35 products were found matching "K04152"!

JNJ-10191584 is a histamine H4 receptor antagonist (Ki = 79. nM). It is selective for the histamine H4 receptor over the histamine H3 receptor (Ki = 3,981 nM). JNJ-10191584 inhibits eosinophil and mast cell chemotaxis (IC50s = 530 and 138 nM, respectively). It decreases colonic injury in a rat model of TNBS-induced...

Description: Adriforant, also known as ZPL-3893787, PF-3893787 and ZPL-389, is a novel histamine H4 receptor antagonist. Adriforant shows an excellent in vitro profile that warrants their further investigation in relevant models of human disease. Histamine H4 receptor (H4R) has become a promising target for...

JNJ-39758979 is a histamine H4 receptor antagonist (Ki = 12.5 nM for the human receptor). It is selective for the histamine H4 receptor over histamine H1, H2, and H3 receptors (Kis = >1,000, >1,000, and 1,043 nM, respectively, for the human receptors), as well as 48 other receptors, ion channels, and transporters at...

Description: Toreforant is an effective and selective histamine H4 receptor antagonist (Ki at the human receptor: 8.4 nM). Target: Histamine Receptor. Smiles: CN1CCC(CCCNc2ncc(-c3nc4cc(C)cc(C)c4[nH]3)c(C)n2)CC1

Host Species: Rabbit. Isotype: IgG. Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. Storage: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. Purification Method: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific...

JNJ-7777120 is a potent and selective histamine H4 receptor antagonist, with a Ki value of approximately 4 nM against the human, mouse, and rat H4 receptors. Its Ki values for the histamine H1-3 receptors exceed 1 µM, regardless of species, and it has no or negligible effects on a range of other receptors and...

VUF10460 is a histamine H4 receptor agonist (Kis = 5.01 and 14.13 nM for the human and rat receptors, respectively). It is selective for the rat histamine H4 receptor over the rat histamine H3 receptor (Kis = 34.67 and 1,778.28 nM, respectively). VUF10460 (10 mg/kg) potentiates the formation of HCl-induced ulcers in...

4-Methylhistamine is a histamine H4 receptor agonist (Ki = 50 nM). It is >100-fold selective for H4 over other histamine receptors. 4-Methylhistamine inhibits CRE-beta-galactosidase activity induced by forskolin (Cay-11018) with an EC50 value of 39.8 nM in SK-N-MC cells transfected with the human H4 receptor. It...

Imetit is a histamine H3 and H4 receptor agonist (Kis = 0.3 and 2.7 nM, respectively, in radioligand binding assays). It is selective for histamine H3 and H4 receptors over H1 and H2 receptors at concentrations up to 100 µM, as well as the serotonin (5-HT) receptor subtype 5-HT3 (Ki = 240 nM). Imetit reduces...

VUF8430 is a histamine H4 receptor agonist (Ki = 31.6 nM). It is selective for histamine H4 over H1 and H3 receptors in radioligand binding assays (Kis = >1 and 1 µM, respectively) and is less active in isolated guinea pig atria, which endogenously expresses high levels of H2 receptors (pD2 = 3.8). VUF8430 inhibits...

Histamine is a biogenic amine. It is produced from histidine in basophils, mast cells, gastric enterochromaffin-like (ECL) cells, and histaminergic neurons by histidine decarboxylase (HDC). Histamine activates the G protein-coupled histamine H1-4 receptors to regulate allergic and inflammatory responses, gastric...

A-943931 is a histamine H4 receptor antagonist (Ki = 3.8 nM). In vivo, A-943931 inhibits scratching induced by clobenpropit (Cay-10011126) in mice (ED50 = 26 µmoles/kg, i.p.).Formal Name: 4-[(3R)-3-amino-1-pyrrolidinyl]-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-d]pyrimidin-2-amine, dihydrochloride, hydrate. Molecular...