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ChemicalBook--->CAS DataBase List--->100130-32-3

100130-32-3

100130-32-3 Structure

100130-32-3 Structure
IdentificationBack Directory
[Name]

2-(diaminomethylideneamino)ethylsulfanylmethanimidamide dihydrobromide
[CAS]

100130-32-3
[Synonyms]

VUF8430 hydrobromide
VUF 8430 dihydrobromide >=97% (NMR)
2-guanidinoethyl carbamimidothioate dihydrobromide
2-[(Aminoiminomethyl)amino]ethyl carbamimidothioic acid ester
2-(diaminomethylideneamino)ethylsulfanylmethanimidamide dihydrobromide
[Molecular Formula]

C4H13Br2N5S
[MDL Number]

MFCD01694605
[MOL File]

100130-32-3.mol
Chemical PropertiesBack Directory
[storage temp. ]

room temp
[solubility ]

deionized water: soluble24mg/mL
[form ]

solid
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P301+P312-P302+P352-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22-36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[RTECS ]

UM6960000
Hazard InformationBack Directory
[Description]

VUF8430 is a histamine H4 receptor agonist (Ki = 31.6 nM). It is selective for histamine H4 over H1 and H3 receptors in radioligand binding assays (Kis = >1 and 1 μM, respectively) and is less active in isolated guinea pig atria, which endogenously expresses high levels of H2 receptors (pD2 = 3.8). VUF8430 inhibits forskolin-induced, cAMP-mediated increases in β-galactosidase activity (EC50 = 50.1 nM). In vivo, VUF8430 (30 mg/kg) enhances HCl-induced formation of gastric lesions in rats. It also reduces mechanical and thermal allodynia in a mouse model of peripheral neuropathy induced by spared nerve injury (SNI).
[Uses]

VUF 8430 Dihydrobromide is an H4 receptor agonist.
[storage]

Desiccate at RT
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