-
1
-
-
0003892409
-
-
Academic Press: New York
-
Sirotnak, F. M., Burchall, J. J., Ensminger, W. B., Montgomery, J. A., Eds. Folate Antagonists as Therapeutic Agents; Academic Press: New York, 1984.
-
(1984)
Folate Antagonists as Therapeutic Agents
-
-
Sirotnak, F.M.1
Burchall, J.J.2
Ensminger, W.B.3
Montgomery, J.A.4
-
2
-
-
0025970198
-
The renewed potential for folate antagonists in contemporary cancer chemotherapy
-
Berman, E. M.; Werbel, L. M. The renewed potential for folate antagonists in contemporary cancer chemotherapy. J. Med. Chem. 1991, 34, 479-485.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 479-485
-
-
Berman, E.M.1
Werbel, L.M.2
-
3
-
-
0025361947
-
Dihydrofolate reductase as a therapeutic target
-
Schweitzer, B. I.; Dicker, A. P.; Bertino, J. R. Dihydrofolate reductase as a therapeutic target. FASEB J. 1990, 4, 2441-2452.
-
(1990)
FASEB J.
, vol.4
, pp. 2441-2452
-
-
Schweitzer, B.I.1
Dicker, A.P.2
Bertino, J.R.3
-
4
-
-
0026619403
-
Antifolates: The next generation
-
Fleming, G. F.; Schilsky, R. L. Antifolates: The next generation. Sem. Oncol. 1993, 11, 707-719.
-
(1993)
Sem. Oncol.
, vol.11
, pp. 707-719
-
-
Fleming, G.F.1
Schilsky, R.L.2
-
5
-
-
0020554087
-
The pharmacology and clinical use of methotrexate
-
Jolivet, J.; Cowan, K. H.; Clendenin, N. J.; Chabner, B. A. The pharmacology and clinical use of methotrexate. N. Engl. J. Med. 1983, 309, 1094-1104.
-
(1983)
N. Engl. J. Med.
, vol.309
, pp. 1094-1104
-
-
Jolivet, J.1
Cowan, K.H.2
Clendenin, N.J.3
Chabner, B.A.4
-
6
-
-
0011087873
-
Design and synthesis of lipophilic antifolates as anticancer agents
-
Sirotnak, F. M., Burchall, J. J., Ensminger, W. B., Montgomery, J. A., Eds.; Academic Press: Orlando, FL
-
Werbel, L. M. Design and synthesis of lipophilic antifolates as anticancer agents. In Folate Antagonists as Therapeutic Agents; Sirotnak, F. M., Burchall, J. J., Ensminger, W. B., Montgomery, J. A., Eds.; Academic Press: Orlando, FL, 1984; Vol. 1, pp 261-287.
-
(1984)
Folate Antagonists as Therapeutic Agents
, vol.1
, pp. 261-287
-
-
Werbel, L.M.1
-
7
-
-
0018138679
-
Lipid-soluble inhibitors of dihydrofolate reductase I. Kinetics, tissue distribution and extent of metabolism of pyrimethamine, metoprine, and etoprine in the rat, dog, and man
-
Cavallito, J. C.; Nichol, C. A.; Brenckman, W. D.; DeAngelis, R. L.; Stickney, D. R.; Simmons, W. S.; Sigel, C. W. Lipid-soluble inhibitors of dihydrofolate reductase I. Kinetics, tissue distribution and extent of metabolism of pyrimethamine, metoprine, and etoprine in the rat, dog, and man. Drug Metab. Disp. 1978, 6, 329-337
-
(1978)
Drug Metab. Disp.
, vol.6
, pp. 329-337
-
-
Cavallito, J.C.1
Nichol, C.A.2
Brenckman, W.D.3
Deangelis, R.L.4
Stickney, D.R.5
Simmons, W.S.6
Sigel, C.W.7
-
8
-
-
0018972242
-
DDMP (2,4-diamino-5-(3′,4′-dichlorophenyl)-6-methylpyrimidine)
-
Hill, B. T.; Price, L. A. DDMP (2,4-diamino-5-(3′,4′-dichlorophenyl)-6-methylpyrimidine). Cancer Treat. Rev. 1980, 7, 95-112.
-
(1980)
Cancer Treat. Rev.
, vol.7
, pp. 95-112
-
-
Hill, B.T.1
Price, L.A.2
-
9
-
-
0020452143
-
Biochemical and chemotherapeutic studies on 2,4-diamino-6-(2,5-dimethoxybenzyl)-5-methylpyrido[2,3-d]pyrimidine (BW301U), a novel lipid-soluble inhibitor of dihydrofolate reductase
-
Duch, D. S.; Edelstein, M. P.; Bowers, S. W.; Nichol, C. A. Biochemical and chemotherapeutic studies on 2,4-diamino-6-(2,5-dimethoxybenzyl)-5-methylpyrido[2,3-d]pyrimidine (BW301U), a novel lipid-soluble inhibitor of dihydrofolate reductase. Cancer Res. 1982, 42, 3987-3994.
-
(1982)
Cancer Res.
, vol.42
, pp. 3987-3994
-
-
Duch, D.S.1
Edelstein, M.P.2
Bowers, S.W.3
Nichol, C.A.4
-
10
-
-
0010246116
-
Preclinical biochemical pharmacology and toxicology of piritrexim, a lipophilic inhibitor of dihydrofolate reductase
-
Sigel, C. W.; Macklin, A. W.; Woolley, J. L., Jr.; Johnson, N. W.; Collier, M. A.; Blum, M. R.; Clendenin, N. J.; Everitt, B. J. M.; Grebe, G.; Mackars, A.; Foss, R. G.; Duch, D. S.; Bowers, S. W.; Nichol, C. A. Preclinical biochemical pharmacology and toxicology of piritrexim, a lipophilic inhibitor of dihydrofolate reductase. Natl. Cancer Instit. Monogr. 1897, 5, 27-35.
-
(1897)
Natl. Cancer Instit. Monogr.
, vol.5
, pp. 27-35
-
-
Sigel, C.W.1
Macklin, A.W.2
Woolley Jr., J.L.3
Johnson, N.W.4
Collier, M.A.5
Blum, M.R.6
Clendenin, N.J.7
Everitt, B.J.M.8
Grebe, G.9
Mackars, A.10
Foss, R.G.11
Duch, D.S.12
Bowers, S.W.13
Nichol, C.A.14
-
11
-
-
0021049802
-
Folate antagonists. 20. Synthesis, antitumor, and antimalarial properties of trimetrexate and related 6-[(phenylamino)methyl]-2,4-quinazolinediamines
-
Elslager, E. F.; Johnson, J. L.; Werbel, L. M. Folate antagonists. 20. Synthesis, antitumor, and antimalarial properties of trimetrexate and related 6-[(phenylamino)methyl]-2,4-quinazolinediamines. J. Med. Chem. 1983, 26, 1753-1760.
-
(1983)
J. Med. Chem.
, vol.26
, pp. 1753-1760
-
-
Elslager, E.F.1
Johnson, J.L.2
Werbel, L.M.3
-
12
-
-
0025816073
-
Update on trimetrexate, a folate antagonist with antineoplastic and antiprotozoal properties
-
Lin, J. T.; Bertino, J. R. Update on trimetrexate, a folate antagonist with antineoplastic and antiprotozoal properties. Cancer Invest. 1991, 9, 159-172.
-
(1991)
Cancer Invest.
, vol.9
, pp. 159-172
-
-
Lin, J.T.1
Bertino, J.R.2
-
13
-
-
0018876119
-
Inhibition of histamine-metabolising enzymes and elevation of histamine levels in tissues by lipid-soluble anticancer folate antagonists
-
Duch, D. S.; Edelstein, M. P.; Nichol, C. A. Inhibition of histamine-metabolising enzymes and elevation of histamine levels in tissues by lipid-soluble anticancer folate antagonists. Mol. Pharmacol. 1980, 18, 100-104.
-
(1980)
Mol. Pharmacol.
, vol.18
, pp. 100-104
-
-
Duch, D.S.1
Edelstein, M.P.2
Nichol, C.A.3
-
14
-
-
0022589150
-
Cross resistance of pleiotropically drug resistant P388 leukemia cells to the lipophilic antifolates trimetrexate and BW 301U
-
Klohs, W. D.; Steinkampf, R. W.; Besserer, J. A.; Fry, D. W. Cross resistance of pleiotropically drug resistant P388 leukemia cells to the lipophilic antifolates trimetrexate and BW 301U. Cancer Lett. 1986, 31, 253-260.
-
(1986)
Cancer Lett.
, vol.31
, pp. 253-260
-
-
Klohs, W.D.1
Steinkampf, R.W.2
Besserer, J.A.3
Fry, D.W.4
-
15
-
-
0024538964
-
Cross-resistance to the lipid-soluble antifolate trimetrexate in human carcinoma cells with the multidrug resistant phenotype
-
Assaraf, Y. G.; Molina, A.; Schimke, R. T. Cross-resistance to the lipid-soluble antifolate trimetrexate in human carcinoma cells with the multidrug resistant phenotype. J. Natl. Cancer Inst. 1989, 81, 291-294.
-
(1989)
J. Natl. Cancer Inst.
, vol.81
, pp. 291-294
-
-
Assaraf, Y.G.1
Molina, A.2
Schimke, R.T.3
-
16
-
-
0027218689
-
Biochemistry of multidrug resistance mediated by the multidrug transporter
-
Gottesman, M. M.; Pastan, I. Biochemistry of multidrug resistance mediated by the multidrug transporter. Annu. Rev. Biochem. 1993, 62, 385-427.
-
(1993)
Annu. Rev. Biochem.
, vol.62
, pp. 385-427
-
-
Gottesman, M.M.1
Pastan, I.2
-
17
-
-
0010271345
-
Multiple drug resistance and its relationship to brain penetration by lipophilic dihydrofolate reductase inhibitors
-
Baccanari, D. P.; Tansik, R. L. Multiple drug resistance and its relationship to brain penetration by lipophilic dihydrofolate reductase inhibitors. Proc. Am. Assoc. Cancer Res. 1990, 31, 339.
-
(1990)
Proc. Am. Assoc. Cancer Res.
, vol.31
, pp. 339
-
-
Baccanari, D.P.1
Tansik, R.L.2
-
18
-
-
13344275848
-
High affinity inhibitors of dihydrofolate reductase: Antimicrobial and anticancer activities of 7,8-dialkyl-1,3-diaminopyrrolo[3,2-f]quinazolines with small molecular size
-
Kuyper, L. F.; Baccanari, D. P.; Jones, M. L.; Hunter, R. N.; Tansik, R. L.; Joyner, S. S.; Boytos, C. M.; Rudolph, S. K.; Knick, V.; Wilson, H. R.; Caddell, J. M.; Friedman, H. S.; Comley, J. C. W.; Stables, J. N. High affinity inhibitors of dihydrofolate reductase: antimicrobial and anticancer activities of 7,8-dialkyl-1,3-diaminopyrrolo[3,2-f]quinazolines with small molecular size. J. Med. Chem. 1996, 39, 892-903.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 892-903
-
-
Kuyper, L.F.1
Baccanari, D.P.2
Jones, M.L.3
Hunter, R.N.4
Tansik, R.L.5
Joyner, S.S.6
Boytos, C.M.7
Rudolph, S.K.8
Knick, V.9
Wilson, H.R.10
Caddell, J.M.11
Friedman, H.S.12
Comley, J.C.W.13
Stables, J.N.14
-
19
-
-
0027177889
-
Identification of highly potent and selective inhibitors of Toxoplasma gondii dihydrofolate reductase
-
Chio, L.; Queener, S. F. Identification of highly potent and selective inhibitors of Toxoplasma gondii dihydrofolate reductase. Antimicrob. Agents Chemother. 1993, 37, 1914-1923.
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 1914-1923
-
-
Chio, L.1
Queener, S.F.2
-
20
-
-
0025836272
-
Pneumocystis carinii dihydrofolate reductase used to screen potential antipneumocystis drugs
-
Broughton, M. C.; Queener, S. F. Pneumocystis carinii dihydrofolate reductase used to screen potential antipneumocystis drugs. Antimicrob. Agents Chemother. 1991, 35, 1348-1355.
-
(1991)
Antimicrob. Agents Chemother.
, vol.35
, pp. 1348-1355
-
-
Broughton, M.C.1
Queener, S.F.2
-
21
-
-
0028044707
-
More choices in treating AIDS-related pneumonia
-
Voelker, R. More choices in treating AIDS-related pneumonia. J. Am. Med. Assoc. 1994, 271, 176-177.
-
(1994)
J. Am. Med. Assoc.
, vol.271
, pp. 176-177
-
-
Voelker, R.1
-
22
-
-
0025103250
-
Trimetrexate-leucovorin dosage evaluation study for the treatment of Pneumocystis carinii pneumonia
-
Sattler, F. R.; Allegra, C. J.; Verdegem, T. D. Trimetrexate-leucovorin dosage evaluation study for the treatment of Pneumocystis carinii pneumonia. J. Infect. Dis. 1990, 161, 91-96.
-
(1990)
J. Infect. Dis.
, vol.161
, pp. 91-96
-
-
Sattler, F.R.1
Allegra, C.J.2
Verdegem, T.D.3
-
23
-
-
0028823974
-
New drug developments for opportunistic infections in immunosuppressed patients: Pneumocystis carinii
-
Queener, S. F. New drug developments for opportunistic infections in immunosuppressed patients: Pneumocystis carinii. J. Med. Chem. 1995, 38, 4739-4759.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4739-4759
-
-
Queener, S.F.1
-
24
-
-
0024432032
-
Structural studies on bioactive compounds. Part 8. Synthesis, crystal structure, and biological properties of a new series of 2,4-diamino-5-aryl-6-ethylpyrimidine dihydrofolate reductase inhibitors with in vivo activity against a methotrexate-resistant cell line
-
Griffin, R. J.; Meek, M. A.; Schwalbe, C. H.; Stevens, M. F. G. Structural studies on bioactive compounds. Part 8. Synthesis, crystal structure, and biological properties of a new series of 2,4-diamino-5-aryl-6-ethylpyrimidine dihydrofolate reductase inhibitors with in vivo activity against a methotrexate-resistant cell line. J. Med. Chem. 1989, 32, 2468-2474.
-
(1989)
J. Med. Chem.
, vol.32
, pp. 2468-2474
-
-
Griffin, R.J.1
Meek, M.A.2
Schwalbe, C.H.3
Stevens, M.F.G.4
-
26
-
-
0002406093
-
Structural studies on bioactive compounds. Part 3. Re-examination of the hydrolysis of the antimalarial drug pyrimethamine and related derivatives and crystal structure of a hydrolysis product
-
Griffin, R. J.; Schwalbe, C. H.; Stevens, M. F. G.; Wong, K. P. Structural studies on bioactive compounds. Part 3. Re-examination of the hydrolysis of the antimalarial drug pyrimethamine and related derivatives and crystal structure of a hydrolysis product. J. Chem. Soc., Perkin Trans, 1 1985, 2267-2276.
-
(1985)
J. Chem. Soc., Perkin Trans
, vol.1
, pp. 2267-2276
-
-
Griffin, R.J.1
Schwalbe, C.H.2
Stevens, M.F.G.3
Wong, K.P.4
-
27
-
-
4344562867
-
Strychnine and Brucine, Part II
-
Clemo, G. R.; Perkin, W. H.; Robinson, R. Strychnine and Brucine, Part II. J. Chem. Soc. 1924, 725, 1751-1804.
-
(1924)
J. Chem. Soc.
, vol.725
, pp. 1751-1804
-
-
Clemo, G.R.1
Perkin, W.H.2
Robinson, R.3
-
28
-
-
0345329013
-
Copper assisted nucleophilic substitution of aryl halogen
-
Lindley, J. Copper assisted nucleophilic substitution of aryl halogen. Tetrahedron 1984, 40, 1433-1456.
-
(1984)
Tetrahedron
, vol.40
, pp. 1433-1456
-
-
Lindley, J.1
-
29
-
-
3142614563
-
Anomalous halogen to dimethylamino replacement with N,N-dimethylformamide catalyzed by ethylenediamine or 2-aminoethanol
-
Yamamoto, H. Anomalous halogen to dimethylamino replacement with N,N-dimethylformamide catalyzed by ethylenediamine or 2-aminoethanol. Bull. Chem. Soc. Jpn. 1982, 55, 2685-2686.
-
(1982)
Bull. Chem. Soc. Jpn.
, vol.55
, pp. 2685-2686
-
-
Yamamoto, H.1
-
30
-
-
37049067076
-
Structural studies on bioactive compounds. Part 5. Synthesis and properties of 2,4-diaminopyrimidine dihydrofolate reductase inhibitors bearing lipophilic azido groups
-
Bliss, E. A.; Griffin, R. J.; Stevens, M. F. G. Structural studies on bioactive compounds. Part 5. Synthesis and properties of 2,4-diaminopyrimidine dihydrofolate reductase inhibitors bearing lipophilic azido groups. J. Chem. Soc., Perkin Trans, 1 1987, 2217-2228.
-
(1987)
J. Chem. Soc., Perkin Trans
, vol.1
, pp. 2217-2228
-
-
Bliss, E.A.1
Griffin, R.J.2
Stevens, M.F.G.3
-
31
-
-
0342738155
-
The synthetic utility of oxazolines in aromatic substitution
-
Reuman, M.; Myers, A. I. The synthetic utility of oxazolines in aromatic substitution. Tetrahedron 1985, 41, 837-860.
-
(1985)
Tetrahedron
, vol.41
, pp. 837-860
-
-
Reuman, M.1
Myers, A.I.2
-
32
-
-
0001621191
-
A novel ring cleavage reaction of oxazolines
-
Levin, J. I.; Weinreb, S. M. A novel ring cleavage reaction of oxazolines. Tetrahedron Lett. 1982, 23, 2347-2350.
-
(1982)
Tetrahedron Lett.
, vol.23
, pp. 2347-2350
-
-
Levin, J.I.1
Weinreb, S.M.2
-
33
-
-
0007105451
-
Regioselective reductions of 2,3-epoxyacetals with zinc-chlorotrimethylsilane and lithium aluminum-hydride. Convenient synthesis of 1,2- and 1,3-diones
-
Vankar, Y. D.; Chaudhuri, N. C.; Rao, C. T. Regioselective reductions of 2,3-epoxyacetals with zinc-chlorotrimethylsilane and lithium aluminum-hydride. Convenient synthesis of 1,2- and 1,3-diones. Tetrahedron Lett. 1987, 28, 551-554.
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 551-554
-
-
Vankar, Y.D.1
Chaudhuri, N.C.2
Rao, C.T.3
-
34
-
-
0027056649
-
Structural studies on bio-active compounds. Part 21. Acid-promoted debenzylations in antitumor 2,4-diamino-5-[4-(N-alkylbenzylamino)-3-nitrophenyl-6-ethylpyrimidines
-
Griffin, R. J.; Stevens, M. F. G. Structural studies on bio-active compounds. Part 21. Acid-promoted debenzylations in antitumor 2,4-diamino-5-[4-(N-alkylbenzylamino)-3-nitrophenyl)-6-ethylpyrimidines. Anti-Cancer Drug Des. 1992, 7, 443-449.
-
(1992)
Anti-Cancer Drug Des.
, vol.7
, pp. 443-449
-
-
Griffin, R.J.1
Stevens, M.F.G.2
-
35
-
-
0020450983
-
Synthesis and anti-tumor activity of 10-alkyl-10-deazaminopterins. A convenient synthesis of 10-deazaminopterin
-
DeGraw, J. I.; Brown, V. H.; Tagawa, H.; Kisliuk, R. L.; Gaumont, Y.; Sirotnak, F. M. Synthesis and anti-tumor activity of 10-alkyl-10-deazaminopterins. A convenient synthesis of 10-deazaminopterin. J. Med. Chem. 1982, 25, 1227-1230.
-
(1982)
J. Med. Chem.
, vol.25
, pp. 1227-1230
-
-
Degraw, J.I.1
Brown, V.H.2
Tagawa, H.3
Kisliuk, R.L.4
Gaumont, Y.5
Sirotnak, F.M.6
-
36
-
-
0027403420
-
Design of thymidylate synthase inhibitors using protein crystal structures. the synthesis and biological evaluation of a novel class of 5-substituted quinazolinones
-
Webber, S. E.; Bleckman, T. M.; Attard, J.; Deal, J. G.; Kathardekar, V.; Welsh, K. M.; Webber, S.; Janson, C. A.; Matthews, D. A.; Smith, W. W.; Freer, S. T.; Jordan, S. R.; Bacquet, R. C.; Howland, E. F.; Booth, C. L. J.; Ward, R. W.; Hermann, S. M.; White, J.; Morse, C. A.; Hilliard, J. A.; Barlett, C. A. Design of thymidylate synthase inhibitors using protein crystal structures. The synthesis and biological evaluation of a novel class of 5-substituted quinazolinones. J. Med. Chem. 1993, 36, 733-746.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 733-746
-
-
Webber, S.E.1
Bleckman, T.M.2
Attard, J.3
Deal, J.G.4
Kathardekar, V.5
Welsh, K.M.6
Webber, S.7
Janson, C.A.8
Matthews, D.A.9
Smith, W.W.10
Freer, S.T.11
Jordan, S.R.12
Bacquet, R.C.13
Howland, E.F.14
Booth, C.L.J.15
Ward, R.W.16
Hermann, S.M.17
White, J.18
Morse, C.A.19
Hilliard, J.A.20
Barlett, C.A.21
more..
-
37
-
-
0027177889
-
Identification of highly potent and selective inhibitors of Toxoplasma gondii dihydrofolate reductase
-
Chio, L.; Queener, S. F. Identification of highly potent and selective inhibitors of Toxoplasma gondii dihydrofolate reductase. Antimicrob. Agents Chemother. 1993, 37, 1914-1923.
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 1914-1923
-
-
Chio, L.1
Queener, S.F.2
-
38
-
-
0029072232
-
Novel 2,4-diamino-5-substituted-pyrrolo[2,3-d]pyrimidines as classical and nonclassical antifolate inhibitors of dihydrofolate reductase
-
Gangjee, A.; Mavandadi, F.; Queener, S. F.; McGuire, J. J. Novel 2,4-diamino-5-substituted-pyrrolo[2,3-d]pyrimidines as classical and nonclassical antifolate inhibitors of dihydrofolate reductase J. Med. Chem. 1995, 38, 2158-2165.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 2158-2165
-
-
Gangjee, A.1
Mavandadi, F.2
Queener, S.F.3
McGuire, J.J.4
-
39
-
-
0017112240
-
Intrinsic resistance to methotrexate of cultured mammalian cells in relation to the inhibition kinetics of their dihydrofolate reductases
-
Jackson, R. C.; Hart, L. I.; Harrap, K. R. Intrinsic resistance to methotrexate of cultured mammalian cells in relation to the inhibition kinetics of their dihydrofolate reductases. Cancer Res. 1976, 36, 1991-1997.
-
(1976)
Cancer Res.
, vol.36
, pp. 1991-1997
-
-
Jackson, R.C.1
Hart, L.I.2
Harrap, K.R.3
-
40
-
-
0020030888
-
Biochemical correlates of responsiveness and collatoral sensitivity of some methotrexate-resistant murine tumors to the lipophilic antifolate, metoprine
-
Sirotnak, F. M.; Moccio, D. M.; Goutas, L. J.; Kelleher, L. E.; Montgomery, J. A. Biochemical correlates of responsiveness and collatoral sensitivity of some methotrexate-resistant murine tumors to the lipophilic antifolate, metoprine. Cancer Res. 1982, 42, 924-928.
-
(1982)
Cancer Res.
, vol.42
, pp. 924-928
-
-
Sirotnak, F.M.1
Moccio, D.M.2
Goutas, L.J.3
Kelleher, L.E.4
Montgomery, J.A.5
-
41
-
-
9844239316
-
-
Unpublished results
-
Rachedi, A.; Sansom, C. E.; Groom, C. R.; Thillet, J.; Griffin, R. J.; Geddes, A. J. Unpublished results.
-
-
-
Rachedi, A.1
Sansom, C.E.2
Groom, C.R.3
Thillet, J.4
Griffin, R.J.5
Geddes, A.J.6
-
42
-
-
0026723496
-
Structural studies on bioactive compounds. 20. Molecular modeling and crystallographic studies on methylbenzoprim, a potent inhibitor of dihydrofolate reductase
-
Denny, B. J.; Ringan, N. S.; Schwalbe, C. H.; Lambert, P. A.; Meek, M. A.; Griffin, R. J.; Stevens, M. F. G. Structural studies on bioactive compounds. 20. Molecular modeling and crystallographic studies on methylbenzoprim, a potent inhibitor of dihydrofolate reductase. J. Med. Chem. 1992, 35, 2315-2320.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 2315-2320
-
-
Denny, B.J.1
Ringan, N.S.2
Schwalbe, C.H.3
Lambert, P.A.4
Meek, M.A.5
Griffin, R.J.6
Stevens, M.F.G.7
-
43
-
-
0017868645
-
Synthesis of 3- and 4-amidinobenzaldehyde hydrochloride
-
Richter, P.; Wagner, G. Synthesis of 3- and 4-amidinobenzaldehyde hydrochloride. Pharmazie 1978, 33, 39-41.
-
(1978)
Pharmazie
, vol.33
, pp. 39-41
-
-
Richter, P.1
Wagner, G.2
-
44
-
-
33947087912
-
Lithium triethylborohydride. An exceptionally powerful nucleophile in displacement reactions with organic halides
-
Brown, H. C.; Krishnamurthy, S. Lithium triethylborohydride. An exceptionally powerful nucleophile in displacement reactions with organic halides. J. Am. Chem. Soc. 1973, 95, 1669-1671.
-
(1973)
J. Am. Chem. Soc.
, vol.95
, pp. 1669-1671
-
-
Brown, H.C.1
Krishnamurthy, S.2
-
45
-
-
0000336105
-
Technique for the study of resistance to folic acid antagonists
-
Bertino, J. R.; Fischer, G. A. Technique for the study of resistance to folic acid antagonists. Methods Med. Res. 1964, 10, 297-299.
-
(1964)
Methods Med. Res.
, vol.10
, pp. 297-299
-
-
Bertino, J.R.1
Fischer, G.A.2
-
46
-
-
0021982971
-
Comparative activity of rat liver dihydrofolate reductase with 7,8-dihydrofolate and other 7,8-dihydropteridines
-
Webber, S.; Whiteley, J. M. Comparative activity of rat liver dihydrofolate reductase with 7,8-dihydrofolate and other 7,8-dihydropteridines. Arch. Biochem. Biophys. 1985, 236, 681-690.
-
(1985)
Arch. Biochem. Biophys.
, vol.236
, pp. 681-690
-
-
Webber, S.1
Whiteley, J.M.2
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