所有图片(3)
About This Item
经验公式（希尔记法）:
C10H14N2O5
CAS号:
分子量:
242.23
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
NACRES:
NA.51
检测方案
≥98% (HPLC)
质量水平
形式
powder
旋光性
[α]25/D 5.0 to 8.0°, c = 2.0% in water
溶解性
water: 50 mg/mL, clear, colorless
SMILES字符串
CC1=CN(C2CC(O)C(CO)O2)C(=O)NC1=O
InChI
1S/C10H14N2O5/c1-5-3-12(10(16)11-9(5)15)8-2-6(14)7(4-13)17-8/h3,6-8,13-14H,2,4H2,1H3,(H,11,15,16)
InChI key
IQFYYKKMVGJFEH-UHFFFAOYSA-N
应用
α-Thymidine (α-Thymidine) is the unnatural epimer of thymidine.
其他说明
Unnatural epimer
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Carolina H Andrade et al.
Journal of chemical information and modeling, 49(4), 1070-1078 (2009-03-20)
Thymidine monophosphate kinase (TMPK) has emerged as an attractive target for developing inhibitors of Mycobacterium tuberculosis growth. In this study the receptor-independent (RI) 4D-QSAR formalism has been used to develop QSAR models and corresponding 3D-pharmacophores for a set of 5'-thiourea-substituted
Y Sato et al.
Nucleic acids symposium series, 44(44), 31-32 (2003-08-09)
In this paper, we report the synthesis of hydroxymethylphosphonate alpha-DNAs and related compounds by use of the H-phosphonate method. These modified alpha-DNAs were designed to improve the inherent poor solubility of well-known methylphosphonate alpha-DNAs by introduction of a more hydrophilic
Sara Van Poecke et al.
Bioorganic & medicinal chemistry, 19(24), 7603-7611 (2011-11-09)
We report on Mycobacterium tuberculosis thymidine monophosphate kinase (TMPKmt) inhibitory activities of a series of new 3'- and 5'-modified thymidine analogues including α- and β-derivatives. In addition, several analogues were synthesized in which the 4-oxygen was replaced by a more
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