2097887-21-1 (MM-589 TFA | Histone Methyltransferase,N-[(12R)-6-Ethyl-12-methyl-9-[3-[(N'-methylcarbamimidoyl)amino]propyl]-2,5,8,11-tetraoxo-3-phenyl-1,4,7,10-tetrazacyclotetradec-12-yl]-2-methylpropanamide;2,2,2-trifluoroacetic acid)

快速询单

结构式：

MM-589 TFA | Histone MethyltransferaseMOL文件

CAS号：

2097887-21-1

中文名称：

MM-589 TFA | Histone Methyltransferase

英文名称：

N-[(12R)-6-Ethyl-12-methyl-9-[3-[(N'-methylcarbamimidoyl)amino]propyl]-2,5,8,11-tetraoxo-3-phenyl-1,4,7,10-tetrazacyclotetradec-12-yl]-2-methylpropanamide;2,2,2-trifluoroacetic acid

分子式：

C₃₀H₄₅F₃N₈O₇

分子量：

686.722917318344

MM-589 TFA | Histone Methyltransferase(2097887-21-1)名称与标识符

名称

英文别名：

N-[(12R)-6-Ethyl-12-methyl-9-[3-[(N'-methylcarbamimidoyl)amino]propyl]-2,5,8,11-tetraoxo-3-phenyl-1,;MM-589 TFA;

标识符

InChIKey：

NARXNZHWAWPJIY-LVENEOMWSA-N

Inchi：

1S/C28H44N8O5.C2HF3O2/c1-6-19-23(38)35-21(18-11-8-7-9-12-18)25(40)31-16-14-28(4,36-22(37)17(2)3)26(41)34-20(24(39)33-19)13-10-15-32-27(29)30-5;3-2(4,5)1(6)7/h7-9,11-12,17,19-21H,6,10,13-16H2,1-5H3,(H,31,40)(H,33,39)(H,34,41)(H,35,38)(H,36,37)(H3,29,30,32);(H,6,7)/t19?,20?,21?,28-;/m1./s1

SMILES：

FC(C(=O)O)(F)F.O=C1[C@@](C)(CCNC(C(C2C=CC=CC=2)NC(C(CC)NC(C(CCCN/C(=N/C)/N)N1)=O)=O)=O)NC(C(C)C)=O

MM-589 TFA | Histone Methyltransferase(2097887-21-1)物化性质

计算特性

氢键供体数量 : 8
氢键受体数量 : 11
可旋转化学键数量 : 9
重原子数量 : 48
复杂度 : 1050
拓扑分子极性表面积 : 233

MM-589 TFA | Histone Methyltransferase(2097887-21-1)安全信息

储存条件： (BD767580)

MM-589 TFA | Histone Methyltransferase(2097887-21-1)推荐厂家更多厂家(6)

公司名称	手机号/电话	联系人	QQ	询单
杭州肽佳生物科技有限公司	13336049365 0571-87213919	来经理	3007955256	询单
上海超岚化工科技中心	13301690235	linda	3027278462	询单
MedChemExpress（MCE 中国）	13611715263 021-58955995	MCE生命科学试剂	2881321772	询单
四川维克奇生物科技有限公司	13348961525	杨洋	2851167780	询单
上海吉至生化科技有限公司	18117592386 021-57481218	吉至试剂	3007522982	询单
天津普西唐生物医药科技有限公司	15801484223 15801484223	唐召锋	3003463702	询单

MM-589 TFA | Histone Methyltransferase(2097887-21-1)相关文献

1. Formation and characterization of the radical cation of pentamethylbenzyl trifluoroacetate from the oxidation of hexamethyl (Dewar benzene) by thallium(III) trifluoroacetate in trifluoroacetic acid—a slow and complex reaction
Lennart Eberson,Michael P. Hartshorn,Ola Persson,Jan O. Svensson J. Chem. Soc. Perkin Trans. 2 1995 1253
2. Formation and characterization of the radical cation of pentamethylbenzyl trifluoroacetate from the oxidation of hexamethyl (Dewar benzene) by thallium(III) trifluoroacetate in trifluoroacetic acid—a slow and complex reaction
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3. Synthesis of oligomers related to nylon 6
Gerald M. Brooke,Shahid Mohammed,Mark C. Whiting J. Chem. Soc. Perkin Trans. 1 1997 3371
4. Reactions of lead tetra-acetate. Part XXI. Acyloxylation, plumbylation, and oxidative dimerisation of some benzenoid compounds in the presence of trifluoro- or trichloro-acetic acid
R. O. C. Norman,C. B. Thomas,J. S. Willson J. Chem. Soc. B 1971 518
5. 669. Studies of trifluoroacetic acid. Part XV. Further investigations on the reactions of acyl trifluoroacetates with hydroxycompounds
E. J. Bourne,M. Stacey,J. C. Tatlow,R. Worrall J. Chem. Soc. 1958 3268
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9. On cysteine and cystine peptides. Part V. S-trityl- and S-diphenylmethyl-cysteine and -cysteine peptides
I. Photaki,J. Taylor-Papadimitriou,C. Sakarellos,P. Mazarakis,L. Zervas J. Chem. Soc. C 1970 2683
10. 1,1,1,3,3,3-Hexafluoropropan-2-ol as a solvent for the generation of highly persistent radical cations
Lennart Eberson,Michael P. Hartshorn,Ola Persson J. Chem. Soc. Perkin Trans. 2 1995 1735

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