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                  Page - 1 of 1                  Record - 1 of 18   [TOP]
Compound ID2856
Compound StructureN/A
Plant SourceLippia origanoides     Common Name:Wild Marjoram
Source FamilyVerbenaceae
OriginColombia
Plant Part UsedLeaf, stem
ExtractLeaf and stem (3.1 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMTT assay
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml125 ± 0.01 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - Assisted Hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorKeya Mukherjee, reshmi

                  Record - 2 of 18   [TOP]
Compound ID2857
Compound StructureN/A
Plant SourceLippia origanoides     Common Name:Wild Marjoram
Source FamilyVerbenaceae
OriginColombia
Plant Part UsedLeaf, stem
ExtractLeaf and stem (3.1 %)
Target BacteriaMycobacterium tuberculosis H37Rv
Assay / Test DoneMTT assay
Positive Control Used (conc.)Isoniazid (0.19 ± 0.07 µg/ml), Rifampin (0.3 ± 0.21 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml125 ± 0.01 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedMixture of Essential oils (Mixture)
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]19753839
Extract PreparationMicrowave - Assisted Hydrodistillation (30 min, 250 ml water), using a Clevenger - type distillation apparatus and a Dean - Stark distillation trap in a domestic microwave oven (Kendo, MO-124, 2.5 GHz, 800 W) (9). Sodium sulfate was added as a drying agent to the decanted essential oil
Chemical Classification [Active Compound]Mixture
Media / Broth Used [Antimicrobial Assay/Test]Lowenstein Jensen (L-J) medium and Middlebrook 7H9 broth
Cytotoxicity Assay [AID]NR
Reference(s)1) Bueno-Sánchez JG, Martínez-Morales JR, Stashenko EE, Ribón W.Anti-tubercular activity of eleven aromatic and medicinal plants occurring in Colombia.Biomedica. 2009 Mar;29(1):51-60

CuratorKeya Mukherjee, reshmi

                  Record - 3 of 18   [TOP]
Compound ID3563
Compound Structure
DOWNLOAD:
Plant SourceCryptolepis sanguinolenta     Common Name:Nibima
Source FamilyApocynaceae
OriginWest Africa
Plant Part UsedRoot
ExtractAmmonia moistened chloroform
Target BacteriaMycobacterium fortuitum
Assay / Test DoneMTT Assay
Positive Control Used (conc.)Ethambutol (8 µg/ml), Isoniazid (0.5 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml16 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCryptolepine hydrochloride
PubChem ID   156093
Ethnomedicinal InformationAntimycobacterial, antimalarial
PubMed ID [Source Literature]12722159
Extract PreparationCryptolepine was isolated from Cryptolepis sanguinolenta roots and crystallized as the hydrochloride salt
Chemical Classification [Active Compound]Aromatic, Quinoline, Alkaloid, Indole
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton broth, Colombia blood agar, 7H9 Middle Brook medium
Cytotoxicity Assay [AID]NR
Molecular Weight232.100
Molecular FormulaC16H13ClN2
SMILESCl.n1(c2c(nc3c2cccc3)cc2c1cccc2)C
XLogP4.596
PSA15.600
H-bond Donor0
H-bond Acceptor1
No. of Rotatable Bond Count0
No. of Rings4
No. of N2
No. of O0
No. of S0
Reference(s)1) Gibbons S, Fallah F, Wright CW.Cryptolepine hydrochloride: a potent antimycobacterial alkaloid derived from Cryptolepis sanguinolenta.Phytother Res. 2003 Apr;17(4):434-6

CuratorWvarsha, rachanake

                  Record - 4 of 18   [TOP]
Compound ID3564
Compound Structure
DOWNLOAD:
Plant SourceCryptolepis sanguinolenta     Common Name:Nibima
Source FamilyApocynaceae
OriginWest Africa
Plant Part UsedRoot
ExtractAmmonia moistened chloroform
Target BacteriaMycobacterium smegmatis (ATCC 14468)
Assay / Test DoneMTT Assay
Positive Control Used (conc.)Ethambutol (0.25 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml8 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCryptolepine hydrochloride
PubChem ID   156093
Ethnomedicinal InformationAntimycobacterial, antimalarial
PubMed ID [Source Literature]12722159
Extract PreparationCryptolepine was isolated from Cryptolepis sanguinolenta roots and crystallized as the hydrochloride salt
Chemical Classification [Active Compound]Aromatic, Quinoline, Alkaloid, Indole
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton broth, Colombia blood agar, 7H9 Middle Brook medium
Cytotoxicity Assay [AID]NR
Molecular Weight232.100
Molecular FormulaC16H13ClN2
SMILESCl.n1(c2c(nc3c2cccc3)cc2c1cccc2)C
XLogP4.596
PSA15.600
H-bond Donor0
H-bond Acceptor1
No. of Rotatable Bond Count0
No. of Rings4
No. of N2
No. of O0
No. of S0
Reference(s)1) Gibbons S, Fallah F, Wright CW.Cryptolepine hydrochloride: a potent antimycobacterial alkaloid derived from Cryptolepis sanguinolenta.Phytother Res. 2003 Apr;17(4):434-6

CuratorWvarsha, rachanake

                  Record - 5 of 18   [TOP]
Compound ID3565
Compound Structure
DOWNLOAD:
Plant SourceCryptolepis sanguinolenta     Common Name:Nibima
Source FamilyApocynaceae
OriginWest Africa
Plant Part UsedRoot
ExtractAmmonia moistened chloroform
Target BacteriaMycobacterium phlei
Assay / Test DoneMTT Assay
Positive Control Used (conc.)Ethambutol (1 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml4 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCryptolepine hydrochloride
PubChem ID   156093
Ethnomedicinal InformationAntimycobacterial, antimalarial
PubMed ID [Source Literature]12722159
Extract PreparationCryptolepine was isolated from Cryptolepis sanguinolenta roots and crystallized as the hydrochloride salt
Chemical Classification [Active Compound]Aromatic, Quinoline, Alkaloid, Indole
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton broth, Colombia blood agar, 7H9 Middle Brook medium
Cytotoxicity Assay [AID]NR
Molecular Weight232.100
Molecular FormulaC16H13ClN2
SMILESCl.n1(c2c(nc3c2cccc3)cc2c1cccc2)C
XLogP4.596
PSA15.600
H-bond Donor0
H-bond Acceptor1
No. of Rotatable Bond Count0
No. of Rings4
No. of N2
No. of O0
No. of S0
Reference(s)1) Gibbons S, Fallah F, Wright CW.Cryptolepine hydrochloride: a potent antimycobacterial alkaloid derived from Cryptolepis sanguinolenta.Phytother Res. 2003 Apr;17(4):434-6

CuratorWvarsha, rachanake

                  Record - 6 of 18   [TOP]
Compound ID3566
Compound Structure
DOWNLOAD:
Plant SourceCryptolepis sanguinolenta     Common Name:Nibima
Source FamilyApocynaceae
OriginWest Africa
Plant Part UsedRoot
ExtractAmmonia moistened chloroform
Target BacteriaMycobacterium abscessus
Assay / Test DoneMTT Assay
Positive Control Used (conc.)Ethambutol (128 µg/ml), Isoniazid (32 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml32 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCryptolepine hydrochloride
PubChem ID   156093
Ethnomedicinal InformationAntimycobacterial, antimalarial
PubMed ID [Source Literature]12722159
Extract PreparationCryptolepine was isolated from Cryptolepis sanguinolenta roots and crystallized as the hydrochloride salt
Chemical Classification [Active Compound]Aromatic, Quinoline, Alkaloid, Indole
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton broth, Colombia blood agar, 7H9 Middle Brook medium
Cytotoxicity Assay [AID]NR
Molecular Weight232.100
Molecular FormulaC16H13ClN2
SMILESCl.n1(c2c(nc3c2cccc3)cc2c1cccc2)C
XLogP4.596
PSA15.600
H-bond Donor0
H-bond Acceptor1
No. of Rotatable Bond Count0
No. of Rings4
No. of N2
No. of O0
No. of S0
Reference(s)1) Gibbons S, Fallah F, Wright CW.Cryptolepine hydrochloride: a potent antimycobacterial alkaloid derived from Cryptolepis sanguinolenta.Phytother Res. 2003 Apr;17(4):434-6

CuratorWvarsha, rachanake

                  Record - 7 of 18   [TOP]
Compound ID3567
Compound Structure
DOWNLOAD:
Plant SourceCryptolepis sanguinolenta     Common Name:Nibima
Source FamilyApocynaceae
OriginWest Africa
Plant Part UsedRoot
ExtractAmmonia moistened chloroform
Target BacteriaMycobacterium aurum
Assay / Test DoneMTT Assay
Positive Control Used (conc.)Ethambutol (1 µg/ml), Isoniazid (2 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml2 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCryptolepine hydrochloride
PubChem ID   156093
Ethnomedicinal InformationAntimycobacterial,AntimalAerial
PubMed ID [Source Literature]12722159
Extract PreparationCryptolepine was isolated from Cryptolepis sanguinolenta roots and crystallized as the hydrochloride salt
Chemical Classification [Active Compound]Aromatic, Quinoline, Alkaloid, Indole
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton broth, Colombia blood agar, 7H9 Middle Brook medium
Cytotoxicity Assay [AID]NR
Molecular Weight232.100
Molecular FormulaC16H13ClN2
SMILESCl.n1(c2c(nc3c2cccc3)cc2c1cccc2)C
XLogP4.596
PSA15.600
H-bond Donor0
H-bond Acceptor1
No. of Rotatable Bond Count0
No. of Rings4
No. of N2
No. of O0
No. of S0
Reference(s)1) Gibbons S, Fallah F, Wright CW.Cryptolepine hydrochloride: a potent antimycobacterial alkaloid derived from Cryptolepis sanguinolenta.Phytother Res. 2003 Apr;17(4):434-6

CuratorWvarsha, rachanake

                  Record - 8 of 18   [TOP]
Compound ID3568
Compound Structure
DOWNLOAD:
Plant SourceCryptolepis sanguinolenta     Common Name:Nibima
Source FamilyApocynaceae
OriginWest Africa
Plant Part UsedRoot
ExtractAmmonia moistened chloroform
Target BacteriaMycobacterium bovis (BCG - Bacillus Calmette Guerin)
Assay / Test DoneMTT Assay
Positive Control Used (conc.)Streptomycin sulphate (6.25 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml12.5 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedCryptolepine hydrochloride
PubChem ID   156093
Ethnomedicinal InformationAntimycobacterial,AntimalAerial
PubMed ID [Source Literature]12722159
Extract PreparationCryptolepine was isolated from Cryptolepis sanguinolenta roots and crystallized as the hydrochloride salt
Chemical Classification [Active Compound]Aromatic, Quinoline, Alkaloid, Indole
Media / Broth Used [Antimicrobial Assay/Test]Mueller - Hinton broth, Colombia blood agar, 7H9 Middle Brook medium
Cytotoxicity Assay [AID]NR
Molecular Weight232.100
Molecular FormulaC16H13ClN2
SMILESCl.n1(c2c(nc3c2cccc3)cc2c1cccc2)C
XLogP4.596
PSA15.600
H-bond Donor0
H-bond Acceptor1
No. of Rotatable Bond Count0
No. of Rings4
No. of N2
No. of O0
No. of S0
Reference(s)1) Gibbons S, Fallah F, Wright CW.Cryptolepine hydrochloride: a potent antimycobacterial alkaloid derived from Cryptolepis sanguinolenta.Phytother Res. 2003 Apr;17(4):434-6

CuratorWvarsha, rachanake

                  Record - 9 of 18   [TOP]
Compound ID3778
Compound StructureNR
Plant SourceEvodia elleryana (Melicope elleryana)     Common Name:Sehit
Source FamilyRutaceae
OriginKurti region of Manus Island, Papua New Guinea
Plant Part UsedBark
ExtractHexane
Target BacteriaMycobacterium tuberculosis H37Ra (ATCC 25177)
Assay / Test DoneMTT assay
Positive Control Used (conc.)Rifampin (5 µg/ml), Isoniazid (50 µg/ml)
Inhibition [%]>= 70 % (50 µg/ml)
Activity [MIC] µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedNR
PubChem IDNR
Ethnomedicinal InformationCough, fever, whooping cough, occasionally used to control fertility in women
PubMed ID [Source Literature]17350179
Extract PreparationSoxhlet extracts (hexane, ethyl acetate and methanol in sequence) of bark, stem and leaves
Chemical Classification [Active Compound]
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]Against Human T cells
Reference(s)1) Barrows LR, Powan E, Pond CD, Matainaho T.Anti-TB activity of Evodia elleryana bark extract.Fitoterapia. 2007 Apr;78(3):250-2. Epub 2007 Feb 3

CuratorVikramjitmandal, rachanake

                  Record - 10 of 18   [TOP]
Compound ID3780
Compound StructureNR
Plant SourceEvodia elleryana (Melicope elleryana)     Common Name:Sehit
Source FamilyRutaceae
OriginKurti region of Manus Island, Papua New Guinea
Plant Part UsedBark
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra (ATCC 25177)
Assay / Test DoneMTT assay
Positive Control Used (conc.)Rifampin (5 µg/ml), Isoniazid (50 µg/ml)
Inhibition [%]< 30 % (50 µg/ml)
Activity [MIC] µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedNR
PubChem IDNR
Ethnomedicinal InformationCough, fever, whooping cough, occasionally used to control fertility in women
PubMed ID [Source Literature]17350179
Extract PreparationSoxhlet extracts (hexane, ethyl acetate and methanol in sequence) of bark, stem and leaves
Chemical Classification [Active Compound]
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]Against Human T cells
Reference(s)1) Barrows LR, Powan E, Pond CD, Matainaho T.Anti-TB activity of Evodia elleryana bark extract.Fitoterapia. 2007 Apr;78(3):250-2. Epub 2007 Feb 3

CuratorVikramjitmandal, rachanake

                  Record - 11 of 18   [TOP]
Compound ID3782
Compound StructureNR
Plant SourceEvodia elleryana (Melicope elleryana)     Common Name:Sehit
Source FamilyRutaceae
OriginKurti region of Manus Island, Papua New Guinea
Plant Part UsedBark
ExtractEthyl acetate
Target BacteriaMycobacterium tuberculosis H37Ra (ATCC 25177)
Assay / Test DoneMTT assay
Positive Control Used (conc.)Rifampin (5 µg/ml), Isoniazid (50 µg/ml)
Inhibition [%]>= 70 % (50 µg/ml)
Activity [MIC] µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedNR
PubChem IDNR
Ethnomedicinal InformationCough, fever, whooping cough, occasionally used to control fertility in women
PubMed ID [Source Literature]17350179
Extract PreparationSoxhlet extracts (hexane, ethyl acetate and methanol in sequence) of bark, stem and leaves
Chemical Classification [Active Compound]
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]Against Human T cells
Reference(s)1) Barrows LR, Powan E, Pond CD, Matainaho T.Anti-TB activity of Evodia elleryana bark extract.Fitoterapia. 2007 Apr;78(3):250-2. Epub 2007 Feb 3

CuratorVikramjitmandal, rachanake

                  Record - 12 of 18   [TOP]
Compound ID3784
Compound StructureNR
Plant SourceEvodia elleryana (Melicope elleryana)     Common Name:Sehit
Source FamilyRutaceae
OriginKurti region of Manus Island, Papua New Guinea
Plant Part UsedStem
ExtractHexane
Target BacteriaMycobacterium tuberculosis H37Ra (ATCC 25177)
Assay / Test DoneMTT assay
Positive Control Used (conc.)Rifampin (5 µg/ml), Isoniazid (50 µg/ml)
Inhibition [%]< 70 % and >= 30 % (50 µg/ml)
Activity [MIC] µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedNR
PubChem IDNR
Ethnomedicinal InformationCough, fever, whooping cough, occasionally used to control fertility in women
PubMed ID [Source Literature]17350179
Extract PreparationSoxhlet extracts (hexane, ethyl acetate and methanol in sequence) of bark, stem and leaves
Chemical Classification [Active Compound]
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]Against Human T cells
Reference(s)1) Barrows LR, Powan E, Pond CD, Matainaho T.Anti-TB activity of Evodia elleryana bark extract.Fitoterapia. 2007 Apr;78(3):250-2. Epub 2007 Feb 3

CuratorVikramjitmandal, rachanake

                  Record - 13 of 18   [TOP]
Compound ID3786
Compound StructureNR
Plant SourceEvodia elleryana (Melicope elleryana)     Common Name:Sehit
Source FamilyRutaceae
OriginKurti region of Manus Island, Papua New Guinea
Plant Part UsedStem
ExtractEthyl acetate
Target BacteriaMycobacterium tuberculosis H37Ra (ATCC 25177)
Assay / Test DoneMTT assay
Positive Control Used (conc.)Rifampin (5 µg/ml), Isoniazid (50 µg/ml)
Inhibition [%]< 30 % (50 µg/ml)
Activity [MIC] µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedNR
PubChem IDNR
Ethnomedicinal InformationCough, fever, whooping cough, occasionally used to control fertility in women
PubMed ID [Source Literature]17350179
Extract PreparationSoxhlet extracts (hexane, ethyl acetate and methanol in sequence) of bark, stem and leaves
Chemical Classification [Active Compound]
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]Against Human T cells
Reference(s)1) Barrows LR, Powan E, Pond CD, Matainaho T.Anti-TB activity of Evodia elleryana bark extract.Fitoterapia. 2007 Apr;78(3):250-2. Epub 2007 Feb 3

CuratorVikramjitmandal, rachanake

                  Record - 14 of 18   [TOP]
Compound ID3788
Compound StructureNR
Plant SourceEvodia elleryana (Melicope elleryana)     Common Name:Sehit
Source FamilyRutaceae
OriginKurti region of Manus Island, Papua New Guinea
Plant Part UsedStem
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra (ATCC 25177)
Assay / Test DoneMTT assay
Positive Control Used (conc.)Rifampin (5 µg/ml), Isoniazid (50 µg/ml)
Inhibition [%]< 30 % (50 µg/ml)
Activity [MIC] µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedNR
PubChem IDNR
Ethnomedicinal InformationCough, fever, whooping cough, occasionally used to control fertility in women
PubMed ID [Source Literature]17350179
Extract PreparationSoxhlet extracts (hexane, ethyl acetate and methanol in sequence) of bark, stem and leaves
Chemical Classification [Active Compound]
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]Against Human T cells
Reference(s)1) Barrows LR, Powan E, Pond CD, Matainaho T.Anti-TB activity of Evodia elleryana bark extract.Fitoterapia. 2007 Apr;78(3):250-2. Epub 2007 Feb 3

CuratorVikramjitmandal, rachanake

                  Record - 15 of 18   [TOP]
Compound ID3790
Compound StructureNR
Plant SourceEvodia elleryana (Melicope elleryana)     Common Name:Sehit
Source FamilyRutaceae
OriginKurti region of Manus Island, Papua New Guinea
Plant Part UsedLeaf
ExtractHexane
Target BacteriaMycobacterium tuberculosis H37Ra (ATCC 25177)
Assay / Test DoneMTT assay
Positive Control Used (conc.)Rifampin (5 µg/ml), Isoniazid (50 µg/ml)
Inhibition [%]< 70 % and >= 30 % (50 µg/ml)
Activity [MIC] µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedNR
PubChem IDNR
Ethnomedicinal InformationCough, fever, whooping cough, occasionally used to control fertility in women
PubMed ID [Source Literature]17350179
Extract PreparationSoxhlet extracts (hexane, ethyl acetate and methanol in sequence) of bark, stem and leaves
Chemical Classification [Active Compound]
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]Against Human T cells
Reference(s)1) Barrows LR, Powan E, Pond CD, Matainaho T.Anti-TB activity of Evodia elleryana bark extract.Fitoterapia. 2007 Apr;78(3):250-2. Epub 2007 Feb 3

CuratorVikramjitmandal, rachanake

                  Record - 16 of 18   [TOP]
Compound ID3792
Compound StructureNR
Plant SourceEvodia elleryana (Melicope elleryana)     Common Name:Sehit
Source FamilyRutaceae
OriginKurti region of Manus Island, Papua New Guinea
Plant Part UsedLeaf
ExtractEthyl acetate
Target BacteriaMycobacterium tuberculosis H37Ra (ATCC 25177)
Assay / Test DoneMTT assay
Positive Control Used (conc.)Rifampin (5 µg/ml), Isoniazid (50 µg/ml)
Inhibition [%]< 30 % (50 µg/ml)
Activity [MIC] µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedNR
PubChem IDNR
Ethnomedicinal InformationCough, fever, whooping cough, occasionally used to control fertility in women
PubMed ID [Source Literature]17350179
Extract PreparationSoxhlet extracts (hexane, ethyl acetate and methanol in sequence) of bark, stem and leaves
Chemical Classification [Active Compound]
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]Against Human T cells
Reference(s)1) Barrows LR, Powan E, Pond CD, Matainaho T.Anti-TB activity of Evodia elleryana bark extract.Fitoterapia. 2007 Apr;78(3):250-2. Epub 2007 Feb 3

CuratorVikramjitmandal, rachanake

                  Record - 17 of 18   [TOP]
Compound ID3794
Compound StructureNR
Plant SourceEvodia elleryana (Melicope elleryana)     Common Name:Sehit
Source FamilyRutaceae
OriginKurti region of Manus Island, Papua New Guinea
Plant Part UsedLeaf
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra (ATCC 25177)
Assay / Test DoneMTT assay
Positive Control Used (conc.)Rifampin (5 µg/ml), Isoniazid (50 µg/ml)
Inhibition [%]< 30 % (50 µg/ml)
Activity [MIC] µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedNR
PubChem IDNR
Ethnomedicinal InformationCough, fever, whooping cough, occasionally used to control fertility in women
PubMed ID [Source Literature]17350179
Extract PreparationSoxhlet extracts (hexane, ethyl acetate and methanol in sequence) of bark, stem and leaves
Chemical Classification [Active Compound]
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]Against Human T cells
Reference(s)1) Barrows LR, Powan E, Pond CD, Matainaho T.Anti-TB activity of Evodia elleryana bark extract.Fitoterapia. 2007 Apr;78(3):250-2. Epub 2007 Feb 3

CuratorVikramjitmandal, rachanake

                  Record - 18 of 18   [TOP]
Compound ID3861
Compound Structure
DOWNLOAD:
Plant SourceRhus taitensis Guill.     Common Name:Pumac
Source FamilyAnacardiaceae
OriginPapua New Guinea
Plant Part UsedLeaf, twig
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Ra (ATCC 25177)
Assay / Test DoneMTT Assay
Positive Control Used (conc.)Rifampin (0.0025 - 0.0079 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml10 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedTetrahydroxysqualene
PubChem ID   25058109
Ethnomedicinal InformationNR
PubMed ID [Source Literature]18710283
Extract PreparationAir - dried leaves and twigs (108.6 g) of Rhus taitensis were ground and extracted with 250 ml MeOH (3 × 24 hours) at room temperature. The crude extract (1.7 g) was filtered and concentrated in vacuo. 5 grams of the crude extract were dissolved in MeOH and mixed with 5 g of HP20SS and dried. The mixture was then poured into a column and fractionated using 100 % water, 75 % H2O / 25 % 2 - propanol, 50 % H2O / 50 % 2 - propanol, 25 % H2O / 75 % 2 - propanol, and 100 % MeOH to yield five fractions designated FW, F1, F2, F3, F4, respectively. The fractions were collected and the solvents evaporated using a centrifugal evaporator
Chemical Classification [Active Compound]Aliphatic, Alkene, Terpene, Triterpene, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]ADC (Remel) supplemented 7H9 medium
Cytotoxicity Assay [AID]Against Human T cells
Molecular Weight474.371
Molecular FormulaC30H50O4
SMILESOCC(=CCC/C(=C/CC/C(=C/CC/C=C(/CC/C=C(/CCC=C(CO)CO)C)C)/C)/C)CO
XLogP5.646
PSA80.920
H-bond Donor4
H-bond Acceptor4
No. of Rotatable Bond Count19
No. of Rings0
No. of N0
No. of O4
No. of S0
Reference(s)1) Noro JC, Barrows LR, Gideon OG, Ireland CM, Koch M, Matainaho T, Piskaut P, Pond CD, Bugni TS.Tetrahdroxysqualene from Rhus taitensis shows antimycobacterial activity against Mycobacterium tuberculosis.J Nat Prod. 2008 Sep;71(9):1623-4. Epub 2008 Aug 19

CuratorKeyaMukherjee, Farzana Shamsudeen, gppreetha


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