Methyl trifluoromethanesulfonate | CAS:333-27-7
Methyl trifluoromethanesulfonate
- 名称:三氟甲烷磺酸甲酯 | Methyl trifluoromethanesulfonate
- CAS号:333-27-7
- 别名:
- 分子式:C2H3F3O3S
- 分子量:164.10
- EINESC号:206-371-7
产品描述
物理化学性质
| 沸点 | 95 ºC |
|---|---|
| 闪点 | 38 ºC |
| 密度 | 1.45 |
| 折射率 | 1.325-1.327 |
安全数据
| 危险品标志 | C |
|---|---|
| 危险类别码 | R10;R20/21/22;R34 |
| 安全说明书 | S16;S26;S36/37/39;S45 |
产品合成路线
| 名称 | CAS号 |
|---|
更多
文章
同行评议文献
Crystallization and preliminary crystallographic studies of human indoleamine 2,3-dioxygenase.Shun-ichiro Oda et al.Acta crystallographica. Section F, Structural biology and crystallization communications, 62(Pt 3), 221-223 (2006-03-03)
Inhibition and binding modes of low-molecular-weight inhibitors of porcine pancreatic alpha-amylase.H Yamashita et al.Journal of biochemistry, 111(2), 182-185 (1992-02-01)
Small-molecule scaffolds for CYP51 inhibitors identified by high-throughput screening and defined by X-ray crystallography.Larissa M Podust et al.Antimicrobial agents and chemotherapy, 51(11), 3915-3923 (2007-09-12)
Theoretical study of the ligand-CYP2B4 complexes: effect of structure on binding free energies and heme spin state.Danni L Harris et al.Proteins, 55(4), 895-914 (2004-05-18)
Ligand-assisted inhibition in cytochrome P450 158A2 from Streptomyces coelicolor A3(2).Bin Zhao et al.Biochemistry, 45(24), 7493-7500 (2006-06-14)
Spectral and metabolic properties of liver microsomes from imidazole-pretreated rabbits.K K Hajek et al.Biochemical and biophysical research communications, 108(2), 664-672 (1982-09-30)
New imidazoles as probes of the active site topology and potent inhibitors of beta-glucosidase.Y K Li et al.Journal of biochemistry, 123(3), 416-422 (1998-05-30)
Crystal structure of human indoleamine 2,3-dioxygenase: catalytic mechanism of O2 incorporation by a heme-containing dioxygenase.Hiroshi Sugimoto et al.Proceedings of the National Academy of Sciences of the United States of America, 103(8), 2611-2616 (2006-02-16)
Amino acid residues critical for differential inhibition of CYP2B4, CYP2B5, and CYP2B1 by phenylimidazoles.M Spatzenegger et al.Molecular pharmacology, 59(3), 475-484 (2001-02-17)
Imidazole derivatives as inhibitors of cytochrome P-450-dependent oxidation and activators of epoxide hydrolase in hepatic microsomes from a marine fish.P J Little et al.Biochemical pharmacology, 30(20), 2876-2880 (1981-10-01)
Enzyme kinetic and spectroscopic studies of inhibitor and effector interactions with indoleamine 2,3-dioxygenase. 1. Norharman and 4-phenylimidazole binding to the enzyme as inhibitors and heme ligands.M Sono et al.Biochemistry, 28(13), 5392-5399 (1989-06-27)
Inhibition of beta-glucosidase by imidazoles.Y K Li et al.Biochimica et biophysica acta, 999(3), 227-232 (1989-12-21)
Structural and catalytic properties of the peroxygenase P450 enzyme CYP152K6 from Bacillus methanolicus.Hazel M Girvan et al.Journal of inorganic biochemistry, 188, 18-28 (2018-08-18)
Calmodulin-dependent nitric-oxide synthase. Mechanism of inhibition by imidazole and phenylimidazoles.D J Wolff et al.The Journal of biological chemistry, 268(13), 9425-9429 (1993-05-05)
Novel synthetic pyridyl analogues of CDDO-Imidazolide are useful new tools in cancer prevention.Martine Cao et al.Pharmacological research, 100, 135-147 (2015-08-05)
Bindings of axial ligands to cytochrome P-450d mutants: a difference absorption spectral study.T Shimizu et al.Biochimica et biophysica acta, 995(2), 116-121 (1989-04-06)
Crystal structure of cytochrome P450 14alpha -sterol demethylase (CYP51) from Mycobacterium tuberculosis in complex with azole inhibitors.L M Podust et al.Proceedings of the National Academy of Sciences of the United States of America, 98(6), 3068-3073 (2001-03-15)
Conformational flexibility of mammalian cytochrome P450 2B4 in binding imidazole inhibitors with different ring chemistry and side chains. Solution thermodynamics and molecular modeling.B K Muralidhara et al.The Journal of biological chemistry, 281(12), 8051-8061 (2006-01-28)
4-Phenyl-1H-imidazole (a low-temperature redetermination), 1-benzyl-1H-imidazole and 1-mesityl-1H-imidazole.David J Nielsen et al.Acta crystallographica. Section C, Crystal structure communications, 60(Pt 8), o542-o544 (2004-08-06)
Crystal structure of a thermophilic cytochrome P450 from the archaeon Sulfolobus solfataricus.J K Yano et al.The Journal of biological chemistry, 275(40), 31086-31092 (2000-06-22)
Crystal structure and properties of CYP231A2 from the thermoacidophilic archaeon Picrophilus torridus.Winny W Ho et al.Biochemistry, 47(7), 2071-2079 (2008-01-17)
X-RAY STUDIES AND ANTIBACTERIAL ACTIVITY IN COPPER AND COBALT COMPLEXES WITH IMIDAZOLE DERIVATIVE LIGANDS.ATRIA a, et al. Journal of the Chilean Chemical Society, 56(3), 786-792 (2011)
Structure-activity relationship of a series of phenylureas linked to 4-phenylimidazole. Novel potent inhibitors of acyl-CoA:cholesterol O-acyltransferase with antiatherosclerotic activity. 2.T Kimura et al.Journal of medicinal chemistry, 36(11), 1641-1653 (1993-05-28)
备注
Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
| 名称 | CAS号 |
|---|
相关产品
相关资讯
问
热门标签
询 单
请 填 写 相 关 信 息
- 请填写产品名称!
- CAS号
- 请正确填写公司名称!
- 请正确填写联系人!
- 请正确填写联系电话!
- 请正确填写联系邮箱!
- 请描述您的问题!