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- 英文名:
2-Amino-1,2,3,4-tetrahydrocyclopenta[b]indole-7-carbonitrile
- 库存:
98
- 供应商:
北京孚博
- CAS号:
1029691-09-5
- 规格:
1g
CAS:1029691-09-5
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文献和实验QSAR and Metabolic Assessment Tools in the Assessment of Genotoxicity
tools to two case-study compounds—2-amino-9H-pyrido[2,3-b]indole (AαC) and 2-aminoacetophenone (2-AAP). The first case study compound (AαC) is an environment pollutant and a food contaminant that can be formed during the cooking of protein-rich food
of xenobiotic carboxylic acids are metabolized to their amino acid conjugates via a pathway that exists primarily in liver and kidney. This conjugation occurs in a two?step pathway catalyzed by two distince types of enzymes, ligases and transferases
Chemistry of Minor Groove Binder–Oligonucleotide Conjugates
‐type MBs of various lengths were prepared with zero to five MPC subunits and conjugated to dT8 or G/C‐rich 8‐mer ODNs. (A ) TTTTTTTT‐MPC n ( n = 0 to 5). (B ) CATCCGCT‐MPC n ( n =0,1,3,4,5). The A/T‐rich duplex shows a stepwise increase in duplex
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