|  Home  |Search   |  Browse  |Similarity   |Data Visualization  |Submission  |Contact Us  |  













                  Page - 1 of 1                  Record - 1 of 1   [TOP]
Compound ID3662
Compound Structure
DOWNLOAD:
Plant SourceChrysanthemum morifolium RAMAT.     Common Name:Chrysanthemum
Source FamilyAsteraceae (Compositae)
OriginAsia and Northeastern Europe
Plant Part UsedFlower
ExtractMethanol
Target BacteriaMycobacterium tuberculosis H37Rv (ATCC 27 294)
Assay / Test DoneMicroplate Alamar Blue Assay (MABA)
Positive Control Used (conc.)Rifampin (0.25 µg/ml)
Inhibition [%]NR
Activity [MIC] µg/ml> 64 µg/ml
Activity (In terms of dilution)NR
Activity (Zone of inhibition in mm)NR
Active Compound Identified(24S) - 25 - Methoxycycloartane - 3β, 24-diol
PubChem ID   5270669
Ethnomedicinal InformationAnti - inflammatory, analgesic, antipyretic
PubMed ID [Source Literature]15635183
Extract PreparationNR
Chemical Classification [Active Compound]Alicyclic, Pentacyclic, Terpene, Triterpene,Cycloartane, Alcohol
Media / Broth Used [Antimicrobial Assay/Test]Middlebrook 7H12 medium
Cytotoxicity Assay [AID]Against Vero cells (ATCCCCL- 81) in the CellTiter 96 aqueous nonradioactive cell proliferation assay
Molecular Weight474.407
Molecular FormulaC31H54O3
SMILESO[C@@H]1C([C@H]2[C@@]3([C@@]4(C3)[C@H]([C@]3([C@](CC4)([C@H](CC3)[C@@H](CC[C@H](O)C(OC)(C)C)C)C)C)CC2)CC1)(C)C
XLogP10.091
PSA49.690
H-bond Donor2
H-bond Acceptor3
No. of Rotatable Bond Count6
No. of Rings5
No. of N0
No. of O3
No. of S0
Reference(s)1) Akihisa T, Franzblau SG, Ukiya M, Okuda H, Zhang F, Yasukawa K, Suzuki T, Kimura Y.Antitubercular activity of triterpenoids from Asteraceae flowers.Biol Pharm Bull. 2005 Jan;28(1):158-60

CuratorVikramjitmandal


Developed by: CSIR- OSDD Unit, Delhi, India and Hosted by: Bioinformatics Centre,   Institute of Microbial Technology, Sec-39A, Chandigarh, India.
The website has been tested on the latest version of Google Chrome (34.0.1847.137 m) and Mozilla Firefox (29.0.1)