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                  Page - 1 of 1                  Record - 1 of 13   [TOP]
Compound ID1175
Compound Structure
Plant SourceAnaemopegma chrysoleucum (H.B.K.) Sandwith     Common Name:
Source FamilyBignoniaceae
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 - 2 of 13   [TOP]
Compound ID1176
Compound Structure
Plant SourceAnaemopegma paraense Bureau & Schumann     Common Name:
Source FamilyBignoniaceae
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 - 3 of 13   [TOP]
Compound ID1208
Compound Structure
Plant SourceArrabidaea cinnamomea (A. DC.) Sandw     Common Name:
Source FamilyBignoniaceae
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 13   [TOP]
Compound ID1339
Compound Structure
Plant SourceCallichlamys latifolia (Richard) Schumann     Common Name:
Source FamilyBignoniaceae
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 - 5 of 13   [TOP]
Compound ID1551
Compound Structure
Plant SourceCrescentia amazonica Ducke     Common Name:
Source FamilyBignoniaceae
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 - 6 of 13   [TOP]
Compound ID1581
Compound Structure
Plant SourceCydista lilacina A. Gentry     Common Name:
Source FamilyBignoniaceae
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 - 7 of 13   [TOP]
Compound ID2090
Compound Structure
Plant SourceLundia corymbifera (Vahl) Sandw     Common Name:
Source FamilyBignoniaceae
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 13   [TOP]
Compound ID2144
Compound Structure
Plant SourceMartinella obovata (H.B.K.) Bureau & Schum     Common Name:
Source FamilyBignoniaceae
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 - 9 of 13   [TOP]
Compound ID2644
Compound Structure
Plant SourceStereospermum kunthianum Cham.     Common Name:Pink Jacaranda
Source FamilyBignoniaceae
OriginNigeria
Plant Part UsedStem bark
ExtractCrude methanol
Target BacteriaMycobacterium tuberculosis clinical isolate
Assay / Test DoneBroth Microdilution Method (BMM)
Positive Control Used (conc.)Ethambutol (2 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml> 2500 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationCancer, tuberculosis
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) A Mann, J O Amupitan, A O Oyewale, J I Okogun, K Ibrahim.An ethnobotanical survey of indigenous flora for treating tuberculosis and other respiratory diseases in Niger State, Nigeria.JOPAT Vol. 12 2007: pp. 1-21

2) Mann A, Gbate M, Nda-Umar A. Medicinal and Economic Plants of Nupeland. Bida, Niger State, Nigeria: Jube-Evans Books and Publications; 2003. p. 276

3) http://www.zimbabweflora.co.zw/speciesdata/species.php?species_id=152430

Curator

                  Record - 10 of 13   [TOP]
Compound ID2687
Compound Structure
Plant SourceTanacium nocternum (Barb. Rodr.) Bureau & Schum     Common Name:
Source FamilyBignoniaceae
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 - 11 of 13   [TOP]
Compound ID4034
Compound Structure
DOWNLOAD:
Plant SourceRadermachera boniana     Common Name:
Source FamilyBignoniaceae
Origin
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml16.8 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedBonianic acid A
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, Prenylated, O-Acetyl, Acid
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight484.355
Molecular FormulaC31H48O4
SMILES[C@H]12[C@](C)(C(=O)O)[C@@H](OC(=O)C)CC[C@@]31[C@@]1(C3)C([C@@H]3CC[C@H]([C@@H](CCC=C(C)C)C)[C@@]3(C)CC1)CC2
XLogP10.616
PSA63.600
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count7
No. of Rings5
No. of N0
No. of O4
No. of S0
Reference(s)1) In silico Comparison of Antimycobacterial Natural Products with Known Antituberculosis Drugs. Marlene Espinoza-Moraga, Nicholas M. Njuguna, Grace Mugumbate, Julio Caballero, and Kelly Chibale. Journal of Chemical Information and Modeling 2013 53 (3), 649-660

2) García, A., Bocanegra-García, V., Palma-Nicolás, J. P., Rivera, G. Vennerstrom, J. L. Recent Advances in Antitubercular Natural Products. Eur. J. Med. Chem. 2012, 49, 1-23

Curator

                  Record - 12 of 13   [TOP]
Compound ID4035
Compound Structure
DOWNLOAD:
Plant SourceRadermachera boniana     Common Name:
Source FamilyBignoniaceae
Origin
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml5 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedBonianic acid B
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene, O-Acetyl, Acid
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight500.350
Molecular FormulaC31H48O5
SMILES[C@H]12[C@](C)(C(=O)O)[C@@H](OC(=O)C)CC[C@@]31[C@@]1(C3)C([C@@H]3CC[C@H]([C@@H](CCC(=O)C(C)C)C)[C@@]3(C)CC1)CC2
XLogP8.764
PSA80.670
H-bond Donor1
H-bond Acceptor5
No. of Rotatable Bond Count8
No. of Rings5
No. of N0
No. of O5
No. of S0
Reference(s)1) In silico Comparison of Antimycobacterial Natural Products with Known Antituberculosis Drugs. Marlene Espinoza-Moraga, Nicholas M. Njuguna, Grace Mugumbate, Julio Caballero, and Kelly Chibale. Journal of Chemical Information and Modeling 2013 53 (3), 649-660

2) García, A., Bocanegra-García, V., Palma-Nicolás, J. P., Rivera, G. Vennerstrom, J. L. Recent Advances in Antitubercular Natural Products. Eur. J. Med. Chem. 2012, 49, 1-23

Curator

                  Record - 13 of 13   [TOP]
Compound ID4039
Compound Structure
DOWNLOAD:
Plant SourceRadermachera boniana     Common Name:
Source FamilyBignoniaceae
Origin
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml39.5 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identifiedβ-Sitostenone
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Alicyclic, Tetracyclic, Steroid, Ketone
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight410.355
Molecular FormulaC29H46O
SMILESC[C@]12C(=CC(=O)CC2)CCC2[C@@H]3CC[C@H]([C@H](C)CC[C@H](C(C)C)CC)[C@@]3(C)CC=C12
XLogP11.136
PSA17.070
H-bond Donor0
H-bond Acceptor1
No. of Rotatable Bond Count6
No. of Rings4
No. of N0
No. of O1
No. of S0
Reference(s)1) In silico Comparison of Antimycobacterial Natural Products with Known Antituberculosis Drugs. Marlene Espinoza-Moraga, Nicholas M. Njuguna, Grace Mugumbate, Julio Caballero, and Kelly Chibale. Journal of Chemical Information and Modeling 2013 53 (3), 649-660

2) García, A., Bocanegra-García, V., Palma-Nicolás, J. P., Rivera, G. Vennerstrom, J. L. Recent Advances in Antitubercular Natural Products. Eur. J. Med. Chem. 2012, 49, 1-23

Curator


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