y 2

BMY 25368 HCl is a competitive histamine H2 receptor antagonist that antagonizes gastric secretion stimulated by pentagastrin, ethacrynic choline, and food.

5-[(2R)-2-Aminopropyl]-1-[3-(benzoyloxy)propyl]-2,3-dihydro-1H-indole-7-carbonitrile (2R,3R)-2,3-dihydroxybutanedioate is a natural product that can be used as reference standards.

2-[(1R,2R)-3-oxo-2-[(2Z)-5-(sulfooxy)pent-2-en-1-y is a useful organic compound for research related to life sciences. The catalog number is T125738 and the CAS number is 155408-18-7.

Neuropeptide Y (2-36) (porcine) is a pig-sourced peptide closely resembling its rat and human counterparts with 97.14% homology. It acts as an agonist for rat neuropeptide receptors Y5, Y2, and Y1, with EC50 values of 1.2, 1.6, and 3.4 nM, respectively. This compound is utilized in research on obesity and eating disorders [1].

BAY 2416964 is a small molecule inhibitor that selectively targets aromatic receptor (AhR) with an IC50 of 341 nM and is commonly used in cancer immunotherapy research.

CY 208-243 is a selective dopamine D1 receptor agonist with anti-Parkinson disease activity.

FOY 251 free base acts as a proteinase inhibitor. FOY 251 free base is an anti-proteolytic active metabolite camostate.

LY 222306, a glycinamide ribonucleotide formyltransferase (GARFT) inhibitor, has a Ki of 0.77 nM.

LY 254155, an antifolate,binds to mFBP and inhibits hGARFT with Kis of 1.7±0.1 and 2.1±0.2 nM, respectively.

PROTAC BET-binding moiety 2 is an inhibitor of the BET bromodomain.

(Rac)-LY 255262 is a pyrazolone derivative known for its antibacterial activity.

LY2389575 hydrochloride is an mGlu3 negative allosteric modulator (NAM) that is selective and non-competitive, with an IC50 value of 190 nM. LY2389575 hydrochloride induces an increase in the level of Mrc1, which amplifies the toxicity of β-amyloid (Aβ), and can be used to study Alzheimer's disease. It can be used to study Alzheimer's disease.

Allosteric potentiator of α7, α4β2 and α4β4 nAChRs

5-HT2 5-HT7 receptor antagonist

LY 225910 is a CCK2 receptor antagonist.

LY 231617 is an antioxidant.

LY 233053 is a Competitive NMDA receptor antagonist.

LY 235959 is a NMDA receptor antagonist.

glycine transporter 1 (GlyT1) inhibitor

LY 272015 hydrochloride is an orally active and selective 5-HT2B receptor antagonist that displays antihypertensive effects in DOCA-salt hypertensive rats.LY 272015 hydrochloride inhibits 5-HT- or BW723C86-induced ERK2 phosphorylation and attenuates MVIC and Tissue downstream cellular effects of 5HT signaling and can be used to study hepatocellular carcinoma.

Y-23684 is an anxiolytic drug with a novel chemical structure. It has similar effects to benzodiazepine drugs and is classed as a nonbenzodiazepine anxiolytic.

LY 288601 is the 5,6-dihydro analog of LY231514 that has antitumor activity.

LY 201409 is a potent benzamide anticonvulsant.

LY 203647 is a antagonist of leukotriene D4 and E4 receptor.