SML0103

AMTB hydrate

≥98% (HPLC)

• Sinônimo(s): N-(3-aminopropyl)-2-[(3-methylphenyl)methoxy]-N-(2-thienylmethyl)-benzamide hydrochloride (1:1) hyclate
• Fórmula empírica (Notação de Hill): C₂₃H₂₆N₂O₂S·HCl · xH₂O
• Número CAS: 926023-82-7
• Peso molecular: 430.99 (anhydrous basis)
• Código UNSPSC: 12352200
• ID de substância PubChem: 329825160
• NACRES: NA.77

Propriedades

• Nível de qualidade: 100
• Ensaio: ≥98% (HPLC)
• Formulário: powder
• condição de armazenamento: desiccated
• cor: white to tan
• solubilidade: DMSO: ≥10 mg/mL
• temperatura de armazenamento: 2-8°C
• cadeia de caracteres SMILES: O=C(C1=C(OCC2=C(C)C=CC=C2)C=CC=C1)N(CCCN)CC3=CC=CS3.Cl.O
• InChI: 1S/C23H26N2O2S.ClH.H2O/c1-18-8-2-3-9-19(18)17-27-22-12-5-4-11-21(22)23(26)25(14-7-13-24)16-20-10-6-15-28-20;;/h2-6,8-12,15H,7,13-14,16-17,24H2,1H3;1H;1H2
• chave InChI: RTYVTAQFASBIDN-UHFFFAOYSA-N

Descrição

Aplicação

AMTB hydrate has been used as an inhibitor of transient receptor potential cation channel, subfamily melastatin, member 8 (TRPM8) in breast cancer cells[1] and murine T cells.[2]

Ações bioquímicas/fisiológicas

AMTB is a 2-benzyloxy-benzoic acid amide derivative,[1] which also inhibits voltage-gated sodium channels (Nav) and their isoforms.[1]

AMTB is a TRPM8 ion channel blocker

AMTB is a TRPM8-selective antagonist with no cross reactivity to TRPV1 or 4. The pIC50 of icilin activation of TRPM8 is 6.23 i.v. administration of AMTB reduced the frequency of rhythmic contractions in volume-loaded bladder and inhibited blood pressure and visceromotor reflex responses to bladder distention.

Informações de segurança

• Código de classe de armazenamento: 11 - Combustible Solids
• Classe de risco de água (WGK): WGK 3
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable