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
EINECS:
Product Categories:Histamine receptor;Amines;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:36376-47-3.mol
4-Methylhistamine dihydrochloride Structure
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
Safety Information
HazardClass IRRITANT
MSDS Information
4-Methylhistamine dihydrochloride Usage And Synthesis
Description4-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.
UsesHistamine 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 Activity4-Methylhistamine dihydrochloride is a potent, high affinity H4 receptor agonist (Ki = 7 nM) that displays > 100-fold selectivity over other human histamine receptor subtypes.
storageDesiccate 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.
4-Methylhistamine dihydrochloride Preparation Products And Raw materials
4-(2,4-DICHLORO-PHENYL)-4,5,6,7-TETRAHYDRO-3H-IMIDAZO[4,5-C]PYRIDINE-6-CARBOXYLIC ACID N-ALPHA-METHYLHISTAMINE DIHYDROCHLORIDE,NA-METHYLHISTAMINE DIHYDROCHLORIDE,Methylhistamine dihydrochloride Nalpha- METHYLHISTAMINE DIHYDROCHLORIDE, N-ALPHA-[METHYL-3H]- (+/-)-5-AMINO-4,5,6,7-TETRAHYDROBENZOIMIDAZOLE DIHYDROCHLORIDE 3-METHYLHISTAMINE DIHYDROCHLORIDE 4-(2,3-DICHLORO-PHENYL)-4,5,6,7-TETRAHYDRO-3H-IMIDAZO[4,5-C]PYRIDINE-6-CARBOXYLIC ACID RARECHEM AN KD 0493 5-amino-4,5,6,7-tetrahydrobenzimidazole 4,5,6,7-Tetrahydro-3H-imidazo[4,5-c]pyridine Alpidem (S)-4,5,6,7-Tetrahydro-3-phenylmethyl-3H-imidazo[4,5-c]pyridine-6-carboxylic acid dihydrochloride 4,5,6,7-TETRAHYDRO-1H-IMIDAZOL[4,5-C]-PYRIDINE DIHYDROCHLORIDE 4-(3,4-DICHLORO-PHENYL)-4,5,6,7-TETRAHYDRO-3H-IMIDAZO[4,5-C]PYRIDINE-6-CARBOXYLIC ACID 2-METHYL-4,5,6,7-TETRAHYDRO-3H-IMIDAZO[4,5-C]PYRIDINE DIHYDROCHLORIDE (r)(-)-α-methylhistamine dihydrochloride,R(-)-ALPHA-METHYLHISTAMINE DIHYDROCHLORIDE,(R)-(-)-A-methylhistamine*dihydrochloride β-Methylhistamine dihydrochloride IFLAB-BB F1824-0006 4-Methylhistamine dihydrochloride

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