Lincomycin (hydrochloride)Lincomycin (hydrochloride) - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-B0417A-01.804-HY-B0417A-01804-HY-B0417A-01Business & Industrial > Science & LaboratoryLincomycin (hydrochloride)
Gentaur
EUR12027-02-20

Lincomycin (hydrochloride)

CAT:
804-HY-B0417A-01
Size:
100 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Lincomycin (hydrochloride) - image 1

Lincomycin (hydrochloride)

  • Description:

    Lincomycin hydrochloride is the salt form of the antibiotic lincomycin. Lincomycin can affect the synthesis of protein, RNA and DNA in the mycelium of the lincomycin-producing organism Act. Roseolus. Lincomycin inhibits protein synthesis in gram-positive and - to a lower degree - also in gram-negative bacteria. Lincomycin binds to the 50S subunits of bacterial ribosomes and act on aminoacyl-tRNA binding and the transpeptidation reaction[1][2][3].
  • Product Name Alternative:

    U10149A
  • UNSPSC:

    12352005
  • Hazard Statement:

    H315, H319, H335
  • Target:

    Antibiotic; Bacterial; DNA/RNA Synthesis
  • Type:

    Natural Products
  • Related Pathways:

    Anti-infection; Cell Cycle/DNA Damage
  • Applications:

    COVID-19-immunoregulation
  • Field of Research:

    Infection
  • Assay Protocol:

    https://www.medchemexpress.com/lincomycin-hydrochloride.html
  • Purity:

    99.29
  • Solubility:

    H2O : 100 mg/mL (ultrasonic)
  • Smiles:

    C[C@@H](O)[C@@]([C@@]([C@@H]([C@H](O)[C@H]1O)O)([H])O[C@@H]1SC)([H])NC([C@@H]2C[C@@H](CCC)CN2C)=O.Cl
  • Molecular Formula:

    C18H35ClN2O6S
  • Molecular Weight:

    443.00
  • Precautions:

    H315, H319, H335
  • References & Citations:

    [1]Griaznova, N.S., et al., [Effect of lincomycin and other protein synthesis inhibitors on the metabolism of Actinomyces roseolus, a producer of lincomycin]. Antibiotiki, 1980. 25 (4) : p. 250-6.|[2]Hummel, H., W. Piepersberg, and A. Bock, Analysis of lincomycin resistance mutations in Escherichia coli. Mol Gen Genet, 1979. 169 (3) : p. 345-7.|[3]Champney, W.S. and C.L. Tober, Specific inhibition of 50S ribosomal subunit formation in Staphylococcus aureus cells by 16-membered macrolide, lincosamide, and streptogramin B antibiotics. Curr Microbiol, 2000. 41 (2) : p. 126-35.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    4°C (Powder, sealed storage, away from moisture)
  • Scientific Category:

    Natural Products
  • Clinical Information:

    Launched
  • Citation 01:

    Chemosphere. 2019 Jun:225:378-387.|Microb Biotechnol. 2021 Nov;14 (6) :2538-2551.|Microbiol Spectr. 2025 Aug 29:e0059025.
  • CAS Number:

    [859-18-7]