| Weight | 406.545 g/mol |
|---|---|
| Formula | C18H34N2O6S |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 7 |
lincomycin (154-21-2)
Lincocin · Lincomycin Hydrochloride · Lincomycin A
Score:
#93 in Microbiology
,
#298 in Biochemistry
,
#1106 in Biology
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#1245 in Chemistry
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- The rate constant of photoinhibition, measured in lincomycin-treated leaves, is directly proportional to light intensity. (Proceedings of the National Academy of Sciences of the United States of America, 1996)
- The oxazolidinone eperezolid binds to the 50S ribosomal subunit and competes with binding of chloramphenicol and lincomycin. (Antimicrobial Agents and Chemotherapy, 1997)
- Molecular characterization of the lincomycin-production gene cluster of Streptomyces lincolnensis 78-11 (Molecular Microbiology, 1995)
- Substrate-and antibiotic-binding sites at the peptidyl-transferase centre of Escherichia coli ribosomes. Studies on the chloramphenicol, lincomycin, and erythromycin sites (FEBS Journal, 1971)
- LINCOMYCIN AS A CAUSE OF PSEUDOMEMBRANOUS COLITIS (The Lancet, 1973)
- Comparative studies of antibacterial activity in vitro and absorption and excretion of lincomycin and clinimycin. (The American Journal of the Medical Sciences, 1968)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Lincocin
- Lincomycin Hydrochloride
- Lincomycin A
- Lincolnensin
- Lincomycin Monohydrochloride, (2S-cis)-Isomer
- Lincomycin Monohydrochloride
- Hemihydrate Lincomycin Monohydrochloride
- Lincomycin Monohydrochloride, (L-threo)-Isomer
- Lincomycin, (2S-cis)-Isomer
- Lincomycin, (L-threo)-Isomer
- Epilincomycin
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SMILESCCCC1CC(N(C1)C)C(=O)NC(C2C(C(C(C(O2)SC)O)O)O)C(C)O
-
InChIKeyOJMMVQQUTAEWLP-UHFFFAOYSA-N
- Pubchem - lincomycin
- Wikipedia - lincomycin
Lincomycin is a lincosamide antibiotic that comes from the actinomycete Streptomyces lincolnensis. A related compound, clindamycin, is derived from lincomycin by using thionyl chloride to replace the 7-hydroxy group with a chlorine atom with inversion of chirality.
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