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Microbiology/Virology

Chemical Structure Cat. No. Product Name CAS No.
Indinavir Chemical Structure
BCP05711 Indinavir 150378-17-9
Indinavir(MK-639; L735524) is a potent and specific HIV protease inhibitor that appears to have good oral bioavailability.
Chloroquine diphosphate Chemical Structure
BCP31956 Chloroquine diphosphate 50-63-5
Chloroquine diphosphate is an inhibitor of autophagy and toll-like receptors (TLRs). Chloroquine diphosphate is an antimalarial and anti-inflammatory drug widely used to treat malaria and rheumatoid arthritis.
Tylvalosin Chemical Structure
BCP31610 Tylvalosin 63409-12-1
Tylvalosin is an antibiotic that shows the activity of gram-positive bacteria.
Cephalosporin c zinc salt Chemical Structure
BCP14370 Cephalosporin c zinc salt 59143-60-1
Cephalosporin C zinc salt is the salt form of cephalosporin C, which is an antibiotic isolated from fungi of the genus Acremonium.
Pirlimycin hydrochloride Chemical Structure
BCP31935 Pirlimycin hydrochloride 78822-40-9
Pirlimycin Hydrochloride is a semi-synthetic lincosaminide antibiotic. Pirlimycin Hydrochloride is a Clindamycin analog.
Pirlimycin Chemical Structure
BCP31934 Pirlimycin 79548-73-5
Pirlimycin is a semi-synthetic lincosamide prepared from clindamycin by hydrolysing the propyl N-methylproline and re-annealing a 4-ethylpipecolic acid; a broad spectrum antibiotic with activity against anaerobic bacteria and protozoans by binding to the 23S ribosomal subunit, blocking protein synthesis
Sitafloxacin hydrate (2:3) Chemical Structure
BCP31925 Sitafloxacin hydrate (2:3) 163253-35-8
Sitafloxacin Hydrate is a new-generation, broad-spectrum oral fluoroquinolone antibiotic.
Deglycosylation Avibactam Chemical Structure
BCP31868 Deglycosylation Avibactam DA
Avibactam is a covalent, reversible non-β-lactam β-lactamase inhibitor, inhibits β-lactamase TEM-1 and CTX-M-15 with IC50 of 8 nM and 5 nM, respectively.
Methyl leucylleucinate hydrochloride Chemical Structure
BCP31707 Methyl leucylleucinate hydrochloride 6491-83-4
L-Leucyl-L-Leucine methyl ester (LLME) is a lysosomal condensation product that has been reported to be cytotoxic towards natural killer cells and CD4 It has also been shown to induce death of monocytes, polymorphonuclear leukocytes, and myeloid tumor cells.
Quinupristin-Dalfopristin mixt Chemical Structure
BCP30272 Quinupristin-Dalfopristin mixt 126602-89-9
Quinupristin-dalfopristin is a 70:30 (w/w) complex of two semi-synthetic analogues marketed as synercid; a highly effective antibiotic, including activity against resistant strains.
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