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62143 Sigma

Lincomycin hydrochloride

≥95.0% (TLC)

Synonym: Lincocin hydrochloride, Methyl 6,8-dideoxy-6-(1-methyl-4-propyl-2-pyrrolidinecarboxamido)-1-thio-D-erythro-α-D-galactooctopyranoside hydrochloride

  • CAS Number 859-18-7

  • Empirical Formula (Hill Notation) C18H34N2O6S · HCl

  • Molecular Weight 443.00

  •  Beilstein Registry Number 4171650

  •  EC Number 212-726-7

  •  MDL number MFCD00083647

  •  PubChem Substance ID 329759714

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Properties

Related Categories Antibacterial, Antibiotics, Antibiotics A to Z, Antibiotics G-M, Biochemicals and Reagents,
material   white to off-white
InChI Key   POUMFISTNHIPTI-BOMBIWCESA-N
assay   ≥95.0% (TLC)
form   solid
impurities   ≤5% water
solubility   H2O: soluble50 mg/mL, clear, colorless
Mode of action   protein synthesis | interferes
antibiotic activity spectrum   Gram-positive bacteria
storage temp.   2-8°C

Description

Biochem/physiol Actions

Mode of action: Lincomycin inhibits bacterial protein synthesis by forming cross-links within the peptidyl transferase loop region of the 23S rRNA.†

Antimicrobial spectrum: Lincomycin hydrochloride is effective against gram-positive bacteria.

Packaging

1, 5 g in glass bottle

Preparation Note

This product is soluble in water at 50 mg/mL, yielding a clear, colorless solution.

Price and Availability

Suggested Laboratory Gloves


Laboratory GlovesThis substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.



Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
2
RTECS 
RH6315000
Protocols & Articles

Articles

Inhibition of Protein Synthesis by Antibiotics

Protein synthesis is a complex, multi-step process involving many enzymes as well as conformational alignment. However, the majority of antibiotics that block bacterial protein synthesis interfere wi...
BioFiles 2006, 1.4, 17.
Keywords: Antibiotics, Environmental, Peptide synthesis

Peer-Reviewed Papers
15

References

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