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1-萘乙酸

中文名称:
1-萘乙酸
中文同义词:
佐芬普利-D5;1-萘乙酸(NAA),FOR PLANT CELL CULTURE,≥96%;1-萘乙酸(NAA),96%;佐芬普利;佐芬普利杂质;4S-1-[D-3-(苯甲酰硫基)-2-甲基丙酰]-4-(苯硫基)-L-脯氨酸
英文名称:
Zofenopril-d5
英文同义词:
1-NAPHTHYLACETICACIDα-NAPHTHYLACETICACID;1-[(S)-3-(Benzoylthio)-2-methyl-1-oxopropyl]-4α-(phenylthio)-L-proline;S-Benzoyl-4-phenylthiocaptopril;(4S)-N-[3-(Benzoylsulfanyl)-2(S)-methylpropionyl]-4-(phenylsulfanyl)-L-proline;Zofenopril;NAA(R);NAA(TM);NAA
CAS号:
81872-10-8
分子式:
C22H23NO4S2
分子量:
429.55
EINECS号:
201-705-8
相关类别:
Mol文件:
81872-10-8.mol
熔点 
129-131.5 °C(lit.)
比旋光度 
D25 -36.5° (c = 1 in methanol)
沸点 
646.3±55.0 °C(Predicted)
密度 
1.34±0.1 g/cm3(Predicted)
储存条件 
2-8°C
酸度系数(pKa)
pK1:4.236 (25°C)
形态
crystalline
颜色
light yellow
CAS 数据库
81872-10-8(CAS DataBase Reference)
生物活性
Zofenopril 是一个 angiotensin-converting enzyme (ACE) 抑制剂,其 IC50 值为 81 μM。
靶点
IC50: 81 μM (ACE)
体外研究
Kinetic analyses demonstrate that enalapril inhibits the uptake of GlySar in a competitive manner (K i approximately 6 mM). Fosinopril and Zofenopril have the greatest inhibitory potency (IC 50 values of 55 and 81μM, respectively) while the other ACE inhibitors exhibit low-affinity interactions with the renal peptide transporter.
体内研究
Zofenopril, a sulphydrylic compound, at doses higher than 70 mg/kg i.p. produces significant protection (i.e. at 70 mg/kg, P=0.044, F=2.17, d.f.=18; at higher concentration P<0.05) against the tonic phase of the audiogenic seizure response. Pretreatment with Zofenopril (15 mg/kg, i.p.) is able to produce a consistent shift to the left of the dose-response curves and a significant reduction of ED 50 values against clonus of some AEDs with the exceptions of diazepam, felbamate, phenobarbital and phenytoin compare with concurrent groups, suggesting an increase in anticonvulsant activity.
危险品标志 
Xn,Xi
危险类别码 
22-37/38-41
安全说明 
23-24/25
WGK Germany 
3
RTECS号
QJ0875000
HazardClass 
IRRITANT
价       格:请咨询卖家
CAS    号: 81872-10-8
规       格:10g/20g/100g/1kg
咨询电话:15623309010
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正规发票
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详细介绍
英文名:
Zofenopril-d5
外观:
纯度:
请咨询卖家
分子式:
C22H23NO4S2
分子量:
429.55
中文名称:
1-萘乙酸
中文同义词:
佐芬普利-D5;1-萘乙酸(NAA),FOR PLANT CELL CULTURE,≥96%;1-萘乙酸(NAA),96%;佐芬普利;佐芬普利杂质;4S-1-[D-3-(苯甲酰硫基)-2-甲基丙酰]-4-(苯硫基)-L-脯氨酸
英文名称:
Zofenopril-d5
英文同义词:
1-NAPHTHYLACETICACIDα-NAPHTHYLACETICACID;1-[(S)-3-(Benzoylthio)-2-methyl-1-oxopropyl]-4α-(phenylthio)-L-proline;S-Benzoyl-4-phenylthiocaptopril;(4S)-N-[3-(Benzoylsulfanyl)-2(S)-methylpropionyl]-4-(phenylsulfanyl)-L-proline;Zofenopril;NAA(R);NAA(TM);NAA
CAS号:
81872-10-8
分子式:
C22H23NO4S2
分子量:
429.55
EINECS号:
201-705-8
相关类别:
Mol文件:
81872-10-8.mol
熔点 
129-131.5 °C(lit.)
比旋光度 
D25 -36.5° (c = 1 in methanol)
沸点 
646.3±55.0 °C(Predicted)
密度 
1.34±0.1 g/cm3(Predicted)
储存条件 
2-8°C
酸度系数(pKa)
pK1:4.236 (25°C)
形态
crystalline
颜色
light yellow
CAS 数据库
81872-10-8(CAS DataBase Reference)
生物活性
Zofenopril 是一个 angiotensin-converting enzyme (ACE) 抑制剂,其 IC50 值为 81 μM。
靶点
IC50: 81 μM (ACE)
体外研究
Kinetic analyses demonstrate that enalapril inhibits the uptake of GlySar in a competitive manner (K i approximately 6 mM). Fosinopril and Zofenopril have the greatest inhibitory potency (IC 50 values of 55 and 81μM, respectively) while the other ACE inhibitors exhibit low-affinity interactions with the renal peptide transporter.
体内研究
Zofenopril, a sulphydrylic compound, at doses higher than 70 mg/kg i.p. produces significant protection (i.e. at 70 mg/kg, P=0.044, F=2.17, d.f.=18; at higher concentration P<0.05) against the tonic phase of the audiogenic seizure response. Pretreatment with Zofenopril (15 mg/kg, i.p.) is able to produce a consistent shift to the left of the dose-response curves and a significant reduction of ED 50 values against clonus of some AEDs with the exceptions of diazepam, felbamate, phenobarbital and phenytoin compare with concurrent groups, suggesting an increase in anticonvulsant activity.
危险品标志 
Xn,Xi
危险类别码 
22-37/38-41
安全说明 
23-24/25
WGK Germany 
3
RTECS号
QJ0875000
HazardClass 
IRRITANT
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