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Infection

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN250113 Tegobuvir 1000787-75-6

    Tegobuvir is a specific, covalent inhibitor of theHCV NS5B polymerase.

  • YN250088 AAI101 1001404-83-6

    AAI101 is an extended-spectrum β-lactamase inhibitor, against many resistant Gram-negative pathogens.

  • YN251947 RPW-24 1001625-82-6

    RPW-24 protectsC. elegansfrom bacterial infection by stimulating the host immune response of the nematode. RPW-24 has antibacterial activity.

  • YN370311 Cobicistat 1004316-88-4

    Cobicistat (GS-9350) is a potent and selective inhibitor of CYP3A with IC50 of 30-285 nM.

  • YN250471 Monodes(N-carboxymethyl)vali... 1007884-60-7

    Monodes(N-carboxymethyl)valine Daclatasvir (Daclatasvir Impurity A) is the main degradation product of Daclatasvir. Daclatasvir is a potent HCV NS5A protein inhibitor.

  • YN250108 Daclatasvir 1009119-64-5

    Daclatasvir (BMS-790052) is a highly selective inhibitor of HCV NS5A with EC50 of 9-50 pM, for a broad range of HCV replicon genotypes and the JFH-1 genotype 2a infectious virus in cell culture. Phase 3.

  • YN250107 Daclatasvir dihydrochloride 1009119-65-6

    Daclatasvir is an orally available antiviral agent that inhibits the NS5A region of the hepatitis C virus (HCV) used for the treatment of chronic HCV genotype 1 and 3 infection.

  • YN360309 GSK369796 Dihydrochloride 1010411-21-8

    GSK369796 Dihydrochloride is an inhibitor of hERG potassium ion channel repolarization with IC50 of 7.5 μM. GSK369796 Dihydrochloride is an affordable and effective 4-aminoquinoline antimalarial.

  • YN250460 AMOZ-d5 1017793-94-0

    AMOZ-d5 is a deuterium labeled AMOZ. AMOZ, a tissue bound metabolite of Furaltadone, Furaltadone is a synthetic nitrofuran antibiotic widely used.

  • YN250813 Sitamaquine tosylate 1019640-33-5

    Sitamaquine (WR 6026) tosylate, an orally active 8-aminoquinoline analog, is an antileishmanial agent. Sitamaquine is a lipophilic weak base that rapidly accumulates in acidic compartments ofLeishmaniaspp., mainly in acidocalcisomes.

  • YN250978 Sulfadiazine D4 1020719-78-1

    Sulfadiazine D4 is a deuterium labeled Sulfadiazine. Sulfadiazine is a sulfonamide antibiotic used for the treatment of toxoplasmosis.

  • YN251011 Sulfadimethoxine D4 1020719-80-5

    Sulfadimethoxine D4 is a deuterium labeled Sulfadimethoxine (Sulphadimethoxine). Sulfadimethoxine is a sulfonamide antibiotic used to treat many infections including treatment of respiratory, urinary tract, enteric, and soft tissue i...

  • YN250903 Sulfamethazine-D4 1020719-82-7

    Sulfamethazine-D4 (Sulfadimidine-D4) is a deuterium labeled Sulfamethazine (Sulfadimidine). Sulfamethazine is an antimicrobial that is widely used to treat and prevent various animal diseases (such as gastrointestinal and respira...

  • YN251000 Sulfamethoxazole D4 1020719-86-1

    Sulfamethoxazole D4 (Ro 4-2130 D4) is a deuterium labeled Sulfamethoxazole (Ro 4-2130). Sulfamethoxazole is a sulfonamide bacteriostatic antibiotic.

  • YN251073 Sulfathiazole D4 1020719-89-4

    Sulfathiazole D4 is a deuterium labeled Sulfathiazole. Sulfathiazole, an organosulfur compound, is used as a short-acting sulfonamide antibiotic.

  • YN250024 Cadazolid 1025097-10-2

    Cadazolid (ACT-179811) is a new oxazolidinone antibiotic with potent activity against Clostridium difficile.

  • YN250839 Lomibuvir 1026785-55-6

    Lomibuvir (VX-222), a selective, non-nucleoside polymerase inhibitor, targets thumb pocket 2 of theHCV NS5B polymerase (RdRp)with aKdof 17nM. Lomibuvir inhibits the 1b/Con1HCVsubgenomic replicon with an EC50 of 5.2nM. L...

  • YN250681 Artefenomel 1029939-86-3

    Artefenomel (OZ439) is a synthetic antimalarial agent with the artemisinin pharmacophore. Artefenomel (OZ439) is a long-acting artemisinin-related agent.

  • YN250571 Sarecycline hydrochloride 1035979-44-2

    Sarecycline hydrochloride is a narrow-spectrum tetracycline-classantibiotic. Sarecycline hydrochloride possesses anti-inflammatory properties and potent activity against Gram-positive bacteria, including activity against multiple strai...

  • YN250262 Purfalcamine 1038620-68-6

    Purfalcamine is an orally active, selectivePlasmodium falciparumcalcium-dependent protein kinase 1 (PfCDPK1)inhibitor with an IC50 of 17nM and an EC50 of 230nM. Purfalcamine has antimalarial activity and causes malaria par...

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