SCH-202676 hydrobromide

• 产品号: S4063
• 分子式: C15H14BrN3S
• 分子量: 348.26076
• 纯 度: 98%

产品别名

• 标题: SCH-202676 hydrobromide
• IUPAC标准名: N-methyl-2,3-diphenyl-2,5-dihydro-1,2,4-thiadiazol-5-imine hydrobromide
• IUPAC传统名: N-methyl-2,3-diphenyl-1,2,4-thiadiazol-5-imine hydrobromide
• 别名: N-(2,3-diphenyl-1,2,4-thiadiazol-5-(2H)-ylidene)methanamine hydrobromide

产品登记号

• PubChem SID: 24278706
• MDL号: MFCD06671539

产品性质

• Empirical Formula (Hill Notation): C15H16BrN3S
• 纯度: 98%
• 熔点: 240.0-240.8 °C(lit.)
• 溶解度: DMSO: soluble40 mg/mL
• 溶解度: H2O: insoluble
• GHS警示词: Warning
• GHS危险声明: H315-H319-H335
• 欧盟危险性物质标志: 刺激性(Irritant) (Xi)
• 个人保护装置: dust mask type N95 (US), Eyeshields, Gloves
• GHS警示性声明: P261-P305 + P351 + P338
• 危险公开号: 36/37/38
• 安全公开号: 26-36
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Biochem/physiol Actions
Allosteric agonist and antagonist of G-protein coupled receptors (GPCRs).
General description
Shown to modulate radioligand binding to various GPCRs including the human μ-, δ-, and κ-opiod, α- and β-adrenergic, muscarinic M1 and M2, and dopaminergic D1 and D2 receptors. Modulation is G-protein independent and is both selective and reversible.

详细说明 (简体中文)

Biochem/physiol Actions
Allosteric agonist and antagonist of G-protein coupled receptors (GPCRs).
General description
Shown to modulate radioligand binding to various GPCRs including the human μ-, δ-, and κ-opiod, α- and β-adrenergic, muscarinic M1 and M2, and dopaminergic D1 and D2 receptors. Modulation is G-protein independent and is both selective and reversible.