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                  Page - 1 of 2                  Record - 1 of 46   [TOP]
Compound ID1247
Compound Structure
Plant SourceBeilschmiedia tawa     Common Name:Tawa
Source FamilyLauraceae
OriginNew Zealand
Plant Part UsedLeaf
Extract
Target BacteriaMycobacterium smegmatis
Assay / Test Done96 well - plate format assay for bacteriostatic activity, two - fold serial dilution to measure any background optical density or fluorescence associated with the extract
Positive Control Used (conc.)Rifampin (100 µM), Streptomycin (100 µM)
Inhibition [%]
Activity [MIC] µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationSore throat, colds, cough
PubMed ID [Source Literature]20537175
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) Earl EA, Altaf M, Murikoli RV, Swift S, O Toole R.Native New Zealand plants with inhibitory activity towards Mycobacterium tuberculosis.BMC Complement Altern Med. 2010 Jun 10;10:25

Curator

                  Record - 2 of 46   [TOP]
Compound ID1448
Compound Structure
Plant SourceCinnamomum camphora (L.) Nees & Eberm     Common Name:Camphor tree (English), Karpura, Ghanasaara, Chandra (Sanskrit)
Source FamilyLauraceae
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)1:80 and 1:1280 dilutions
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationLeprosy
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) Sharma, S.K., 1998. Medicinal Plants Used in Ayurveda. National Academy of Ayurveda, Ministry of Health and Family Welfare, Govt. of India, New Delhi, India

Curator

                  Record - 3 of 46   [TOP]
Compound ID1449
Compound Structure
Plant SourceCinnamomum triplinerve (R.& P.) Kostermans     Common Name:
Source FamilyLauraceae
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 46   [TOP]
Compound ID1450
Compound Structure
Plant SourceCinnamomum zeylandicum Breyn.     Common Name:Cinnamon, Ceylon Cinnamon (English), Tvak, Daaruchini (Sanskrit)
Source FamilyLauraceae
OriginSri Lanka, Sumatra, Eastern Islands, Brazil, Mauritius, India, Jamaica
Plant Part UsedBark
ExtractMethanol (9.41 %)
Target BacteriaMycobacterium avium
Assay / Test DoneBroth Microdilution Method (BMM)
Positive Control Used (conc.)Streptomycin (IC50 value 1.14)
Inhibition [%]
Activity [MIC] µg/ml> 500 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationAntiseptic and used to treat gonorrhoea, asthma, diabetes, diseases of oral cavity, bronchitis, expectorant
PubMed ID [Source Literature]11744296
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) Newton SM, Lau C, Gurcha SS, Besra GS, Wright CW.The evaluation of forty-three plant species for in vitro antimycobacterial activities; isolation of active constituents from Psoralea corylifolia and Sanguinaria canadensis.J Ethnopharmacol. 2002 Jan;79(1):57-67

Curator

                  Record - 5 of 46   [TOP]
Compound ID1451
Compound Structure
Plant SourceCinnamomum zeylandicum Breyn.     Common Name:Cinnamon, Ceylon Cinnamon (English),Tvak, Daaruchini (Sanskrit)
Source FamilyLauraceae
OriginSri Lanka, Sumatra, Eastern Islands, Brazil, Mauritius, India, Jamaica, Malaysia
Plant Part UsedBark
ExtractMethanol (9.41 %)
Target BacteriaMycobacterium smegmatis
Assay / Test DoneBroth Microdilution Method (BMM)
Positive Control Used (conc.)Streptomycin (IC50 value 0.17)
Inhibition [%]
Activity [MIC] µg/ml> 500 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationAntiseptic and used to treat gonorrhoea, asthma, diabetes, diseases of oral cavity, bronchitis, expectorant
PubMed ID [Source Literature]11744296
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) Newton SM, Lau C, Gurcha SS, Besra GS, Wright CW.The evaluation of forty-three plant species for in vitro antimycobacterial activities; isolation of active constituents from Psoralea corylifolia and Sanguinaria canadensis.J Ethnopharmacol. 2002 Jan;79(1):57-67

Curator

                  Record - 6 of 46   [TOP]
Compound ID1452
Compound Structure
Plant SourceCinnamomum zeylanicum Breyn.     Common Name:Cinnamon, Ceylon Cinnamon (English),Tvak, Daaruchini (Sanskrit)
Source FamilyLauraceae
OriginSri Lanka, Sumatra, Eastern Islands, Brazil, Mauritius, India, Jamaica
Plant Part UsedLeaf
ExtractWater
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneBroth Dilution Assay
Positive Control Used (conc.)
Inhibition [%]100 %
Activity [MIC] µg/ml1:640 dilution
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationAntiseptic and used to treat gonorrhoea, asthma, diabetes, diseases of oral cavity, bronchitis, expectorant
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) Kirtikar, K.R., Basu, B.D., 1935. Indian Medicinal Plants, vols. 14. Lalit Mohan Basu, Allahabad, India

Curator

                  Record - 7 of 46   [TOP]
Compound ID1453
Compound Structure
Plant SourceCinnamomum zeylanicum Breyn.     Common Name:Cinnamon, Ceylon Cinnamon (English),Tvak, Daaruchini (Sanskrit)
Source FamilyLauraceae
OriginSri Lanka, Sumatra, Eastern Islands, Brazil, Mauritius, India, Jamaica, Malaysia
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 InformationAntiseptic and used to treat gonorrhoea, asthma, diabetes, diseases of oral cavity, bronchitis, expectorant
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) Ong, T., 2008. Rahsia Herba, 2nd ed. Alaf 21 Sdn Bhd, Shah Alam, Selangor, Malaysia

2) http://parisaramahiti.kar.nic.in/Medicinal_plants_new/med%20plants/p52.html

Curator

                  Record - 8 of 46   [TOP]
Compound ID1565
Compound Structure
Plant SourceCryptocarya latifolia Sond.     Common Name:Broad - Leaved Quince
Source FamilyLauraceae
OriginAfrica
Plant Part UsedBark
ExtractAcetone
Target BacteriaMycobacterium tuberculosis
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml0.001 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationChest ailments, 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) Lall, N., Meyer, J.J., Wang, Y., Bapela, N.B., van Rensburg, C.E.J., Fourie, B., Franzblau, S.G..Characterization of Intracellular Activity of Antitubercular Constituents the Roots of Euclea natalensis.Pharmaceutical Biology (Formerly International Journal of Pharmacognosy), Volume 43, Number 4, June 2005 , pp. 353-357

2) http://www.growwild.co.za/node/223

Curator

                  Record - 9 of 46   [TOP]
Compound ID1566
Compound Structure
Plant SourceCryptocarya latifolia Sond.     Common Name:Broad - Leaved Quince
Source FamilyLauraceae
OriginAfrica
Plant Part UsedBark
ExtractWater
Target BacteriaMycobacterium tuberculosis
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml0.005 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationChest ailments, 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) Lall, N., Meyer, J.J., Wang, Y., Bapela, N.B., van Rensburg, C.E.J., Fourie, B., Franzblau, S.G..Characterization of Intracellular Activity of Antitubercular Constituents the Roots of Euclea natalensis.Pharmaceutical Biology (Formerly International Journal of Pharmacognosy), Volume 43, Number 4, June 2005 , pp. 353-357

2) http://www.growwild.co.za/node/223

Curator

                  Record - 10 of 46   [TOP]
Compound ID2237
Compound Structure
Plant SourceNectandra cuneato-cordata Mez     Common Name:
Source FamilyLauraceae
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 46   [TOP]
Compound ID2238
Compound Structure
Plant SourceNectandra hihua (R. & P.) Rowher     Common Name:
Source FamilyLauraceae
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 [%]98 %
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 - 12 of 46   [TOP]
Compound ID2239
Compound Structure
Plant SourceNectandra sp.     Common Name:
Source FamilyLauraceae
OriginPeru
Plant Part UsedBark, root
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 - 13 of 46   [TOP]
Compound ID2265
Compound Structure
Plant SourceOcotea cernua s.l. (Nees) Mez     Common Name:
Source FamilyLauraceae
OriginPeru
Plant Part UsedBark, root
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 - 14 of 46   [TOP]
Compound ID2312
Compound Structure
Plant SourcePersea americana Mill     Common Name:Avocado, Alligator Pear
Source FamilyLauraceae
OriginMexico
Plant Part UsedLeaf
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]82 - 100 %
Activity [MIC] µg/ml125 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationDigestive, emmenagogue, antibacterial, antioxidant, antifungal, pectoral, stomachic, anthelmintic, antiperiodic, antidiarrheal
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) R. Gomez-Flores, C. Arzate-Quintana, R. Quintanilla-Licea, P. Tamez-Guerra, R. Tamez-Guerra, E. Monreal-Cuevas and C. Rodríguez-Padilla.Antimicrobial Activity of Persea americana Mill (Lauraceae) (Avocado) and Gymnosperma glutinosum (Spreng.) Less (Asteraceae) Leaf Extracts and Active Fractions Against Mycobacterium tuberculosis.American-Eurasian Journal of Scientific Research 3 (2): 188-194, 2008

2) http://www.stuartxchange.org/Abukado.html

Curator

                  Record - 15 of 46   [TOP]
Compound ID2313
Compound Structure
Plant SourcePersea americana Mill     Common Name:Avocado, Alligator Pear
Source FamilyLauraceae
OriginMexico
Plant Part UsedLeaf
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]53 - 100 %
Activity [MIC] µg/ml62.5 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationDigestive, emmenagogue, antibacterial, antioxidant, antifungal, pectoral, stomachic, anthelmintic, antiperiodic, antidiarrheal
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) R. Gomez-Flores, C. Arzate-Quintana, R. Quintanilla-Licea, P. Tamez-Guerra, R. Tamez-Guerra, E. Monreal-Cuevas and C. Rodríguez-Padilla.Antimicrobial Activity of Persea americana Mill (Lauraceae) (Avocado) and Gymnosperma glutinosum (Spreng.) Less (Asteraceae) Leaf Extracts and Active Fractions Against Mycobacterium tuberculosis.American-Eurasian Journal of Scientific Research 3 (2): 188-194, 2008

2) http://www.stuartxchange.org/Abukado.html

Curator

                  Record - 16 of 46   [TOP]
Compound ID2314
Compound Structure
Plant SourcePersea americana Mill     Common Name:Avocado, Alligator Pear
Source FamilyLauraceae
OriginMexico
Plant Part UsedLeaf
ExtractSoxhlet hexane
Target BacteriaMycobacterium tuberculosis H37Ra
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]18 - 100 %
Activity [MIC] µg/ml31.2 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationDigestive, emmenagogue, antibacterial, antioxidant, antifungal, pectoral, stomachic, anthelmintic, antiperiodic, antidiarrheal
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) R. Gomez-Flores, C. Arzate-Quintana, R. Quintanilla-Licea, P. Tamez-Guerra, R. Tamez-Guerra, E. Monreal-Cuevas and C. Rodríguez-Padilla.Antimicrobial Activity of Persea americana Mill (Lauraceae) (Avocado) and Gymnosperma glutinosum (Spreng.) Less (Asteraceae) Leaf Extracts and Active Fractions Against Mycobacterium tuberculosis.American-Eurasian Journal of Scientific Research 3 (2): 188-194, 2008

2) http://www.stuartxchange.org/Abukado.html

Curator

                  Record - 17 of 46   [TOP]
Compound ID2315
Compound Structure
Plant SourcePersea americana Mill     Common Name:Avocado, Alligator Pear
Source FamilyLauraceae
OriginMexico
Plant Part UsedLeaf
ExtractSoxhlet hexane
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]84 - 100 %
Activity [MIC] µg/ml31.2 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal InformationDigestive, emmenagogue, antibacterial, antioxidant, antifungal, pectoral, stomachic, anthelmintic, antiperiodic, antidiarrheal
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) R. Gomez-Flores, C. Arzate-Quintana, R. Quintanilla-Licea, P. Tamez-Guerra, R. Tamez-Guerra, E. Monreal-Cuevas and C. Rodríguez-Padilla.Antimicrobial Activity of Persea americana Mill (Lauraceae) (Avocado) and Gymnosperma glutinosum (Spreng.) Less (Asteraceae) Leaf Extracts and Active Fractions Against Mycobacterium tuberculosis.American-Eurasian Journal of Scientific Research 3 (2): 188-194, 2008

2) http://www.stuartxchange.org/Abukado.html

Curator

                  Record - 18 of 46   [TOP]
Compound ID2410
Compound Structure
Plant SourcePleurotherium parviflorum Ducke     Common Name:
Source FamilyLauraceae
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) and 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 - 19 of 46   [TOP]
Compound ID3596
Compound Structure
Plant SourceNectandra hihua (R. & P.) Rowher     Common Name:
Source FamilyLauraceae
OriginPeru
Plant Part UsedBark
ExtractDichloromethane
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 27294)
Assay / Test DoneRadiometric assay using BACTEC 460 system
Positive Control Used (conc.)Rifampin (2 µg/ml), Ethambutol (7.5 µg/ml)
Inhibition [%]
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]13678239
Extract Preparation
Chemical Classification [Active Compound]
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
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

CuratorRachana, vikramjitmandal

                  Record - 20 of 46   [TOP]
Compound ID3984
Compound Structure
DOWNLOAD:
Plant SourceCinnamomum kotoense     Common Name:
Source FamilyLauraceae
Origin
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml2.8 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound IdentifiedLincomolide B
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Alicyclic, Butenolides, Fattyacid, Lactone, Ether, Alcohol, Alkene, Alkyne,
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight278.188
Molecular FormulaC17H26O3
SMILESC[C@@H]1OC(=O)/C(=C/CCCCCCCCCC#C)/[C@@H]1O
XLogP5.004
PSA46.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count9
No. of Rings1
No. of N0
No. of O3
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) Rogoza, L. N.; Salakhutdinov, N. F.; Tolstikov, G. A. Anti-tubercular Activity of Natural Products: Recent Developments. In Opportunity, Challenge and Scope of Natural Products in Medicinal Chemistry; Tiwari, V. K. Ed.; Research Signpost: India, 2011; pp 103-120

Curator

                  Record - 21 of 46   [TOP]
Compound ID3762
Compound Structure
DOWNLOAD:
Plant SourceLaurus novocanariensis     Common Name:
Source FamilyLauraceae
Origin
Plant Part UsedRipe fruit
ExtractLaurel oil
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 27294)
Assay / Test DoneFluorometric Alamar Blue Microassay (FMABA)
Positive Control Used (conc.)
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCostunolide
PubChem ID   5281437
Ethnomedicinal InformationAnti-inflammatory, skin infections, anti-rheumatic, vulnerary, blood depurative, stomachic, haemostatic, influenza, apoplexy, constipation
PubMed ID [Source Literature]17218447
Extract PreparationVolatile components were removed by hydrodistillation of the oil in a Clevenger - type apparatus to yield the essential oil and an odourless residue containing the lipids and other non - volatile compounds. The residue was partitioned between n - hexane and methanol to separate the lipid fraction from the more polar compounds, including the lactones. The methanolic fraction containing mainly the lactones costunolide (1) and dehydrocostuslactone (2) was further fractioned by column chromatography. 1 and 2 were identified by their mass spectra, and proton and carbon NMR spectra and their purity established as > 95 % by gas chromatography
Chemical Classification [Active Compound]Alicyclic, Bicyclic, Terpene, Sesquiterpene, Lactone
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight232.146
Molecular FormulaC15H20O2
SMILESO1[C@H]2[C@@H](CC/C(=C/CC/C(=C/2)/C)/C)C(=C)C1=O
XLogP3.308
PSA26.300
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count0
No. of Rings2
No. of N0
No. of O2
No. of S0
Reference(s)1) Luna-Herrera J, Costa MC, González HG, Rodrigues AI, Castilho PC.Synergistic antimycobacterial activities of sesquiterpene lactones from Laurus spp.J Antimicrob Chemother. 2007 Mar;59(3):548-52

CuratorVikramjitmandal

                  Record - 22 of 46   [TOP]
Compound ID3763
Compound Structure
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Plant SourceLaurus novocanariensis     Common Name:
Source FamilyLauraceae
Origin
Plant Part UsedRipe fruit
ExtractLaurel oil
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 35822) (Isoniazid resistant)
Assay / Test DoneFluorometric Alamar Blue Microassay (FMABA)
Positive Control Used (conc.)
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCostunolide
PubChem ID   5281437
Ethnomedicinal InformationAnti-inflammatory, skin infections, anti-rheumatic, vulnerary, blood depurative, stomachic, haemostatic, influenza, apoplexy, constipation
PubMed ID [Source Literature]17218447
Extract PreparationVolatile components were removed by hydrodistillation of the oil in a Clevenger - type apparatus to yield the essential oil and an odourless residue containing the lipids and other non - volatile compounds. The residue was partitioned between n - hexane and methanol to separate the lipid fraction from the more polar compounds, including the lactones. The methanolic fraction containing mainly the lactones costunolide (1) and dehydrocostuslactone (2) was further fractioned by column chromatography. 1 and 2 were identified by their mass spectra, and proton and carbon NMR spectra and their purity established as > 95 % by gas chromatography
Chemical Classification [Active Compound]Alicyclic, Bicyclic, Terpene, Sesquiterpene, Lactone
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight232.146
Molecular FormulaC15H20O2
SMILESO1[C@H]2[C@@H](CC/C(=C/CC/C(=C/2)/C)/C)C(=C)C1=O
XLogP3.308
PSA26.300
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count0
No. of Rings2
No. of N0
No. of O2
No. of S0
Reference(s)1) Luna-Herrera J, Costa MC, González HG, Rodrigues AI, Castilho PC.Synergistic antimycobacterial activities of sesquiterpene lactones from Laurus spp.J Antimicrob Chemother. 2007 Mar;59(3):548-52

CuratorVikramjitmandal

                  Record - 23 of 46   [TOP]
Compound ID3764
Compound Structure
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Plant SourceLaurus novocanariensis     Common Name:
Source FamilyLauraceae
Origin
Plant Part UsedRipe fruit
ExtractLaurel oil
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 35838) (Rifampin resistant)
Assay / Test DoneFluorometric Alamar Blue Microassay (FMABA)
Positive Control Used (conc.)
Inhibition [%]NR
Activity [MIC] µg/ml6.25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCostunolide
PubChem ID   5281437
Ethnomedicinal InformationAnti-inflammatory, skin infections, anti-rheumatic, vulnerary, blood depurative, stomachic, haemostatic, influenza, apoplexy, constipation
PubMed ID [Source Literature]17218447
Extract PreparationVolatile components were removed by hydrodistillation of the oil in a Clevenger - type apparatus to yield the essential oil and an odourless residue containing the lipids and other non - volatile compounds. The residue was partitioned between n - hexane and methanol to separate the lipid fraction from the more polar compounds, including the lactones. The methanolic fraction containing mainly the lactones costunolide (1) and dehydrocostuslactone (2) was further fractioned by column chromatography. 1 and 2 were identified by their mass spectra, and proton and carbon NMR spectra and their purity established as > 95 % by gas chromatography
Chemical Classification [Active Compound]Alicyclic, Bicyclic, Terpene, Sesquiterpene, Lactone
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight232.146
Molecular FormulaC15H20O2
SMILESO1[C@H]2[C@@H](CC/C(=C/CC/C(=C/2)/C)/C)C(=C)C1=O
XLogP3.308
PSA26.300
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count0
No. of Rings2
No. of N0
No. of O2
No. of S0
Reference(s)1) Luna-Herrera J, Costa MC, González HG, Rodrigues AI, Castilho PC.Synergistic antimycobacterial activities of sesquiterpene lactones from Laurus spp.J Antimicrob Chemother. 2007 Mar;59(3):548-52

CuratorVikramjitmandal

                  Record - 24 of 46   [TOP]
Compound ID3765
Compound Structure
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Plant SourceLaurus novocanariensis     Common Name:
Source FamilyLauraceae
Origin
Plant Part UsedRipe fruit
ExtractLaurel oil
Target BacteriaMycobacterium tuberculosis H37Rv (Streptomycin resistant)
Assay / Test DoneFluorometric Alamar Blue Microassay (FMABA)
Positive Control Used (conc.)
Inhibition [%]NR
Activity [MIC] µg/ml25 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCostunolide
PubChem ID   5281437
Ethnomedicinal InformationAnti-inflammatory, skin infections, anti-rheumatic, vulnerary, blood depurative, stomachic, haemostatic, influenza, apoplexy, constipation
PubMed ID [Source Literature]17218447
Extract PreparationVolatile components were removed by hydrodistillation of the oil in a Clevenger - type apparatus to yield the essential oil and an odourless residue containing the lipids and other non - volatile compounds. The residue was partitioned between n - hexane and methanol to separate the lipid fraction from the more polar compounds, including the lactones. The methanolic fraction containing mainly the lactones costunolide (1) and dehydrocostuslactone (2) was further fractioned by column chromatography. 1 and 2 were identified by their mass spectra, and proton and carbon NMR spectra and their purity established as > 95 % by gas chromatography
Chemical Classification [Active Compound]Alicyclic, Bicyclic, Terpene, Sesquiterpene, Lactone
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight232.146
Molecular FormulaC15H20O2
SMILESO1[C@H]2[C@@H](CC/C(=C/CC/C(=C/2)/C)/C)C(=C)C1=O
XLogP3.308
PSA26.300
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count0
No. of Rings2
No. of N0
No. of O2
No. of S0
Reference(s)1) Luna-Herrera J, Costa MC, González HG, Rodrigues AI, Castilho PC.Synergistic antimycobacterial activities of sesquiterpene lactones from Laurus spp.J Antimicrob Chemother. 2007 Mar;59(3):548-52

CuratorVikramjitmandal

                  Record - 25 of 46   [TOP]
Compound ID3766
Compound Structure
DOWNLOAD:
Plant SourceLaurus novocanariensis     Common Name:
Source FamilyLauraceae
Origin
Plant Part UsedRipe fruit
ExtractLaurel oil
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 35837) (Ethambutol resistant)
Assay / Test DoneFluorometric Alamar Blue Microassay (FMABA)
Positive Control Used (conc.)
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCostunolide
PubChem ID   5281437
Ethnomedicinal InformationAnti-inflammatory, skin infections, anti-rheumatic, vulnerary, blood depurative, stomachic, haemostatic, influenza, apoplexy, constipation
PubMed ID [Source Literature]17218447
Extract PreparationVolatile components were removed by hydrodistillation of the oil in a Clevenger - type apparatus to yield the essential oil and an odourless residue containing the lipids and other non - volatile compounds. The residue was partitioned between n - hexane and methanol to separate the lipid fraction from the more polar compounds, including the lactones. The methanolic fraction containing mainly the lactones costunolide (1) and dehydrocostuslactone (2) was further fractioned by column chromatography. 1 and 2 were identified by their mass spectra, and proton and carbon NMR spectra and their purity established as > 95 % by gas chromatography
Chemical Classification [Active Compound]Alicyclic, Bicyclic, Terpene, Sesquiterpene, Lactone
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]NR
Molecular Weight232.146
Molecular FormulaC15H20O2
SMILESO1[C@H]2[C@@H](CC/C(=C/CC/C(=C/2)/C)/C)C(=C)C1=O
XLogP3.308
PSA26.300
H-bond Donor0
H-bond Acceptor2
No. of Rotatable Bond Count0
No. of Rings2
No. of N0
No. of O2
No. of S0
Reference(s)1) Luna-Herrera J, Costa MC, González HG, Rodrigues AI, Castilho PC.Synergistic antimycobacterial activities of sesquiterpene lactones from Laurus spp.J Antimicrob Chemother. 2007 Mar;59(3):548-52

CuratorVikramjitmandal


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