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- 文献和实验
- 技术资料
- 保存条件:
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- 保质期:
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- 英文名:
4-[[5-[[(Cyclopentyloxy)carbonyl]amino]-1-methyl-1H-indol-3-yl]methyl]-3-methoxy-benzoic Acid Methyl Ester
- 库存:
100+
- 供应商:
上海维亦特生物
- CAS号:
107754-19-8
4-[[5-[[(Cyclopentyloxy)carbonyl]amino]-1-methyl-1H-indol-3-yl]methyl]-3-methoxy-benzoic Acid Methyl Ester
107754-19-8
C25H28N2O5
436.5
No Data Available
No Data Available
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文献和实验4-[[5-[[(Cyclopentyloxy)carbonyl]amino]-1-methyl-1H-indol-3-yl]methyl]-3-methoxy-benzoic Acid Methyl Ester
107754-19-8
C25H28N2O5
436.5
No Data Available
No Data Available
: 2‐(N ‐(2‐(4‐((N ‐(2‐(Bis(4‐methoxyphenyl)(phenyl)methoxy)ethyl)‐2‐(uracil‐1‐)acetamido)methyl)‐1H‐1,2,3‐triazol‐1‐yl)ethyl)‐2‐(uracil‐1‐yl)acetami‐do)ethyl (2‐cyanoethyl) diisopropylphosphoramidite (24 ; Basic Protocol
) 0.25 M 5‐ethylthio‐1H ‐tetrazole in dry acetonitrile (ETT/MeCN; Glen Research) 3H ‐1,2‐Benzodithiol‐3‐one 1,1‐dioxide (Glen Research
Synthesis of Peptide‐Oligonucleotide Conjugates by Diels‐Alder Cycloaddition in Water
?oligonucleotide conjugates incorporating all the nucleobases and trifunctional amino acids are obtained by Diels?Alder reaction between diene?modified oligonucleotides (2??deoxyribo? or ribo?) and malemide?derivatized peptides. Both reagents are easily synthesized
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