258504
N4-苯甲酰基-5′-O-(4,4′-二甲氧基三苯基)-2′-脱氧胞苷
95%
别名:
Bz-DMT-dC
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关于此项目
经验公式（希尔记法）:
C37H35N3O7
化学文摘社编号:
分子量:
633.69
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
266-605-9
Beilstein/REAXYS Number:
601627
MDL number:
Assay:
95%
Form:
solid
form
solid
InChI key
MYSNCIZBPUPZMQ-VOTWKOMSSA-N
InChI
1S/C37H35N3O7/c1-44-29-17-13-27(14-18-29)37(26-11-7-4-8-12-26,28-15-19-30(45-2)20-16-28)46-24-32-31(41)23-34(47-32)40-22-21-33(39-36(40)43)38-35(42)25-9-5-3-6-10-25/h3-22,31-32,34,41H,23-24H2,1-2H3,(H,38,39,42,43)/t31-,32+,34+/m0/s1
SMILES string
COc1ccc(cc1)C(OC[C@H]2O[C@H](C[C@@H]2O)N3C=CC(NC(=O)c4ccccc4)=NC3=O)(c5ccccc5)c6ccc(OC)cc6
assay
95%
functional group
amide, ether, hydroxyl, phenyl
storage temp.
2-8°C
General description
The 3′-O-(2-cyanoethyl)-N,N-diisopropylphosphoramidite derivatives of N4-benzoyl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxycytidine (DMT-dCBz) participates in Diels-Alder reaction between diene-modified oligonucleotides and maleimide-derivatized peptides.
Application
N4-Benzoyl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxycytidine has been used as research tool for anti-viral and anti-cancer studies.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2
存储类别
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Vicente Marchán et al.
Nucleic acids research, 34(3), e24-e24 (2006-02-16)
The Diels-Alder reaction between diene-modified oligonucleotides and maleimide-derivatized peptides afforded peptide-oligonucleotide conjugates with high purity and yield. Synthesis of the reagents was easily accomplished by on-column derivatization of the corresponding peptides and oligonucleotides. The cycloaddition reaction was carried out in
Aldrichimica Acta, 20, 52-52 (1987)
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