-
1
-
-
0000833934
-
Peptide decomposition in the neutral Ph region via the formation of diketopiperazines
-
Steinberg SM, Bada JL. Peptide decomposition in the neutral Ph region via the formation of diketopiperazines. J Org Chem 1983;48:2295-2298
-
(1983)
J Org Chem
, vol.48
, pp. 2295-2298
-
-
Steinberg, S.M.1
Bada, J.L.2
-
2
-
-
0031897939
-
Kinetics of diketopiperazine formation using model peptides
-
Chimanlal G, Ronals TB. Kinetics of diketopiperazine formation using model peptides. J Pharm Sci 1998;87:283-288
-
(1998)
J Pharm Sci
, vol.87
, pp. 283-288
-
-
Chimanlal, G.1
Ronals, T.B.2
-
3
-
-
37049133921
-
Piperazinedione formation from esters of dipeptides containing glycine, alanine and sarcosine: The kinetics in aqueous solution
-
Purdie JE, Benoiton NL. Piperazinedione formation from esters of dipeptides containing glycine, alanine and sarcosine: The kinetics in aqueous solution. Chem Soc Perkin Trans 2. 1973;13:1845-1852
-
(1973)
Chem Soc Perkin Trans 2
, vol.13
, pp. 1845-1852
-
-
Purdie, J.E.1
Benoiton, N.L.2
-
4
-
-
0019433424
-
Diketopiperazine formation during investigations of aminoacid racemization in dipeptides
-
Steinberg SM, Bada JL. Diketopiperazine formation during investigations of aminoacid racemization in dipeptides. Science 1981;213:544-545
-
(1981)
Science
, vol.213
, pp. 544-545
-
-
Steinberg, S.M.1
Bada, J.L.2
-
5
-
-
34249848236
-
-
US Patent No. 4,344, 949, August 17
-
Hoefle ML, Klutchko S. Substituted acyl derivatives of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids. US Patent No. 4,344, 949, August 17, 1982.
-
(1982)
Substituted Acyl Derivatives of 1, 2,3,4-tetrahydroisoquinoline-3- carboxylic Acids
-
-
Hoefle, M.L.1
Klutchko, S.2
-
6
-
-
71049167534
-
-
GB Patent No. 2, 095, 252, September 29
-
Jiyon TS, Jiefurii EB, Jiyon AR. N-(substituted aminoalkanoyl) heterocyclic compounds. GB Patent No. 2,095,252, September 29, 1982
-
(1982)
N-(substituted Aminoalkanoyl) Heterocyclic Compounds
-
-
Jiyon, T.S.1
Jiefurii, E.B.2
Jiyon, A.R.3
-
7
-
-
71049119299
-
-
EP Patent No. 0, 065, 301, November 24
-
Patchett AA, Wu MT. Isoquinoline carboxylic acid derivates, process for preparing and pharmaceutical composition containing the same. EP Patent No. 0,065,301, November 24, 1982.
-
(1982)
Isoquinoline Carboxylic Acid Derivates, Process for Preparing and Pharmaceutical Composition Containing the Same
-
-
Patchett, A.A.1
Wu, M.T.2
-
8
-
-
0033971208
-
Physical characteristics and chemical degradation of amorphous quinapril hydrochloride
-
Guo Y, Byrn SR, Zografi G. Physical characteristics and chemical degradation of amorphous quinapril hydrochloride. J Pharm Sci 2000;89:128-143
-
(2000)
J Pharm Sci
, vol.89
, pp. 128-143
-
-
Guo, Y.1
Byrn, S.R.2
Zografi, G.3
-
9
-
-
84890662885
-
The importance of solvates
-
Hilfiker R, editor. Weinheim: Wiley-VCH
-
Ulrich JG. The importance of solvates. In: Hilfiker R, editor. Polymorphism in pharmaceutical Industry. Weinheim: Wiley-VCH; 2006. p. 211-233
-
(2006)
Polymorphism in Pharmaceutical Industry
, pp. 211-233
-
-
Ulrich, J.G.1
-
10
-
-
53549119401
-
Polymorphism and solvatomorphism 2006
-
Brittain HG. Polymorphism and solvatomorphism 2006. J Pharm Sci 2007;97:3611-3636
-
(2007)
J Pharm Sci
, vol.97
, pp. 3611-3636
-
-
Brittain, H.G.1
-
11
-
-
33645999665
-
Identification, preparation, and characterization of several polymorphs and solvates of terazosin hydrochloride
-
Baure J, Morley J, Spanton S, Leusen FJ, Henry R, Hollis S, et al. Identification, preparation, and characterization of several polymorphs and solvates of terazosin hydrochloride. J Pharm Sci 2006;95:917-928
-
(2006)
J Pharm Sci
, vol.95
, pp. 917-928
-
-
Baure, J.1
Morley, J.2
Spanton, S.3
Leusen, F.J.4
Henry, R.5
Hollis, S.6
-
12
-
-
0036276280
-
Physicochemical characterization of hydrated and anhydrous crystal forms of amlodipine besylate
-
Rollinger JM, Burger A. Physicochemical characterization of hydrated and anhydrous crystal forms of amlodipine besylate. J Thermal Anal Calorimetry 2002;68:361-372
-
(2002)
J Thermal Anal Calorimetry
, vol.68
, pp. 361-372
-
-
Rollinger, J.M.1
Burger, A.2
-
13
-
-
0001317352
-
Mechanism of several solid-solid transformations between dihydrated and anhydrous copper(II) 8-hydroxyquinolinates. proposition for a unified model for the dehydration of molecular crystals
-
Petit S, Coquerel G. Mechanism of several solid-solid transformations between dihydrated and anhydrous copper(II) 8-hydroxyquinolinates. proposition for a unified model for the dehydration of molecular crystals. Chem Materials 1996;8:2247-2258
-
(1996)
Chem Materials
, vol.8
, pp. 2247-2258
-
-
Petit, S.1
Coquerel, G.2
-
14
-
-
0036145187
-
Effects of a citrate buffer system on the solidstate chemical stability of lyophilized quinapril preparations
-
Li J, Guo Y, Zugrufi G. Effects of a citrate buffer system on the solidstate chemical stability of lyophilized quinapril preparations. Pharm Res 2002;19:20-26
-
(2002)
Pharm Res
, vol.19
, pp. 20-26
-
-
Li, J.1
Guo, Y.2
Zugrufi, G.3
-
15
-
-
71049180192
-
-
US Patent No. 4, 743, 450, May 10
-
Harris M, Hokanson G, Murthy K, Reisch R, Waldman F. Stabilized compositions. US Patent No. 4,743,450, May 10, 1988.
-
(1988)
Stabilized Compositions
-
-
Harris, M.1
Hokanson, G.2
Murthy, K.3
Reisch, R.4
Waldman, F.5
-
17
-
-
71049164567
-
-
US Patent Application No. 20040052835, March 18
-
Klokkers K, Kramer KT, Fischer W, Sendl-Lang A. Matrix controlled transdermal system for stabile derivatives of ace inhibitors. US Patent Application No. 20040052835, March 18, 2004.
-
(2004)
Matrix Controlled Transdermal System for Stabile Derivatives of Ace Inhibitors
-
-
Klokkers, K.1
Kramer, K.T.2
Fischer, W.3
Sendl-Lang, A.4
-
19
-
-
0036143366
-
The solid-state stability of amorphous quinapril in the presence of beta cyclodextrins
-
Li J, Guo Y, Zografi G. The solid-state stability of amorphous quinapril in the presence of beta cyclodextrins. J Pharm Sci 2002;91:229-243
-
(2002)
J Pharm Sci
, vol.91
, pp. 229-243
-
-
Li, J.1
Guo, Y.2
Zografi, G.3
-
20
-
-
71049165028
-
-
US Patent No. 4, 761, 479, August 2
-
Goel OP, Krolls U. Crystalline quinapril and a process for producing the same. US Patent No. 4,761,479, August 2, 1988.
-
(1988)
Crystalline Quinapril and A Process for Producing the Same
-
-
Goel, O.P.1
Krolls, U.2
-
23
-
-
37049077608
-
The use of co-crystallization as a method of studying hydrogen bond p of 2-aminopyridine
-
Etter MC, Adsmond DA. The use of co-crystallization as a method of studying hydrogen bond p of 2-aminopyridine. J Chem Soc Chem Commun 1990;589-591
-
(1990)
J Chem Soc Chem Commun
, pp. 589-591
-
-
Etter, M.C.1
Adsmond, D.A.2
-
24
-
-
84903185610
-
Graph-set analysis of hydrogen-bond patterns in organic crystals
-
Etter MC. Graph-set analysis of hydrogen-bond patterns in organic crystals. Acta Crystallogr B 1990;46:256-262
-
(1990)
Acta Crystallogr B
, vol.46
, pp. 256-262
-
-
Etter, M.C.1
-
25
-
-
11944250136
-
Hydrogen bond directed co crystallization and molecular recognition properties of diarylureas
-
Etter MC, Urbanczyk-Lipkowska Z, Zia-Ebrahima M, Panunto TW. Hydrogen bond directed co crystallization and molecular recognition properties of diarylureas. J Am Chem Soc 1990;112:8415-8426
-
(1990)
J Am Chem Soc
, vol.112
, pp. 8415-8426
-
-
Etter, M.C.1
Urbanczyk-Lipkowska, Z.2
Zia-Ebrahima, M.3
Panunto, T.W.4
-
26
-
-
0040601673
-
On the inclusion of solvent molecules in the crystal structures of organic compounds
-
Carl HG, Hans PH On the inclusion of solvent molecules in the crystal structures of organic compounds. Acta Crystallogr B 2000;56:525-534
-
(2000)
Acta Crystallogr B
, vol.56
, pp. 525-534
-
-
Carl, H.G.1
Hans, P.H.2
-
27
-
-
0012359444
-
Molecular complexes of some mono- and dicarboxylic acids with trans-l,4,-dithiane-l,4-dioxide
-
SenthilKumar VS, Nangia A. Molecular complexes of some mono- and dicarboxylic acids with trans-l,4,-dithiane-l,4-dioxide. Crystal Growth Design 2002;2:325-328
-
(2002)
Crystal Growth Design
, vol.2
, pp. 325-328
-
-
Senthilkumar, V.S.1
Nangia, A.2
-
28
-
-
8844275016
-
Crystal and co-crystal
-
Desiraju GR. Crystal and co-crystal. Crystal Engg Commun 2003;5:466-467
-
(2003)
Crystal Engg Commun
, vol.5
, pp. 466-467
-
-
Desiraju, G.R.1
-
29
-
-
77951280457
-
-
US Patent Appl. 20070059356, March 15
-
Almarsson O, Bourghol HM, Peterson M, Zaworotko MJ, Moulton B, Rodriguez-Hornedo N. Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothiazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen. US Patent Appl. 20070059356, March 15, 2007.
-
(2007)
Pharmaceutical Co-crystal Compositions of Drugs Such As Carbamazepine, Celecoxib, Olanzapine, Itraconazole, Topiramate, Modafinil, 5-fluorouracil, Hydrochlorothiazide, Acetaminophen, Aspirin, Flurbiprofen, Phenytoin and Ibuprofen
-
-
Almarsson, O.1
Bourghol, H.M.2
Peterson, M.3
Zaworotko, M.J.4
Moulton, B.5
Rodriguez-Hornedo, N.6
-
31
-
-
71049185896
-
-
US patent No. 6, 617, 457, September 9
-
Monsalvatje LM, Bartra SM, Tomas NJ, Puig TS. Process for obtaining quinapril hydrochloride and solvates useful for isolating and purifying quinapril hydrochloride. US patent No. 6,617,457, September 9, 2003.
-
(2003)
Process for Obtaining Quinapril Hydrochloride and Solvates Useful for Isolating and Purifying Quinapril Hydrochloride
-
-
Monsalvatje, L.M.1
Bartra, S.M.2
Tomas, N.J.3
Puig, T.S.4
-
38
-
-
33744498094
-
Mercury: Visualization and analysis of crystal structures
-
Macrae CF, Edgington PR, McCabe P, Pidcock E, Shields GP, Taylor R, et al. Mercury: visualization and analysis of crystal structures. J Applied Crystallogr 2006;39:453-457
-
(2006)
J Applied Crystallogr
, vol.39
, pp. 453-457
-
-
MacRae, C.F.1
Edgington, P.R.2
McCabe, P.3
Pidcock, E.4
Shields, G.P.5
Taylor, R.6
-
39
-
-
0026035414
-
Molecular and crystal structure of MDL27,467A hydrochloride and quinapril hydrochloride, two ester derivatives of potent angiotensin converting enzyme inhibitors
-
Hausin RJ, Codding PW. Molecular and crystal structure of MDL27,467A Hydrochloride and Quinapril Hydrochloride, Two Ester Derivatives of Potent Angiotensin Converting Enzyme Inhibitors. J Med Chem 1991;34:511-517
-
(1991)
J Med Chem
, vol.34
, pp. 511-517
-
-
Hausin, R.J.1
Codding, P.W.2
-
40
-
-
71049193795
-
-
The Cambridge Structural Database (CSD)- The Cambridge Crystallographic Data Centre, Copyright ©
-
The Cambridge Structural Database (CSD)- The world repository of small molecule crystal structures The Cambridge Crystallographic Data Centre, Copyright © 2004-2008.
-
(2004)
The World Repository of Small Molecule Crystal Structures
-
-
-
41
-
-
33749286804
-
Calculation of ring puckering parameters
-
Boeyens JCA. Calculation of ring puckering parameters. J crystallogr Mol Structure 1978;8:317.
-
(1978)
J Crystallogr Mol Structure
, vol.8
, pp. 317
-
-
Boeyens, J.C.A.1
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