前往化源商城

3-甲基-2-苯基-N-((1S)-1-苯基丙基)喹啉-4-甲酰胺

更新时间:2025-08-26 22:49:14

3-甲基-2-苯基-N-((1S)-1-苯基丙基)喹啉-4-甲酰胺结构式
3-甲基-2-苯基-N-((1S)-1-苯基丙基)喹啉-4-甲酰胺结构式
品牌特惠专场
常用名 3-甲基-2-苯基-N-((1S)-1-苯基丙基)喹啉-4-甲酰胺 英文名 SB-222200
CAS号 174635-69-9 分子量 380.48200
密度 1.142g/cm3 沸点 553.5ºC at 760 mmHg
分子式 C26H24N2O 熔点 N/A
MSDS 美版 闪点 288.6ºC

 用途


SB 222200是可逆的竞争性人NK受体抑制剂,对hNK-3受体的Ki为4.4 nM,能透过血脑屏障。

 名称

中文名 3-甲基-2-苯基-N-((1S)-1-苯基丙基)喹啉-4-甲酰胺
英文名 3-methyl-2-phenyl-N-[(1S)-1-phenylpropyl]quinoline-4-carboxamide
英文别名 更多

 物理化学性质

密度 1.142g/cm3
沸点 553.5ºC at 760 mmHg
分子式 C26H24N2O
分子量 380.48200
闪点 288.6ºC
精确质量 380.18900
PSA 41.99000
LogP 6.48220
InChIKey MQNYRKWJSMQECI-QFIPXVFZSA-N
SMILES CCC(NC(=O)c1c(C)c(-c2ccccc2)nc2ccccc12)c1ccccc1
蒸汽压 2.7E-12mmHg at 25°C
折射率 1.633
储存条件 2-8℃

 MSDS

 安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
危险品运输编码 NONH for all modes of transport

 文献3

更多文献
Nonpeptide tachykinin receptor antagonists. II. Pharmacological and pharmacokinetic profile of SB-222200, a central nervous system penetrant, potent and selective NK-3 receptor antagonist.

J. Pharmacol. Exp. Ther. 295(1) , 373-81, (2000)

The pharmacological and pharmacokinetic profile of SB-222200 [(S)-(-)-N-(alpha-ethylbenzyl)-3-methyl-2-phenylquinoline-4-car boxami de], a human NK-3 receptor (hNK-3R) antagonist, was determined. SB-2...

In vitro and in vivo characterization of NK3 receptors in the rabbit eye by use of selective non-peptide NK3 receptor antagonists.

Br. J. Pharmacol. 122 , 469-476, (1997)

1. Inhibition of NK3 receptor agonist-induced contraction in the rabbit isolated iris sphincter muscle was used to assess the in vitro functional activity of three 2-phenyl-4-quinolinecarboxamides, me...

Expression of neurokinin B/NK3 receptor and kisspeptin/KISS1 receptor in human granulosa cells.

Hum. Reprod. 29(12) , 2736-46, (2014)

Are neurokinin B (NKB), NK3 receptor (NK3R), kisspeptin (KISS1) and kisspeptin receptor (KISS1R) expressed in human ovarian granulosa cells?The NKB/NK3R and kisspeptin/KISS1R systems are co-expressed ...

 靶点实验

查看更多实验

实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:Thermal Shift Assay. Domain: start/stop: M1-L298
来源:ChEMBL
靶标:Cyclin-dependent kinase 2
External Id:CHEMBL5062802
实验名称:Inhibition of neurosphere proliferation of mouse neural precursor cells by MTT assay
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1266185
实验名称:Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
来源:NCGC
External Id:SNCA-p-activity-luciferase
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:Tocris HTS for Inhibitors of Aerobactin Synthetase lucA
来源:23265
External Id:IucA Pilot Assay Tocris Library
实验名称:Incucyte cell viability with HEK293T
来源:ChEMBL
靶标:HEK-293T
External Id:CHEMBL5058565
实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
共265条,当前第1页,共27页
1
2
3
4
5

 英文别名

Lopac-S-5192
Tocris-1393
SB-222200
本网页内容来自不同专业数据源,如对内容有疑义,欢迎联系service1@chemsrc.com。