Lincomycin
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Lincomycin
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CAS No:
154-21-2
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Formula:
C18H34N2O6S
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Chemical Name:
Lincomycin
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Synonyms:
D-erythro-α-D-galacto-Octopyranoside,methyl 6,8-dideoxy-6-[[[(2S,4R)-1-methyl-4-propyl-2-pyrrolidinyl]carbonyl]amino]-1-thio-;D-erythro-D-galacto-Octopyranoside,methyl 6,8-dideoxy-6-(1-methyl-4-propyl-L-2-pyrrolidinecarboxamido)-1-thio-,trans-α-;D-erythro-α-D-galacto-Octopyranoside,methyl 6,8-dideoxy-6-[[(1-methyl-4-propyl-2-pyrrolidinyl)carbonyl]amino]-1-thio-,(2S-trans)-;Lincomycin;Methyl 6,8-dideoxy-6-[[[(2S,4R)-1-methyl-4-propyl-2-pyrrolidinyl]carbonyl]amino]-1-thio-D-erythro-α-D-galacto-octopyranoside;U 10,149A;Lincomycin A;Lincolcina;Cillimycin;Jiemycin;U 10149;Lincolnensin;Medoglycine;12768-69-3;16977-76-7
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CAS No:
Description
White Crystalline SolidChEBI: A carbohydrate-containing antibiotic produced by the actinomyces Streptomyces lincolnensis.
Characteristics
148
0.20
White crystalline solid
1.1704 (rough estimate)
148-150°C
646.8±55.0 °C(Predicted)
345ºC
1.6510 (estimate)
In water, 927 mg/L at 25 deg C (est)
Lincomycin hydrochloride injection should be stored at 20-25 deg C; freezing should be avoided.
1.34X10-17 mm Hg at 25 deg C (est)
LD50 oral in rat: 1gm/kg
Lincomycin Use and Manufacturing
Streptomyces (Streptomyces lincolnensis) mutant strain produced by fermentation.
Lincomycin is a polar, water soluble, broad spectrum antibiotic first isolated from Streptomyces licolnensis by researchers at Upjohn in 1962. Lincomycin was the first of a unique structural class, the lincosamides, containing a rare amino acid, 4-propyl-N-methylproline, coupled to an equally rare aminomethylthio-octopyranoside sugar. Lincomycin and semi-synthetic analogues are often incorrectly considered to be aminoglycosides but share little or no structural similarity. Lincomycin is a broad spectrum antibiotic with activity against anaerobic bacteria and protozoans. Lincomycin acts by binding to the 23S ribosomal subunit, blocking protein synthesis. Lincomycin has been extensively studied with over 7,000 literature citations.
Drug Function and Efficacy
Antibiotics, with an antibacterial spectrum similar to erythromycin, mainly have high antibacterial activity against Gram-positive bacteria, and its mechanism of action is to inhibit bacterial protein synthesis
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