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Cat. No. Product Name Field of Application Chemical Structure
DC1103 Hesperadin Featured Hesperadin inhibits Aurora B and T. brucei Aurora kinase-1 (TbAUK1) with IC50 of 250 nM and 40 nM, respectively.
DCAPI1218 Hesperidin Hesperidin
DC10967 HET0016 HET0016 (HET-0016) is a potent, selective inhibitor of CYP4A, potently inhibits the formation of 20-HETE with IC50 of 8.9 nM in human renal microsomes.
DC12717 Hetrombopag Hetrombopag is a potent, selective, orally-active Thrombopoietin (TPO) receptor agonist.
DC12227 Hexacosanoic acid Hexacosanoic acid is a long-chain fatty acid related to various diseases such as adrenoleukodystrophy (ALD), adrenomyeloneuropathy (AMN) and atherosclerosis.
DC12195 Hexadimethrine bromide Featured Hexadimethrine bromide is a cationic polymer discovered to enhance retroviral transduction.
DC12306 Hexamethylquercetagetin Hexamethylquercetagetin is a polymethoxylated flavone in peels of citrus cultivars.
DC8680 Hexaminolevulinate hydrochloride Hexaminolevulinate hydrochloride is a fluorescent agent, has approved for cystoscopic detection of papillary bladder cancer.
DC12707 Hexokinase 2 modulator Comp-1 Hexokinase 2 modulator Comp-1 is a potent, selective small molecule modulator of Hexokinase 2 (HK2) interaction with the mitochondria, selectively dissociates HK2 from VDAC1 in vitro with IC50 of 92 nM.
DC21904 HG-12-6 HG-12-6 is a small-molecule inhibitor that bind preferentially to unphosphorylated IRAK4 with IC50 of 165.1 nM, displays 15-fold selectivity over phosphorylated IRAK4 (IC50=2876 nM).
DC10652 HG-14-10-04 Featured HG-14-10-04 is a potent and specific ALK inhibitor with IC50 of 20 nM.
DC23141 HG6-64-1 HG6-64-1 is a potent dual TAK1 and MAP4K2 ((germinal center kinase, GCK)) inhibitor with IC50 of 41 nM and 98 nM, respectively.
DC20405 HG-7-27-01 HG-7-27-01 is a potent, selective c-Fes protein-tyrosine kinase inhibitor with IC50 of 224 nM, displays intermediate selectivity profiles (selectivity score=0.16) against 442 kinases..
DC21379 HG-7-92-01(NG25) Featured HG-7-92-01 is a potent, selective c-Fes protein-tyrosine kinase inhibitor with IC50 of 292 nM, displays intermediate selectivity profiles (selectivity score=0.18) against 353 kinases..
DC10108 HG-9-91-01 Featured HG-9-91-01 is a potent and highly selective salt-inducible kinase (SIKs) inhibitor with IC50s of 0.92 nM, 6.6 nM and 9.6 nM for SIK1, SIK2 and SIK3 respectively.
DC26060 gly-arg p-nitroanilide dihydrochloride Featured H-Gly-Arg-pNA is a colorimetric substrate for thrombin.
DC8846 HhAntag Featured HhAntag is a GLI1-Mediated transcription inhibitor.
DC20406 HIF2α-IN-2 HIF2α-IN-2 is a potent, selective, allosteric inhibitor of HIF-2α PAS-B domain with Kd of 81 nM, shows high selectivity and does not affect HIF-1 function.
DC7148 LY 379268 Featured Highly selective group II mGlu receptor agonist (EC50 values are 2.69 and 4.48 nM for hmGlu2 and hmGlu3 respectively) that displays > 80-fold selectivity over group I and group III receptors.
DC20083 H-Ile-Pro-Pro-OH Featured H-Ile-Pro-Pro-OH, a milk-derived peptide, inhibits angiotensin-converting enzyme (ACE) with an IC50 of 5 μM. Antihypertensive tripeptides.
DC23298 Hinokitiol Hinokitiol (4-Isopropyltropolone.
DC23710 Hippuristanol Hippuristanol is a potent, steroid inhibitor of eukaryotic initiation factor 4A (eIF4A), results in cell cycle arrest at G1 phase, and induces caspases activation and apoptosis.
DC10585 Hispidol Featured Hispidol ((Z)-Hispidol) is a potential therapeutic for inflammatory bowel disease; inhibits TNF-α induced adhesion of monocytes to colon epithelial cells with an IC50 of 0.50 µM.
DC10171 Hispidulin Featured Hispidulin is a natural flavone with a broad spectrum of biological activities. Hispidulin is a Pim-1 inhibitor with an IC50 of 2.71 μM.
DCAPI1505 Darunavir Featured Darunavir(TMC114) is an HIV protease inhibitor,showed potent activity against COVID-19(SARS-COV-2) .
DC8163 Fostemsavir(BMS-663068) Featured HIV-1 attachment inhibitor,a prodrug of the small-molecule inhibitor BMS-626529
DC23258 HIV-1 inhibitor 18A HIV-1 inhibitor 18A is a novel broad HIV-1 inhibitor that blocks envelope glycoprotein transitions critical for entry, specifically inhibits the entry of a wide range of HIV-1 isolates with mean IC50 of 6.4 uM.
DC9473 HIV-1 integrase inhibitor HIV-1 integrase inhibitor ((Z)-4-(3-(azidomethyl)phenyl)-2-hydroxy-4-oxobut-2-enoic acid) is uesful for anti-HIV.
DC23263 HIV-1 Integrase Inhibitor 7 HIV-1 Integrase Inhibitor 7 is an allosteric HIV-1 integrase inhibitor that inhibits the LEDGF/p75-integrase interaction with IC50 of 0.58 uM, antiviral activity EC50 of 0.76 uM..
DC9472 HIV-1 integrase inhibitor 2 HIV-1 integrase inhibitor, in the treatment of human immunodeficiency virus (HIV) infection.

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