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Infection

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN250686 AFN-1252 620175-39-5

    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 ...

  • YN250359 iKIX1 656222-54-7

    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.

  • YN250435 RSV604 676128-63-5

    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.

  • YN330187 SKF1 678997-25-6

    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...

  • YN483797 HEX3 688805-40-5

    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 .

  • YN250596 Nesbuvir 691852-58-1

    Nesbuvir is a nonnucleoside inhibitor of the hepatitis C virus (HCV) nonstructural protein 5B (NS5B) polymerase.

  • YN330715 RO8191 691868-88-9

    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.

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