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  9. (R)-(-)-α-Methylhistamine dihydrobromide, Tocris Bioscience™ 

(R)-(-)-α-Methylhistamine dihydrobromide, Tocris Bioscience™ Available on GSA/VA Contract for Federal Government customers only.

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Quantity:
10mg
50mg
This item is not returnable. View return policy
868698-49-1
C6H13Br2N3
286.999
RWHNAAABSGVRDT-ZJIMSODOSA-N
r---alpha-methylhistamine dihydrobromide,r---?-methylhistamine dihydrobromide,r---,a-methylhistamine dihydrobromide,r---alpha-methylhisamine dihydrochloride,r-1-1h-imidazol-4-yl propan-2-amine dihydrobromide,r---?-methyl-1h-imidazole-4-ethanamine dihydrobromide,2r-1-1h-imidazol-4-yl propan-2-amine dihydrobromide
45037031
(2R)-1-(1H-imidazol-5-yl)propan-2-amine;dihydrobromide
CC(CC1=CN=CN1)N.Br.Br
This item is not returnable. View return policy
868698-49-1
C6H13Br2N3
286.999
RWHNAAABSGVRDT-ZJIMSODOSA-N
r---alpha-methylhistamine dihydrobromide,r---?-methylhistamine dihydrobromide,r---,a-methylhistamine dihydrobromide,r---alpha-methylhisamine dihydrochloride,r-1-1h-imidazol-4-yl propan-2-amine dihydrobromide,r---?-methyl-1h-imidazole-4-ethanamine dihydrobromide,2r-1-1h-imidazol-4-yl propan-2-amine dihydrobromide
45037031
(2R)-1-(1H-imidazol-5-yl)propan-2-amine;dihydrobromide
CC(CC1=CN=CN1)N.Br.Br

Description

Potent, standard H3 agonist

Very potent, high affinity H3 agonist (KD = 50.3 nM) that displays > 200-fold selectivity over H4 receptors. Inhibits H3-mediated histamine synthesis and release in the CNS and stimulates H4-mediated eosinophil shape change (EC50 = 66 nM).

Available as part of the Histamine H3 Receptor Tocriset™ . S-enantiomer also available.

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Quantity 10mg
Formula Weight 287
Percent Purity >99%
Chemical Name or Material (R)-(-)-α-Methylhistamine dihydrobromide

Safety and Handling

Recommended Storage : Desiccate at Room Temperature