| Weight | 424.991 g/mol |
|---|---|
| Formula | C18H33ClN2O5S |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 7 |
clindamycin (18323-44-9)
Cleocin · Clindamycin Hydrochloride · Dalacin C
Score:
#51 in Microbiology
,
#690 in Biology
,
#744 in Chemistry
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- Streptococcus pneumoniae and Streptococcus pyogenes resistant to macrolides but sensitive to clindamycin: a common resistance pattern mediated by an efflux system. (Antimicrobial Agents and Chemotherapy, 1996)
- Letter: Clindamycin and pseudomembranous colitis. (The Lancet, 1974)
- Clindamycin-associated colitis. A prospective study. (Annals of Internal Medicine, 1974)
- The Eagle Effect Revisited: Efficacy of Clindamycin, Erythromycin, and Penicillin in the Treatment of Streptococcal Myositis (The Journal of Infectious Diseases, 1988)
- Clindamycin-Associated Colitis Due to a Toxin-Producing Species of Clostridium in Hamsters (The Journal of Infectious Diseases, 1977)
- Practical Disk Diffusion Method for Detection of Inducible Clindamycin Resistance in Staphylococcus aureus and Coagulase-Negative Staphylococci (Journal of Clinical Microbiology, 2003)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Cleocin
- Clindamycin Hydrochloride
- Dalacin C
- Chlolincocin
- Clindamycin Monohydrochloride
- 7-Chloro-7-deoxylincomycin
- Chlorlincocin
- 7 Chloro 7 deoxylincomycin
- Monohydrate Clindamycin Monohydrochloride
-
SMILESCCCC1CC(N(C1)C)C(=O)NC(C2C(C(C(C(O2)SC)O)O)O)C(C)Cl
-
InChIKeyKDLRVYVGXIQJDK-UHFFFAOYSA-N
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