| Company Name: |
Sigma-Aldrich |
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021-61415566 800-8193336 |
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orderCN@merckgroup.com |
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| | Histamine dihydrochloride r(-)-α-methyl Basic information |
| | Histamine dihydrochloride r(-)-α-methyl Chemical Properties |
| Melting point | 169-173°C | | storage temp. | desiccated | | solubility | H2O: soluble | | form | Powder | | color | white to off-white | | Optical Rotation | [α]22/D 4°, c = 0.8 in H2O(lit.) | | Water Solubility | H2O: soluble | | Sensitive | Hygroscopic | | InChI | 1S/C6H11N3.2ClH/c1-5(7)2-6-3-8-4-9-6;;/h3-5H,2,7H2,1H3,(H,8,9);2*1H/t5-;;/m1../s1 | | InChIKey | IZHCNQFUWDFPCW-ZJIMSODOSA-N | | SMILES | Cl.Cl.C[C@@H](N)Cc1c[nH]cn1 |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2 Skin Irrit. 2 STOT SE 3 |
| | Histamine dihydrochloride r(-)-α-methyl Usage And Synthesis |
| Uses | Potent, selective H3 histamine receptor agonist which crosses the blood-brain barrier; inhibits histamine synthesis and release. | | Uses | R(-)-α-Methyl Histamine Dihydrochloride is a potent and selective H3 histamine receptor agonist that inhibits the synthesis and release of histamine (1,2,3,4). R(-)-α-Methyl Histamine Dihydrochloride is a blood-brain barrier penetrant. | | Biochem/physiol Actions | Potent, selective H3 histamine receptor agonist which crosses the blood-brain barrier; inhibits histamine synthesis and release. | | in vivo | Pretreatment with (R)-(-)-α-Methylhistamine dihydrochloride (RAMH; 10 mg/kg; i.p.; 60 min before training) reverses Propofol‐induced (25 mg/kg; i.p.; 30 min before training) memory retention[5].
(R)-(-)-α-Methylhistamine dihydrochloride (6.3 mg/kg; i.p.) significantly decreases the steady-state t-MH level in the mouse brain, whereas these compounds produced no significant changes in the HA level[3].
| Animal Model: | Male Sprague‐Dawley rats (10-12 week)[3] | | Dosage: | 10 mg/kg | | Administration: | IP; 60 min before training | | Result: | Reversed propofol‐induced memory retention.
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| | IC 50 | H3 receptor: 50.3 nM (Kd) |
| | Histamine dihydrochloride r(-)-α-methyl Preparation Products And Raw materials |
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