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6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮

更新时间:2025-09-01 09:11:49

6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮结构式
6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮结构式
委托求购
常用名 6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮 英文名 6-pyridin-3-yl-3,4-dihydro-1H-quinolin-2-one
CAS号 99471-41-7 分子量 224.25800
密度 N/A 沸点 N/A
分子式 C14H12N2O 熔点 N/A
MSDS N/A 闪点 N/A

 6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮名称

中文名 6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮
英文名 6-pyridin-3-yl-3,4-dihydro-1H-quinolin-2-one
英文别名 更多

 6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮物理化学性质

分子式 C14H12N2O
分子量 224.25800
精确质量 224.09500
PSA 45.48000
LogP 2.71840
InChIKey MPGBYGNPFRLHAO-UHFFFAOYSA-N
SMILES O=C1CCc2cc(-c3cccnc3)ccc2N1

 6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮合成线路

~69%

6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮结构式

6-(吡啶-3-基)-3,4-...

99471-41-7

文献:Martinez; Walker; Hirschfeld; Bruno; Yang; Maloney Journal of Medicinal Chemistry, 1992 , vol. 35, # 4 p. 620 - 628

~%

6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮结构式

6-(吡啶-3-基)-3,4-...

99471-41-7

文献:Martinez; Walker; Hirschfeld; Bruno; Yang; Maloney Journal of Medicinal Chemistry, 1992 , vol. 35, # 4 p. 620 - 628

~%

6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮结构式

6-(吡啶-3-基)-3,4-...

99471-41-7

文献:MERCK SHARP and DOHME CORP.; ElexoPharm GmbH; HOYT, Scott, B.; PETRILLI, Whitney Lane; LONDON, Clare; XIONG, Yusheng; TAYLOR, Jerry Andrew; ALI, Amjad; LO, Michael; HENDERSON, Timothy, J.; HU, Qingzhong; HARTMANN, Rolf; YIN, Lina; HEIM, Ralf; BEY, Emmanuel; SAXENA, Rohit; SAMANTA, Swapan Kumar; KULKARNI, Bheemashankar, A. Patent: WO2012/148808 A1, 2012 ; WO 2012/148808 A1

~94%

6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮结构式

6-(吡啶-3-基)-3,4-...

99471-41-7

文献:Universitat des Saarlandes Patent: US2011/112067 A1, 2011 ; Location in patent: Page/Page column 34; 35 ; US 20110112067 A1

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6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮结构式

6-(吡啶-3-基)-3,4-...

99471-41-7

文献:MERCK SHARP and DOHME CORP.; ElexoPharm GmbH; HOYT, Scott, B.; PETRILLI, Whitney Lane; LONDON, Clare; XIONG, Yusheng; TAYLOR, Jerry Andrew; ALI, Amjad; LO, Michael; HENDERSON, Timothy, J.; HU, Qingzhong; HARTMANN, Rolf; YIN, Lina; HEIM, Ralf; BEY, Emmanuel; SAXENA, Rohit; SAMANTA, Swapan Kumar; KULKARNI, Bheemashankar, A. Patent: WO2012/148808 A1, 2012 ; WO 2012/148808 A1

~%

6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮结构式

6-(吡啶-3-基)-3,4-...

99471-41-7

文献:Alabaster; Bell; Campbell; Ellis; Henderson; Roberts; Ruddock; Samuels; Stefaniak Journal of Medicinal Chemistry, 1988 , vol. 31, # 10 p. 2048 - 2056

 6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮上下游产品

6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮上游产品  6

6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮下游产品  0

 6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮靶点实验

查看更多实验

实验名称:Inhibition of human CYP11B2 expressed in hamster V79 MZh cells assessed as conversion...
来源:ChEMBL
靶标:Cytochrome P450 11B2, mitochondrial
External Id:CHEMBL1768362
实验名称:Percentage increase in dP/dt maximum observed with 4-[4-[2-(1,1-dioxo-2-isothiazolidi...
来源:ChEMBL
靶标:Canis lupus familiaris
External Id:CHEMBL667664
实验名称:Intrinsic activity calculated as the ratio of the maximum response to the compound to...
来源:ChEMBL
靶标:Cavia porcellus
External Id:CHEMBL687848
实验名称:Inhibition of human CYP11B2 expressed in hamster V79 MZh cells
来源:ChEMBL
靶标:Cytochrome P450 11B2, mitochondrial
External Id:CHEMBL989835
实验名称:Inhibition of human CYP11B2 expressed in hamster V79 MZh cells at 500 nM
来源:ChEMBL
靶标:Cytochrome P450 11B2, mitochondrial
External Id:CHEMBL989834
实验名称:Selectivity ratio, IC50 for human CYP11B1 to IC50 for human CYP11B2
来源:ChEMBL
靶标:N/A
External Id:CHEMBL989837
实验名称:Inhibition of human CYP11B1 expressed in hamster V79 MZh cells
来源:ChEMBL
靶标:Cytochrome P450 11B1, mitochondrial
External Id:CHEMBL989836
实验名称:Protection against mortality in pulmonary thromboembolism model in mice at 10 mg/kg
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL729595
实验名称:Inhibition of human recombinant CYP1A2 expressed in baculovirus-infected insect micro...
来源:ChEMBL
靶标:Cytochrome P450 1A2
External Id:CHEMBL989843
实验名称:Protection against mortality in pulmonary thromboembolism model in mice at 1 mg/kg
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL728712
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 6-(吡啶-3-基)-3,4-二氢喹啉-2(1H)-酮英文别名

6-pyridin-3-yl-3,4-dihydroquinolin-2(1H)-one
6-(pyridin-3-yl)-3,4-dihydrocarbostyril
6-(3-pyridyl)-3,4-dihydrocarbostyril
6-Pyridin-3-yl-3,4-dihydroquinolin-2(1H)-on
2(1H)-Quinolinone,3,4-dihydro-6-(3-pyridinyl)
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