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Clindamycin hydrochloride

SIGMA/C5269 - lincosamide antibiotic

Synonym: (7S)-7-Chloro-7-deoxylincomycin hydrochloride; Cleocin

CAS Number: 21462-39-5
Empirical Formula (Hill Notation): C18H33ClN2O5S · HCl
Molecular Weight: 461.44
MDL Number: MFCD07793327
Linear Formula: C18H33ClN2O5S · HCl
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-C5269-10MG 10 mg
$110.00
1/EA
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45-C5269-50MG 50 mg
$314.00
1/EA
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45-C5269-100MG 100 mg
$528.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: C5269-100MG
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: C5269-10MG

 

antibiotic activity spectrum Gram-negative bacteria
  Gram-positive bacteria
form powder or crystals
impurities ≤13%
InChI 1S/C18H33ClN2O5S.ClH/c1-5-6-10-7-11(21(3)8-10)17(25)20-12(9(2)19)16-14(23)13(22)15(24)18(26-16)27-4;/h9-16,18,22-24H,5-8H2,1-4H3,(H,20,25);1H/t9-,10+,11-,12+,13-,14+,15+,16+,18+;/m0./s1
InChI key AUODDLQVRAJAJM-XJQDNNTCSA-N
mode of action protein synthesis | interferes
Quality Level 200 
SMILES string Cl.CCC[C@@H]1C[C@H](N(C)C1)C(=O)N[C@H]([C@H](C)Cl)C2O[C@H](SC)[C@H](O)[C@@H](O)[C@H]2O
solubility H2O: 50 mg/mL
storage temp. 2-8°C
Application: Clindamycin is used to study bacterial infections, such as group B streptococcal disease, bacterial resistance and plasma protein binding.
Application: Used to study bacterial protein synthesis.
Biochem/physiol Actions: Clindamycin hydrochloride is highly effective against anaerobic species.
Biochem/physiol Actions: Clindamycin is a semi-synthetic, lincosamide antibiotic that is prepared from lincomycin. It inhibits bacterial protein synthesis by hydrogen bond interactions with the 23S rRNA component of the 50S ribosomal subunit thus inducing dissociation of the peptidyl-t-RNA complex. It has antibacterial activity against Gram-positive cocci and antiprotozoal activity against Taxoplasma.
General description: Chemical structure: macrolide
Other Notes: Antibacterial and antiprotozoal antibiotic of the lincosamide class.
Other Notes: Keep container tightly closed in a dry and well-ventilated place.
Packaging: 10 mg in poly bottle
Packaging: 50, 100 mg in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 2
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Storage Temp. 2-8°C
UNSPSC 51102829

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