CAS 58207-19-5
:Clindamycin alcoholate
Description:
Clindamycin alcoholate, with the CAS number 58207-19-5, is a chemical compound derived from clindamycin, an antibiotic used primarily to treat bacterial infections. This substance is characterized by its structural modification, which involves the addition of an alcohol moiety to the clindamycin framework. Clindamycin itself is a lincosamide antibiotic that works by inhibiting bacterial protein synthesis, making it effective against anaerobic bacteria and certain protozoa. The alcoholate form may exhibit altered solubility and stability compared to its parent compound, potentially influencing its pharmacokinetic properties. Typically, clindamycin and its derivatives are administered in various forms, including oral and topical preparations, and are known for their effectiveness against skin infections, respiratory tract infections, and certain types of bone infections. As with many antibiotics, the use of clindamycin alcoholate may be accompanied by considerations regarding resistance, side effects, and interactions with other medications. Overall, this compound represents an important aspect of antibiotic chemistry and pharmacology.
Formula:C18H34Cl2N2O5S
InChI:InChI=1/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?;/m1./s1
Synonyms:- Clindamycin Hydrochloride Monohydrate
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Found 8 products.
Clindamycin Hydrochloride Monohydrate
CAS:Formula:C18H33ClN2O5S·HCl·H2OPurity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:479.46Clindamycin hydrochloride monohydrate
CAS:<p>Clindamycin hydrochloride (HCl) monohydrate, 58207-19-5, is a salt form of clindamycin, a semi-synthetic lincosamide antibiotic with broad-spectrum activity. Learn more.</p>Formula:C18H34Cl2N2O5SColor and Shape:White to cream, Powder or crystals or crystalline powderMolecular weight:461.44Clindamycin Hydrochloride
CAS:<p>Antibiotics nesoi</p>Formula:C18H33ClN2O5S·HCl·H2OColor and Shape:White Off-White PowderMolecular weight:478.16711L-threo-α-D-galacto-Octopyranoside, methyl 7-chloro-6,7,8-trideoxy-6-[[(1-methyl-4-propyl-2-pyrrolidinyl)carbonyl]amino]-1-thio-, monohydrochloride, monohydrate, (2S-trans)-
CAS:Formula:C18H36Cl2N2O6SPurity:98%Color and Shape:SolidMolecular weight:479.4592Clindamycin hydrochloride monohydrate
CAS:<p>Clindamycin HCl monohydrate inhibits Staph aureus protein synthesis, suppresses virulence factors, resistance via 50S rRNA methylation.</p>Formula:C18H36Cl2N2O6SPurity:99.80%Color and Shape:SolidMolecular weight:479.46Clindamycin hydrochloride monohydrate
CAS:<p>Clindamycin hydrochloride monohydrate</p>Purity:≥98%Molecular weight:479.46g/mol(7S)-7-Chloro-7-deoxylincomycin hydrochloride monohydrate
CAS:Formula:C18H34Cl2N2O5SPurity:≥98%Color and Shape:White to very pale yellow crystal powderMolecular weight:461.44Clindamycin hydrochloride monohydrate
CAS:<p>Clindamycin is a lincosamide antibiotic that inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit. It is used for the treatment of streptococcal pharyngitis. Clindamycin hydrochloride monohydrate has been shown to inhibit human polymorphonuclear leukocytes (PMN) migration in vitro, which may be due to its anti-inflammatory properties. Clindamycin also has an effect on oral pathogens. This drug binds to the 30S ribosomal subunit and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. Clindamycin hydrochloride monohydrate has been shown to inhibit Streptococcus mutans, Streptococcus sobrinus, and Enterococcus faecalis growth in vitro.</p>Formula:C18H36Cl2N2O6SPurity:Min. 95%Molecular weight:479.5 g/mol
