-
1
-
-
64349088294
-
Discovery of (R)-6-cyclopentyl-6-(2-(2,6-diethylpyridin-4-yl)ethyl)-3-((5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)methyl)-4-hydroxy-5,6-dihydropyran-2-one (PF-00868554) as a potent and orally available hepatitis C virus polymerase inhibitor
-
Hui L., Tatlock J., Linton A., Gonzalez J., Jewell T., Patel L., Ludlum S., Drowns M., Rahavendran S.V., Skor H., Hunter R., Shi S.T., Herlihy K.J., Parge H., Hickey M., Yu X., Chau F., Nonomiya J., Lewis C. Discovery of (R)-6-cyclopentyl-6-(2-(2,6-diethylpyridin-4-yl)ethyl)-3-((5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)methyl)-4-hydroxy-5,6-dihydropyran-2-one (PF-00868554) as a potent and orally available hepatitis C virus polymerase inhibitor. J. Med. Chem. 2009, 52:1255-1258.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1255-1258
-
-
Hui, L.1
Tatlock, J.2
Linton, A.3
Gonzalez, J.4
Jewell, T.5
Patel, L.6
Ludlum, S.7
Drowns, M.8
Rahavendran, S.V.9
Skor, H.10
Hunter, R.11
Shi, S.T.12
Herlihy, K.J.13
Parge, H.14
Hickey, M.15
Yu, X.16
Chau, F.17
Nonomiya, J.18
Lewis, C.19
-
2
-
-
33746884722
-
Development of a synthetic process towards a hepatitis C polymerase inhibitor
-
Camp D., Matthews C.F., Neville S.T., Rouns M., Scott R.W., Truong Y. Development of a synthetic process towards a hepatitis C polymerase inhibitor. Org. Process Res. Dev. 2006, 10:814-821.
-
(2006)
Org. Process Res. Dev.
, vol.10
, pp. 814-821
-
-
Camp, D.1
Matthews, C.F.2
Neville, S.T.3
Rouns, M.4
Scott, R.W.5
Truong, Y.6
-
6
-
-
33645840463
-
A rationale for determining, testing, and controlling specific impurities in pharmaceuticals that possess potential for genotoxicity
-
Muller L., Mauthe R.J., Riley C.M., Andino M.A., De Antonis D., Beels C., DeGeorge J., De Knaep A.G.M., Ellison D., Fagerland J.A., Frank R., Fritschel B., Galloway S., Harpur E., Humfrey C.D.N., Jacks A.S., Jagota N., Mackinnon J., Mohan G., Ness D.K., O'Donovan M.R., Smith M.D., Vudathala G., Yotti L. A rationale for determining, testing, and controlling specific impurities in pharmaceuticals that possess potential for genotoxicity. Regul. Toxicol. Pharmacol. 2006, 44:198-211.
-
(2006)
Regul. Toxicol. Pharmacol.
, vol.44
, pp. 198-211
-
-
Muller, L.1
Mauthe, R.J.2
Riley, C.M.3
Andino, M.A.4
De Antonis, D.5
Beels, C.6
DeGeorge, J.7
De Knaep, A.G.M.8
Ellison, D.9
Fagerland, J.A.10
Frank, R.11
Fritschel, B.12
Galloway, S.13
Harpur, E.14
Humfrey, C.D.N.15
Jacks, A.S.16
Jagota, N.17
Mackinnon, J.18
Mohan, G.19
Ness, D.K.20
O'Donovan, M.R.21
Smith, M.D.22
Vudathala, G.23
Yotti, L.24
more..
-
7
-
-
84862796606
-
-
Committee for Medicinal Products for Human Use (CHMP), European Medicines Agency, (EMA/CHMP/SWP/431994/2007)
-
Questions & Answers on the " Guideline on the Limits of Genotoxic Impurities" 2010, Committee for Medicinal Products for Human Use (CHMP), European Medicines Agency, (EMA/CHMP/SWP/431994/2007).
-
(2010)
Questions & Answers on the " Guideline on the Limits of Genotoxic Impurities"
-
-
-
8
-
-
84873066366
-
-
Deductive Estimation of Risk from Existing Knowledge (DEREK), marketed by LHASA Ltd., Leeds, UK, .
-
Deductive Estimation of Risk from Existing Knowledge (DEREK), marketed by LHASA Ltd., Leeds, UK, https://www.lhasalimited.org/.
-
-
-
-
9
-
-
0026745007
-
Mutagenicity of nitroxyl compounds: structure-activity relationships
-
Gallez B., De Meester C., Debuyst R., Dejehet F., Dumont P. Mutagenicity of nitroxyl compounds: structure-activity relationships. Toxicol. Lett. 1992, 63:35-45.
-
(1992)
Toxicol. Lett.
, vol.63
, pp. 35-45
-
-
Gallez, B.1
De Meester, C.2
Debuyst, R.3
Dejehet, F.4
Dumont, P.5
-
10
-
-
0033952204
-
Cyto- and genotoxic effects of novel aromatic nitroxide radicals in vitro
-
Damiani E., Greci L., Hrella P. Cyto- and genotoxic effects of novel aromatic nitroxide radicals in vitro. Free Radic. Biol. Med. 2000, 28:330-336.
-
(2000)
Free Radic. Biol. Med.
, vol.28
, pp. 330-336
-
-
Damiani, E.1
Greci, L.2
Hrella, P.3
-
11
-
-
77955401057
-
A systematic method development strategy for determination of pharmaceutical genotoxic impurities
-
Sun M., Liu D.Q., Kord A.S. A systematic method development strategy for determination of pharmaceutical genotoxic impurities. Org. Process Res. Dev. 2010, 14:977-985.
-
(2010)
Org. Process Res. Dev.
, vol.14
, pp. 977-985
-
-
Sun, M.1
Liu, D.Q.2
Kord, A.S.3
-
12
-
-
72749101941
-
Recent advances in trace analysis of pharmaceutical genotoxic impurities
-
Liu D.Q., Sun M., Kord A.S. Recent advances in trace analysis of pharmaceutical genotoxic impurities. J. Pharm. Biomed. Anal. 2010, 51:999-1014.
-
(2010)
J. Pharm. Biomed. Anal.
, vol.51
, pp. 999-1014
-
-
Liu, D.Q.1
Sun, M.2
Kord, A.S.3
-
13
-
-
79955468501
-
Strategies for the identification, control and determination of genotoxic impurities in drug substances: a pharmaceutical industry perspective
-
Raman N.V.V.S.S., Prasad A.V.S.S., Reddy K.R. Strategies for the identification, control and determination of genotoxic impurities in drug substances: a pharmaceutical industry perspective. J. Pharm. Biomed. Anal. 2011, 55:662-667.
-
(2011)
J. Pharm. Biomed. Anal.
, vol.55
, pp. 662-667
-
-
Raman, N.V.1
Prasad, A.V.2
Reddy, K.R.3
-
14
-
-
65949108606
-
Approaches to assessment, testing decisions, and analytical determination of genotoxic impurities in drug substances
-
Pierson D.A., Olsen B.A., Robbins D.K., DeVries K.M., Varie D.L. Approaches to assessment, testing decisions, and analytical determination of genotoxic impurities in drug substances. Org. Process Res. Dev. 2009, 13:285-291.
-
(2009)
Org. Process Res. Dev.
, vol.13
, pp. 285-291
-
-
Pierson, D.A.1
Olsen, B.A.2
Robbins, D.K.3
DeVries, K.M.4
Varie, D.L.5
-
15
-
-
77955380706
-
Control of genotoxic impurities in active pharmaceutical ingredients: a review and perspective
-
Robinson D.I. Control of genotoxic impurities in active pharmaceutical ingredients: a review and perspective. Org. Process Res. Dev. 2010, 14:946-959.
-
(2010)
Org. Process Res. Dev.
, vol.14
, pp. 946-959
-
-
Robinson, D.I.1
-
16
-
-
77955347744
-
Risk assessment of potentially genotoxic impurities within the framework of quality by design
-
Looker A.R., Ryan M.P., Neubert-Langille B.J., Naji R. Risk assessment of potentially genotoxic impurities within the framework of quality by design. Org. Process Res. Dev. 2010, 14:1032-1036.
-
(2010)
Org. Process Res. Dev.
, vol.14
, pp. 1032-1036
-
-
Looker, A.R.1
Ryan, M.P.2
Neubert-Langille, B.J.3
Naji, R.4
-
17
-
-
0000307530
-
A versatile and highly selective hypervalent iodine (III)/2,2,6,6-tetramethyl-1-piperidinyloxyl-mediated oxidation of alcohols to carbonyl compounds
-
De Mico A., Margarita R., Parlanti L., Vescovi A., Piancatelli G. A versatile and highly selective hypervalent iodine (III)/2,2,6,6-tetramethyl-1-piperidinyloxyl-mediated oxidation of alcohols to carbonyl compounds. J. Org. Chem. 1997, 62:6974-6977.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6974-6977
-
-
De Mico, A.1
Margarita, R.2
Parlanti, L.3
Vescovi, A.4
Piancatelli, G.5
-
18
-
-
0041363221
-
Thermolysis of N-tetramethylpiperidinyl triphenylacetate: hemolytic fragmentation of a TEMPO ester
-
Henry-Riyad H., Tidwell T.T. Thermolysis of N-tetramethylpiperidinyl triphenylacetate: hemolytic fragmentation of a TEMPO ester. J. Phys. Org. Chem. 2003, 16:559-563.
-
(2003)
J. Phys. Org. Chem.
, vol.16
, pp. 559-563
-
-
Henry-Riyad, H.1
Tidwell, T.T.2
-
19
-
-
33845280113
-
Oxoiminium ions for N-demethylation: 1-oxo-2,2,6,6-teteramethylpiperidinium chloride
-
Hunter D.H., Racok J.S., Rey A.W., Ponce Y.Z. Oxoiminium ions for N-demethylation: 1-oxo-2,2,6,6-teteramethylpiperidinium chloride. J. Org. Chem. 1988, 53:1278-1281.
-
(1988)
J. Org. Chem.
, vol.53
, pp. 1278-1281
-
-
Hunter, D.H.1
Racok, J.S.2
Rey, A.W.3
Ponce, Y.Z.4
-
20
-
-
33845184317
-
The mechanism of formation of Grignard reagents: trapping of free alkyl radical intermediates by reaction with tetramethylpiperidine-N-oxyl
-
Root K.S., Hill C.L., Lawrence L.M., Whitesides G.M. The mechanism of formation of Grignard reagents: trapping of free alkyl radical intermediates by reaction with tetramethylpiperidine-N-oxyl. J. Am. Chem. Soc. 1989, 111:5405-5412.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 5405-5412
-
-
Root, K.S.1
Hill, C.L.2
Lawrence, L.M.3
Whitesides, G.M.4
-
21
-
-
0041889408
-
2,2,6,6-Tetramethylpiperidin-1-oxyl
-
John Wiley & Sons, New York, L.A. Paquette (Ed.)
-
Montanari F., Quici S. 2,2,6,6-Tetramethylpiperidin-1-oxyl. Encyclopedia of Reagents for Organic Synthesis 1995, 4821-4823. John Wiley & Sons, New York. L.A. Paquette (Ed.).
-
(1995)
Encyclopedia of Reagents for Organic Synthesis
, pp. 4821-4823
-
-
Montanari, F.1
Quici, S.2
-
22
-
-
23944435696
-
Development and validation of a sensitive GC-MS method for the determination of trace levels of an alkylating reagent in a β-lactam active pharmaceutical ingredient
-
Li H., Sluggett G.W. Development and validation of a sensitive GC-MS method for the determination of trace levels of an alkylating reagent in a β-lactam active pharmaceutical ingredient. J. Pharm. Biomed. Anal. 2005, 39:486-494.
-
(2005)
J. Pharm. Biomed. Anal.
, vol.39
, pp. 486-494
-
-
Li, H.1
Sluggett, G.W.2
-
23
-
-
77955373387
-
A tool for the semiquantitative assessment of potentially genotoxic impurity (PGI) carryover into API using physicochemical parameters and process conditions
-
Teasdale A., Fenner S., Ray A., Ford A., Phillips A. A tool for the semiquantitative assessment of potentially genotoxic impurity (PGI) carryover into API using physicochemical parameters and process conditions. Org. Process Res. Dev. 2010, 14:943-945.
-
(2010)
Org. Process Res. Dev.
, vol.14
, pp. 943-945
-
-
Teasdale, A.1
Fenner, S.2
Ray, A.3
Ford, A.4
Phillips, A.5
|