Home > Products

Products

You can also try the following methods, and our professionals will serve you Customized Consultation
Cat. No. Product Name Field of Application Chemical Structure
DC7705 HTH-01-015 Featured HTH-01-015 is a selective inhibitor of NUAK1 kinase with an IC50 value of 100 nM.
DC20409 HTH-01-091 HTH-01-091 is a potent and selective, cell-permeable, ATP-competitive MELK inhibitor with biochemical IC50 of 10.5 nM.
DC9960 HTHQ Featured HTHQ, which is a hydroquinone monoalkyl ether, is a potent anti-oxidative agent, even at low dose levels.
DC21128 HTS 01037 HTS01037 is a highly potent ligand of adipocyte fatty acid binding protein (A-FABP/aP2) with Ki of 0.67 uM.
DC9697 HUHS015 Featured HUHS015 is a prostate cancer antigen (PCA)-1/AlkB homologue 3 (ALKBH3) inhibitor.
DC9329 (±)-Huperzine A Huperzine A, an active Lycopodium alkaloid extracted from traditional Chinese herb, is a potent, selective and reversible acetylcholinesterase (AChE) inhibitor and has been widely used in China for the treatment of Alzheimer's disease (AD).
DC12262 H-Val-Pro-Pro-OH TFA Featured H-Val-Pro-Pro-OH (TFA) is a trifluoroacetate (TFA) salt form of the tripeptide H-Val-Pro-Pro-OH, which is derived from milk proteins. This peptide is known for its ability to inhibit Angiotensin I Converting Enzyme (ACE), a key enzyme in the renin-angiotensin system (RAS) that regulates blood pressure. The TFA salt form is commonly used in research and pharmaceutical applications to improve the solubility and stability of the peptide.
DC20081 H-Val-Pro-Pro-OH Featured H-Val-Pro-Pro-OH is a tripeptide derived from milk proteins, specifically a proline-rich peptide, and is known for its inhibitory activity against Angiotensin I Converting Enzyme (ACE). ACE is a key enzyme in the renin-angiotensin system (RAS), which regulates blood pressure by converting angiotensin I to angiotensin II, a potent vasoconstrictor. Inhibition of ACE leads to reduced angiotensin II levels, resulting in vasodilation and lowered blood pressure.
DC10580 hVEGF-IN-1 Featured hVEGF-IN-1 represses human VEGF-A translation and shows antitumor activity.
DC11167 HX600 HX600 (HX-600) is a synthetic agonist of RXR-Nurr1 heterodimer complex, also selectively activate NGFI-B/RXR heterodimers.
DC20281 Hycanthone Featured Hycanthone, the most potent mutagen in a series of nine thiaxanthenones, is a potent inducer of nuclear immunoreactivity to antinucleoside antibodies in HeLa cells.
DCAPI1149 Hydralazine HCl Hydralazine HCl
DC20410 Hydrazinocurcumin Featured Hydrazinocurcumin is a synthetic curcumin derivative that inhibits the proliferation of bovine aortic endothelial cells (BAECs) with IC50 of 520 nM without cytotoxicity, inhibits STAT3 phosphorylation and downregulates an array of STAT3 downstream targets.
DCAPI1269 Hydrochlorothiazide Hydrochlorothiazide
DCAPI1198 Hydrocortisone (Cortisol) Hydrocortisone (Cortisol)
DC10227 Hydroquinidine Hydroquinidine is an antiarrhythmic agent.
DC9614 Hydroxyfasudil (hydrochloride) Featured Hydroxyfasudil Hcl(HA1100 Hcl), metabolite of Fasudil, is a potent Rho-kinase inhibitor and vasodilator.
DC20277 Hydroxyfasudil free base Featured Hydroxy-Fasudil is a metabolite of Fasudil, acting as a potent Rho-kinase inhibitor and vasodilator.
DCAPI1226 Hydroxyflutamide (Hydroxyniphtholide) Hydroxyflutamide (Hydroxyniphtholide)
DC10848 Hydroxyhexamide Featured Hydroxyhexamide is a pharmacologically active metabolite of Acetohexamide, used as a hypoglycemic agents.
DC10237 Hydroxyprogesterone caproate Hydroxyprogesterone Caproate is a synthetic progestational agent. It binds to and activates nuclear progesterone receptors in the reproductive system and inhibits ovulation and an alteration in the cervical mucus and endometrium.
DCAPI1045 Hydroxyurea (Cytodrox) Hydroxyurea (Cytodrox)
DC11328 Hydroxyzine Hydroxyzine is a histamine H1 receptor antagonist (Ki = 1.9 nM).
DCAPI1564 Hyoscyamine Sulfate Hyoscyamine Sulfate
DC9913 Hypericin Hypericin is a photosensitive antiviral with anticancer and antidepressant agent derived from Hypericum perforatum. It can inhibit tyrosine kinases with IC50 of 7.5 μM.
DC23001 Hypocrellin B Featured Hypocrellin B is an apoptosis inducer. The hypocrellins are pigments isolated from the fungi Hypocrella bambusae and Shiraia bambusicola. They are used as photosensitizers for photodynamic therapy of cancer.
DC8166 Molidustat(BAY 85-3934) Featured Hypoxia-inducible factor prolyl hydroxylase inhibitor
DC21129 HZ05 HZ05 is a potent DHODH inhibitor with IC50 of 32 nM, accumulates cancer cells in S-phase, increases p53 synthesis, and synergizes with an inhibitor of p53 degradation (Nutlin-3a) to reduce tumor growth in vivo..
DC8834 HZ-1157 Featured HZ-1157 is a novel potent inhibitor of HCV NS3/4A protease; Potent Dengue virus inhibitor
DC11118 HZ-166 HZ-166 (HZ166) is a GABAA receptor subtype-selective benzodiazepine site ligand with preferential activity at α2- and α3-GABA(A) receptors.

Customized Consultation X

Your information is safe with us. * Required Fields.

Your name
Company
Email
Procuct Name
Cat. No.
Remark
Verification code
Please fill out the characters in the picture
X