790305-00-9Relevant articles and documents
Water-soluble poly(l -serine)s with elongated and charged side-chains: Synthesis, conformations, and cell-penetrating properties
Tang, Haoyu,Yin, Lichen,Lu, Hua,Cheng, Jianjun
, p. 2609 - 2615 (2012)
Water-soluble poly(l-serine)s bearing long side-chain with terminal charge groups were synthesized via ring-opening polymerization of O-pentenyl-l-serine N-carboxyanhydride followed by thiol-ene reactions. These side-chain modified poly(l-serine)s adopt β
Genetically encoded alkenes in yeast
Ai, Hui-Wang,Shen, Weijun,Brustad, Eric,Schultz, Peter G.
, p. 935 - 937 (2010)
(Figure Presented) Olefin-containing amino acids have been genetically introduced into proteins in Saccharomyces cerevisiae by orthogonal tRNA/aminoacyl-tRNA synthetase pairs. These nonnatural amino acids can be used for selective protein modification thr
Stable helical ionic polypeptides
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Page/Page column 119-121, (2016/02/12)
The invention provides polymers comprising Formula I: wherein monomer is a repeating unit comprising 2, 3, 4, 5, 6 or 7 carbon atoms and the monomers are linked together through amide or ester bonds; n is about 6 to about 1000; and Linker is an optionally
A concise synthesis of the HCV protease inhibitor BILN 2061 and its P3 modified analogs
Liu, Dejun,Dong, Jingchao,Yin, Yunxing,Ma, Rujian,Shi, Yifeng,Wu, Hao,Chen, Shuhui,Li, Ge
experimental part, p. 1489 - 1502 (2011/11/01)
A concise synthesis of BILN 2061 was achieved through more efficient installation of P2 4-quinoline moiety via SN2 displacement of the β-OBs group located on the 4-hydroxyl proline intermediate, which was prepared from 4-α-hydroxyl proline analog via Mitsunobu reaction with inversion of stereochemistry. In addition, a short and practical synthesis for P3 unit is also described herein. Final assembly of four fragments for BILN 2061 was achieved with an overall yield of 58% in 4 steps from P1 to 15a. Furthermore several analogs of BILN 2061 (WX-1-WX-5) containing modifications on P3 unit were synthesized successfully using the same synthetic route as described for the parent inhibitor BILN 2061. Copyright
Inhibitors of Hepatitis C Virus
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Page/Page column 41, (2008/12/04)
Macrocyclic peptides are disclosed having the general formula: wherein R3, R3′, R4, R6, R′, X, Q and W are described. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.
MACROCYCLIC PEPTIDES AS HEPATITIS C VIRUS INHIBITORS
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Page/Page column 84, (2008/12/05)
Macrocyclic peptides having the general formula (I): are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.
Inhibitors of Hepatitis C Virus
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Page/Page column 39, (2008/12/04)
Macrocyclic peptides are disclosed having the general formula: wherein R3, R3′, R4, R6, R′, X, Q and W are described. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.
Inhibitors of Hepatitis C Virus
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Page/Page column 40, (2008/12/04)
Macrocyclic peptides are disclosed having the general formula: wherein R3, R′3, R4, R6, R′, X, Q and W are described. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.
MACROCYCLIC PEPTIDES AS HEPATITIS C VIRUS INHIBITORS
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Page/Page column 81, (2008/12/05)
Macrocyclic peptides having the general formula are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.
Hepatitis C virus inhibitors
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Page/Page column 54-55, (2010/11/26)
Hepatitis C virus inhibitors having the general formula are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.