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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 H 3 agonist (K D = 50.3 nM) that displays > 200-fold selectivity over H 4 receptors. Inhibits H 3 -mediated histamine synthesis and release in the CNS and stimulates H 4 -mediated eosinophil shape change (EC 50 = 66 nM). Available as part of the Histamine H 3 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