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N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺

N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺

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?N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺名称
















中文名

N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺
英文名

N-[4-(3-bromoanilino)quinazolin-6-yl]prop-2-enamide
英文别名
更多





?N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺生物活性














































描述
PD168393是一个强的,不可逆转的EGFR抑制剂,IC50是0.7 nM.
相关类别



靶点

EGFR:0.7 nM (IC50)


溶解度

体外:

DMSO:≥30mg / mL(81.25 mM)

* “≥”表示可溶,但饱和度未知。


储备液

1 mM 2.7084 mL 13.5421 mL 27.0841 mL
5 mM 0.5417 mL 2.7084 mL 5.4168 mL
10 mM 0.2708 mL 1.3542 mL 2.7084 mL


存储

粉末 -20℃下 3年
4℃下 2年
在溶剂中 -80℃下 6个月
-20℃下 1个月


运输

室温;可能会有所不同
SMILES

C=CC(NC1=CC2=C(NC3=CC=CC(Br)=C3)N=CN=C2C=C1)=O
参考文献

[1]. Fry DW et al. Specific, irreversible inactivation of the epidermal growth factor receptor and erbB2, by a new class of tyrosine kinase inhibitor. Proc Natl Acad Sci U S A. 1998 Sep 29;95(20):12022-7.

[2]. Sun X et al. The activation of EGFR promotes myocardial tumor necrosis factor-α production and cardiac failure in endotoxemia. Oncotarget. 2015 Nov 3;6(34):35478-95.

[3]. Li G et al. Modulation of ErbB2 blockade in ErbB2-positive cancers: the role of ErbB2 Mutations and PHLDA1. PLoS One. 2014 Sep 19;9(9):e106349.

[4]. White KJ et al. Irritant activation of epithelial cells is mediated via protease-dependent EGFR activation. J Invest Dermatol. 2011 Feb;131(2):435-42.


相关活性
小分子




奥希替尼



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酪氨酸磷酸化抑制剂AG 490



|

来那替尼



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金雀异黄酮



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(-)-表没食子儿茶素没食子酸酯



|

4-(3-氯苯胺)-6,7-二甲氧基喹唑啉盐酸盐



|

达克替尼



|

图卡蒂尼(伊尔比尼替尼,ONT-380)



|

波齐奥替尼(HM781-36B)



|

N-[3-[[2-[[4-(4-甲基-1-哌嗪基)苯基]氨基]噻吩并[3,2-d]嘧啶-4-基]氧基]苯基]-2-丙烯酰胺



|

AZD 8931



|

AZD-3759



|

吡咯替尼



|

卡纽替尼二盐酸盐



|

(3R,4R)-4-氨基-1-[[4-[(3-甲氧基苯基)氨基]吡咯并[2,1-f][1,2,4]三嗪-5-基]甲基]哌啶-3-醇






?N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺物理化学性质







































密度 1.6±0.1 g/cm3
沸点 571.1±50.0 °C at 760 mmHg
熔点 279℃
分子式 C17H13BrN4O
分子量 369.215
闪点 299.2±30.1 °C
精确质量 368.027252
PSA 70.40000
LogP 3.72
蒸汽压 0.0±1.6 mmHg at 25°C
折射率 1.744
储存条件 -20°C






?N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺安全信息
















危险品运输编码 NONH for all modes of transport





?N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺合成线路
































~43%







N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺结构式

N-[4-[(3-溴苯基)氨基...

194423-15-9






文献:Warner-Lambert Company Patent: US6344459 B1, 2002 ; Location in patent: Page column 48 ; US 6344459 B1





~84%







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文献:Wyeth Patent: EP1100788 B1, 2005 ; Location in patent: Page/Page column 7 ;





~56%







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文献:Wyeth Patent: EP1100788 B1, 2005 ; Location in patent: Page/Page column 9-10 ;





~49%







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文献:Wyeth Patent: EP1100788 B1, 2005 ; Location in patent: Page/Page column 8 ;









~11%







N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺结构式” />						
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文献:Pawar, Vijaykumar G.; Sos, Martin L.; Rode, Haridas B.; Rabiller, Matthias; Heynck, Stefanie; Van Otterlo, Willem A. L.; Thomas, Roman K.; Rauh, Daniel Journal of Medicinal Chemistry, 2010 , vol. 53, # 7 p. 2892 - 2901





~%







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文献:American Cyanamid Company Patent: EP787722 A1, 1997 ; Title/Abstract Full Text Show Details Wyeth Holdings Corporation Patent: EP980244 B1, 2003 ;





~%







N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺结构式” />						
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文献:Tsou; Mamuya; Johnson; Reich; Gruber; Ye; Nilakantan; Shen; Discafani; DeBlanc; Davis; Koehn; Greenberger; Wang; Wissner Journal of Medicinal Chemistry, 2001 , vol. 44, # 17 p. 2719 - 2734





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文献:Tsou; Mamuya; Johnson; Reich; Gruber; Ye; Nilakantan; Shen; Discafani; DeBlanc; Davis; Koehn; Greenberger; Wang; Wissner Journal of Medicinal Chemistry, 2001 , vol. 44, # 17 p. 2719 - 2734







?N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺上下游产品













N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺上游产品? 5

N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺下游产品? 0















?N-[4-[(3-溴苯基)氨基]-6-喹唑啉]-2-丙酰胺英文别名



























2-Propenamide (N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]


nchembio866-comp2


pd 168393


2-Propenamide, N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-


N-{4-[(3-Bromophenyl)amino]-6-quinazolinyl}acrylamide


PD168393








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