SDZ-201106 (±), (DPI-201106)

SDZ-201106 (±), (DPI-201106)CAS号: 97730-95-5分子式: C29H30N4O2分子量: 466.6描述应用纯度使用方法储存/保存方法密度熔点沸点折射率PK值Ki 数据可溶性/溶解性PubChem CID

产品描述
描述

SDZ-201106 (±), (DPI-201106) is a Diphenylpiperazinylindole derivative. Positive inotropic and calcium sensitizing agent. Increases action potential duration (APD) of heart muscle. DPI 201-106 has been shown to increase the probability of the open state of the Na+ channel, thus increasing the force of the contraction. Used to study mechanisms of restoring the myofibrillar Ca2+ sensitivity and myosin enzymatic activity in diseased human hearts. Has both electron-donor and electron-acceptor activity.

应用
A positive inotropic and calcium sensitizing agent
纯度
99%
使用方法
Store solutions at 20°C for up to 3 months.
储存/保存方法
Store at -20° C
基本信息
密度
1.29 g/cm3 (Predicted)
熔点
282.96° C (Predicted)
沸点
702.59° C at 760 mmHg (Predicted)
折射率
n20D 1.69 (Predicted)
PK值
pKa: 13.99, pKb: 6.57
Ki 数据
Beta-2 adrenergic receptor: Ki= 57.3 nM (human)
可溶性/溶解性
Soluble in water (700 mg/L at 25 °C), chloroform (44.51 g/100mL at 25 °C), dichloromethane (19.20 g/100mL at 25 °C), methanol (9.98 g/100mL at 25 °C), DMSO (50 mM), ethanol (1.28 g/100mL at 25 °C)
PubChem CID
5190

SDZ 220-040

SDZ 220-040CAS号: 174575-40-7分子式: C16H16Cl2NO6P分子量: 420.18描述应用储存/保存方法形态密度熔点沸点折射率PK值Ki 数据可溶性/溶解性MDLPubChem CID

产品描述
描述
SDZ 220-040 is a potent and competitive antagonist at the NMDA receptor (pKi = 8.5). It is selective over a range of other receptor sites.
应用
A potent competitive antagonist at the NMDA receptor
储存/保存方法
Store at room temperature
形态
Solid
基本信息
密度
~1.6 g/cm3 (Predicted)
熔点
304.03° C (Predicted)
沸点
~653.5° C at 760 mmHg (Predicted)
折射率
n20D 1.66 (Predicted)
PK值
pKa: 0.66 (Predicted), pKb: 9.07 (Predicted)
Ki 数据
Cruzipain: Ki= 77 µM (Trypanosoma cruzi); beta-lactamase AmpC: Ki= 160 µM; chymotrypsin: Ki= 270 µM; malate dehydrogenase: Ki>600 µM
可溶性/溶解性
Soluble in DMSO (100 mM).
MDL
MFCD02262130
PubChem CID
6604839

SDZ 220-581 (hydrochloride)

SDZ 220-581 (hydrochloride)CAS号: 179411-93-9分子式: C16H18Cl2NO5P分子量: 406.1976描述纯度储存/保存方法外观

产品描述
描述
SDZ 220-581 Hcl is a potent, competitive antagonist at the NMDA glutamate receptor subtype(pKi= 7.7).
纯度
>98%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
外观
Powder

分子结构图

SDZ 220-581 (hydrochloride)

SDZ-202 791 R(-)

SDZ-202 791 R(-)CAS号: 97217-84-0分子式: C17H18N4O5分子量: 358.4描述应用使用方法储存/保存方法别名密度沸点折射率可溶性/溶解性MDLPubChem CID

产品描述
描述
SDZ-202 791 R(-) is a dihydropyridine-type voltage-sensitive (L-type) calcium channel blocker.
应用
A dihydropyridine-type voltage-sensitive calcium channel blocker
使用方法
Store, as supplied, at room temperature for up to 1 year. Store solutions at –
20°C for up to 3 months.
储存/保存方法
Store at room temperature
基本信息
别名
SAN 202791
密度
1.36 g/cm3 (Predicted)
沸点
504.88° C at 760 mmHg (Predicted)
折射率
n20D 1.62 (Predicted)
可溶性/溶解性
Soluble in water (700 mg/L at 25 °C), chloroform (44.51 g/100mL at 25 °C), dichloromethane (19.20 g/100mL at 25 °C), methanol (9.98 g/100mL at 25 °C), DMSO (50 mM), ethanol (1.28 g/100mL at 25 °C)
MDL
MFCD00802535
PubChem CID
122292

SDZ 220-581 Ammonium salt

SDZ 220-581 Ammonium saltCAS号: 179411-94-0分子式: C16H20ClN2O5P分子量: 386.77描述纯度储存/保存方法可溶性/溶解性

产品描述
描述

SDZ 220-581 ammonium salt is a potent, competitive antagonist at the NMDA glutamate receptor subtype(pKi= 7.7).

纯度
>98%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
可溶性/溶解性
DMSO: < 3.9 mg/mL

分子结构图

SDZ 220-581 Ammonium salt