Application of tert-Butylchlorodiphenylsilane
Tert butyl diphenylchlorosilane known as silane protector, is used to replace the active hydrogen in silane based compounds (such as hydrogen in hydroxyl, carboxyl and amino groups) to form stable int
Mar 21，2022 Organic Synthesis Intermediate
The role of glyphosate
Glyphosate is a biocide herbicide developed by the famous American company Monsanto.
Mar 21，2022 API
Toxicity of Garenoxacin
Garenoxacin is a desfluoro quinolone which, as such, lacks a fluorine at the C-6 position in comparison with other fluoroquinolones, such as ciprofloxacin, moxifloxacin, and levofloxacin, and has a di
Mar 18，2022 API
Toxicity of Gatifloxacin
Gatifloxacin is an 8-methoxy fluoroquinolone and is marketed by Bristol Myers Squibb as Tequint. Three formulations are available: oral, ophthalmic, and intravenous. Like other members of this class,
Mar 18，2022 APIThe steroid antibiotics---?Fusidic acid
Fusidic acid was developed by Leo Laboratories in Copenhagen and obtained from the fungus Fusidium coccineum.
Mar 18，2022 APIWhat is Fosfomycin?
Fosfomycin is a phosphoenolpyruvate analogue produced by Streptomyces fradiae and by some Pseudomonas spp., but is now mostly obtained synthetically. It is a broad-spectrum antibiotic with bactericida
Mar 18，2022 API
Ampicillin–Sulbactam: Antimicrobial Activity, Susceptibility, Administration and Dosage, Clinical Uses etc.
Ampicillin–sulbactam (AMP/S) is a beta-lactam/beta-lactamase inhibitor that was developed to overcome the increasing resistance of various bacteria to ampicillin. AMP/S is marketed under various trad
Mar 18，2022 APIInstructions of ?Pristinamycin
?Pristinamycin is a mixture of water-insoluble pristinamycin IA (PIA, 90–97%) and pristinamycin IIA (PIIA, 3–10%), derived from S. pristinaespiralis.
Mar 18，2022 APILinezolid:U-100766
Linezolid (previously U-100766) is the first in a new class of completely synthetic antimicrobial agents, the oxazolidinones.
Mar 18，2022 APIThe first glycylcycline---Tigecycline
Tigecycline is produced by Wyeth under the trade name of Tygacils. The modification of the tetracycline nucleus led to a reduction in tetracycline-specific efflux and ribosomal protection.
Mar 18，2022 API