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Chemical Structure Cat. No. Product Name CAS No.
LYS228 Chemical Structure
BCP38938 LYS228 1810051-96-7
LYS228 is a potent antibiotics with Activity against Carbapenem-Resistant Enterobacteriaceae (MIC90 = 2 uM/mL).
Ethambutol Chemical Structure
BCP39004 Ethambutol 74-55-5
Ethambutol is an antitubercular agent that inhibits the transfer of mycolic acids into the cell wall of the tubercle bacillus. It may also inhibit the synthesis of spermidine in mycobacteria. The action is usually bactericidal, and the drug can penetrate human cell membranes to exert its lethal effect.
Seco Rapamycin Chemical Structure
BCP38974 Seco Rapamycin 147438-27-5
Seco Rapamycin is the ring-opened product of Rapamycin.
2-O-(alpha-D-Glucopyranosyl)glycerol Chemical Structure
BCP38973 2-O-(alpha-D-Glucopyranosyl)glycerol 22160-26-5
2-O-(alpha-D-glucopyranosyl)glycerol is a glucosylglycerol consisting of an alpha-D-glucosyl residue attached at position 2 of glycerol via a glycosidic bond.
AT-130 Chemical Structure
BCP38969 AT-130 211364-06-6
AT-130 is a HBV virus inhibitor.
Methicillin Sodium Salt Chemical Structure
BCP38900 Methicillin Sodium Salt 132-92-3
Methicillin Sodium is the sodium salt of Meticillin, a β-lactam antibiotic, could be obtained through semi-synthetic and used as an antibacterial agent especially against Gram-positive bacteria.
N-Acetyl-D-Glucosamine Chemical Structure
BCP38887 N-Acetyl-D-Glucosamine 7512-17-6
N-acetyl-D-glucosamine is the D isomer of N-acetylglucosamine.
Islatravir Chemical Structure
BCP38832 Islatravir 865363-93-5
Islatravir is a potential antiviral drug for the treatment of HIV infection.
5-Hydroxymethyl-2'-deoxyuridine Chemical Structure
BCP38821 5-Hydroxymethyl-2'-deoxyuridine 5116-24-5
5-Hydroxymethyl-2'-deoxyuridine is a pyrimidine 2'-deoxyribonucleoside composed of 2'-deoxyuridine having a 5-hydroxymethyl substituent. It derives from a 5-hydroxymethyluracil.
R-1479 Chemical Structure
BCP38817 R-1479 478182-28-4
R1479 is a potent and highly specific inhibitor of HCV replication in cell culture, and that its triphosphate is a potent and highly selective inhibitor of NS5B mediated RNA synthesis, the HCV encoded RNA polymerase.
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