N-[3-[(4AS,7AS)-2-氨基-4A,5-二氢-4H-呋喃并[3,4-D][1,3]噻嗪-7A(7H)-基]-4-氟苯基]-5-氟-2-吡啶甲酰胺结构式
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常用名 | N-[3-[(4AS,7AS)-2-氨基-4A,5-二氢-4H-呋喃并[3,4-D][1,3]噻嗪-7A(7H)-基]-4-氟苯基]-5-氟-2-吡啶甲酰胺 | 英文名 | LY2886721 |
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| CAS号 | 1262036-50-9 | 分子量 | 390.407 | |
| 密度 | 1.6±0.1 g/cm3 | 沸点 | N/A | |
| 分子式 | C18H16F2N4O2S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
用途LY2886721是BACE抑制剂,在临床前实验中对阿尔茨海默病有效。 |
| 中文名 | N-[3-[(4AS,7AS)-2-氨基-4A,5-二氢-4H-呋喃并[3,4-D][1,3]噻嗪-7A(7H)-基]-4-氟苯基]-5-氟-2-吡啶甲酰胺 |
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| 英文名 | N-[3-[(4aS,7aS)-2-amino-4,4a,5,7-tetrahydrofuro[3,4-d][1,3]thiazin-7a-yl]-4-fluorophenyl]-5-fluoropyridine-2-carboxamide |
| 英文别名 | 更多 |
| 密度 | 1.6±0.1 g/cm3 |
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| 分子式 | C18H16F2N4O2S |
| 分子量 | 390.407 |
| 精确质量 | 390.096191 |
| PSA | 112.40000 |
| LogP | 0.80 |
| InChIKey | NIDRNVHMMDAAIK-YPMLDQLKSA-N |
| SMILES | NC1=NC2(c3cc(NC(=O)c4ccc(F)cn4)ccc3F)COCC2CS1 |
| 折射率 | 1.706 |
| 储存条件 | -20°C |
| 危害码 (欧洲) | Xi |
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实验名称:Inhibition of BACE1 in alzheimer's disease patient assessed as reduction of CSF Abeta...
来源:ChEMBL
靶标:Homo sapiens
External Id:CHEMBL2399144
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实验名称:Inhibition of BACE1 in alzheimer's disease patient assessed as reduction of CSF Abeta...
来源:ChEMBL
靶标:Homo sapiens
External Id:CHEMBL2399143
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实验名称:Cytotoxicity counterscreen for inhibitors of SARS-CoV-2 cell entry
来源:NCGC
靶标:N/A
External Id:TRND-SARS-CoV-2-cytotox-48hr
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实验名称:Primary qHTS to identify inhibitors of SARS-CoV-2 cell entry
来源:NCGC
External Id:TRND-SARS-CoV-2-PP
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实验名称:Inhibition of human BACE1 (1 to 460 residues) expressed in HEK293 cells using mcaFRET...
来源:ChEMBL
靶标:Beta-secretase 1
External Id:CHEMBL4614135
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实验名称:Inhibition of recombinant human BACE1 using (MCA)-S-E-V-N-L-D-A-E-F-R-K(dinitrophenol...
来源:ChEMBL
靶标:Beta-secretase 1
External Id:CHEMBL5034186
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实验名称:qHTS drug screen for cell cycle checkpoint inhibitors in PARPi-resistant BRCA-mutant ...
来源:NCGC
External Id:FGL-PARP_PEO-CTG96h-MIPE5.0-p1
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| LY-2886721 |
| cc-426 |
| S2156_Selleck |
| UNII:2CQ62IWB67 |
| LY2886721 |
| UNII-2CQ62IWB67 |
| LY 2886721 |