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Home >> Signaling Pathways >> Neuroscience >> Histamine Receptor

Histamine Receptor

Histamine receptor has 4 subtypes (H1,H2,H3 and H4) which mediates various biological fuctions, including allergic reaction, gastric acid secretion and inflammation etc.

Products for  Histamine Receptor

  1. Cat.No. Product Name Information
  2. GC61256 Rupatadine D4 fumarate Rupatadine D4 fumarate (UR-12592 D4 fumarate) is a deuterium labeled Rupatadine fumarate. Rupatadine D4 fumarate Chemical Structure
  3. GC11033 Rupatadine Fumarate Inhibitor of PAF and histamine (H1) receptor Rupatadine Fumarate Chemical Structure
  4. GC31105 S 38093 S 38093 is a brain-penetrant, orally active antagonist of H3 receptor, with Kis of 8.8, 1.44 and 1.2 ?M for rat, mouse and human H3 receptors, respectively. S 38093 Chemical Structure
  5. GC64084 Samelisant Samelisant (SUVN-G3031) is a potent and selective histamine H3 receptor (H3R) inverse agonist with good brain penetration and oral bioavailability. Samelisant Chemical Structure
  6. GC68014 Seliforant Seliforant Chemical Structure
  7. GC31800 SUN 1334H SUN 1334H is a potent, orally active, highly selective H1 receptor antagonist, with Ki of 9.7 nM. SUN 1334H Chemical Structure
  8. GC64545 Tecastemizole Tecastemizole (Norastemizole), a major metabolite of Astemizole, is a potent and selective H1 receptor antagonist. Tecastemizole Chemical Structure
  9. GC10978 Terfenadine Histamine H1-receptor antagonist Terfenadine Chemical Structure
  10. GC64934 Thiethylperazine Thiethylperazine, a phenothiazine derivate, is an orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist. Thiethylperazine Chemical Structure
  11. GC64935 Thiethylperazine dimaleate Thiethylperazine dimaleate, a phenothiazine derivate, is an orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist. Thiethylperazine dimaleate Chemical Structure
  12. GC13496 Thioperamide histamine H3 and H4 antagonist/inverse agonist Thioperamide Chemical Structure
  13. GC11330 Tiotidine Potent histamine H2-receptor antagonist Tiotidine Chemical Structure
  14. GC31220 Toreforant (JNJ-38518168) Toreforant (JNJ-38518168) is a potent and selective histamine H4 receptor (H4R) antagonist, with a Ki at the human receptor of 8.4 nM. Toreforant (JNJ-38518168) Chemical Structure
  15. GC13266 trans-Triprolidine hydrochloride trans-Triprolidine hydrochloride is an orally active histamine H1 antagonist. trans-Triprolidine hydrochloride Chemical Structure
  16. GC17488 Trimipramine (maleate) potent antagonist of histamine H1 receptor Trimipramine (maleate) Chemical Structure
  17. GC12061 Tripelennamine HCl Tripelennamine HCl, an ethylenediamine derivative, is a potent histamine H1-receptor antagonist. Tripelennamine HCl Chemical Structure
  18. GC39735 Triprolidine hydrochloride monohydrate Triprolidine hydrochloride monohydrate, a first-generation antihistamine, is an oral active histamine H1 antagonist. Triprolidine hydrochloride monohydrate Chemical Structure
  19. GC17585 VUF 10460 histamine H4 receptor agonist VUF 10460 Chemical Structure
  20. GC16018 VUF 5681 dihydrobromide histamine H3 receptor silent antagonist VUF 5681 dihydrobromide Chemical Structure
  21. GC17564 VUF 8430 dihydrobromide histamine H4 receptor full agonist VUF 8430 dihydrobromide Chemical Structure
  22. GC31824 Wy 49051 Wy 49051 is a potent, orally active H1 receptor antagonist, with IC50 of 44 nM. Wy 49051 Chemical Structure
  23. GC37959 Zaltidine Zaltidine(CP-57361) is a H2-receptor antagonist, which has the antisecretory action. Zaltidine Chemical Structure
  24. GC13388 Zolantidine dimaleate H2 receptor antagonist Zolantidine dimaleate Chemical Structure

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