4-[(2,6-dimethylmorpholin-4-yl)methyl]-N-phenyl-1,3-thiazol-2-amine结构式
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常用名 | 4-[(2,6-dimethylmorpholin-4-yl)methyl]-N-phenyl-1,3-thiazol-2-amine | 英文名 | 4-[(2,6-dimethylmorpholin-4-yl)methyl]-N-phenyl-1,3-thiazol-2-amine |
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| CAS号 | 871105-94-1 | 分子量 | 303.4 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C16H21N3OS | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 4-[(2,6-dimethylmorpholin-4-yl)methyl]-N-phenyl-1,3-thiazol-2-amine |
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| 分子式 | C16H21N3OS |
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| 分子量 | 303.4 |
| InChIKey | ALTOSZLWPBXEHC-UHFFFAOYSA-N |
| SMILES | CC1CN(Cc2csc(Nc3ccccc3)n2)CC(C)O1 |
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实验名称:ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania ...
来源:ChEMBL
靶标:Glucose transporter
External Id:CHEMBL3436044
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实验名称:Biochemical screen of P. falciparum CDPK1
来源:1187
靶标:Calcium-Dependent Protein Kinase 1 (CDPK1)
External Id:PfalCDPK1
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实验名称:ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania ...
来源:ChEMBL
靶标:Solute carrier family 2, facilitated glucose transporter member 1
External Id:CHEMBL3436042
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实验名称:ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania ...
来源:ChEMBL
靶标:Hexose transporter 1
External Id:CHEMBL3436043
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实验名称:Biochemical screen of P. falciparum MAPK2
来源:1187
靶标:mitogen-activated protein kinase 2 (MAP2 or MAPK2)
External Id:PfalMAPK2
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实验名称:Biochemical screen of P. falciparum CDPK4
来源:1187
靶标:Calcium-Dependent Protein Kinase 4 (CDPK4)
External Id:PfalCDPK4
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实验名称:Luciferase/luciferin-expressing antifolate-resistant parasites were used to infect a ...
来源:ChEMBL
靶标:HepG2-CD81
External Id:CHEMBL4483864
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实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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