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Compound ID3742
Compound Structure
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Plant SourceSwartzia polyphylla DC     Common Name:Cumaseba
Source FamilyFabaceae
OriginPeru
Plant Part UsedBark
ExtractEthanol (95 %)
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 27 294)
Assay / Test DoneTetrazolium Microplate Assay (TEMA)
Positive Control Used (conc.)NR
Inhibition [%]NR
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedT-cadinol
PubChem ID   160799
Ethnomedicinal InformationLarvicidal, antifungal, aphrodisiac, antiseptic, tonic, bad eyesight, bone fractures, childbirth, colds, dislocations, fatigue, fungal infections, laziness, optic nerve injuries, rheumatism, and yeast infections. It also inhibits the in vitro growth of the dermatophyte Trichophyton mentagrophytes, and was active against the larvae of the mosquito Culex quinquefasciatus
PubMed ID [Source Literature]16462085
Extract Preparation
Chemical Classification [Active Compound]Alicyclic, Bicyclic, Terpene, Sesquiterpene, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight222.198
Molecular FormulaC15H26O
SMILESO[C@@]1([C@H]2[C@H]([C@@H](CC1)C(C)C)C=C(CC2)C)C
XLogP4.476
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count1
No. of Rings2
No. of N0
No. of O1
No. of S0
Reference(s)1) Rojas R, Bustamante B, Ventosilla P, Fernádez I, Caviedes L, Gilman RH, Lock O, Hammond GB.Larvicidal, antimycobacterial and antifungal compounds from the bark of the Peruvian plant Swartzia polyphylla DC.Chem Pharm Bull (Tokyo). 2006 Feb;54(2):278-9

CuratorVikramjitmandal

                  Record - 2 of 2   [TOP]
Compound ID3743
Compound Structure
DOWNLOAD:
Plant SourceSwartzia polyphylla DC     Common Name:Cumaseba
Source FamilyFabaceae
OriginPeru
Plant Part UsedBark
ExtractEthanol (95 %)
Target BacteriaMulti - drug resistant Mycobacterium tuberculosis strain (Clinical isolate, strain 02 tuberculosis DM039EP097)
Assay / Test DoneTetrazolium Microplate Assay (TEMA)
Positive Control Used (conc.)NR
Inhibition [%]NR
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedT-cadinol
PubChem ID   160799
Ethnomedicinal InformationLarvicidal, antifungal, aphrodisiac, antiseptic, tonic, bad eyesight, bone fractures, childbirth, colds, dislocations, fatigue, fungal infections, laziness, optic nerve injuries, rheumatism, and yeast infections. It also inhibits the in vitro growth of the dermatophyte Trichophyton mentagrophytes, and was active against the larvae of the mosquito Culex quinquefasciatus
PubMed ID [Source Literature]16462085
Extract Preparation
Chemical Classification [Active Compound]Alicyclic, Bicyclic, Terpene, Sesquiterpene, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight222.198
Molecular FormulaC15H26O
SMILESO[C@@]1([C@H]2[C@H]([C@@H](CC1)C(C)C)C=C(CC2)C)C
XLogP4.476
PSA20.230
H-bond Donor1
H-bond Acceptor1
No. of Rotatable Bond Count1
No. of Rings2
No. of N0
No. of O1
No. of S0
Reference(s)1) Rojas R, Bustamante B, Ventosilla P, Fernádez I, Caviedes L, Gilman RH, Lock O, Hammond GB.Larvicidal, antimycobacterial and antifungal compounds from the bark of the Peruvian plant Swartzia polyphylla DC.Chem Pharm Bull (Tokyo). 2006 Feb;54(2):278-9

CuratorVikramjitmandal


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