MED CHEM EXPRESS Non-Antibody Products — page 1 of 807
Non-Antibody Products
Page 1 of 807
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| 653-47 | 653-47, a potentiator, significantly potentiates the cAMP-response element… | 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | HY-134598 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 360A | 360A is a selective stabilizer of G-quadruplex, and also inhibits telomera… | n/a | HY-15595 | More Info |
| 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 | More Info |
| 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 | More Info |
| A 419259 | A 419259 is a broad-spectrum pyrrolo-pyrimidine inhibitor, designed to enh… | n/a | HY-15764 | More Info |
| 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 | More Info |
| A 71915 | A 71915 is a highly potent and competitive natriuretic peptide receptor A… | n/a | HY-P2026 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| A-192621 | A-192621 is a potent, nonpeptide, orally active and selective endothelin B… | 5 mg | HY-120295 | More Info |
| 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 | More Info |
| A-205804 | A-205804 is an orally bioavailable, potent and selective lead inhibitor of… | 10 mM - 1 mL, 10 mg, 50 mg | HY-100226 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| A-317567 | A-317567 is a potent acid-sensing ion channel 3 (ASIC-3) inhibitor with an… | n/a | HY-122135 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| A40926 | A40926, the precursor of Dalbavancin, is a second-generation glycopeptide… | 5 mg, 10 mg, 25 mg, 50 mg, 100 mg | HY-107833 | More Info |
| A-437203 | A-437203 is a selective D3 receptor antagonist with Ki of 71, 1. 6, and 62… | n/a | HY-U00185 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| A68930 | A68930, as a dopamine D1 receptor agonist, can be used for the research of… | n/a | HY-120687 | More Info |
| A-69412 | A-69412 is a reversible, specific inhibitor of the 5-lipoxygenase (5-LO).… | n/a | HY-101945 | More Info |
| A7132 | A7132 is an antibacterial agent. A7132 possess broad and potent antibacter… | n/a | HY-U00225 | More Info |
| A71623 | A71623, a CCK-4-based peptide, is a potent and highly selective CCK-A full… | n/a | HY-P1096 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| 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 | More Info |
| A81988 | A81988 is a potent, competitive, non-peptidic antagonist of angiotensin AT… | n/a | HY-U00188 | More Info |
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