5-(4-Chlorophenyl)-6-methylpyrimidine-2,4-diamine结构式
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常用名 | 5-(4-Chlorophenyl)-6-methylpyrimidine-2,4-diamine | 英文名 | 5-(4-Chlorophenyl)-6-methylpyrimidine-2,4-diamine |
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| CAS号 | 3275-44-3 | 分子量 | 234.68 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C11H11ClN4 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
本表展示该化学物质的中文名称、英文系统名、各类中文与英文别名信息。
| 英文名 | 5-(4-Chlorophenyl)-6-methylpyrimidine-2,4-diamine |
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本表包含该物质理化参数,如熔点、沸点、密度、溶解度、旋光性等理化指标,无数据项标记为N/A。
| 分子式 | C11H11ClN4 |
|---|---|
| 分子量 | 234.68 |
| InChIKey | SNBBQZGVKQEBQT-UHFFFAOYSA-N |
| SMILES | CC1=C(C(=NC(=N1)N)N)C2=CC=C(C=C2)Cl |
本表记录该化合物靶点、体外体内实验、生物测定实验相关实验数据。
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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: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:Ratio of Inhibition of the C59R+S108N mutant of dihydrofolate reductase (DHFR) to inh...
来源:ChEMBL
靶标:Bifunctional dihydrofolate reductase-thymidylate synthase
External Id:CHEMBL849932
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实验名称:Ratio of Inhibition of the S108N mutant of dihydrofolate reductase (DHFR) to inhibiti...
来源:ChEMBL
靶标:Bifunctional dihydrofolate reductase-thymidylate synthase
External Id:CHEMBL848232
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实验名称:Inhibition of human placental HexA using pNPGlcNAc substrate
来源:ChEMBL
靶标:Beta-hexosaminidase subunit beta
External Id:CHEMBL3579956
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实验名称:Inhibition constant against Plasmodium falciparum dihydrofolate reductase
来源:ChEMBL
靶标:Bifunctional dihydrofolate reductase-thymidylate synthase
External Id:CHEMBL828776
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实验名称:Inhibition of the C59R+S108N mutant of dihydrofolate reductase (DHFR)
来源:ChEMBL
靶标:Bifunctional dihydrofolate reductase-thymidylate synthase
External Id:CHEMBL668409
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实验名称:Inhibition of the S108N mutant of dihydrofolate reductase (DHFR)
来源:ChEMBL
靶标:Bifunctional dihydrofolate reductase-thymidylate synthase
External Id:CHEMBL668410
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实验名称:Inhibition of the wild-type dihydrofolate reductase (DHFR)
来源:ChEMBL
靶标:Bifunctional dihydrofolate reductase-thymidylate synthase
External Id:CHEMBL668411
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本部分为该化合物相关常见问答,包含基础参数、性状、储存条件等高频咨询问题与对应答案。
| Q: 3275-44-3的中文名称是什么? |
| A: 3275-44-3的中文名称为3275-44-3。 |
| Q: 3275-44-3的英文名称是什么? |
| A: 3275-44-3英文名称为5-(4-Chlorophenyl)-6-methylpyrimidine-2,4-diamine。 |
| Q: 3275-44-3的InChIKey是什么? |
| A: 3275-44-3InChIKey为SNBBQZGVKQEBQT-UHFFFAOYSA-N。 |
| Q: 3275-44-3的CAS号是多少? |
| A: 3275-44-3CAS号为3275-44-3。 |
| Q: 3275-44-3的SMILES表达式是什么? |
| A: 3275-44-3SMILES表达式为CC1=C(C(=NC(=N1)N)N)C2=CC=C(C=C2)Cl。 |
| Q: 3275-44-3的分子式是什么? |
| A: 3275-44-3分子式为C11H11ClN4。 |
| Q: 3275-44-3的分子量是多少? |
| A: 3275-44-3分子量为234.68。 |