2-[(4-Chlorophenyl)amino]nicotinic acid结构式
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常用名 | 2-[(4-Chlorophenyl)amino]nicotinic acid | 英文名 | DHODH-IN-17 |
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| CAS号 | 16344-26-6 | 分子量 | 248.67 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C12H9ClN2O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
用途DHODH-IN-17是一种2-苯胺基烟酸,是一种人体DHODH抑制剂(IC50=0.40μM)。DHODH-IN-17可用于急性髓系白血病(AML)的研究[1]。 |
| 中文名 | 2-[(4-氯苯基)氨基]-3-吡啶羧酸 |
|---|---|
| 英文名 | 2-(4-chloroanilino)pyridine-3-carboxylic acid |
| 英文别名 | 更多 |
| 描述 | DHODH-IN-17是一种2-苯胺基烟酸,是一种人体DHODH抑制剂(IC50=0.40μM)。DHODH-IN-17可用于急性髓系白血病(AML)的研究[1]。 |
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| 相关类别 | |
| 靶点实验 |
IC50: 0.4 μM (DHODH)[1] |
| 体外研究 | DHODH-IN-17是一种2-苯胺基烟酸,是一种人体DHODH抑制剂,IC50值为0.40μM[1]。 |
| 参考文献 |
| 分子式 | C12H9ClN2O2 |
|---|---|
| 分子量 | 248.67 |
| 精确质量 | 248.03500 |
| PSA | 62.22000 |
| LogP | 3.24980 |
| InChIKey | YEXIXVLEDGNAKM-UHFFFAOYSA-N |
| SMILES | O=C(O)c1cccnc1Nc1ccc(Cl)cc1 |
| 外观性状 | 固体 |
| 储存条件 | 2-8°C,密封,干燥 |
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~99%
2-[(4-Chlorophe... 16344-26-6 |
| 文献:Kamal, Ahmed; Srikanth; Naseer Ahmed Khan; Ashraf, Md.; Kashi Reddy; Sultana, Farheen; Kaur, Tandeep; Chashoo, Gousia; Suri, Nitasha; Sehar, Irum; Wani, Zahoor A.; Saxena, Arpita; Sharma, Parduman R.; Bhushan, Shashi; Mondhe, Dilip M.; Saxena, Ajit K. Bioorganic and Medicinal Chemistry, 2011 , vol. 19, # 23 p. 7136 - 7150 |
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~92%
2-[(4-Chlorophe... 16344-26-6 |
| 文献:Li, Zhenghua; Xiao, Shangyou; Liang, Ronghui; Xia, Zhining Research on Chemical Intermediates, 2012 , vol. 38, # 7 p. 1691 - 1697 |
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~%
2-[(4-Chlorophe... 16344-26-6 |
| 文献:Kamal, Ahmed; Srikanth, Yellamelli Valli Venkata; Khan, Mohammed Naseer Ahmed; Ashraf, Mohammed; Sehar, Irum; Chashoo, Gousia; Sharma, Parduman Raj; Dar, Abid Hamid; Shashi, Bhushan; Singh, Shashank Kumar; Mondhe, Dilip Manikrao; Saxena, Ajit Kumar Patent: US2013/324734 A1, 2013 ; |
|
~%
2-[(4-Chlorophe... 16344-26-6 |
| 文献:Kamal, Ahmed; Srikanth, Yellamelli Valli Venkata; Khan, Mohammed Naseer Ahmed; Ashraf, Mohammed; Sehar, Irum; Chashoo, Gousia; Sharma, Parduman Raj; Dar, Abid Hamid; Shashi, Bhushan; Singh, Shashank Kumar; Mondhe, Dilip Manikrao; Saxena, Ajit Kumar Patent: US2013/324734 A1, 2013 ; |
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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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实验名称:Dose response of compounds that promote myeloid differentiation with HOXA9ER cells wi...
来源:NMMLSC
External Id:UNMCMD_HOXA9_MYELOIDDIFFERENTIATION_HOXA9ER_SAR01
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实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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实验名称:Rescue cell viability in cybrid cells with a genetic mutation in complex 1 of the mit...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1315
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实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
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实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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| 2-[(4-chlorophenyl)amino]-3-pyridinecarboxylic acid |
| HMS2655G09 |
| 2-(4-chloro-anilino)-nicotinic acid |
| 2-(4-Chloro-phenylamino)-nicotinic acid |
| 2-(p-Chloranilino)-nicotinsaeure |
| 2-[(4-chlorophenyl)amino]pyridine-3-carboxylic acid |