基本信息 物理化学性质 苯甲酸 (2Z)-2-(1-己基-1,2-二氢-2-氧代-3H-吲哚-3-亚基)肼价格(试剂级) 常见问题列表 供应商 相关产品
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1048973-47-2

中文名称 苯甲酸 (2Z)-2-(1-己基-1,2-二氢-2-氧代-3H-吲哚-3-亚基)肼
英文名称 MDA 19
CAS 1048973-47-2
分子式 C21H23N3O2
分子量 349.43
MOL 文件 1048973-47-2.mol
结构式 1048973-47-2 结构式

基本信息

中文别名 N'-(1-己基-2-氧代吲哚啉-3-基亚甲基)苯甲酰肼
苯甲酸 (2Z)-2-(1-己基-1,2-二氢-2-氧代-3H-吲哚-3-亚基)肼
英文别名 MDA 19
MDA19
MDA-19
N'-(1-Hexyl-2-oxoindolin-3-ylidene)benzohydrazide
(Z)-N'-(1-hexyl-2-oxoindolin-3-ylidene)benzohydrazide
N-[(Z)-(1-Hexyl-2-oxo-indolin-3-ylidene)aMino]benzaMide
N'-[(3Z)-1-Hexyl-2-oxo-1,2-dihydro-3H-indol-3-ylidene]benzohydrazide
Benzoic acid (2Z)-2-(1-hexyl-1,2-dihydro-2-oxo-3H-indol-3-ylidene)hydrazide
MDA 19 (Z)-N'-(1-hexyl-2-oxoindolin-3-ylidene)benzohydrazide

物理化学性质

密度 1.16±0.1 g/cm3 (20 ºC 760 Torr)
储存条件 -20°C储存
溶解度 DMF: 20 mg/ml; DMSO: 10 mg/ml; Ethanol: 3 mg/ml; Methanol: 1 mg/ml
酸度系数(pKa) 10.45±0.20(Predicted)
形态 结晶固体
颜色 Light yellow to yellow

苯甲酸 (2Z)-2-(1-己基-1,2-二氢-2-氧代-3H-吲哚-3-亚基)肼价格(试剂级)

报价日期产品编号产品名称CAS号包装价格
2026/09/15HY-15451R苯甲酸 (2Z)-2-(1-己基-1,2-二氢-2-氧代-3H-吲哚-3-亚基)肼
MDA 19 (Standard)
1048973-47-25 mg2000元
2026/09/15HY-15451苯甲酸 (2Z)-2-(1-己基-1,2-二氢-2-氧代-3H-吲哚-3-亚基)肼
MDA 19
1048973-47-25mg880元
2026/09/15HY-15451R苯甲酸 (2Z)-2-(1-己基-1,2-二氢-2-氧代-3H-吲哚-3-亚基)肼
MDA 19 (Standard)
1048973-47-210 mg3200元

常见问题列表

生物活性
MDA 19 是一种有效和选择性的人类大麻素受体 2 (CB2) 激动剂,Ki 值为 43.3 nM。MDA 19 在神经性疼痛的大鼠模型中具有抗痛觉过敏作用,并且不影响大鼠的运动能力。
体外研究

MDA19 displayed 4-fold-higher affinity at the human CB(2) than at the human CB1 receptor (K(i) = 43.3 +/- 10.3 vs 162.4 +/- 7.6 nM) and nearly 70-fold-higher affinity at the rat CB2 than at the rat CB1 receptor (K(i) = 16.3 +/- 2.1 vs 1130 +/- 574 nM). In guanosine triphosphate (GTP)gamma[(35)S] functional assays, MDA19 behaved as an agonist at the human CB1 and CB2 receptors and at the rat CB1 receptor but as an inverse agonist at the rat CB2 receptor. In 3',5'-cyclic adenosine monophosphate (cAMP) assays, MDA19 behaved as an agonist at the rat CB1 receptor and exhibited no functional activity at the rat CB(2) receptor. In extracellular signal-regulated kinases 1 and 2 activation assays.

体内研究

MDA19 behaved as an agonist at the rat CB2 receptor. MDA19 attenuated tactile allodynia produced by spinal nerve ligation or paclitaxel in a dose-related manner in rats and CB2(+/+) mice but not in CB2(-/-) mice, indicating that CB2 receptors mediated the effects of MDA19. MDA19 did not affect rat locomotor activity.

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