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Compound ID3588
Compound Structure
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Plant SourceCaleolaria pinnifolia Cav.     Common Name:NR
Source FamilyScrophulariaceae
OriginNR
Plant Part UsedAerial
ExtractDichloromethane:Methanol
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 27 294)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.06 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 Identified19 - Malonyloxydehydroabietinol
PubChem IDNR
Ethnomedicinal InformationNR
PubMed ID [Source Literature]12898418
Extract PreparationNR
Chemical Classification [Active Compound]Alicyclic, Tricyclic, Terpene, Diterpene, Malonyl
Media / Broth Used [Antimicrobial Assay/Test]NR
Cytotoxicity Assay [AID]NR
Molecular Weight372.230
Molecular FormulaC23H32O4
SMILESC1CC[C@](C2[C@@]1(c1c(CC2)cc(cc1)C(C)C)C)(C)COC(=O)CC(=O)O
XLogP8.774
PSA63.600
H-bond Donor1
H-bond Acceptor4
No. of Rotatable Bond Count6
No. of Rings3
No. of N0
No. of O4
No. of S0
Reference(s)1) Woldemichael GM, Franzblau SG, Zhang F, Wang Y, Timmermann BN.Inhibitory effect of sterols from Ruprechtia triflora and diterpenes from Calceolaria pinnifolia on the growth of Mycobacterium tuberculosis.Planta Med. 2003 Jul;69(7):628-31

CuratorReshmi, vikramjitmandal


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