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Compound ID4018
Compound Structure
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Plant SourceAnisochilus harmandii     Common Name:
Source FamilyLamiaceae
Origin
Plant Part Used
Extract
Target BacteriaMycobacterium tuberculosis
Assay / Test Done
Positive Control Used (conc.)
Inhibition [%]
Activity [MIC] µg/ml50 µg/ml
Activity (In terms of dilution)
Activity (Zone of inhibition in mm)
Active Compound Identified15-hydroxydehydroabietic acid
PubChem IDNR
Ethnomedicinal Information
PubMed ID [Source Literature]
Extract Preparation
Chemical Classification [Active Compound]Alicyclic, Tricyclic, Terpene, Diterpene, Acid, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]
Cytotoxicity Assay [AID]
Molecular Weight316.204
Molecular FormulaC20H28O3
SMILESC[C@]12[C@@H](CCc3cc(C(C)(O)C)ccc13)[C@](C)(C(=O)O)CCC2
XLogP5.770
PSA57.530
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count2
No. of Rings3
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) 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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