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N-(苄氧基)-n-((3s,4r)-6-氰基-3-羟基-2,2-二甲基苯并二氢吡喃-4-基)乙酰胺

更新时间:2025-08-21 18:41:18

N-(苄氧基)-n-((3s,4r)-6-氰基-3-羟基-2,2-二甲基苯并二氢吡喃-4-基)乙酰胺结构式
N-(苄氧基)-n-((3s,4r)-6-氰基-3-羟基-2,2-二甲基苯并二氢吡喃-4-基)乙酰胺结构式
品牌特惠专场
常用名 N-(苄氧基)-n-((3s,4r)-6-氰基-3-羟基-2,2-二甲基苯并二氢吡喃-4-基)乙酰胺 英文名 Y-27152
CAS号 127408-30-4 分子量 366.41
密度 1.28g/cm3 沸点 513.4ºC at 760mmHg
分子式 C21H22N2O4 熔点 N/A
MSDS N/A 闪点 264.3ºC

 用途


Y-27152 是KATP (Kir6)通道开放剂Y-26763的前体药物,是长效的K+ 通道开放剂,在高血压大鼠和狗在清醒状态下发挥降压作用的同时,具有更低的心动过速作用。

 名称

中文名 N-(苄氧基)-n-((3s,4r)-6-氰基-3-羟基-2,2-二甲基苯并二氢吡喃-4-基)乙酰胺
英文名 N-[(3S,4R)-6-Cyano-3,4-dihydro-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-yl]-N-(phenylmethoxy)acetamide
英文别名 更多

 生物活性

描述 Y-27152 是KATP (Kir6)通道开放剂Y-26763的前体药物,是长效的K+ 通道开放剂,在高血压大鼠和狗在清醒状态下发挥降压作用的同时,具有更低的心动过速作用。
相关类别
靶点实验

K+ channel[1].

参考文献

[1]. Nakajima T, et al. Y-27152, a long-acting K+ channel opener with less tachycardia: antihypertensive effects in hypertensive rats and dogs in conscious state. J Pharmacol Exp Ther. 1992 May;261(2):730-6.

[2]. Fukunari A, et al. Y-26763 protects the canine heart from a stunning injury through opening of the KATP channels. Eur J Pharmacol. 1997 Apr 4;323(2-3):197-204.

 物理化学性质

密度 1.28g/cm3
沸点 513.4ºC at 760mmHg
分子式 C21H22N2O4
分子量 366.41
闪点 264.3ºC
精确质量 366.15800
PSA 82.79000
LogP 3.11158
InChIKey RHFUXPCCELGMFC-UXHICEINSA-N
SMILES CC(=O)N(OCc1ccccc1)C1c2cc(C#N)ccc2OC(C)(C)C1O
蒸汽压 2.29E-11mmHg at 25°C
折射率 1.617

 毒性和生态

 靶点实验

查看更多实验

实验名称:Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident pro...
来源:NCGC
靶标:N/A
External Id:SERCaMPGLuc-p1-antagonist
实验名称:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Enzymatic assay of human HDAC6 with commercial peptide substrate
来源:ChEMBL
靶标:Histone deacetylase 6
External Id:CHEMBL4808149
实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
实验名称:EZH2/PRC2 methyltransferase inhibitors Measured in Biochemical System Using Plate Rea...
来源:Broad Institute
靶标:histone-lysine N-methyltransferase EZH2 isoform a [Homo sapiens]
External Id:2125-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Enzymatic assay of human HDAC6 with custom peptide substrate
来源:ChEMBL
靶标:Histone deacetylase 6
External Id:CHEMBL4808150
实验名称:High Throughput Screening for Foot and Mouth Disease Virus Antivirals
来源:NCGC
靶标:N/A
External Id:StopGo1
实验名称:Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of VER...
来源:ChEMBL
靶标:Severe acute respiratory syndrome coronavirus 2
External Id:CHEMBL4513082
实验名称:Rescue cell viability in cybrid cells with a genetic mutation in complex 1 of the mit...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1315
实验名称:Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of Cac...
来源:ChEMBL
靶标:Severe acute respiratory syndrome coronavirus 2
External Id:CHEMBL4303805
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 英文别名

Conantokin-R
Y-27152
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