4-Methylhistamine dihydrochloride
4-Methylhistamine dihydrochloride Basic information
- Product Name:
- 4-Methylhistamine dihydrochloride
- Synonyms:
-
- 5-(2-AMINOETHYL)-4-METHYLIMIDAZOLE DIHYDROCHLORIDE
- 4-METHYLHISTAMINE DIHYDROCHLORIDE
- SKF-71517
- 1H-Imidazole-4-ethanamine, 5-methyl-, dihydrochloride (9ci)
- 4-(2-Aminoethyl)-5-methylimidazole dihydrochloride
- 5-Methyl-1H-imidazole-4-ethanamine dihydrochloride
- 5-Methylhistamine dihydrochloride
- Imidazole, 4-(2-aminoethyl)-5-methyl-, dihydrochloride
- CAS:
- 36376-47-3
- MF:
- C6H14Cl2N3
- MW:
- 199.10146
- Product Categories:
-
- Histamine receptor
- Amines
- Heterocycles
- Intermediates & Fine Chemicals
- Pharmaceuticals
- Mol File:
- 36376-47-3.mol
4-Methylhistamine dihydrochloride Chemical Properties
- Melting point:
- 231-233℃ (ethanol )
- storage temp.
- Desiccate at RT
- solubility
- DMSO (Slightly, Heated), Methanol (Slightly)
- form
- Solid
- color
- White to Pale Beige
- Water Solubility
- Soluble to 50 mM in water
4-Methylhistamine dihydrochloride Usage And Synthesis
Description
4-Methylhistamine (dihydrochloride) is the potent agonist of histamine 4 receptor (H4R). 4-Methylhistamine (dihydrochloride) has the potential for the research of immune-related diseases such as cancer and autoimmune disorders.
Uses
Histamine H2 receptor agonist, antagonist and antineoplastic agent on the in vitro growth of peripheral blood CFU-GM from normal individuals and HL-60 leukemia cells.
Biological Activity
4-Methylhistamine dihydrochloride is a potent, high affinity H4 receptor agonist (Ki = 7 nM) that displays > 100-fold selectivity over other human histamine receptor subtypes.
storage
Desiccate at RT
References
[1]. lim hd, van rijn rm, ling p, et al. evaluation of histamine h1-, h2-, and h3-receptor ligands at the human histamine h4 receptor: identification of 4-methylhistamine as the first potent and selective h4 receptor agonist. journal of pharmacology and experimental therapeutics, 2005, 314(3): 1310-1321.
[2]. ahmad sf, ansari ma, zoheir kma, et al. regulation of tnf-α and nf-κb activation through the jak/stat signaling pathway downstream of histamine 4 receptor in a rat model of lps-induced joint inflammation. immunobiology, 2015, 220(7): 889-898.
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