2-(1-hydroxycyclohexyl)-2-phenyl-acetic acid结构式
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常用名 | 2-(1-hydroxycyclohexyl)-2-phenyl-acetic acid | 英文名 | 2-(1-hydroxycyclohexyl)-2-phenyl-acetic acid |
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| CAS号 | 5449-68-3 | 分子量 | 234.29100 | |
| 密度 | 1.219g/cm3 | 沸点 | 398ºC at 760 mmHg | |
| 分子式 | C14H18O3 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 208.7ºC |
| 英文名 | 2-(1-hydroxycyclohexyl)-2-phenylacetic acid |
|---|---|
| 英文别名 | 更多 |
| 密度 | 1.219g/cm3 |
|---|---|
| 沸点 | 398ºC at 760 mmHg |
| 分子式 | C14H18O3 |
| 分子量 | 234.29100 |
| 闪点 | 208.7ºC |
| 精确质量 | 234.12600 |
| PSA | 57.53000 |
| LogP | 2.55000 |
| InChIKey | AOHSAQWYEVFRKD-UHFFFAOYSA-N |
| SMILES | O=C(O)C(c1ccccc1)C1(O)CCCCC1 |
| 折射率 | 1.586 |
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~94%
2-(1-hydroxycyc... 5449-68-3 |
| 文献:Black, T. Howard; Maluleka, Stephen L. Tetrahedron Letters, 1989 , vol. 30, # 5 p. 531 - 534 |
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~92%
2-(1-hydroxycyc... 5449-68-3 |
| 文献:Black, T. Howard; Eisenbeis, Shane A.; McDermott, Todd S.; Maluleka, Stephen L. Tetrahedron, 1990 , vol. 46, p. 2307 - 2316 |
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~61%
2-(1-hydroxycyc... 5449-68-3 |
| 文献:Mladenova, M.; Blagoev, B.; Gaudemar, M.; Gaudemar-Bardone, F.; Lallemand, J. Y. Tetrahedron, 1981 , vol. 37, p. 2157 - 2164 |
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~10%
2-(1-hydroxycyc... 5449-68-3 |
| 文献:Toullec, Jean; Mladenova, Margarita; Gaudemar-Bardone, Francoise; Blagoev, Blagoi Journal of Organic Chemistry, 1985 , vol. 50, # 14 p. 2563 - 2569 |
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~%
2-(1-hydroxycyc... 5449-68-3 |
| 文献:Phalnikar; Nargund Journal of the Indian Chemical Society, 1937 , vol. 14, p. 736,745 Full Text Show Details Ivanoff; Spassoff Bulletin de la Societe Chimique de France, 1931 , vol. <4> 49, p. 377 |
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~%
2-(1-hydroxycyc... 5449-68-3 |
| 文献:Treves; Testa Journal of the American Chemical Society, 1952 , vol. 74, p. 46 Full Text View citing articles Show Details Maillard et al. Bulletin de la Societe Chimique de France, 1958 , p. 244,248 |
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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: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:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
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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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实验名称:Identifying Sarm1 TIR NADase inhibitors through high throughput HPLC assay
来源:24386
靶标:N/A
External Id:Sarm1 TIR NADase inhibitors
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| (1-Hydroxy-cyclohexyl)-phenyl-essigsaeure |
| (1-hydroxycyclohexyl)(phenyl)acetic acid |
| HMS2882L21 |