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Clindamycin

Clindamycin Structure
CAS No.
18323-44-9
Chemical Name:
Clindamycin
Synonyms
clindamycine;CLDM;7-cdl;U-21251;sobelin;dalacinc;clinimycin;CLINDAMYCIN;chlolincocin;Clindamycin Base
CBNumber:
CB4399999
Molecular Formula:
C18H33ClN2O5S
Molecular Weight:
424.98
MOL File:
18323-44-9.mol
MSDS File:
SDS
Modify Date:
2024/7/14 20:44:35

Clindamycin Properties

alpha D +214° (chloroform)
Boiling point 134°C (rough estimate)
Density 1.1184 (rough estimate)
refractive index 1.6100 (estimate)
storage temp. Store at -20°C
solubility DMSO:52.5(Max Conc. mg/mL);123.54(Max Conc. mM)
DMF:30.0(Max Conc. mg/mL);70.59(Max Conc. mM)
Ethanol:52.5(Max Conc. mg/mL);123.54(Max Conc. mM)
PBS (pH 7.2):0.2(Max Conc. mg/mL);0.47(Max Conc. mM)
form A crystalline solid
pka 7.6(at 25℃)
color White to light yellow
BCS Class 1
Stability Hygroscopic
CAS DataBase Reference 18323-44-9(CAS DataBase Reference)
EPA Substance Registry System L-threo-?-D-galacto-Octopyranoside, methyl 7-chloro-6,7,8-trideoxy-6-[[[(2S,4R)-1-methyl-4-propyl-2-pyrrolidinyl]carbonyl]amino]-1-thio- (18323-44-9)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08
Signal word  Warning
Hazard statements  H362-H319
Precautionary statements  P201-P260-P263-P264-P270-P308+P313-P264-P280-P305+P351+P338-P337+P313P
Toxicity LD50 subcutaneous in rat: 2618mg/kg
NFPA 704
0
2 0

Clindamycin Chemical Properties,Uses,Production

Description

Clindamycin, a derivative of lincomycin, was first isolated from Streptomyces lincolnesis in 1962 and became commercially available in 1966. The name originates from Lincoln, Nebraska, where the organism was first isolated from a soil sample. The parent compound of clindamycin is lincomycin, which is produced by actinomycete, Streptomyces liconelnensis, which belongs to the order of Actinobacteria. It replaced lincomycin use because of its better absorption and clinical spectrum. Lincomycin belongs to the lincosamides, which is a class of antibiotics. The compounds use as antibiotic agents stems from their ability to interfere with the protein synthesis of bacteria. The chemical modification of lincomycin, clindamycin, has proven to be superior to the natural product for clinical applications. Clindamycin is better absorbed from the gastrointestinal tract and food does not interfere with its absorption. It is also eight times more active against aerobic gram-positive cocci, and it has proven activity against gram-positive and gram-negative anaerobic bacteria as well as protozoal organisms like Toxoplasma and Plasmodium species.

Uses

Clindamycin is a semi-synthetic analogue of lincomycin, prepared by chloride substitution of the exocyclic sugar hydroxy group. This affords a more hydrophobic compound with improved pharmacodynamics. Like other members of the lincosamide family, clindamycin is a broad spectrum antibiotic with activity against anaerobic bacteria and protozoans. Clindamycin acts by binding to the 23S ribosomal subunit, blocking protein synthesis. Clindamycin has been extensively studied with over 8,000 literature citations.

Indications

Clindamycin (Cleocin), 300 to 450 mg/day, is an extremely effective agent for acne.

Definition

ChEBI: Clindamycin is a carbohydrate-containing antibiotic that is the semisynthetic derivative of lincomycin, a natural antibiotic. The physiologic effect of clindamycin is by means of Decreased Sebaceous Gland Activity, and Neuromuscular Blockade.

Contact allergens

This lincosanide antibiotic is used in topical form for acne, or systemically has been responsible for exanthematous rashes and acute generalized exanthematous pustulosis.

Mechanism of action

Clindamycin inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit. The use of clindamycin with macrolides is not recommended since both of them compete for binding sites to the 50S subunit.

Clinical Use

Clindamycin is effective in the treatment of most infections secondary to anaerobes and gram-positive cocci. It can be used for anaerobic pulmonary, intra-abdominal, gynecologic, pelvic, diabetic foot, and decubitus ulcer infections. Another appropriate agent should be added since the majority of these infections are polymicrobial. It can also be used as an alternative agent for patients with severe penicillin allergy. It is also used to treat Clostridium perfringens infection.
Oral preparations of clindamycin and vaginal cream are alternatives to metronidazole for the treatment of bacterial vaginosis. Topical solution is used for treatment of acne vulgaris and rosacea.
Clindamycin is extensively metabolized by the liver and the half-life is prolonged in patients with cirrhosis and hepatitis. Dose reductions are recommended in patients with acute liver disease.

Side effects

The most commonly observed adverse effect is diarrhea. The reported incidence of C. difficile colitis in patients treated with clindamycin varies from 0.1 to 10%. The syndrome may be fatal. If the patient develops C. difficile colitis, clindamycin should be discontinued and the patient should be treated for C. difficile . Other side effects include rash, nausea, vomiting, diarrhea, flatulence, abdominal distension, anorexia, and transient elevation of liver enzymes. Other less common events, such as fever, neutropenia, thrombocytopenia, and eosinophilia have been reported.

Clindamycin Preparation Products And Raw materials

Global( 203)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CHEMXTREE STANDARDS +919872732255 Punjab, India 96 58 Inquiry
PROTECH TELELINKS +91-8571891912 +91-9855060837 Himachal Pradesh, India 62 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Triveni chemicals 08048762458 New Delhi, India 6093 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Jigs Chemical Limited +91 80 4290 2764 Ahmedabad, India 235 58 Inquiry
Mahir Technologies Inc. 09930610606 Mumbai, India 38 58 Inquiry
Chemland Ind 08046075772 Gujarat, India 95 58 Inquiry
Karthik Enterprises 08048971098 Mumbai, India 14 58 Inquiry
Taj Mahal Vision Chemicals Private Limited 07942557933 Mumbai, India 206 58 Inquiry

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Clindamycin Spectrum

Clindamycin (base and/or unspecified salts) (2S,4R)-N-[(1S,2S)-2-Chloro-1-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methylsulfanyloxan-2-yl]propyl]-1-methyl-4-propylpyrrolidine-2-carboxamide CLDM Methyl 7-chloro-6,7,8-trideoxy-6-[[[(2S)-1-methyl-4β-propyl-2-pyrrolidinyl]carbonyl]amino]-1-thio-L-threo-α-D-galacto-octopyranoside Methyl 7-chloro-6,7,8-trideoxy-6-[[[(2S,4R)-1-methyl-4-propyl-2-pyrrolidinyl]carbonyl]amino]-1-thio-L-threo-α-D-galacto-octopyranoside U-21251 Clindamycin Base 7-Chloro-7-deoxylincoMycin, 7-ChlorolincoMycin L-threo-a-D-galacto-Octopyranoside, Methyl7-chloro-6,7,8-trideoxy-6-[[[(2S,4R)-1-Methyl-4-propyl-2-pyrrolidinyl]carbonyl]aMino]-1-thio- L-threo-α-D-galacto-Octopyranoside, methyl 7-chloro-6,7,8-trideoxy-6-[[[(2S,4R)-1-methyl-4-propyl-2-pyrrolidinyl]carbonyl]amino]-1-thio- methyl 7-chloro-6,7,8-trideoxy-6-({[(2S,4R)-1-methyl-4-propyl-2-pyrrolidinyl]carbonyl}amino)-1-thio-L-threo-alpha-D-galacto-octopyranoside Clindamycin (free base) CLINDAMYCIN -1-thio-trans-alpha-l-threo-d-galacto-octopyranoside 7-cdl 7-chloro-7-deoxylincomycin 7-chlorodeoxylincomycin 7-chlorolincomycin 7-deoxy-7(s)-chlorolincomycin chlolincocin clinimycin clinimycin(rescinded) dalacinc methyl7-chloro-6,7,8-trideoxy-6-(1-methyl-4-l-threo-d-galacto-octopyranosid methyl7-chloro-6,7,8-trideoxy-6-(1-methyl-4-propyl-l-2-pyrrolidinecarboxamido) sobelin trans-alpha-propyl-l-2-pyrrolidinecarboxamido)-1-thio L-threo-.alpha.-D-galacto-Octopyranoside, methyl 7-chloro-6,7,8-trideoxy-6-(2S,4R)-1-methyl-4-propyl-2-pyrrolidinylcarbonylamino-1-thio- CLINDAMYCIN-HYDROCHLORIDE-ETHANOL(INTERMEDIATE) Clindamycin - Dalacine | U 21251 Clindamycin Solution, 1000ppm Clindamycin Solution, 100ppm Clindamycin USP/EP/BP ClindamycinQ: What is Clindamycin Q: What is the CAS Number of Clindamycin Q: What is the storage condition of Clindamycin clindamycine methyl7-chloro-6,7,8-trideoxy-6-[[[(2S,4R)-1-methyl-4-propylpyrrolidin-2-yl]carbonyl]amino]-4-O-phosphono-1-thio-L-threo-α-d-galacto-octopyranoside(clindamycin4-phosphate) (2S,4R)-N-((1S,2S)-2-Chloro-1-((2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(methylthio)tetrahydro-2H-pyran-2-yl)propyl)-1-methyl-4-propylpyrrolidine-2-carboxamide 18323-44-9 21463-39-5 C18H33ClN2O5S Inhibitors