Chemical structure
Cat.No.
Product Name
CAS no.
Target
AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (FabI), inhibited all clinical isolates of Staphylococcus aureus and Staphylococcus epidermidis at concentrations of ≤0.12 μg/ml.
YN372204 Asunaprevir 630420-16-5
Asunaprevir is an orally bioavailable inhibitor of the hepatitis C virus enzyme serine protease NS3 that is necessary for protein processing required for viral replication.
YN250683 Censavudine 634907-30-5
Censavudine (OBP-601; BMS-986001), anucleoside analog, is anucleoside reverse transcriptaseinhibitor. Censavudine is a potentHIVinhibitor withEC50ranges from 30nM to 81nM and 450nM to 890nM forHIV-2 and HIV-1, respe...
YN372426 Darunavir (Ethanolate) 635728-49-3
Darunavir Ethanolate (DRV) is a nonpeptidic HIV protease inhibitor, used to treat HIV infection.
YN484255 Tauroxicum 648922-41-2
Tauroxicum can be used as a nontoxic, non-antimicrobial agent that can replace or supplement the use of antibiotics in the animal husb and ry of livestock animals to increase health and general well-being, productivity, feed efficiency ...
iKIX1 is anantifungal agent and resensitizes drug-resistantC. glabratato azole antifungals in vitro. iKIX1 inhibits the interaction between the KIX domain of the mediator subunitCgGal11A and the activation domain ofCgPdr1, ...
YN250277 Fluopyram 658066-35-4
Fluopyram is asuccinate dehydrogenaseinhibitor fungicide, inhibits the growth ofF. virguliformeisolates with mean EC50of 3.35 µg/mL.
YN250167 Arterolane 664338-39-0
Arterolane is an antimalarial agent, with IC50 of both 1.1nM againstP. falciparumRo73 and W2, respectively.
YN420211 BIO-acetoxime 667463-85-6
BIO-acetoxime is a potent dual GSK3α/β inhibitor with IC50 of 10 nM, >240-fold selectivity over CDK5/p25, CDK2/cyclin A and CDK1/cyclin B.
YN484044 Histone H4 (2-21) 667899-73-2
Histone H4 (2-21) is the core histones associated with chromatinization of herpes simplex virus 1 (HSV-1) genomes.
YN483818 Hexa-D-arginine 673202-67-0
Hexa-D-arginine (Furin Inhibitor II) is a stablefurininhibitor with Ki values 106nM, 580nM and 13.2μM forfurin, PACE4 and prohormone convertase-1 (PC1), respectively. Hexa-D-arginine blocksPseudomonas exotoxinA and...
YN250229 DSHS00884 675104-49-1
DSHS00884 is a potenthuman papillomavirus E6inhibitor with an IC50 of 10μM.
RSV604, a novel benzodiazepine, is an inhibitor of respiratory syncytial virus (RSV) with EC50 of 0.86 μM. RSV604 has significant potential for the effective treatment of RSV disease. Phase 2.
SKF1 is aFK506suppressor, causes a mitochondrially induced death in low salt, concomitant with the release ofreactive oxygen species (ROS).
YN250214 RR-11a analog 685543-66-2
RR-11a analog is a potent and selective inhibitors ofasparaginyl endopeptidases (AE) (Legumain), with IC50 values of 4.5nM, 4.5nM and 31nM for AE1 inTrichomonas Vaginalis, AE inIxodes ricinus and AE inSchistosoma ma...
HEX3 is a fragment of the adenoviral hexon. Hexon is the major capsid protein of adenovirion and is comprised of three identical polypeptide chains.
YN250105 Balapiravir 690270-29-2
Balapiravir (Ro 4588161; R1626) is an orally active prodrug of a nucleoside analogue inhibitor of the RNA-dependent RNA polymerase (RdRp) of HCV (R1479; 4'-Azidocytidine). Balapiravir has anti-HCVactivity .
Nesbuvir is a nonnucleoside inhibitor of the hepatitis C virus (HCV) nonstructural protein 5B (NS5B) polymerase.
RO8191 (RO4948191), an imidazonaphthyridine compound, is an orally active and potentinterferon (IFN) receptoragonist. RO8191 activates IFN-stimulated genes (ISGs) expression and JAK/STATphosphorylation. RO8191 sho...
YN484054 TAT-amide 697226-52-1
TAT-amide is a cell penetrating peptide. Cell-penetrating peptides (CPPs) are short amino acid sequences able to enter different cells.
TELL : +86-020-82000279
Add:Room 519, Block F, Guangzhou International Business Incubator, No.3 Lanyue Road, Science Town, Huangpu District, Guangzhou, China.