653-47 |
653-47, a potentiator, significantly potentiates the cAMP-response element… |
5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-134598 |
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666-15 |
666-15 is a potent and selective CREB inhibitor with an IC50 of 81 nM. 666… |
10 mM - 1 mL, 5 mg, 10 mg, 25 mg, 50 mg |
HY-101120 |
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10074-A4 |
10074-A4 is a c-Myc inhibitor. 10074-A4 could bind to c-Myc370-409 at diff… |
5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-124129 |
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1A-116 |
1A-116 is a Rac1 inhibitor, with antitumoral and antimetastatic effects in… |
10 mM - 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-104064 |
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360A |
360A is a selective stabilizer of G-quadruplex, and also inhibits telomera… |
n/a |
HY-15595 |
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A 1070722 |
A 1070722 is a potent and selective glycogen synthase kinase 3 (GSK-3) inh… |
10 mM - 1 mL, 10 mg, 50 mg |
HY-107531 |
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A 1120 |
A 1120 is a high-affinity nonretinoid retinol-binding protein 4 (RBP4) ant… |
10 mM - 1 mL, 5 mg, 10 mg, 25 mg, 50 mg |
HY-107633 |
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A 419259 |
A 419259 is a broad-spectrum pyrrolo-pyrimidine inhibitor, designed to enh… |
n/a |
HY-15764 |
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A 438079 |
A 438079 is a potent, and selective P2X7 receptor antagonist with pIC50 of… |
10 mM - 1 mL, 10 mg, 50 mg, 100 mg |
HY-15488 |
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A 71915 |
A 71915 is a highly potent and competitive natriuretic peptide receptor A… |
n/a |
HY-P2026 |
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A 77-01 |
A 77-01 is a potent inhibitor of transforming growth factor (TGF)-β t… |
10 mM - 1 mL, 5 mg, 10 mg |
HY-78349 |
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A 779 |
A 779 is a specific antagonist of G-protein coupled receptor (Mas receptor… |
10 mM - 1 mL, 1 mg, 5 mg |
HY-P0216 |
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A 83-01 |
A 83-01 is a potent inhibitor of TGF-β type I receptor ALK5 kinase, t… |
5 mg, 10 mg, 50 mg |
HY-10432 |
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A 839977 |
A 839977 is a P2X7 selective antagonist; it blocks BzATP-evoked calcium in… |
10 mM - 1 mL, 10 mg, 50 mg |
HY-13954 |
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A 922500 |
A 922500 (DGAT-1 Inhibitor 4a) is a potent, selective, and orally bioavail… |
10 mM - 1 mL, 5 mg, 10 mg, 50 mg, 100 mg |
HY-10038 |
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A-1155463 |
A-1155463 is a highly potent and selective BCL-XL inhibitor with an EC50 o… |
10 mM - 1 mL, 5 mg, 10 mg, 50 mg, 100 mg |
HY-19725 |
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A-1165442 |
A-1165442 is a potent, competitive and orally available TRPV1 antagonist w… |
10 mM - 1 mL, 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-12428 |
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A-1210477 |
A-1210477 is a potent and selective inhibitor of MCL-1 with a Ki of 0. 45… |
5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-12468 |
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A-1331852 |
A-1331852 is an orally available BCL-XL selective inhibitor with a Ki of l… |
10 mM - 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-19741 |
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A1874 |
A1874 is a nutlin-based (MDM2 ligand) and BRD4-degrading PROTAC with a DC5… |
5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-114305 |
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A-192621 |
A-192621 is a potent, nonpeptide, orally active and selective endothelin B… |
5 mg |
HY-120295 |
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A-196 |
A-196 is a potent and selective inhibitor of SUV420H1 and SUV420H2 with IC… |
10 mM - 1 mL, 5 mg, 10 mg, 50 mg, 100 mg |
HY-100201 |
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A-205804 |
A-205804 is an orally bioavailable, potent and selective lead inhibitor of… |
10 mM - 1 mL, 10 mg, 50 mg |
HY-100226 |
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A2793 |
A2793 is an efficient dual TWIK-related acid-sensitive K+ channel (TASK)-1… |
10 mM - 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-137563 |
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A-286982 |
A-286982 is a potent and allosteric LFA-1 / ICAM-1 interaction inhibitor w… |
5 mg, 10 mg, 25 mg, 50 mg |
HY-107587 |
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A-317491 |
A-317491 is a potent, selective and non-nucleotide antagonist of P2X3 and… |
10 mM - 1 mL, 5 mg, 10 mg, 50 mg |
HY-15568 |
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A-317567 |
A-317567 is a potent acid-sensing ion channel 3 (ASIC-3) inhibitor with an… |
n/a |
HY-122135 |
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A3334 |
A3051 is a potent and orally active inhibtor of CXXC5-DVL extracted from p… |
10 mM - 1 mL, 5 mg, 10 mg, 50 mg, 100 mg |
HY-131448 |
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A-366 |
A-366 is a potent, highly selective, peptide-competitive histone methyltra… |
10 mM - 1 mL, 5 mg, 10 mg, 50 mg |
HY-12583 |
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A-381393 |
A-381393 is a potent, selective, brain penetrate dopamine D4 receptor anta… |
10 mM - 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-116941 |
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A-385358 |
A-385358 is a selective inhibitor of Bcl-XL with Kis of 0. 80 and 67 nM fo… |
10 mM - 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-16014 |
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A-395 |
A-395 is an antagonist of polycomb repressive complex 2 (PRC2) protein-pro… |
10 mM - 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-101512 |
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A40926 |
A40926, the precursor of Dalbavancin, is a second-generation glycopeptide… |
5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-107833 |
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A-437203 |
A-437203 is a selective D3 receptor antagonist with Ki of 71, 1. 6, and 62… |
n/a |
HY-U00185 |
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A-443654 |
A-443654 is a pan-Akt inhibitor and has equal potency against Akt1, Akt2,… |
10 mM - 1 mL, 1 mg, 5 mg, 10 mg |
HY-10425 |
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A-484954 |
A-484954 is a highly selective eukaryotic elongationfactor-2 (eEF2) inhibi… |
10 mM - 1 mL, 5 mg, 10 mg, 25 mg, 50 mg |
HY-110096 |
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A-485 |
A-485 is a potent and selective catalytic inhibitor of p300 / CBP with IC5… |
10 mM - 1 mL, 1 mg, 5 mg, 10 mg, 50 mg, 100 mg |
HY-107455 |
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A66 |
A66 is a highly specific and selective p110α inhibitor with an IC50… |
10 mM - 1 mL, 5 mg, 10 mg, 50 mg, 100 mg |
HY-13261 |
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A-674563 |
A-674563 is an orally active and selective Akt1 inhibitor with a Ki of 11… |
5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-13254 |
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A68930 |
A68930, as a dopamine D1 receptor agonist, can be used for the research of… |
n/a |
HY-120687 |
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A-69412 |
A-69412 is a reversible, specific inhibitor of the 5-lipoxygenase (5-LO).… |
n/a |
HY-101945 |
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A7132 |
A7132 is an antibacterial agent. A7132 possess broad and potent antibacter… |
n/a |
HY-U00225 |
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A71623 |
A71623, a CCK-4-based peptide, is a potent and highly selective CCK-A full… |
n/a |
HY-P1096 |
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A-740003 |
A-740003 is a potent, selective and competitive P2X7 receptor antagonist w… |
10 mM - 1 mL, 10 mg, 50 mg, 100 mg |
HY-50697 |
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A-769662 |
A-769662 is a potent, reversible AMPK activator with EC50 of 0. 8 µM… |
10 mM - 1 mL, 5 mg, 10 mg, 50 mg, 100 mg |
HY-50662 |
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A-770041 |
A-770041 is selective and orally active Src-family Lck inhibitor; A-770041… |
10 mM - 1 mL, 5 mg, 10 mg |
HY-11011 |
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A-802715 |
A802715 is a methylxanthine derivative. A802715 has a TD50 (toxic dose of… |
10 mM - 1 mL, 1 mg, 5 mg, 10 mg, 20 mg |
HY-U00142 |
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A-803467 |
A-803467 is a potent and selective tetrodotoxin-resistant Nav1. 8 sodium c… |
10 mM - 1 mL, 10 mg, 50 mg |
HY-11079 |
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A-804598 |
A-804598 is a CNS penetrant, competitive and selective P2X7 receptor antag… |
10 mM - 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
HY-100483 |
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A81988 |
A81988 is a potent, competitive, non-peptidic antagonist of angiotensin AT… |
n/a |
HY-U00188 |
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