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Submit ReviewClindamycin hydrochloride is a lincosamide antibiotic. Inhibits protein synthesis by binding to the 50S ribosomal subunit and preventing early peptide chain elongation in bacteria.
Sold for research purposes under agreement from Pfizer Inc.
M. Wt | 461.44 |
Formula | C18H33ClN2O5S.HCl |
Storage | Store at -20°C |
Purity | ≥98% (HPLC) |
CAS Number | 21462-39-5 |
PubChem ID | 16051951 |
InChI Key | AUODDLQVRAJAJM-XJQDNNTCSA-N |
Smiles | CN1[C@H]([C@@](N[C@@]([H])([C@@]2([H])O[C@H](SC)[C@H](O)[C@@H](O)[C@H]2O)[C@@H](Cl)C)=O)C[C@@H](CCC)C1.Cl |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
References are publications that support the biological activity of the product.
Champney and Tober (2000) Specific inhibition of 50S ribosomal subunit formation in Staphylococcus aureus cells by 16-membered macrolide, lincosamide, and streptogramin B antibiotics. Curr.Microbiol. 41 126 PMID: 10856379
Dhawan and Thadepalli (1982) Clindamycin: a review of fifteen years of experience. Rev.Infect.Dis. 4 1133 PMID: 6818656
Keywords: Clindamycin hydrochloride, Clindamycin hydrochloride supplier, Lincosamide, antibiotics, bacterial, infections, inhibitors, inhibits, protein, synthesis, 50S, ribosomal, ribosome, bacteria, Antibiotics, 4822, Tocris Bioscience
Citations are publications that use Tocris products.
Currently there are no citations for Clindamycin hydrochloride.
Average Rating: 5 (Based on 1 Review.)
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