| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC26053 | Benzamil (hydrochloride) Featured | Benzamil hydrochloride is a specific and potent sodium channel (ENaC) blocker. |
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| DC22184 | Benzarone | Benzarone (NSC 82134) is a small molecule inhibitor of Eyes Absen (EYA) protein tyrosine phosphatase activity (IC50=17 uM, EYA3), exhibits selectivity for EYA over PTP1B. |
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| DC8895 | benzbromaron Featured | Benzbromarone is a highly effective and well tolerated non-competitive inhibitor of xanthine oxidase, used as an uricosuric agent, used in the treatment of gout. |
|
| DC9885 | Benzenesulfonamide | Benzenesulfonamide ia an inhibitor of carbonic anhydrases |
|
| DC20028 | Benznidazole (Synonyms: Benznidazol; Ro 07-1051; Ro 71051) Featured | Benznidazole (Ro 07-1051) is an antiparasitic medication, with an IC50 of 20.35 μM for Colombian T. cruzi strains, and has been used in the treatment of Chagas disease. |
|
| DC10223 | Benzocaine hydrochloride | Benzocaine hydrochloride is a surface anesthetic that acts by preventing transmission of impulses along nerve fibers and at nerve endings. |
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| DC12173 | Benzyl alcohol (Benzenemethanol) | Benzyl alcohol is an aromatic alcohol; a colorless liquid with a mild pleasant aromatic odor. |
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| DC20216 | Benzylcetyldimethylammonium chloride hydrate | Benzylcetyldimethylammonium chloride hydrate is a chemical. |
|
| DC22482 | Bephenium hydroxynaphthoate | Bephenium hydroxynaphthoate is an anthelmintic compound that acts as an activiator of nematode B-type nAChR, is used in the treatment of hookworm infections and ascariasis.. |
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| DC22478 | Bephenium | Bephenium is an anthelmintic compound that acts as an activiator of nematode B-type nAChR, is used in the treatment of hookworm infections and ascariasis.. |
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| DCAPI1500 | Bepotastine Besilate Featured | Bepotastine Beslilate (Bepreve) is a histamine H1 receptor anatagonist. |
|
| DC8898 | Bepotastine Featured | Bepotastine is a non-sedating, selective antagonist of the histamine 1 (H1) receptor. |
|
| DC11403 | Bepridil hydrochloride Featured | Bepridil hydrochloride is a calcium channel blocker, with antianginal activity. |
|
| DC21868 | Berotralstat | Berotralstat is a potent human plasma kallikrein inhibitor. |
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| DC4143 | Besifloxacin HCl Featured | Besifloxacin HCl is a fourth-generation fluoroquinolone antibiotic. |
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| DC21519 | Besifovir | Besifovir (PMCDG Dipivoxil, NA-380, LB-80380) is a potent, selective, orally available anti-HBV agent, the prodrug of PMCDG (EC50=4 uM).. |
|
| DC11042 | BET inhibitor CF53 | BET inhibitor CF53 is a highly potent, orally active inhibitor of bromodomain and extra-terminal (BET) with Ki of <1 nM (BRD4 BD1). |
|
| DC21382 | EIDD-1931(NHC) Featured | EIDD-1931 (β-d-N4-Hydroxycytidine, NHC) inhibits both murine hepatitis virus (MHV) (EC50 of 0.17 μM) and Middle East respiratory syndrome CoV (MERS-CoV) (EC50 of 0.56 μM) with minimal cytotoxicity. It also inhibits SARS-CoV-2 and multiple 2 endemic, epide |
|
| DC10655 | 3-Guanidinopropionic acid Featured | Beta-guanidinopropionic acid is a novel creatine kinase inhibitor. |
|
| DC8967 | Betahistine Dihydrochloride | Betahistine Dihydrochloride is a histamine H3 receptors inhibitor used as an antivertigo drug. |
|
| DC8830 | Betahistine Featured | Betahistine is a strong affinity histamine H3 receptor antagonist and weak affinity agonist of histamine H1 receptors. |
|
| DC7905 | beta-Lapachone (ARQ-501, CO-501) Featured | Beta-Lapachone is a selective DNA topoisomerase I inhibitor, exhibiting no inhibitory activities against DNA topoisomerase II or ligase. Phase 2. |
|
| DCAPI1169 | Betamethasone (Celestone) | Betamethasone (Celestone) |
|
| DC12320 | Betanin | Betanin has potent antioxidant and anti-inflammatory effect, that could inhibit peroxynitrite (ONOO-), with an IC50 of 19.2 μM. Betanin is a red glycoside obtained from beets that can be used as colorant. |
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| DCAPI1040 | Betapar(Meprednisone) | Betapar(Meprednisone) |
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| DC11105 | Umibecestat Featured | beta-secretase inhibitor. |
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| DC8556 | BET-BAY 002 | BET-BAY 002 is a potent BET inhibitor; shows efficacy in a multiple myeloma model. |
|
| DC11566 | BETd-260 Featured | BETd-260 (ZBC260, BETd260) is a novel PROTAC BET degrader that tether HJB97 to a ligand for the E3 ubiquitin ligase VHL. |
|
| DC11567 | BETd-260 trifluoroacetate | BETd-260 trifluoroacetate (ZBC260, BETd 260 TFA) is a novel PROTAC BET degrader that tether HJB97 to a ligand for the E3 ubiquitin ligase VHL. |
|
| DC7373 | Betrixaban Featured | Betrixaban (PRT-054021) is a highly potent, selective, and orally efficacious factor Xa inhibitor with IC50 of 1.2 nM(inhibition of Factor 10a). |
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