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Compound ID3072
Compound Structure
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Plant SourceCostus     Common Name:NR
Source FamilyCostaceae
OriginNR
Plant Part UsedNR
ExtractNR
Target BacteriaMycobacterium tuberculosis
Assay / Test DoneRadiorespirometric Bioassay
Positive Control Used (conc.)NR
Inhibition [%]NR
Activity [MIC] µg/ml128 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedPumilin
PubChem ID   6436294
Ethnomedicinal InformationNR
PubMed ID [Source Literature]9784148
Extract PreparationNR
Chemical Classification [Active Compound]Alicyclic, Tricyclic, Terpene, Sesquiterpene, Lactone , Acyl, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]NR
Molecular Weight374.137
Molecular FormulaC20H22O7
SMILESO1[C@H]2[C@@H]([C@@H](O)[C@H](OC(=O)/C(=CC)/C)C(=C3[C@]2(O)C(=CC3=O)C)C)C(=C)C1=O
XLogP-0.432
PSA110.130
H-bond Donor2
H-bond Acceptor7
No. of Rotatable Bond Count3
No. of Rings3
No. of N0
No. of O7
No. of S0
Reference(s)1) Cantrell CL, Nuņez IS, Castaņeda-Acosta J, Foroozesh M, Fronczek FR, Fischer NH, Franzblau SG.Antimycobacterial activities of dehydrocostus lactone and its oxidation products.J Nat Prod. 1998 Oct;61(10):1181-6

CuratorFarzana-shamsudeen, gppreetha

                  Record - 2 of 2   [TOP]
Compound ID3073
Compound Structure
DOWNLOAD:
Plant SourceCostus     Common Name:NR
Source FamilyCostaceae
OriginNR
Plant Part UsedNR
ExtractNR
Target BacteriaMycobacterium avium
Assay / Test DoneRadiorespirometric Bioassay
Positive Control Used (conc.)NR
Inhibition [%]NR
Activity [MIC] µg/ml128 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound IdentifiedPumilin
PubChem ID   6436294
Ethnomedicinal Information
PubMed ID [Source Literature]9784148
Extract PreparationNR
Chemical Classification [Active Compound]Alicyclic, Tricyclic, Terpene, Sesquiterpene, Lactone , Acyl, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]
Molecular Weight374.137
Molecular FormulaC20H22O7
SMILESO1[C@H]2[C@@H]([C@@H](O)[C@H](OC(=O)/C(=CC)/C)C(=C3[C@]2(O)C(=CC3=O)C)C)C(=C)C1=O
XLogP-0.432
PSA110.130
H-bond Donor2
H-bond Acceptor7
No. of Rotatable Bond Count3
No. of Rings3
No. of N0
No. of O7
No. of S0
Reference(s)1) Cantrell CL, Nuņez IS, Castaņeda-Acosta J, Foroozesh M, Fronczek FR, Fischer NH, Franzblau SG.Antimycobacterial activities of dehydrocostus lactone and its oxidation products.J Nat Prod. 1998 Oct;61(10):1181-6

Curator


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