| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V4406 | ABT-239 | 460746-46-7 | ABT-239 is a novel, highly efficacious, non-imidazole class of H3R antagonist and a transient receptor potential vanilloid type 1 (TRPV1) antagonist/inverse agonist developed by Abbott with stimulant and nootropic effects, and has been investigated as a treatment for ADHD, Alzheimer's disease, and schizophrenia. |
|
V97373 | Aminopotentidine | 140873-26-3 | Aminopotentidine is a histamine H2 receptor antagonist with KB values of 220 and 280 nM for human and guinea pig H2 receptors, respectively. |
|
V103940 | Arpromidine | 106669-71-0 | Apromidine (BU-E-50) is a histamine H2 receptor agonist and histamine H1 receptor antagonist. |
|
V115308 | D-20133 | 146764-26-3 | D-20133 is an orally effective cetylphosphocholine analogue. |
|
V107689 | Elbanizine | 110629-41-9 | Albanizine inhibits histamine, bradykinin activity, histamine release from rat mast cells (IC50 0.26 μM), and IgE-mediated passive cutaneous anaphylaxis (PCA). |
|
V135865 | Fenspiride-d5 hydrochloride | 1246815-28-0 | Fenspiride-d5 hydrochloride is a deuterated fenspiride hydrochloride. |
|
V2939 | GSK189254A | 720690-73-3 | GSK189254A (also known as GSK189254) is a novel histamine H(3) receptor antagonist with high affinity for human (pK(i) = 9.59 -9.90) and rat (pK(i) = 8.51-9.17) H(3) receptors. |
|
V137057 | H3R antagonist 5 | 879368-27-1 | H3R antagonist 5 is a selective histamine H3 receptor inverse agonist with an IC50 value of 0.54 nM and the ability to cross the blood-brain barrier. |
|
V94342 | Impromidine hydrochloride | 65573-02-6 | Imoprodine is a potent histamine H2 receptor agonist. |
|
V1239 | JNJ-7777120 | 459168-41-3 | JNJ-7777120 (JNJ7777120; JNJ 7777120), an indole analog, is a potent and selective non-imidazole-based histamine H4R receptor antagonist that can reduce allergic and asthmatic symptoms. |
|
V29682 | N-Acetylhistamine | 673-49-4 | N-Acetylhistamine is a histamine metabolite. |
|
V109135 | Propiomazine maleate | 3568-23-8 | Promethazine maleate is an effective oral antihistamine. |
|
V2789 | S 38093 | 862896-30-8 | S 38093 is a novel brain-penetrant antagonist (inverse agonist) of the H3 (histamine H3) receptor with Kiof 8.8, 1.44 and 1.2 µM for rat, mouse and human H3 receptors, respectively. |
|
V144669 | SCH 79687 | 224585-45-9 | SCH 79687 is an orally effective histamine H3 receptor antagonist with a Ki value of 1.9 nM in rats and 13 nM in guinea pigs. |
|
V85156 | Spinacetin | 3153-83-1 | |
|
V147152 | Wy 45086 | 87476-50-4 | Wy 45086 is a histamine H2 receptor antagonist. |
|
V147195 | XmAb-7195 | XmAb-7195 is a human monoclonal antibody (mAb) that targets IGH. | |
|
V117117 | Zolantidine | 104076-38-2 | Zolantidine (SKF 95282) is a potent, selective, blood-brain barrier-crossing histamine H2 receptor antagonist. |
|
V147782 | σ1R/H3R ligand-1 | σ1R/H3R ligand-1 is a dual σ1R/H3R antagonist with a Ki value of 8.8 nM for σ1R and 31.2 nM for H3R. | |
|
V29268 | Epinastine (WAL801) | 80012-43-7 | Epinastine (also known as WAL-801CL HCl) is a potent antihistamine H1 without sedative activity and a mast cell stabilizer that is used in eye drops for the treatment of allergic conjunctivitis. |