
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 58207-19-5 |
| Catalog No. | 2A-9009831 |
| Chinese Name | 克林霉素盐酸盐 一水合物 |
| Synonyms | clindamycin hydrochloride hydrate |
| Molecular Formula | C18H36Cl2N2O6S |
| Molecular Weight | 479.47 |
| Purity | 98 |
| Boiling Point | 647ºC at 760 mmHg |
| Melting Point | 143ºC |
| Appearance | White crystalline solid |
| Water Solubility | Soluble in water |
| Storage Condition | Room Temperature |
| Application | Clindamycin hydrochloride monohydrate is an orally available protein synthesis inhibitor with the ability to express virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MI |
| HTC | 29419090 |
| MDL Number | C18H36Cl2N2O6S |
| SMILES | CCCC1CC(C(=O)NC(C(C)Cl)C2OC(SC)C(O)C(O)C2O)N(C)C1.Cl.O |
| InChI Key | KWMXKEGEOADCEQ-WNNJHRBUSA-N |
| MSDS | msds/9831_1_58207_19_5.pdf |
| Bioactivity | Clindamycin hydrochloride monohydrate is an oral protein synthesis inhibitory agent that has the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin hydrochloride monohydrate resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin hydrochloride monohydrate decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1) or alpha-haemolysin (Hla)[1]. Related Catalog Research Areas >> Infection Signaling Pathways >> Anti-infection >> Bacterial References [1]. Hodille E, et al. Clindamycin suppresses virulence expression in inducible clindamycin-resistant Staphylococcus aureus strains. Ann Clin Microbiol Antimicrob. 2018 Oct 20;17(1):38. Chemical & Physical Properties Boiling Point 647ºC at 760 mmHg Melting Point 143ºC Molecular Formula C18H36Cl2N2O6S Molecular Weight 479.459 Flash Point 345.1ºC Exact Mass 478.167114 PSA 136.79000 LogP 1.45600 Index of Refraction 143 ° (C=2, H2O) InChIKey KWMXKEGEOADCEQ-WNNJHRBUSA-N SMILES CCCC1CC(C(=O)NC(C(C)Cl)C2OC(SC)C(O)C(O)C2O)N(C)C1.Cl.O Water Solubility Soluble in water |
| Use of | Clindamycin hydrochloride monohydrate is an oral protein synthesis inhibitory agent that has the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin hydrochloride monohydrate resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin hydrochloride monohydrate decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1) or alpha-haemolysin (Hla)[1]. Properties Articles47 Name Clindamycin Hydrochloride Monohydrate Synonym More Synonyms clindamycin hydrochloride Biological Activity Description Clindamycin hydrochloride monohydrate is an oral protein synthesis inhibitory agent that has the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin hydrochloride monohydrate resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin hydrochloride monohydrate decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1) or alpha-haemolysin (Hla)[1]. Related Catalog Research Areas >> Infection Signaling Pathways >> Anti-infection >> Bacterial References [1]. Hodille E, et al. Clindamycin suppresses virulence expression in inducible clindamycin-resistant Staphylococcus aureus strains. Ann Clin Microbiol Antimicrob. 2018 Oct 20;17(1):38. Chemical & Physical Properties Exact Mass 478.167114 PSA 136.79000 LogP 1.45600 InChIKey KWMXKEGEOADCEQ-WNNJHRBUSA-N Water Solubility Soluble in water |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified |
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