所有图片(2)
About This Item
经验公式（希尔记法）:
C8H16N2O4S2
CAS号:
分子量:
268.35
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.26
推荐产品
产品名称
D-Homocystine,
方案
≥98% (TLC)
质量水平
表单
powder
颜色
white to off-white
SMILES字符串
N[C@H](CCSSCC[C@@H](N)C(O)=O)C(O)=O
InChI
1S/C8H16N2O4S2/c9-5(7(11)12)1-3-15-16-4-2-6(10)8(13)14/h5-6H,1-4,9-10H2,(H,11,12)(H,13,14)/t5-,6-/m1/s1
InChI key
ZTVZLYBCZNMWCF-PHDIDXHHSA-N
相关类别
生化/生理作用
D-Homocystine may be used in the preparation of carbocyclic nucleoside such as S-aristeromycinyl-L-homocysteine for use in studied on S-adenosylmethionine-dependent methyltransferase inhibitors.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
D M Houston et al.
Journal of medicinal chemistry, 28(4), 478-482 (1985-04-01)
A series of base- and amino acid modified analogues of S-aristeromycinyl-L-homocysteine, a carbocyclic nucleoside, were synthesized and evaluated as inhibitors of S-adenosyl-L-methionine-dependent methyltransferases, including catechol O-methyltransferase, phenylethanolamine N-methyltransferase, and histamine N-methyltransferase. The base-modified analogues (8-azaadenine, 3-deazaadenine, and N6-methyladenine) were prepared
S-Aristeromycinyl-L-homocysteine, a potent inhibitor of S-adenosylmethionine-dependent transmethylations.
R T Borchardt et al.
Journal of medicinal chemistry, 19(1), 197-198 (1976-01-01)
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