Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H26Cl2O2 |
| Molecular Weight | 381.336 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C1=C(O)C(CC2=C(C)C(Cl)=CC(C(C)C)=C2O)=C(C)C(Cl)=C1
InChI
InChIKey=HNOOXWDWUSLXOB-UHFFFAOYSA-N
InChI=1S/C21H26Cl2O2/c1-10(2)14-8-18(22)12(5)16(20(14)24)7-17-13(6)19(23)9-15(11(3)4)21(17)25/h8-11,24-25H,7H2,1-6H3
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/28925466
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28925466
Biclotymol, a phenolic antiseptic has multiple actions: it has bacteriostatic, bactericidal, anti-inflammatory and analgesic activity. Biclotymol is recommended as a prompt, effective and safe first-line option for the treatment of sore throat.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: GO:0044277 Sources: https://www.ncbi.nlm.nih.gov/pubmed/28925466 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Role of biclotymol-based products in the treatment of infectious sore throat. | 2017-08 |
|
| Collective relaxation dynamics and crystallization kinetics of the amorphous Biclotymol antiseptic. | 2015-11-10 |
|
| Overall monotropic behavior of a metastable phase of biclotymol, 2,2'-methylenebis(4-chloro-3-methyl-isopropylphenol), inferred from experimental and topological construction of the related P-T state diagram. | 2008-09 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28925466
5-minute application of a 90% biclotymol-based mouthwash (Hexaspray, biclotymol 2.5%, Laboratoires Bouchara Recordati, France) reduced by 5-log the concentration of Pseudomonas aeruginosa strains (data on fle). Similar results were reported for Escherichia coli and Enterococcus strains.
Route of Administration:
Irrigation
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NCI_THESAURUS |
C28394
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ACTIVE MOIETY