1 of 2                  Record - 1 of 44   [TOP]
Compound ID1286
Compound Structure
Plant SourceBouvardia ternifolia     Common Name:Firecracker Bush
Source FamilyRubiaceae
OriginMexico
Plant Part UsedAerial
ExtractHexane, methanol
Target Bacteria
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml> 200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationCough
PubMed ID [Source Literature]13680821
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) Jimenez-Arellanes A, Meckes M, Ramirez R, Torres J, Luna-Herrera J. Activity against multidrug-resistant Mycobacterium tuberculosis in Mexican plants used to treat respiratory diseases. Phytother Res. 2003 Sep;17(8):903-8

2) Http://www.fireflyforest.com/flowers/271/bouvardia-ternifolia-firecrackerbush/

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                  Record - 2 of 44   [TOP]
Compound ID1341
Compound Structure
Plant SourceCalycophyllum spruceanum (Benth.) Hook.f. ex Schumann     Common Name:
Source FamilyRubiaceae
OriginPeru
Plant Part UsedBark
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

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                  Record - 3 of 44   [TOP]
Compound ID1412
Compound Structure
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Plant SourceCephaelis dichroa     Common Name:
Source FamilyRubiaceae
OriginMexico
Plant Part UsedAerial
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/ml> 50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedStrictosidine
PubChem ID   161336
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Alkaloid, Indole, Pyran, Ester, Sugar
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight530.226
Molecular FormulaC27H34N2O9
SMILESO([C@@H]1OC=C([C@@H](C[C@@H]2NCCc3c2[nH]c2c3cccc2)[C@H]1C=C)C(=O)OC)[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)CO
XLogP1.559
PSA162.730
H-bond Donor6
H-bond Acceptor11
No. of Rotatable Bond Count8
No. of Rings5
No. of N2
No. of O9
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

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                  Record - 4 of 44   [TOP]
Compound ID1413
Compound Structure
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Plant SourceCephaelis dichroa     Common Name:
Source FamilyRubiaceae
OriginMexico
Plant Part UsedAerial
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/ml6.25 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedPeracetyl - Strictosidine Lactam
PubChem IDNR
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Alkaloid, Carbazole, Pyran, Isoquinoline, O-Acetyl, Sugar
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight650.284
Molecular FormulaC35H42N2O10
SMILESC1cccc2c1c1c([nH]2)C2N(CC1)CC1=COC(C(C1C2)C=C)OC1O[C@H]([C@@H]([C@H]([C@@H]1OC(=O)C)CC(=O)C)OC(=O)C)COC(=O)C
XLogP3.192
PSA142.690
H-bond Donor1
H-bond Acceptor12
No. of Rotatable Bond Count12
No. of Rings6
No. of N2
No. of O10
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

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                  Record - 5 of 44   [TOP]
Compound ID1414
Compound Structure
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Plant SourceCephaelis dichroa     Common Name:
Source FamilyRubiaceae
OriginMexico
Plant Part UsedAerial
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/ml100 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedStrictosidine
PubChem ID   161336
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Alkaloid, Indole, Pyran, Ester, Sugar
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight530.226
Molecular FormulaC27H34N2O9
SMILESO([C@@H]1OC=C([C@@H](C[C@@H]2NCCc3c2[nH]c2c3cccc2)[C@H]1C=C)C(=O)OC)[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)CO
XLogP1.559
PSA162.730
H-bond Donor6
H-bond Acceptor11
No. of Rotatable Bond Count8
No. of Rings5
No. of N2
No. of O9
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

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                  Record - 6 of 44   [TOP]
Compound ID1415
Compound Structure
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Plant SourceCephaelis dichroa     Common Name:
Source FamilyRubiaceae
OriginMexico
Plant Part UsedAerial
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 IdentifiedPeracetyl - Strictosidine Lactam
PubChem IDNR
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Alkaloid, Carbazole, Pyran, Isoquinoline, O-Acetyl, Sugar
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight650.284
Molecular FormulaC35H42N2O10
SMILESC1cccc2c1c1c([nH]2)C2N(CC1)CC1=COC(C(C1C2)C=C)OC1O[C@H]([C@@H]([C@H]([C@@H]1OC(=O)C)CC(=O)C)OC(=O)C)COC(=O)C
XLogP3.192
PSA142.690
H-bond Donor1
H-bond Acceptor12
No. of Rotatable Bond Count12
No. of Rings6
No. of N2
No. of O10
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

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                  Record - 7 of 44   [TOP]
Compound ID1416
Compound Structure
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Plant SourceCephaelis dichroa     Common Name:
Source FamilyRubiaceae
OriginMexico
Plant Part UsedAerial
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 IdentifiedStrictosidine
PubChem ID   161336
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Alkaloid, Indole, Pyran, Ester, Sugar
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight530.226
Molecular FormulaC27H34N2O9
SMILESO([C@@H]1OC=C([C@@H](C[C@@H]2NCCc3c2[nH]c2c3cccc2)[C@H]1C=C)C(=O)OC)[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)CO
XLogP1.559
PSA162.730
H-bond Donor6
H-bond Acceptor11
No. of Rotatable Bond Count8
No. of Rings5
No. of N2
No. of O9
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

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                  Record - 8 of 44   [TOP]
Compound ID1417
Compound Structure
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Plant SourceCephaelis dichroa     Common Name:
Source FamilyRubiaceae
OriginMexico
Plant Part UsedAerial
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 IdentifiedPeracetyl - strictosidine lactam
PubChem IDNR
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Alkaloid, Carbazole, Pyran, Isoquinoline, O-Acetyl, Sugar
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight650.284
Molecular FormulaC35H42N2O10
SMILESC1cccc2c1c1c([nH]2)C2N(CC1)CC1=COC(C(C1C2)C=C)OC1O[C@H]([C@@H]([C@H]([C@@H]1OC(=O)C)CC(=O)C)OC(=O)C)COC(=O)C
XLogP3.192
PSA142.690
H-bond Donor1
H-bond Acceptor12
No. of Rotatable Bond Count12
No. of Rings6
No. of N2
No. of O10
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

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                  Record - 9 of 44   [TOP]
Compound ID1418
Compound Structure
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Plant SourceCephaelis dichroa     Common Name:
Source FamilyRubiaceae
OriginMexico
Plant Part UsedAerial
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/ml200 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedStrictosidine
PubChem ID   161336
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Tricyclic, Alkaloid, Indole, Pyran, Ester, Sugar
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight530.226
Molecular FormulaC27H34N2O9
SMILESO([C@@H]1OC=C([C@@H](C[C@@H]2NCCc3c2[nH]c2c3cccc2)[C@H]1C=C)C(=O)OC)[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)CO
XLogP1.559
PSA162.730
H-bond Donor6
H-bond Acceptor11
No. of Rotatable Bond Count8
No. of Rings5
No. of N2
No. of O9
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

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                  Record - 10 of 44   [TOP]
Compound ID1419
Compound Structure
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Plant SourceCephaelis dichroa     Common Name:
Source FamilyRubiaceae
OriginMexico
Plant Part UsedAerial
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 IdentifiedPeracetyl - Strictosidine Lactam
PubChem IDNR
Ethnomedicinal InformationTuberculosis
PubMed ID [Source Literature]
Extract PreparationN/A
Chemical Classification [Active Compound]Aromatic, Pentacyclic, Alkaloid, Carbazole, Pyran, Isoquinoline, O-Acetyl, Sugar
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight650.284
Molecular FormulaC35H42N2O10
SMILESC1cccc2c1c1c([nH]2)C2N(CC1)CC1=COC(C(C1C2)C=C)OC1O[C@H]([C@@H]([C@H]([C@@H]1OC(=O)C)CC(=O)C)OC(=O)C)COC(=O)C
XLogP3.192
PSA142.690
H-bond Donor1
H-bond Acceptor12
No. of Rotatable Bond Count12
No. of Rings6
No. of N2
No. of O10
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

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Compound ID1438
Compound Structure
Plant SourceChomelia malaneoides Muell. Arg.     Common Name:
Source FamilyRubiaceae
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 [%]55 %
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

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Compound ID1736
Compound Structure
Plant SourceFaramea occidentails (L.) A. Rich.     Common Name:
Source FamilyRubiaceae
OriginPuerto 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 [%]56 %
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]11746852
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) 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

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Compound ID1790
Compound Structure
Plant SourceGalium aparine L.     Common Name:Goosegrass, Clivers, Cleavers, Catch Weed (English), Choleretic, Stomachic (Sanskrit)
Source FamilyRubiaceae
OriginIndia
Plant Part UsedWhole plant
ExtractEthyl acetate
Target BacteriaMycobacterium smegmatis
Assay / Test DoneAgar - Well Diffusion Assay
Positive Control Used (conc.)Streptomycin sulphate (1 mg/ml)
Inhibition [%]
Activity [MIC] µg/ml20000 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)5 mm, 20 mm (control)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationAperient, diuretic, refrigerant, antiscorbutic and fruits used as a substitute for coffee
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) James D. Mcchesney, Robert P. Adams.Co-evaluation of plant extracts as petrochemical substitutes and for biologically active compounds.Economic Botany. 12/1984, 39(1):74-86

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Compound ID1791
Compound Structure
Plant SourceGalium aparine L.     Common Name:Goosegrass, Clivers, Cleavers, Catch Weed (English), Choleretic, Stomachic (Sanskrit)
Source FamilyRubiaceae
OriginIndia
Plant Part UsedLeaf
ExtractWater
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneBroth Dilution Assay
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 InformationAperient, diuretic, refrigerant, antiscorbutic and fruits used as a substitute for coffee
PubMed ID [Source Literature]17276637
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) Gautam R, Saklani A, Jachak SM.Indian medicinal plants as a source of antimycobacterial agents.J Ethnopharmacol. 2007 Mar 21;110(2):200-34

2) Chopra, R.N., Nayar, S.L., Chopra, R.C., 1956. Glossary of Indian Medicinal Plants. Council of Scientific and Industrial Research, New Delhi, India.

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Compound ID1833
Compound Structure
Plant SourceGuettarda sp.     Common Name:
Source FamilyRubiaceae
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

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                  Record - 16 of 44   [TOP]
Compound ID2201
Compound Structure
Plant SourceMorinda citrifolia L.     Common Name:Indian Mulberry (English), Ashyuka, Akshi, Atchy (Sanskrit)
Source FamilyRubiaceae
OriginMalaysia, India
Plant Part UsedFruit
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 InformationAsthma, joint pains, immune problems, pain relief, cellular regeneration, tuberculosis, respiratory disorders
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) Chin, W.Y., 2002. A Guide to Medicinal Plants. Singapore Science Centre, Singapore

2) http://www.motherherbs.com/morinda-citrifolia.html

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Compound ID2202
Compound Structure
Plant SourceMorinda citrifolia L.     Common Name:Indian Mulberry (English), Ashyuka, Akshi, Atchy (Sanskrit)
Source FamilyRubiaceae
OriginMalaysia, India
Plant Part UsedLeaf
ExtractEthanol, hexane
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneBroth dilution assay using BACTEC system
Positive Control Used (conc.)Rifampin (0.125 µg/ml)
Inhibition [%]89 and 95 %
Activity [MIC] µg/ml100 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationAsthma, joint pains, immune problems, pain relief, cellular regeneration, tuberculosis, respiratory disorders
PubMed ID [Source Literature]12410555
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) Saludes JP, Garson MJ, Franzblau SG, Aguinaldo AM.Antitubercular constituents from the hexane fraction of Morinda citrifolia Linn. (Rubiaceae).Phytother Res. 2002 Nov;16(7):683-5

2) http://www.motherherbs.com/morinda-citrifolia.html

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                  Record - 18 of 44   [TOP]
Compound ID2203
Compound Structure
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Plant SourceMorinda citrifolia L.     Common Name:Indian Mulberry (English), Ashyuka, Akshi, Atchy (Sanskrit)
Source FamilyRubiaceae
OriginMalaysia, India
Plant Part UsedLeaf
ExtractHexane
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneBroth dilution assay using BACTEC system
Positive Control Used (conc.)Rifampin (0.125 µg/ml)
Inhibition [%]Crude: 89% and Hexane: 95 %
Activity [MIC] µg/ml32 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified(E)-Phytol
PubChem ID   5280435
Ethnomedicinal InformationAsthma, joint pains, immune problems, pain relief, cellular regeneration, tuberculosis, respiratory disorders
PubMed ID [Source Literature]12410555
Extract PreparationN/A
Chemical Classification [Active Compound]Aliphatic, Alkene, Terpene, Diterpene, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight296.308
Molecular FormulaC20H40O
SMILESOC/C=C(/CCC[C@@H](CCC[C@@H](CCCC(C)C)C)C)C
XLogP8.949
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count13
No. of Rings0
No. of N0
No. of O1
No. of S0
Reference(s)1) Saludes JP, Garson MJ, Franzblau SG, Aguinaldo AM.Antitubercular constituents from the hexane fraction of Morinda citrifolia Linn. (Rubiaceae).Phytother Res. 2002 Nov;16(7):683-5

2) http://www.motherherbs.com/morinda-citrifolia.html

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                  Record - 19 of 44   [TOP]
Compound ID2204
Compound Structure
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Plant SourceMorinda citrifolia L.     Common Name:Indian Mulberry (English), Ashyuka, Akshi, Atchy (Sanskrit)
Source FamilyRubiaceae
OriginIndo - Pacific region
Plant Part UsedLeaf
Extract
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneBroth dilution assay using BACTEC system
Positive Control Used (conc.)Rifampin (0.125 µg/ml)
Inhibition [%]Crude ethanol extract - 89 % and hexane fraction - 95 %
Activity [MIC] µg/ml> 64 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedCycloartenol
PubChem ID   17750995
Ethnomedicinal InformationAsthma, joint pains, immune problems, pain relief, cellular regeneration, tuberculosis, respiratory disorders
PubMed ID [Source Literature]12410555
Extract PreparationDried leaves were extracted with ethanol to give a green, syrupy extract which was further partitioned into hexane DCM , EtOAc and n - BuOH fractions
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, Cycloartane, Prenylated, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Bactec 12B broth
Cytotoxicity Assay [AID]N/A
Molecular Weight426.386
Molecular FormulaC30H50O
SMILESO[C@@H]1C([C@H]2[C@@]3([C@]4(C3)[C@H]([C@]3([C@](CC4)([C@H](CC3)[C@@H](CCC=C(C)C)C)C)C)CC2)CC1)(C)C
XLogP11.921
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count4
No. of Rings5
No. of N0
No. of O1
No. of S0
Reference(s)1) Saludes JP, Garson MJ, Franzblau SG, Aguinaldo AM.Antitubercular constituents from the hexane fraction of Morinda citrifolia Linn. (Rubiaceae).Phytother Res. 2002 Nov;16(7):683-5

2) http://www.motherherbs.com/morinda-citrifolia.html

Curator

                  Record - 20 of 44   [TOP]
Compound ID2205
Compound Structure
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Plant SourceMorinda citrifolia L.     Common Name:Indian Mulberry (English), Ashyuka, Akshi, Atchy (Sanskrit)
Source FamilyRubiaceae
OriginIndo - Pacific region
Plant Part UsedLeaf
ExtractEthanol, Hexane
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneRadiorespirometric Bioassay
Positive Control Used (conc.)Rifampin (0.125 µg/ml)
Inhibition [%]Crude ethanol extract - 89 % and hexane fraction - 95 %
Activity [MIC] µg/ml< 2 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedStigmasta - 4 - 22 - Dien - 3 - One
PubChem ID   6479802
Ethnomedicinal InformationAsthma, joint pains, immune problems, pain relief, cellular regeneration, tuberculosis, respiratory disorders
PubMed ID [Source Literature]12410555
Extract PreparationN/A
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Ketone
Media / Broth Used [Antimicrobial Assay/Test]Bactec 12B broth
Cytotoxicity Assay [AID]N/A
Molecular Weight424.371
Molecular FormulaC30H48O
SMILESO=C1CC[C@@]2(C3C([C@]4([C@@]([C@H](CC4)C(C)/C=C/[C@H](C(C)C)CC)(CC3)C)C)CCC2=C1)C
XLogP11.670
PSA17.070
H-bond Donor0
H-bond Acceptor1
No. of Rotatable Bond Count5
No. of Rings4
No. of N0
No. of O1
No. of S0
Reference(s)1) Saludes JP, Garson MJ, Franzblau SG, Aguinaldo AM.Antitubercular constituents from the hexane fraction of Morinda citrifolia Linn. (Rubiaceae).Phytother Res. 2002 Nov;16(7):683-5

2) http://www.motherherbs.com/morinda-citrifolia.html

Curator

                  Record - 21 of 44   [TOP]
Compound ID2206
Compound Structure
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Plant SourceMorinda citrifolia L.     Common Name:Indian Mulberry (English), Ashyuka, Akshi, Atchy (Sanskrit)
Source FamilyRubiaceae
OriginIndo - Pacific region
Plant Part UsedLeaf
ExtractEthanol, Hexane
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneRadiorespirometric Bioassay
Positive Control Used (conc.)Rifampin (0.125 µg/ml)
Inhibition [%]Crude ethanol extract - 89 % and hexane fraction - 95 %
Activity [MIC] µg/ml128 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identifiedβ - sitosterol
PubChem ID   222284
Ethnomedicinal InformationAsthma, joint pains, immune problems, pain relief, cellular regeneration, tuberculosis, respiratory disorders
PubMed ID [Source Literature]12410555
Extract PreparationN/A
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight414.386
Molecular FormulaC29H50O
SMILESO[C@@H]1CC2=CC[C@H]3[C@H]4[C@@]([C@H](CC4)[C@@H](CC[C@H](C(C)C)CC)C)(CC[C@@H]3[C@]2(CC1)C)C
XLogP11.595
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count6
No. of Rings4
No. of N0
No. of O1
No. of S0
Reference(s)1) Saludes JP, Garson MJ, Franzblau SG, Aguinaldo AM.Antitubercular constituents from the hexane fraction of Morinda citrifolia Linn. (Rubiaceae).Phytother Res. 2002 Nov;16(7):683-5

2) http://www.motherherbs.com/morinda-citrifolia.html

Curator

                  Record - 22 of 44   [TOP]
Compound ID2207
Compound Structure
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Plant SourceMorinda citrifolia L.     Common Name:Indian Mulberry (English), Ashyuka, Akshi, Atchy (Sanskrit)
Source FamilyRubiaceae
OriginIndo - Pacific region
Plant Part UsedLeaf
Extract
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneRadiorespirometric Bioassay
Positive Control Used (conc.)Rifampin (0.125 µg/ml)
Inhibition [%]Crude ethanol extract - 89 % and hexane fraction - 95 %
Activity [MIC] µg/ml32 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedStigmasterol
PubChem ID   5280794
Ethnomedicinal InformationAsthma, joint pains, immune problems, pain relief, cellular regeneration, tuberculosis, respiratory disorders
PubMed ID [Source Literature]12410555
Extract PreparationN/A
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]N/A
Cytotoxicity Assay [AID]N/A
Molecular Weight412.371
Molecular FormulaC29H48O
SMILESO[C@@H]1CC2=CC[C@H]3[C@H]4[C@@]([C@H](CC4)[C@H](C)/C=C/[C@H](C(C)C)CC)(CC[C@@H]3[C@]2(CC1)C)C
XLogP11.071
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count5
No. of Rings4
No. of N0
No. of O1
No. of S0
Reference(s)1) Saludes JP, Garson MJ, Franzblau SG, Aguinaldo AM.Antitubercular constituents from the hexane fraction of Morinda citrifolia Linn. (Rubiaceae).Phytother Res. 2002 Nov;16(7):683-5

2) http://www.motherherbs.com/morinda-citrifolia.html

Curator

                  Record - 23 of 44   [TOP]
Compound ID2244
Compound Structure
Plant SourceNeolaugeria resinosa (Vahl) Nichols.     Common Name:
Source FamilyRubiaceae
OriginPuerto Rico
Plant Part UsedLeaf, stem
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMiddlebrook 7H9 Broth using BACTEC 460 System
Positive Control Used (conc.)Rifampin
Inhibition [%]36 and 35 %
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]11746852
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) 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

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                  Record - 24 of 44   [TOP]
Compound ID2284
Compound Structure
Plant SourcePalicourea croceoides Ham     Common Name:
Source FamilyRubiaceae
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

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                  Record - 25 of 44   [TOP]
Compound ID2310
Compound Structure
Plant SourcePentanisia prunelloides Walp     Common Name:Wild Verbena, Broad - Leaved Pentanisia
Source FamilyRubiaceae
OriginAfrica
Plant Part UsedFleshy, tuberous root
Extract
Target Bacteria
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, chest pain
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) Watt, John Mitchell, and Maria Gerdina Breyer-Brandwijk. 1962. The medicinal and poisonous plants of southern and eastern Africa; being an account of their medicinal and other uses, chemical composition, pharmacological effects and toxicology in man and animal. Edinburgh: Livingstone (2nd Edition)

2) http://www.plantzAfrica.com/plantnop/pentanprunel.htm

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