| Cat.No. | Name | Information |
|---|---|---|
| M6098 | Baicalein | Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor, IC50 value of 3.12 mM. |
| M9325 | EGTA | EGTA is a specific calcium chelator with a Kd of 60.5 nM at physiological pH (7.4) and a high specificity for Ca2+ than for Mg2+.EGTA significantly inhibits the substrate adhesion capacity of inflammatory macrophages. |
| M9330 | Brij-35 | Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability. |
| M6154 | 2-PMPA tetrasodium | 2-PMPA (PMPA tetrasodium salt) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC50 of 300 pM. |
| M2250 | Pamidronate disodium | Pamidronate disodium is a nitrogen containing bisphosphonate, used to the research of preventing osteoporosis. |
| M9916 | DPPH | DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a stable free radical that measures the free radical scavenging activity of antioxidants. |
| M9194 | Insulin (human) | Insulin (human) is a polypeptide hormone that regulates the level of sugar (glucose) in the blood and is produced by beta cells of islets. |
| M3409 | Formestane | Formestane is a second generation selective aromatase inhibitor with an IC50 of 80 nM. |
| M9665 | N-(2-amino-2-oxoethyl)acrylamide | N-(2-Amino-2-oxoethyl)acrylamide |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M6436 | AMG 853 | AMG 853 is a potent dual CRTH2 and prostaglandin D 2 (PGD 2) receptor antagonist. |
| M6435 | AMG 837 hemicalcium salt | AMG 837 hemicalcium salt is a potent free fatty acid receptor 1 (FFA1/GPR40) partial agonist. |
| M6432 | AMBMP hydrochloride | AMBMP hydrochloride is a wnt canonical signaling activator; also tubulin polymerization inhibitor. |
| M6431 | AM 92016 hydrochloride | AM 92016 hydrochloride is a k V channel blocker. |
| M6428 | AM 4668 | AM 4668 is a potent FFA1 (GPR40) agonist. |
| M6426 | ALX 5407 hydrochloride | ALX 5407 hydrochloride is a selective non-transportable GlyT1 inhibitor. |
| M6425 | Altanserin hydrochloride | Altanserin hydrochloride is a 5-HT 2A receptor antagonist. |
| M6421 | AL 8697 | AL 8697 is a potent and selective p38α inhibitor. |
| M6419 | AIDA | AIDA is a potent, selective group I mGlu antagonist. |
| M6418 | AI-3 | AI-3 is a aRE activator; induces Nrf2-ARE-dependent transcription. |
| M6412 | AG 556 | AG 556 is a eGFR-kinase inhibitor. |
| M6410 | AG 045572 | AG 045572 is a selective GnRH receptor antagonist. |
| M6409 | AF-DX 384 | AF-DX 384 is a potent M 2/M 4 antagonist. |
| M6408 | AEG 3482 | AEG 3482 is a inhibitor of JNK signaling. |
| M6405 | ACT 335827 | ACT 335827 is a potent and selective OX 1 antagonist. |
| M6403 | ACPT-II | ACPT-II is a competitive mGlu receptor antagonist. |
| M6401 | Acifran | Acifran is a hypolipidemic agent; agonist for the GPR109A (HM74A) and GPR109B receptors. |
| M6400 | ACET | ACET is a potent antagonist of GluR5-containing kainate receptors. |
| M6398 | ACDPP hydrochloride | ACDPP hydrochloride is a selective mGlu 5 receptor antagonist. |
| M6397 | ACBC | ACBC is a nMDA antagonist, acts at glycine site. |
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