-
1
-
-
84882549603
-
-
US 7,029,918 B2, April 18
-
Li, M., Wu, R.S. Tsai, J.S.C. Water-soluble derivatives of lipophilic drugs. US 7,029,918 B2, April 18, 2006.
-
(2006)
Water-soluble derivatives of lipophilic drugs
-
-
Li, M.1
Wu, R.S.2
Tsai, J.S.C.3
-
2
-
-
78651188140
-
Metodos Modernos de Solubilizacion de Medicamentos Organicos
-
Marini-Bettolo G.B. Metodos Modernos de Solubilizacion de Medicamentos Organicos. Ann. Asoc. Quim. Pharm. Urugay. 1948, 50:3-17.
-
(1948)
Ann. Asoc. Quim. Pharm. Urugay.
, vol.50
, pp. 3-17
-
-
Marini-Bettolo, G.B.1
-
4
-
-
0001889919
-
Prodrugs: an overview and definition
-
American Chemical Society, Washington, DC, T. Higuchi, V. Stella (Eds.)
-
Stella V. Prodrugs: an overview and definition. Prodrugs as Novel Drug Delivery Systems 1975, Vol. 14:1-115. American Chemical Society, Washington, DC. T. Higuchi, V. Stella (Eds.).
-
(1975)
Prodrugs as Novel Drug Delivery Systems
, vol.14
, pp. 1-115
-
-
Stella, V.1
-
6
-
-
0004144022
-
-
Chapman and Hall, London, pp. 403-440
-
Albert A. Selective Toxicity 1979, Chapman and Hall, London, pp. 403-440.
-
(1979)
Selective Toxicity
-
-
Albert, A.1
-
7
-
-
0011896187
-
Recent advances in anti-infective agents
-
Academic Press, San Diego, CA, J.A. Bristol (Ed.)
-
Hammond M.L. Recent advances in anti-infective agents. Annu. Rep. Med. Chem. 1993, Vol. 28:119-130. Academic Press, San Diego, CA. J.A. Bristol (Ed.).
-
(1993)
Annu. Rep. Med. Chem.
, vol.28
, pp. 119-130
-
-
Hammond, M.L.1
-
8
-
-
0345449099
-
Drugs interacting with the glycine binding site
-
Verlag Helvetica Chemica Acta/VHC, Basel, Weinheim, B. Testa, E. Kyburz, W. Fuhrer, R. Giger (Eds.)
-
Leeson P.D., Carling R.W., Kulagowski J.J., Mawer I.M., Moore K.W., Moseley A.M., Rowley M., Smith J.D., Stevenson G.I., Williams B.J., Baker R., Foster A.C., Kemp J.A., Tricklebank M.D. Drugs interacting with the glycine binding site. Perspectives in Medicinal Chemistry 1993, 239-257. Verlag Helvetica Chemica Acta/VHC, Basel, Weinheim. B. Testa, E. Kyburz, W. Fuhrer, R. Giger (Eds.).
-
(1993)
Perspectives in Medicinal Chemistry
, pp. 239-257
-
-
Leeson, P.D.1
Carling, R.W.2
Kulagowski, J.J.3
Mawer, I.M.4
Moore, K.W.5
Moseley, A.M.6
Rowley, M.7
Smith, J.D.8
Stevenson, G.I.9
Williams, B.J.10
Baker, R.11
Foster, A.C.12
Kemp, J.A.13
Tricklebank, M.D.14
-
9
-
-
0033916946
-
Water-soluble, core-modified porphyrins as novel, longer-wavelength-absorbing sensitizers for photodynamic therapy
-
Stilts C.E., Nelen M.I., Hilmey D.G., Davies S., Gollnick S.O., Oseroff A.R., Gibson S.L., Hilf R., Detty M.R. Water-soluble, core-modified porphyrins as novel, longer-wavelength-absorbing sensitizers for photodynamic therapy. J. Med. Chem. 2000, 43:2403-2410.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2403-2410
-
-
Stilts, C.E.1
Nelen, M.I.2
Hilmey, D.G.3
Davies, S.4
Gollnick, S.O.5
Oseroff, A.R.6
Gibson, S.L.7
Hilf, R.8
Detty, M.R.9
-
10
-
-
0028323564
-
Second-generation benzodiazepine CCK-B antagonists. Development of subnanomolar analogs with selectivity and water solubility
-
Bock M.G., DiPardo R.M., Mellin E.C., Newton R.C., Veber D.F., Freedman S.B. Second-generation benzodiazepine CCK-B antagonists. Development of subnanomolar analogs with selectivity and water solubility. J. Med. Chem. 1994, 37:722-724.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 722-724
-
-
Bock, M.G.1
DiPardo, R.M.2
Mellin, E.C.3
Newton, R.C.4
Veber, D.F.5
Freedman, S.B.6
-
11
-
-
33845371870
-
Potent and orally bioavailable 8-bicyclo[2.2.2]octylxanthines as adenosine A1 receptor antagonists
-
Kiesman W.F., Zhao J., Conlon P.R., Dowling J.E., Petter R.C., Lutterodt F., Jin X., Smits G., Fure M., Jayarag A. Potent and orally bioavailable 8-bicyclo[2.2.2]octylxanthines as adenosine A1 receptor antagonists. J. Med. Chem. 2006, 49:7119-7131.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 7119-7131
-
-
Kiesman, W.F.1
Zhao, J.2
Conlon, P.R.3
Dowling, J.E.4
Petter, R.C.5
Lutterodt, F.6
Jin, X.7
Smits, G.8
Fure, M.9
Jayarag, A.10
-
13
-
-
33947438473
-
Certain N -alkyl, N -carboxyalkyl and N -hydroxyalkyl derivatives of 4,4 prime; -diaminodiphenyl sulfone
-
Jackson E.L. Certain N -alkyl, N -carboxyalkyl and N -hydroxyalkyl derivatives of 4,4' -diaminodiphenyl sulfone. J. Am. Chem. Soc. 1948, 70:680-684.
-
(1948)
J. Am. Chem. Soc.
, vol.70
, pp. 680-684
-
-
Jackson, E.L.1
-
14
-
-
84882477984
-
-
US Patent 1,993,039 (March 5, 1935, to Winthrop Chemical Company, Inc., New York)
-
J. Reitmann, Aliphatic amine salts of halogenated pyridones containing an acid group. US Patent 1,993,039 (March 5, 1935, to Winthrop Chemical Company, Inc., New York), 1935.
-
(1935)
Aliphatic amine salts of halogenated pyridones containing an acid group
-
-
Reitmann, J.1
-
15
-
-
33947435834
-
Organic compounds in chemotherapy. II. The preparation of formaldehyde sulfoxylate derivatives of sulfanilamide and of amino compounds
-
Bauer H. Organic compounds in chemotherapy. II. The preparation of formaldehyde sulfoxylate derivatives of sulfanilamide and of amino compounds. J. Am. Chem. Soc. 1939, 61:617-618.
-
(1939)
J. Am. Chem. Soc.
, vol.61
, pp. 617-618
-
-
Bauer, H.1
-
16
-
-
0023555532
-
Antimalarial activity of new water-soluble dihydroartemisin derivatives
-
Lin A.J., Klayman D.L., Milhous W. Antimalarial activity of new water-soluble dihydroartemisin derivatives. J. Med. Chem. 1987, 30:2147-2150.
-
(1987)
J. Med. Chem.
, vol.30
, pp. 2147-2150
-
-
Lin, A.J.1
Klayman, D.L.2
Milhous, W.3
-
17
-
-
0030963326
-
Antimalarial activity of new dihydroartemisin derivatives. 7. 4-(p -substituted phenyl)-4(R or S)-[10 ( alpha; or beta;)-dihydroartemisinoxy]butyric acids
-
Lin A.J., Sikry A.B., Kyle D.E. Antimalarial activity of new dihydroartemisin derivatives. 7. 4-(p -substituted phenyl)-4(R or S)-[10 (α or β)-dihydroartemisinoxy]butyric acids. J. Med. Chem. 1997, 40:1396-1400.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 1396-1400
-
-
Lin, A.J.1
Sikry, A.B.2
Kyle, D.E.3
-
18
-
-
0024360869
-
Antimalarial activity of new water-soluble dihydroartemisin derivatives. 2. Stereospecificity of the ether side chain
-
Lin A.J., Lee M., Klayman D.L. Antimalarial activity of new water-soluble dihydroartemisin derivatives. 2. Stereospecificity of the ether side chain. J. Med. Chem. 1989, 32:1249-1252.
-
(1989)
J. Med. Chem.
, vol.32
, pp. 1249-1252
-
-
Lin, A.J.1
Lee, M.2
Klayman, D.L.3
-
19
-
-
0013787343
-
Action of some steroids on the central nervous system of the mouse. I. Synthetic methods
-
Coker J.D., Elks J., May P.J., Nice F.A., Phillips G.H., Wall W.F. Action of some steroids on the central nervous system of the mouse. I. Synthetic methods. J. Med. Chem. 1965, 8:417-425.
-
(1965)
J. Med. Chem.
, vol.8
, pp. 417-425
-
-
Coker, J.D.1
Elks, J.2
May, P.J.3
Nice, F.A.4
Phillips, G.H.5
Wall, W.F.6
-
20
-
-
84882478721
-
Sur l'activite acute; analge acute;sique et antiinflammatoire des 4-(2 prime; -alcoxycarbonyl phe acute;nylamino) quinole acute;i die;nes
-
Allais A., Rousseau G., Girault P., Mathieu J., Peterfalvi M., Branceni D., Azadian-Boulanger G., Chiffl L., Jequier R. Sur l'activité analgésique et antiinflammatoire des 4-(2' -alcoxycarbonyl phénylamino) quinoléïnes. E ur. J. Med. Chem. 1966, 12:65-70.
-
(1966)
E ur. J. Med. Chem.
, vol.12
, pp. 65-70
-
-
Allais, A.1
Rousseau, G.2
Girault, P.3
Mathieu, J.4
Peterfalvi, M.5
Branceni, D.6
Azadian-Boulanger, G.7
Chiffl, L.8
Jequier, R.9
-
21
-
-
0004228420
-
-
American Society of Hospital Pharmacists, Bethesda, MD
-
Trissel L.A. Handbook on Injectable Drugs 2007, American Society of Hospital Pharmacists, Bethesda, MD. 14th Edition.
-
(2007)
Handbook on Injectable Drugs
-
-
Trissel, L.A.1
-
22
-
-
0019475132
-
Initial rate studies of hydrolysis and acyl migration in methylprednisolone 21-hemisuccinate and 17- hemisuccinate
-
Anderson B.D., Taphouse V. Initial rate studies of hydrolysis and acyl migration in methylprednisolone 21-hemisuccinate and 17- hemisuccinate. J. Pharm. Sci. 1981, 70:181-186.
-
(1981)
J. Pharm. Sci.
, vol.70
, pp. 181-186
-
-
Anderson, B.D.1
Taphouse, V.2
-
23
-
-
0021254008
-
Carboxyl group catalysis of acyl transfer reactions in corticosteroid 17- and 21-monoesters
-
Anderson B.D., Conradi R.A., Lambert J.W. Carboxyl group catalysis of acyl transfer reactions in corticosteroid 17- and 21-monoesters. J. Pharm. Sci. 1984, 73:604-611.
-
(1984)
J. Pharm. Sci.
, vol.73
, pp. 604-611
-
-
Anderson, B.D.1
Conradi, R.A.2
Lambert, J.W.3
-
24
-
-
0014747573
-
Rearrangement of chloramphenicol-3-monosuccinate
-
Sandman B., Szulczewski D., Winheuser J., Higuchi T. Rearrangement of chloramphenicol-3-monosuccinate. J. Pharm. Sci. 1970, 59:427-429.
-
(1970)
J. Pharm. Sci.
, vol.59
, pp. 427-429
-
-
Sandman, B.1
Szulczewski, D.2
Winheuser, J.3
Higuchi, T.4
-
25
-
-
0026770939
-
Evidence for an additional intracellular site of action of probucol in the prevention of oxidative modification of low density lipoprotein. Use of a new water-soluble probucol derivative
-
Parthasarathy S. Evidence for an additional intracellular site of action of probucol in the prevention of oxidative modification of low density lipoprotein. Use of a new water-soluble probucol derivative. J. Clin. Invest. 1992, 89:1618-1621.
-
(1992)
J. Clin. Invest.
, vol.89
, pp. 1618-1621
-
-
Parthasarathy, S.1
-
26
-
-
0021956174
-
Strategies in the design of solution-stable, water-soluble prodrugs III: Influence of the pro-moiety on the bioconversion of 21-esters of corticosteroids
-
Anderson B.D., Conradi R.A., Spilman C.H., Forbes A.D. Strategies in the design of solution-stable, water-soluble prodrugs III: Influence of the pro-moiety on the bioconversion of 21-esters of corticosteroids. J. Pharm. Sci. 1985, 74:382-387.
-
(1985)
J. Pharm. Sci.
, vol.74
, pp. 382-387
-
-
Anderson, B.D.1
Conradi, R.A.2
Spilman, C.H.3
Forbes, A.D.4
-
27
-
-
0014867174
-
Factors influencing solvolysis of corticosteroid-21-phosphate esters
-
Flynn G.L., Lamb D.J. Factors influencing solvolysis of corticosteroid-21-phosphate esters. J. Pharm. Sci. 1970, 59:1433-1438.
-
(1970)
J. Pharm. Sci.
, vol.59
, pp. 1433-1438
-
-
Flynn, G.L.1
Lamb, D.J.2
-
28
-
-
33746446182
-
Comparative studies on absorption and metabolic disposal of water-soluble corticosteroid esters
-
Melby J.C., St Cyr M. Comparative studies on absorption and metabolic disposal of water-soluble corticosteroid esters. Metabolism 1961, 10:75-82.
-
(1961)
Metabolism
, vol.10
, pp. 75-82
-
-
Melby, J.C.1
St Cyr, M.2
-
29
-
-
65249169622
-
Synthesis of 3-phosphoric ester of l -ascorbic acid
-
Cutolo E., Larizza A. Synthesis of 3-phosphoric ester of l -ascorbic acid. Gazz. Chim. Ital. 1961, 91:964-972.
-
(1961)
Gazz. Chim. Ital.
, vol.91
, pp. 964-972
-
-
Cutolo, E.1
Larizza, A.2
-
30
-
-
84882528631
-
-
German Patent 1 110 646 (July 13, 1961; E. Merck A.G. Darmstadt)
-
Wenz, A., Göttmann, G., Koop, H. Verfahren zur Herstellung der freien Base und der Salze des Aneurin-orthophosphor-säureesters. German Patent 1 110 646 (July 13, 1961; E. Merck A.G. Darmstadt), 1961.
-
(1961)
Verfahren zur Herstellung der freien Base und der Salze des Aneurin-orthophosphor-säureesters
-
-
Wenz, A.1
Göttmann, G.2
Koop, H.3
-
31
-
-
84882464726
-
-
German Patent 1,130,811 (April 14, 1960 to Sankyo Kabushiki Kaisha, Tokyo)
-
Ito, A. Hamanaka, W. Takagi, H. Wada, T. Kawada, T. Verfahren zur Herstellung eines Acylierungsproduktes von Vitamin-B 1-orthophosphorsäureester und Salzen davon. German Patent 1,130,811 (April 14, 1960 to Sankyo Kabushiki Kaisha, Tokyo), 1960.
-
(1960)
Verfahren zur Herstellung eines Acylierungsproduktes von Vitamin-B 1-orthophosphorsäureester und Salzen davon
-
-
Ito, A.1
Hamanaka, W.2
Takagi, H.3
Wada, T.4
Kawada, T.5
-
32
-
-
0344288058
-
A new thiamine derivative, S -benzoylthiamine O -monophosphate
-
Wada T., Tagaki H., Minakami H., Hamanaka W., Okamoto K., Ito A., Sahashi Y. A new thiamine derivative, S -benzoylthiamine O -monophosphate. Science 1961, 134:195-196.
-
(1961)
Science
, vol.134
, pp. 195-196
-
-
Wada, T.1
Tagaki, H.2
Minakami, H.3
Hamanaka, W.4
Okamoto, K.5
Ito, A.6
Sahashi, Y.7
-
33
-
-
84981839369
-
Einfache Synthese kristallisierter Lactoflavin-5 prime; -phosphorsa die;ure (Coferment des Flavinenzyms)
-
Viscontini M., Ebnoether C., Karrer P. Einfache Synthese kristallisierter Lactoflavin-5' -phosphorsäure (Coferment des Flavinenzyms). Helv. Chim. Acta 1952, 35:457-459.
-
(1952)
Helv. Chim. Acta
, vol.35
, pp. 457-459
-
-
Viscontini, M.1
Ebnoether, C.2
Karrer, P.3
-
34
-
-
84882468662
-
-
US Patent 2,407,823 (September 17, 1946 to Research Corporation, New York)
-
L.F. Fieser, Antihemorrhagic esters and methods for Producing the Same. US Patent 2,407,823 (September 17, 1946 to Research Corporation, New York), 1946.
-
(1946)
Antihemorrhagic esters and methods for Producing the Same
-
-
Fieser, L.F.1
-
35
-
-
0034704822
-
Phosphorylated morpholine acetal human neurokinin-1 receptor antagonists as watersoluble prodrugs
-
Hale J.J., Mills S.G., MacCoss M., Dorn C.P., Finke P.E., Budhu R.J., Reamer R.A., Huskey S.W., Luffer-Atlas D., Dean B.J., McGowan E.M., Feeney W.P., Chiu LeeS.H., Cascieri M.A., Chicchi G.G., Kurtz M.M., Sadowski S., Ber E., Tattersall F.D., Rupniak N.M.J., Williams A.R., Rycroft W., Hargreaves R., Metzger J.M., MacIntyre D.E. Phosphorylated morpholine acetal human neurokinin-1 receptor antagonists as watersoluble prodrugs. J. Med. Chem. 2000, 43:1234-1241.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1234-1241
-
-
Hale, J.J.1
Mills, S.G.2
MacCoss, M.3
Dorn, C.P.4
Finke, P.E.5
Budhu, R.J.6
Reamer, R.A.7
Huskey, S.W.8
Luffer-Atlas, D.9
Dean, B.J.10
McGowan, E.M.11
Feeney, W.P.12
Chiu, L.13
Cascieri, M.A.14
Chicchi, G.G.15
Kurtz, M.M.16
Sadowski, S.17
Ber, E.18
Tattersall, F.D.19
Rupniak, N.M.J.20
Williams, A.R.21
Rycroft, W.22
Hargreaves, R.23
Metzger, J.M.24
MacIntyre, D.E.25
more..
-
36
-
-
0027220895
-
Peptidomimetic HIV protease inhibitors: phosphate prodrugs with improved biological activities
-
Chong K.-T., Ruwart M.J., Hinshaw R.R., Wilkinson K.F., Rush B.D., Yancey M.F., Strohbach J.W., Thaisrivongs S. Peptidomimetic HIV protease inhibitors: phosphate prodrugs with improved biological activities. J. Med. Chem. 1993, 36:2575-2577.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2575-2577
-
-
Chong, K.-T.1
Ruwart, M.J.2
Hinshaw, R.R.3
Wilkinson, K.F.4
Rush, B.D.5
Yancey, M.F.6
Strohbach, J.W.7
Thaisrivongs, S.8
-
38
-
-
18844385474
-
O -Phenylene phosphochloridate. A convenient phosphorylating agent
-
Khawaja T.A., Reese C.B. o -Phenylene phosphochloridate. A convenient phosphorylating agent. J. Am. Chem. Soc. 1966, 88:3446-3447.
-
(1966)
J. Am. Chem. Soc.
, vol.88
, pp. 3446-3447
-
-
Khawaja, T.A.1
Reese, C.B.2
-
39
-
-
37049122339
-
A Convenient general procedure for the conversion of alcohols into their monophosphate esters
-
Khawaja T.A., Reese C.B., Stewart J.C.M. A Convenient general procedure for the conversion of alcohols into their monophosphate esters. J. Chem. Soc. (C) 1970, 2090-2100.
-
(1970)
J. Chem. Soc. (C)
, pp. 2090-2100
-
-
Khawaja, T.A.1
Reese, C.B.2
Stewart, J.C.M.3
-
40
-
-
0016699204
-
2-(N, N -diethylamino)-4-nitrophenyl phosphate and its use in the selective phosphorylation of unprotected nucleosides
-
Taguchi Y., Mushika Y. 2-(N, N -diethylamino)-4-nitrophenyl phosphate and its use in the selective phosphorylation of unprotected nucleosides. Tetrahedron Lett 1975, 24:1913-1916.
-
(1975)
Tetrahedron Lett
, vol.24
, pp. 1913-1916
-
-
Taguchi, Y.1
Mushika, Y.2
-
41
-
-
85004732234
-
Phase-transfer-catalysed halogenation of di- t -butyl phosphite. preparation of di- t -butyl phosphorohalidates
-
Gajda T., Zwierzak A. Phase-transfer-catalysed halogenation of di- t -butyl phosphite. preparation of di- t -butyl phosphorohalidates. Synthesis 1976, 243-244.
-
(1976)
Synthesis
, pp. 243-244
-
-
Gajda, T.1
Zwierzak, A.2
-
42
-
-
79958294731
-
Di- t -butyl phosphorobromidate. A new selective phosphorylating agent containing acid-labile protecting groups
-
Gajda T., Zwierzak A. Di- t -butyl phosphorobromidate. A new selective phosphorylating agent containing acid-labile protecting groups. Synthesis 1977, 623-625.
-
(1977)
Synthesis
, pp. 623-625
-
-
Gajda, T.1
Zwierzak, A.2
-
43
-
-
0000277376
-
2-Cyanoethyl phosphate and its use in the synthesis of phosphate esters
-
Tener G.M. 2-Cyanoethyl phosphate and its use in the synthesis of phosphate esters. J. Am. Chem. Soc. 1961, 83:159-168.
-
(1961)
J. Am. Chem. Soc.
, vol.83
, pp. 159-168
-
-
Tener, G.M.1
-
44
-
-
0000275866
-
The synthesis of orotidine-5 prime; phosphate
-
Moffatt J.G. The synthesis of orotidine-5' phosphate. J. Am. Chem. Soc. 1963, 85:1118-1123.
-
(1963)
J. Am. Chem. Soc.
, vol.85
, pp. 1118-1123
-
-
Moffatt, J.G.1
-
45
-
-
9744275510
-
A direct method for the preparation of steroid-21-phosphates
-
Brownfield R.B., Shultz W. A direct method for the preparation of steroid-21-phosphates. Steroids 1963, 2:597-603.
-
(1963)
Steroids
, vol.2
, pp. 597-603
-
-
Brownfield, R.B.1
Shultz, W.2
-
46
-
-
37049054756
-
Phosphoramidic halides; phosphorylating agents derived from morpholine
-
Montgomery H.A.C., Turnbull J.H. Phosphoramidic halides; phosphorylating agents derived from morpholine. J. Chem. Soc. 1958, 1963-1967.
-
(1958)
J. Chem. Soc.
, pp. 1963-1967
-
-
Montgomery, H.A.C.1
Turnbull, J.H.2
-
48
-
-
33947447339
-
Water-soluble antihemorrhagic esters
-
Fieser L.F., Fry E.M. Water-soluble antihemorrhagic esters. J. Am. Chem. Soc. 1940, 62:228-229.
-
(1940)
J. Am. Chem. Soc.
, vol.62
, pp. 228-229
-
-
Fieser, L.F.1
Fry, E.M.2
-
49
-
-
84882500817
-
-
German Auslegeschrift 1,090,669 (January 11, 1958 to Arzneimittelfabrik Krewel-Leuffen G.m.b. H., Eitorf/Sieg)
-
Stieglitz, E.; M. Matz, Verfahren zur Herstellung von Xanthinalkylschwefelsäuren oder deren Salze. German Auslegeschrift 1,090,669 (January 11, 1958 to Arzneimittelfabrik Krewel-Leuffen G.m.b. H., Eitorf/Sieg), 1958.
-
(1958)
Verfahren zur Herstellung von Xanthinalkylschwefelsäuren oder deren Salze
-
-
Stieglitz, E.1
Matz, M.2
-
50
-
-
0019441202
-
A comparison of the bioavailability and potency of dexamethazone phosphate and sulphate in man
-
Miyabo S., Nakamura T., Kuwazima S., Kishida S. A comparison of the bioavailability and potency of dexamethazone phosphate and sulphate in man. E ur. J. Clin. Pharmacol. 1981, 20:277-282.
-
(1981)
E ur. J. Clin. Pharmacol.
, vol.20
, pp. 277-282
-
-
Miyabo, S.1
Nakamura, T.2
Kuwazima, S.3
Kishida, S.4
-
51
-
-
0020680150
-
Evaluation of the prodrug potential of the sulfate ester of acetaminophen and 3-hydroxymethyl-phenytoin
-
Williams D.B., Varia S.A., Stella V.J., Pitman I.H. Evaluation of the prodrug potential of the sulfate ester of acetaminophen and 3-hydroxymethyl-phenytoin. Int. J. Pharm. 1983, 14:113-120.
-
(1983)
Int. J. Pharm.
, vol.14
, pp. 113-120
-
-
Williams, D.B.1
Varia, S.A.2
Stella, V.J.3
Pitman, I.H.4
-
52
-
-
0015117766
-
The reaction of vitamin K 3 with sodium bisulfite
-
Greenberg F.H., Leung K.K., Leung M. The reaction of vitamin K 3 with sodium bisulfite. J. Chem. Ed. 1971, 48:632-634.
-
(1971)
J. Chem. Ed.
, vol.48
, pp. 632-634
-
-
Greenberg, F.H.1
Leung, K.K.2
Leung, M.3
-
54
-
-
0026564081
-
6 -sulfoalkyl derivatives of adenosine: water-soluble and peripherally selective adenosine agonists
-
6 -sulfoalkyl derivatives of adenosine: water-soluble and peripherally selective adenosine agonists. J. Med. Chem. 1992, 35:4143-4149.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 4143-4149
-
-
Jacobson, K.A.1
Nikodijevic, O.2
Ji, X.-D.3
Berkich, D.A.4
Eveleth, D.5
Dean, R.L.6
Hiramatsu, K.-I.7
Kassel, N.F.8
van Galen, P.J.M.9
Lee, K.S.10
Bartus, R.T.11
Daly, J.D.12
LaNoue, K.F.13
Maillard, M.14
-
55
-
-
84882548768
-
-
Anonymous, German Patent 209,695 (8 May 1907, to Roberto Lepetit, Garessio, Italy)
-
Anonymous. Verfahren zur Darstellung von p-äthoxyphenylaminomethylschwefligsauren Salzen. German Patent 209,695 (8 May 1907, to Roberto Lepetit, Garessio, Italy), 1907.
-
(1907)
Verfahren zur Darstellung von p-äthoxyphenylaminomethylschwefligsauren Salzen
-
-
-
58
-
-
77955551925
-
A new sulphonamide (sulfonamide E.O.S.)
-
Mutch N. A new sulphonamide (sulfonamide E.O.S.). B r. Med. J. 1941, 2:503-507.
-
(1941)
B r. Med. J.
, vol.2
, pp. 503-507
-
-
Mutch, N.1
-
59
-
-
84882508659
-
The preparation of promin
-
(C.A. 40, 4687 7, 1946).
-
Jain B.C., Iyer B.H., Guha P.C. The preparation of promin. Sci. Cult. 1946, 11:568-569. (C.A. 40, 4687 7, 1946).
-
(1946)
Sci. Cult.
, vol.11
, pp. 568-569
-
-
Jain, B.C.1
Iyer, B.H.2
Guha, P.C.3
-
60
-
-
84882509796
-
-
Anonymous. Soluble diphenylsulfone. Swiss Patent 234,108 (December 1, 1944; Aktien-Gesellschaft vorm. B. Siegfried)
-
Anonymous. Soluble diphenylsulfone. Swiss Patent 234,108 (December 1, 1944; Aktien-Gesellschaft vorm. B. Siegfried), 1949.
-
(1949)
-
-
-
61
-
-
84882481973
-
-
US Patent 2,193,788 (March 19, 1940; Winthrop Chemical Company, Inc.)
-
Bockmühl, M., W. Krohs, F. Racke, Windisch, K. N -methylsulphites and N -methanesulphinic acid salts of 1-aryl-2,3-dialkyl-4- alkylaminopyrazolones. US Patent 2,193,788 (March 19, 1940; Winthrop Chemical Company, Inc.), 1940.
-
(1940)
N -methylsulphites and N -methanesulphinic acid salts of 1-aryl-2,3-dialkyl-4- alkylaminopyrazolones
-
-
Bockmühl, M.1
Krohs, W.2
Racke, F.3
Windisch, K.4
-
63
-
-
0014077792
-
Absorption and activity of some derivatives of griseofulvin
-
Fischer L.J., Riegelman S. Absorption and activity of some derivatives of griseofulvin. J. Pharm. Sci. 1967, 56:469-476.
-
(1967)
J. Pharm. Sci.
, vol.56
, pp. 469-476
-
-
Fischer, L.J.1
Riegelman, S.2
-
64
-
-
0023634385
-
Oxime-metabolizing activity of liver aldehyde oxidase
-
Tatsumi K., Ishigai M. Oxime-metabolizing activity of liver aldehyde oxidase. Arch. Biochem. Biophys. 1987, 253:413-418.
-
(1987)
Arch. Biochem. Biophys.
, vol.253
, pp. 413-418
-
-
Tatsumi, K.1
Ishigai, M.2
-
66
-
-
84882516982
-
Basische tricyclische Oximinoa die;ther und ihre pharmakologischen Eigenschaften
-
Aichinger G., Behner O., Hoffmeister F., Schütz S. Basische tricyclische Oximinoäther und ihre pharmakologischen Eigenschaften. Arzneim.-Forsch. 1969, 19:838-845.
-
(1969)
Arzneim.-Forsch.
, vol.19
, pp. 838-845
-
-
Aichinger, G.1
Behner, O.2
Hoffmeister, F.3
Schütz, S.4
-
67
-
-
0026099599
-
Synthesis of watersoluble (aminoalkyl)camptothecin analogues: inhibition of topoisomerase I and antitumor activity
-
Kingsbury W.D., Boehm J.C., Jakas D.R., Holden K.G., Hecht S.M., Gallagher G., Caranfa M.J., McCabe F.L., Faucette L.F., Johnson R.K., Hertzberg R.P. Synthesis of watersoluble (aminoalkyl)camptothecin analogues: inhibition of topoisomerase I and antitumor activity. J. Med. Chem. 1991, 34:98-107.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 98-107
-
-
Kingsbury, W.D.1
Boehm, J.C.2
Jakas, D.R.3
Holden, K.G.4
Hecht, S.M.5
Gallagher, G.6
Caranfa, M.J.7
McCabe, F.L.8
Faucette, L.F.9
Johnson, R.K.10
Hertzberg, R.P.11
-
68
-
-
0028314649
-
High-affinity and potent, water-soluble 5-amino-1,4-benzodiazepine CCKB/gastrin receptor antagonists containing a cationic solubilizing group
-
Showell G.A., Bourrain S., Neduvelil J.G., Fletcher S.R., Freedman S.B., Kemp J.A., Marshall G.R., Patel S., Smith A.J., Matassa V.G. High-affinity and potent, water-soluble 5-amino-1,4-benzodiazepine CCKB/gastrin receptor antagonists containing a cationic solubilizing group. J. Med. Chem. 1994, 37:719-721.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 719-721
-
-
Showell, G.A.1
Bourrain, S.2
Neduvelil, J.G.3
Fletcher, S.R.4
Freedman, S.B.5
Kemp, J.A.6
Marshall, G.R.7
Patel, S.8
Smith, A.J.9
Matassa, V.G.10
-
69
-
-
0022364754
-
Cyclic guanidines. 17. Novel (N -substituted amino)imidazo[2,1- b ] quinazolin-2-ones: water-soluble platelet aggregation inhibitors
-
Ishikawa F., Saegusa J., Inamura K., Sakuma K., Ashida S.-I. Cyclic guanidines. 17. Novel (N -substituted amino)imidazo[2,1- b ] quinazolin-2-ones: water-soluble platelet aggregation inhibitors. J. Med. Chem. 1985, 28:1387-1393.
-
(1985)
J. Med. Chem.
, vol.28
, pp. 1387-1393
-
-
Ishikawa, F.1
Saegusa, J.2
Inamura, K.3
Sakuma, K.4
Ashida, S.-I.5
-
70
-
-
0026783826
-
7,8-Dihydro-8-ethyl-2-(3-noradamantyl)-4-propyl-1H-imidazo[2,1- i ]purin-5(4H)-one: a potent and water-soluble adenosine A1 antagonist
-
Suzuki F., Shimada J., Nonaka H., Ishii A., Shiozaki S., Ichikawa S., Ono E. 7,8-Dihydro-8-ethyl-2-(3-noradamantyl)-4-propyl-1H-imidazo[2,1- i ]purin-5(4H)-one: a potent and water-soluble adenosine A1 antagonist. J. Med. Chem. 1992, 35:3572-3581.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 3572-3581
-
-
Suzuki, F.1
Shimada, J.2
Nonaka, H.3
Ishii, A.4
Shiozaki, S.5
Ichikawa, S.6
Ono, E.7
-
71
-
-
33846928166
-
2 prime; -activated potassium (maxi-K) channels, identification, solubility, and SAR
-
2' -activated potassium (maxi-K) channels, identification, solubility, and SAR. J. Med. Chem. 2007, 50:528-542.
-
(2007)
J. Med. Chem.
, vol.50
, pp. 528-542
-
-
Romine, J.L.1
Martin, S.W.2
Meanwell, S.A.3
Gribkoff, V.K.4
Boissard, C.G.5
Dworetzky, S.I.6
Natale, J.7
Moon, S.8
Ortiz, A.9
Yeleswaram, S.10
Pajor, L.11
Gao, Q.12
Starrett, J.E.13
-
72
-
-
0017672631
-
Peptido-aminobenzophenones-novel latentiated benzo-1,4-diazepines
-
Hassall C.H., Holmes S.W., Johnson W.H., Kröhn A., Smithen C.E., Thomas W.A. Peptido-aminobenzophenones-novel latentiated benzo-1,4-diazepines. Experientia 1977, 33:1492-1493.
-
(1977)
Experientia
, vol.33
, pp. 1492-1493
-
-
Hassall, C.H.1
Holmes, S.W.2
Johnson, W.H.3
Kröhn, A.4
Smithen, C.E.5
Thomas, W.A.6
-
73
-
-
0023677574
-
Cardiovascular effects of new water-soluble derivatives of forskolin
-
Khandelwal Y., Rajeshwari K., Rajagopalan R., Swamy L., Dohadwalla A.N., de Souza N.J., Rupp R.H. Cardiovascular effects of new water-soluble derivatives of forskolin. J. Med. Chem. 1988, 31:1872-1879.
-
(1988)
J. Med. Chem.
, vol.31
, pp. 1872-1879
-
-
Khandelwal, Y.1
Rajeshwari, K.2
Rajagopalan, R.3
Swamy, L.4
Dohadwalla, A.N.5
de Souza, N.J.6
Rupp, R.H.7
-
74
-
-
84918426296
-
Improved rectal and parenteral delivery of allopurinol using the prodrug approach
-
Bundgaard H., Falch E. Improved rectal and parenteral delivery of allopurinol using the prodrug approach. A rch. Pharm. Chem. Sci. Ed. 1985, 13:39-48.
-
(1985)
A rch. Pharm. Chem. Sci. Ed.
, vol.13
, pp. 39-48
-
-
Bundgaard, H.1
Falch, E.2
-
75
-
-
0024367481
-
A novel solution-stable, watersoluble prodrug type for drugs containing a hydroxyl or an NH-acidic group
-
Bundgaard H., Falch E., Jensen E. A novel solution-stable, watersoluble prodrug type for drugs containing a hydroxyl or an NH-acidic group. J. Med. Chem. 1989, 32:2503-2507.
-
(1989)
J. Med. Chem.
, vol.32
, pp. 2503-2507
-
-
Bundgaard, H.1
Falch, E.2
Jensen, E.3
-
76
-
-
0021915751
-
Strategies in the design of solution-stable, water-soluble prodrugs I: a physical-organic approach to pro-moiety selection for 21-esters of corticosteroids
-
Anderson B.D., Conradi R.A., Knuth K.E. Strategies in the design of solution-stable, water-soluble prodrugs I: a physical-organic approach to pro-moiety selection for 21-esters of corticosteroids. J. Pharm. Sci. 1985, 74:365-374.
-
(1985)
J. Pharm. Sci.
, vol.74
, pp. 365-374
-
-
Anderson, B.D.1
Conradi, R.A.2
Knuth, K.E.3
-
77
-
-
0026575017
-
Synthesis, stability, and biological evaluation of water-soluble prodrugs of a new echinocandin lipopeptide. Discovery of a potential clinical agent for the treatment of systemic candidiasis and Pneumocystis carinii pneumonia (PCP)
-
Balkovec J.M., Black R.M., Hammond M.L., Heck J.V., Zambias R.A., Abruzzo G., Bartizal K., Kropp H., Trainor C., Schwartz R.E., McFadden D.C., Nollstadt K.H., Pittarelli L.A., Powles M.A., Schmatz D.M. Synthesis, stability, and biological evaluation of water-soluble prodrugs of a new echinocandin lipopeptide. Discovery of a potential clinical agent for the treatment of systemic candidiasis and Pneumocystis carinii pneumonia (PCP). J. Med. Chem. 1992, 35:194-198.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 194-198
-
-
Balkovec, J.M.1
Black, R.M.2
Hammond, M.L.3
Heck, J.V.4
Zambias, R.A.5
Abruzzo, G.6
Bartizal, K.7
Kropp, H.8
Trainor, C.9
Schwartz, R.E.10
McFadden, D.C.11
Nollstadt, K.H.12
Pittarelli, L.A.13
Powles, M.A.14
Schmatz, D.M.15
-
78
-
-
0011494172
-
Beitrag zur Reaktionsfa die;higheit der 7-Stellung des Theophyllins. 2.Mitt. U die;ber Synthesen in der Theophyllinreihe
-
Klosa J. Beitrag zur Reaktionsfähigheit der 7-Stellung des Theophyllins. 2.Mitt. Über Synthesen in der Theophyllinreihe. Arch. Pharm. 1955, 288:301-303.
-
(1955)
Arch. Pharm.
, vol.288
, pp. 301-303
-
-
Klosa, J.1
-
80
-
-
0026766138
-
Quinolone antibacterial agents. Synthesis and structure-activity relationships of a series of amino acid prodrugs of racemic and chiral 7-(3-amino-1-pyrrolidinyl)quinolones. Highly soluble quinolone prodrugs with in vivo pseudomonas activity
-
Sanchez J.P., Domagala J.M., Heifetz C.L., Priebe S.R., Sesnie J.A., Trehan A.K. Quinolone antibacterial agents. Synthesis and structure-activity relationships of a series of amino acid prodrugs of racemic and chiral 7-(3-amino-1-pyrrolidinyl)quinolones. Highly soluble quinolone prodrugs with in vivo pseudomonas activity. J. Med. Chem. 1992, 35:1764-1773.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1764-1773
-
-
Sanchez, J.P.1
Domagala, J.M.2
Heifetz, C.L.3
Priebe, S.R.4
Sesnie, J.A.5
Trehan, A.K.6
-
81
-
-
0027173188
-
Chemical modification of an antitumor alkaloid, 20(S)-camptothecin: E-lactone ring modified water-soluble derivatives of 7-ethylcamptothecin
-
Sawada S., Yaegashi T., Furuta T., Yokokura T., Miyasaka T. Chemical modification of an antitumor alkaloid, 20(S)-camptothecin: E-lactone ring modified water-soluble derivatives of 7-ethylcamptothecin. Chem. Pharm. Bull. 1993, 41:310-313.
-
(1993)
Chem. Pharm. Bull.
, vol.41
, pp. 310-313
-
-
Sawada, S.1
Yaegashi, T.2
Furuta, T.3
Yokokura, T.4
Miyasaka, T.5
-
82
-
-
0026740226
-
-
Boyd S.A., Fung A.K.L., Baker W.R., Mantei R.A., Armiger Y.-L., Stein H.H., Cohen J., Egan D.A., Barlow J.L., Klinghofer V., Verburg K.M., Martin D.L., Young G.A., Polakowski J.S., Hoffman D.J., Garren K.W., Perun T.J., Kleinert H.D. C-Terminal modifications of nonpeptide renin inhibitors: improved oral bioavailability via modification of physicochemical properties. J. Med. Chem. 1992, 35:1735-1746.
-
(1992)
C-Terminal modifications of nonpeptide renin inhibitors: improved oral bioavailability via modification of physicochemical properties. J. Med. Chem.
, vol.35
, pp. 1735-1746
-
-
Boyd, S.A.1
Fung, A.K.L.2
Baker, W.R.3
Mantei, R.A.4
Armiger, Y.-L.5
Stein, H.H.6
Cohen, J.7
Egan, D.A.8
Barlow, J.L.9
Klinghofer, V.10
Verburg, K.M.11
Martin, D.L.12
Young, G.A.13
Polakowski, J.S.14
Hoffman, D.J.15
Garren, K.W.16
Perun, T.J.17
Kleinert, H.D.18
-
84
-
-
0011441339
-
Zur Darstellung von beta; -Oxyalkyl-dimethyl-purinen; Umsetzung von Theophyllin und Theobromin mit 1,2-Epoxyden
-
Roth H.J. Zur Darstellung von β -Oxyalkyl-dimethyl-purinen; Umsetzung von Theophyllin und Theobromin mit 1,2-Epoxyden. Arch. Pharm. 1959, 292:234-238.
-
(1959)
Arch. Pharm.
, vol.292
, pp. 234-238
-
-
Roth, H.J.1
-
86
-
-
0018889756
-
A new, convenient synthesis of glafenine and floctafenine
-
Mouzin G., Cousse H., Autin J.M. A new, convenient synthesis of glafenine and floctafenine. Synthesis 1980, 12:54-55.
-
(1980)
Synthesis
, vol.12
, pp. 54-55
-
-
Mouzin, G.1
Cousse, H.2
Autin, J.M.3
-
87
-
-
0017691705
-
Zur Chemie von Etofenamat, einem Antiphlogisticum aus der Klasse der N -Arylanthranylsa die;urederivate
-
Boltze K.H., Kreisfeld H. Zur Chemie von Etofenamat, einem Antiphlogisticum aus der Klasse der N -Arylanthranylsäurederivate. Arzneimit.-Forsch.-Drug Des. 1977, 27:1300-1312.
-
(1977)
Arzneimit.-Forsch.-Drug Des.
, vol.27
, pp. 1300-1312
-
-
Boltze, K.H.1
Kreisfeld, H.2
-
88
-
-
84882466992
-
-
US Patent 2,714,608 (August 2, 1955; to Ciba Pharmaceutical Products, Inc., Summit, N.J.)
-
M. Matter, Polyethoxy ethers of isocyclic organic carboxylic acids. US Patent 2,714,608 (August 2, 1955; to Ciba Pharmaceutical Products, Inc., Summit, N.J.), 1955.
-
(1955)
Polyethoxy ethers of isocyclic organic carboxylic acids
-
-
Matter, M.1
-
91
-
-
0015621051
-
Polyethylene glycol derivatives of procaine
-
Weiner B.-Z., Zilkha A. Polyethylene glycol derivatives of procaine. J. Med. Chem. 1973, 16:573-574.
-
(1973)
J. Med. Chem.
, vol.16
, pp. 573-574
-
-
Weiner, B.-Z.1
Zilkha, A.2
-
93
-
-
84882532139
-
-
US Patent 4,349,545 (September 14, 1982; to Roussel-UCLAF)
-
Gouin d'Ambrières, S., A. Lutz, J.C. Gasc, Novel erythromycin a derivatives. US Patent 4,349,545 (September 14, 1982; to Roussel-UCLAF), 1982.
-
(1982)
Novel erythromycin a derivatives
-
-
Gouin d'Ambrières, S.1
Lutz, A.2
Gasc, J.C.3
-
94
-
-
84982058544
-
6. U die;ber Steroide. (33. Mitteilung). U die;ber Glukoside des Desoxy-corticosterons
-
Miescher K., Fischer W.H., Meystre C. 6. Über Steroide. (33. Mitteilung). Über Glukoside des Desoxy-corticosterons. Helv. Chim. Acta 1942, 25:40-42.
-
(1942)
Helv. Chim. Acta
, vol.25
, pp. 40-42
-
-
Miescher, K.1
Fischer, W.H.2
Meystre, C.3
-
95
-
-
84982337600
-
26. U die;ber Steroide. 34. Mitteilung. U die;ber Sacharide des Desoxy-corticosterons II
-
Miescher K., Meystre C. 26. Über Steroide. 34. Mitteilung. Über Sacharide des Desoxy-corticosterons II. H elv. Chim. Acta 1943, 26:224-233.
-
(1943)
H elv. Chim. Acta
, vol.26
, pp. 224-233
-
-
Miescher, K.1
Meystre, C.2
-
96
-
-
84931921358
-
U die;ber Steroide. (35. Mitteilung). Zur Darstellung von Saccharidderivaten der Steroide
-
Meystre C., Miescher K. Über Steroide. (35. Mitteilung). Zur Darstellung von Saccharidderivaten der Steroide. H elv. Chim. Acta 1944, 27:231-236.
-
(1944)
H elv. Chim. Acta
, vol.27
, pp. 231-236
-
-
Meystre, C.1
Miescher, K.2
-
97
-
-
84882472120
-
-
German Offen. 2.242.237 (August 28, 1972; to Toyo Hakka Kogyo Kabushiki Kaishy)
-
T. Higashiyama, I. Sakata, Mentholglykoside, Verfahren zur ihrer Herstellung, ihre Verwendung zur Entwicklung des Pfefferminzgeschmack sowie diese Verbindungen enthaltende Arzneimittel. German Offen. 2.242.237 (August 28, 1972; to Toyo Hakka Kogyo Kabushiki Kaishy), 1972.
-
(1972)
Mentholglykoside, Verfahren zur ihrer Herstellung, ihre Verwendung zur Entwicklung des Pfefferminzgeschmack sowie diese Verbindungen enthaltende Arzneimittel
-
-
Higashiyama, T.1
Sakata, I.2
-
98
-
-
84882512271
-
-
Actualités de Chimie Thérapeutique (Combet-C. Farnoux (Ed.), Société de Chimie Thérapeutique, Châtenay-Malabry
-
C. Chavis, Imbach, J.-L. Sur une méthode de pharmacomodulation: l'utilisation du vecteur sucre. in: Actualités de Chimie Thérapeutique (Combet-C. Farnoux (Ed.), Vol. 5, Société de Chimie Thérapeutique, Châtenay-Malabry, 1977, pp. 3-28.
-
(1977)
Sur une méthode de pharmacomodulation: l'utilisation du vecteur sucre
, vol.5
, pp. 3-28
-
-
Chavis, C.1
Imbach, J.-L.2
-
99
-
-
37049154774
-
N -substituted glycosylamines derived from sulphanilamide and p -aminosalicylic acid
-
Bognar R., Nanasi P. N -substituted glycosylamines derived from sulphanilamide and p -aminosalicylic acid. J. Chem. Soc. 1953, 1703-1708.
-
(1953)
J. Chem. Soc.
, pp. 1703-1708
-
-
Bognar, R.1
Nanasi, P.2
-
100
-
-
33947455546
-
D -Glucuronolactone isonicotinyl hydrazone
-
Sah P. d -Glucuronolactone isonicotinyl hydrazone. J. Am. Chem. Soc. 1953, 75:2512-2513.
-
(1953)
J. Am. Chem. Soc.
, vol.75
, pp. 2512-2513
-
-
Sah, P.1
-
101
-
-
84882515209
-
-
German Patent 2,223,051 (December 13, 1973; to SIR Lab. Chimico Biologici SpA); CA 80, 83529e
-
A. Demetrio, F. Ganzina, M. Magi, E. Serino, E. Paroli, F. Samueli, Antiinflammatory di-(+6/11/2008)glucosamide of 1-(4-chlorobenzoyl)-2-methyl-5-methoxyindole-3-acetic acid. German Patent 2,223,051 (December 13, 1973; to SIR Lab. Chimico Biologici SpA); CA 80, 83529e, 1974.
-
(1974)
Antiinflammatory di-(+6/11/2008)glucosamide of 1-(4-chlorobenzoyl)-2-methyl-5-methoxyindole-3-acetic acid
-
-
Demetrio, A.1
Ganzina, F.2
Magi, M.3
Serino, E.4
Paroli, E.5
Samueli, F.6
-
102
-
-
84882488877
-
-
US Patent 3,701,771 (October 31,1972; to Nyegaard & Co, A/S)
-
T.H. O. Almen, J. Haavaldsen, Nordal, V. N -(2,4,6-triiodobenzoyl)-sugar amines. US Patent 3,701,771 (October 31,1972; to Nyegaard & Co, A/S), 1972.
-
(1972)
N -(2,4,6-triiodobenzoyl)-sugar amines
-
-
Almen, T.H.O.1
Haavaldsen, J.2
Nordal, V.3
-
103
-
-
0017797454
-
Development and evaluation of a new water-soluble iodinated myelographic contrast medium with markedly reduced convulsive effects
-
Hilae S.K., Dauth G.W., Hess K.H., Gilman S. Development and evaluation of a new water-soluble iodinated myelographic contrast medium with markedly reduced convulsive effects. Radiology 1978, 126:417-422.
-
(1978)
Radiology
, vol.126
, pp. 417-422
-
-
Hilae, S.K.1
Dauth, G.W.2
Hess, K.H.3
Gilman, S.4
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