| 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. |
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