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- 文献和实验
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- 英文名:
4-(tert-butyl)-N-(6-hydroxy-5-(2-methoxyphenoxy)-[2,2-bipyrimidin]-4-yl)benzenesulfonamide
- 库存:
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- 供应商:
无锡云萃生物
- CAS号:
174227-14-6
- 规格:
2mg/10mg/500mg/500g
| 规格: | 2mg | 产品价格: | ¥100.0 |
|---|---|---|---|
| 规格: | 10mg | 产品价格: | ¥100.0 |
| 规格: | 500mg | 产品价格: | ¥100.0 |
| 规格: | 500g | 产品价格: | ¥100.0 |
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文献和实验Natural Product Chemistry in Action: The Synthesis of Melatonin Metabolites K1 and K2
melatonin, the kynurenamines N1-acetyl-N2 -formyl-5-methoxykynurenine (K1 ) and N -acetyl-5-methoxykynurenamine (K2 ). The four key synthetic transformations involve (a) conversion of 4-methoxy aniline into the tert -butyl (4-methoxyphenyl)carbamate, (b
Synthesis of Peptidomimetic Conjugates of Cyclic Nucleoside Phosphonates
)‐(L)‐serinate ( S.3 a ) Methyl N ‐(tert ‐butoxycarbonyl)‐(L)‐tyrosinate ( S.3 b ) Methyl N
Characterization of DNA Strand Cleavage by Enzymes That Act at Abasic Sites in DNA
directed toward a modified or nonconventional base in DNA. Some of these N -glycosylases also possess AP lyase activity that cleaves DNA 3′ to an AP site via a β-elimination reaction to leave a 3′ 4-hydroxy-2-pentenal-5-phosphate (Fig. 1 ). An example










