-
1
-
-
0032862077
-
Anti-HIV agents 36. 17-carboxylated steroids as potential anti-HIV agents
-
Submitted
-
Xia, P.; Yang, Z.; Xia, Y.; Zheng, Y.; Cosentino, L. M.; Lee, K. H. Anti-HIV agents 36. 17-Carboxylated steroids as potential anti-HIV agents. Bioorg. Med. Chem. Submitted.
-
Bioorg. Med. Chem.
-
-
Xia, P.1
Yang, Z.2
Xia, Y.3
Zheng, Y.4
Cosentino, L.M.5
Lee, K.H.6
-
2
-
-
0020532060
-
Isolation of a T-cell leukemia virus in acquired immunodeficiency syndrome (AIDS)
-
Gallo, R. C.; Sarin, P. S.; Gelmann, E. P.; Robert-Guroff, M.; Richardson, E.; Kalyanaraman, V. S.; Mann, D.; Sidhu, G. D.; Stahl, R. E.; Zolla-Prazner, S.; Leibowitch, J.; Popovic, M. Isolation of a T-cell leukemia virus in acquired immunodeficiency syndrome (AIDS). Science 1983, 220, 865-867.
-
(1983)
Science
, vol.220
, pp. 865-867
-
-
Gallo, R.C.1
Sarin, P.S.2
Gelmann, E.P.3
Robert-Guroff, M.4
Richardson, E.5
Kalyanaraman, V.S.6
Mann, D.7
Sidhu, G.D.8
Stahl, R.E.9
Zolla-Prazner, S.10
Leibowitch, J.11
Popovic, M.12
-
3
-
-
0020596551
-
Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS)
-
Barre-Sinoussi, F.; Chermann, J. C.; Rey, F.; Nugeyre, M. T.; Chamaret, S.; Gruest, J.; Dauguet, C.; Axler-Blin, C.; Vezinet-Brun, F.; Rouzioux, C.; Rozenbaum, W.; Montagnier, L. Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS). Science 1983, 220, 868-871.
-
(1983)
Science
, vol.220
, pp. 868-871
-
-
Barre-Sinoussi, F.1
Chermann, J.C.2
Rey, F.3
Nugeyre, M.T.4
Chamaret, S.5
Gruest, J.6
Dauguet, C.7
Axler-Blin, C.8
Vezinet-Brun, F.9
Rouzioux, C.10
Rozenbaum, W.11
Montagnier, L.12
-
4
-
-
0029011730
-
Toward improved anti-HIV chemotherapy: Therapeutic strategies for intervention with HIV infections
-
De Clercq, E. Toward improved anti-HIV chemotherapy: Therapeutic strategies for intervention with HIV infections. J. Med. Chem. 1995, 38, 2491-2517.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 2491-2517
-
-
De Clercq, E.1
-
5
-
-
0027949236
-
Future treatment strategies in HIV-infection
-
Dormont, J. Future treatment strategies in HIV-infection. AIDS 1994, 8 (Suppl. 3), S31-S33.
-
(1994)
AIDS
, vol.8
, Issue.3 SUPPL.
-
-
Dormont, J.1
-
6
-
-
0029022257
-
Treatment of AIDS with drugs targeted to inhibit different stages of the HIV life cycle
-
Sarin, P. S.; Goldstein, A. L. Treatment of AIDS with drugs targeted to inhibit different stages of the HIV life cycle. Immunopharmacol. Immunotoxicol. 1995, 17, 217-245.
-
(1995)
Immunopharmacol. Immunotoxicol.
, vol.17
, pp. 217-245
-
-
Sarin, P.S.1
Goldstein, A.L.2
-
7
-
-
0345100148
-
-
Reported by Office of Special Health Issues, Food and Drug Administration. December 22
-
Reported by Office of Special Health Issues, Food and Drug Administration. December 22, 1998.
-
(1998)
-
-
-
8
-
-
0030012398
-
Resistance-related mutations in the HIV-1 protease gene of patients treated for 1 year with the protease inhibitor ritonavir (ABT-538)
-
Schmit, J. C.; Ruiz, L.; Clotet, B.; Raventos, A.; Tor, J.; Leonard, J.; Desmyter, J.; De Clercq, E.; Vandamme, A. M. Resistance-related mutations in the HIV-1 protease gene of patients treated for 1 year with the protease inhibitor ritonavir (ABT-538). AIDS 1996, 10, 995-999.
-
(1996)
AIDS
, vol.10
, pp. 995-999
-
-
Schmit, J.C.1
Ruiz, L.2
Clotet, B.3
Raventos, A.4
Tor, J.5
Leonard, J.6
Desmyter, J.7
De Clercq, E.8
Vandamme, A.M.9
-
9
-
-
0028034266
-
The K65R mutant reverse-transcriptase of HIV-1 cross-resistant to 2′,3′-dideoxycytidine, 2′,3′-dideoxy-3′-thiacytidine, and 2′,3′-dideoxyinosine shows reduced sensitivity to specific dideoxynucleoside triphosphate inhibitors in vitro
-
Gu, Z. X.; Fletcher, R. S.; Arts, E. J.; Wainberg, M. A.; Parniak, M. A. The K65R mutant reverse-transcriptase of HIV-1 cross-resistant to 2′,3′-dideoxycytidine, 2′,3′-dideoxy-3′-thiacytidine, and 2′,3′-dideoxyinosine shows reduced sensitivity to specific dideoxynucleoside triphosphate inhibitors in vitro. J. Biol. Chem. 1994, 269, 28118-28122.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 28118-28122
-
-
Gu, Z.X.1
Fletcher, R.S.2
Arts, E.J.3
Wainberg, M.A.4
Parniak, M.A.5
-
10
-
-
0028051329
-
Natural occurrence of drug-resistance mutations in the reverse-transcriptase of human-immunodeficiency-virus type-1 isolates
-
Najera, I.; Richman, D. D.; Olivares, I.; Rojas, J. M.; Peinado, M. A.; Perucho, M.; Najera, R.; Lopez-Galindez, C. Natural occurrence of drug-resistance mutations in the reverse-transcriptase of human-immunodeficiency-virus type-1 isolates. AIDS Res. Hum. Retroviruses 1994, 10, 1479-1488.
-
(1994)
AIDS Res. Hum. Retroviruses
, vol.10
, pp. 1479-1488
-
-
Najera, I.1
Richman, D.D.2
Olivares, I.3
Rojas, J.M.4
Peinado, M.A.5
Perucho, M.6
Najera, R.7
Lopez-Galindez, C.8
-
11
-
-
0025950055
-
Resistance to DDI and sensitivity to AZT induced by a mutation in HIV-1 reverse-transcriptase
-
Stclair, M. H.; Martin, J. L.; Tudor-Williams, G.; Bach, M. C.; Vavro, C. L.; King, D. M.; Kellam, P.; Kemp, S. D.; Larder, B. A. Resistance to DDI and sensitivity to AZT induced by a mutation in HIV-1 reverse-transcriptase. Science 1991, 253, 1557-1559.
-
(1991)
Science
, vol.253
, pp. 1557-1559
-
-
Stclair, M.H.1
Martin, J.L.2
Tudor-Williams, G.3
Bach, M.C.4
Vavro, C.L.5
King, D.M.6
Kellam, P.7
Kemp, S.D.8
Larder, B.A.9
-
12
-
-
0028013171
-
Generation and characterization of a human-immunodeficiency-virus type-1 (HIV-1) mutant resistant to an HIV-1 protease inhibitor
-
Elfarrash, M. A.; Kuroda, M. J.; Kitazaki, T.; Masuda, T.; Kato, K.; Hatanaka, M.; Harada, S. Generation and characterization of a human-immunodeficiency-virus type-1 (HIV-1) mutant resistant to an HIV-1 protease inhibitor. J. Virol. 1994, 68, 233-239.
-
(1994)
J. Virol.
, vol.68
, pp. 233-239
-
-
Elfarrash, M.A.1
Kuroda, M.J.2
Kitazaki, T.3
Masuda, T.4
Kato, K.5
Hatanaka, M.6
Harada, S.7
-
13
-
-
0030065565
-
Resistance of human immunodeficiency virus type 1 to protease inhibitors: Selection of resistance mutations in the presence and absence of the drug
-
Borman, A. M.; Paulous, S.; Clavel, F. Resistance of human immunodeficiency virus type 1 to protease inhibitors: Selection of resistance mutations in the presence and absence of the drug. J. Gen. Virol. 1996, 77, 419-426.
-
(1996)
J. Gen. Virol.
, vol.77
, pp. 419-426
-
-
Borman, A.M.1
Paulous, S.2
Clavel, F.3
-
14
-
-
0028522491
-
Suksdorfin: An anti-HIV principle from Lomatium suksdorfii, its structure-activity correlation with related coumarins, and synergistic effects with anti-AIDS nucleosides
-
Lee, T. T.-Y.; Kashiwada, Y.; Huang, L.; Snider, J.; Cosentino, L. M.; Lee, K. H. Suksdorfin: An anti-HIV principle from Lomatium suksdorfii, its structure-activity correlation with related coumarins, and synergistic effects with anti-AIDS nucleosides. Bioorg. Med. Chem. 1994, 2, 1051-1056.
-
(1994)
Bioorg. Med. Chem.
, vol.2
, pp. 1051-1056
-
-
Lee, T.T.-Y.1
Kashiwada, Y.2
Huang, L.3
Snider, J.4
Cosentino, L.M.5
Lee, K.H.6
-
15
-
-
0344237915
-
A note on the preliminary phytochemical and biological study of Lomatium suksdorfii
-
Pettinato, F. A.; Fischer, L.; Hall, N. A. A note on the preliminary phytochemical and biological study of Lomatium suksdorfii. J. Am. Pharm. Assoc. 1959, 48, 423-423.
-
(1959)
J. Am. Pharm. Assoc.
, vol.48
, pp. 423-423
-
-
Pettinato, F.A.1
Fischer, L.2
Hall, N.A.3
-
16
-
-
0001293316
-
Isolation, purification, and structure determination of pteryxin and suksdorfin
-
Willette, R. E.; Soine, T. O. Isolation, purification, and structure determination of pteryxin and suksdorfin. J. Pharm. Sci. 1962, 51, 149-156.
-
(1962)
J. Pharm. Sci.
, vol.51
, pp. 149-156
-
-
Willette, R.E.1
Soine, T.O.2
-
17
-
-
0014558431
-
Revised absolute configuration of natural khellactone esters (1)
-
Kemmich, J.; Pederson, P. A.; Nielsen, B. E. Revised absolute configuration of natural khellactone esters (1). Tetrahedron Lett. 1969, 3365-3366.
-
(1969)
Tetrahedron Lett.
, pp. 3365-3366
-
-
Kemmich, J.1
Pederson, P.A.2
Nielsen, B.E.3
-
18
-
-
0027943195
-
Anti-AIDS agents 15. Synthesis and anti-HIV activity of dihydroseselins and related analogues
-
Huang, L.; Kashiwada, Y.; Cosentino, L. M.; Fan, S.; Chen, C. H.; McPhail, A. T.; Fujioka, T.; Mihashi, K.; Lee, K. H. Anti-AIDS agents 15. Synthesis and anti-HIV activity of dihydroseselins and related analogues. J. Med. Chem. 1994, 37, 3947-3955.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3947-3955
-
-
Huang, L.1
Kashiwada, Y.2
Cosentino, L.M.3
Fan, S.4
Chen, C.H.5
McPhail, A.T.6
Fujioka, T.7
Mihashi, K.8
Lee, K.H.9
-
19
-
-
0028210937
-
Anti-AIDS agents 14. 3′,4′-Di-O-(-)-camphanoyl-(+)-cis-khel-lactone and related compounds: A new class of potent anti-HIV agents
-
Huang, L.; Kashiwada, Y.; Cosentino, L. M.; Fan, S.; Lee, K. H. Anti-AIDS agents 14. 3′,4′-Di-O-(-)-camphanoyl-(+)-cis-khel-lactone and related compounds: A new class of potent anti-HIV agents. Bioorg. Med. Chem. 1994, 4, 593-598.
-
(1994)
Bioorg. Med. Chem.
, vol.4
, pp. 593-598
-
-
Huang, L.1
Kashiwada, Y.2
Cosentino, L.M.3
Fan, S.4
Lee, K.H.5
-
20
-
-
0030725569
-
Anti-AIDS agents 28. Synthesis and anti-HIV activity of methoxy substituted 3′,4′-di-O-(-)-camphanoyl-(+)-cis-khellactone (DCK) analogues
-
Takeuchi, Y.; Xie, L.; Cosentino, L. M.; Lee K. H. Anti-AIDS agents 28. Synthesis and anti-HIV activity of methoxy substituted 3′,4′-di-O-(-)-camphanoyl-(+)-cis-khellactone (DCK) analogues. Bioorg. Med. Chem. Lett. 1997, 7, 2573-2578.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 2573-2578
-
-
Takeuchi, Y.1
Xie, L.2
Cosentino, L.M.3
Lee K, H.4
-
21
-
-
0032544137
-
Anti-AIDS agents 33. Synthesis and anti-HIV activity of monomethyl substituted 3′,4′-di-O-(-)-camphanoyl-(+)-cis-khellactone (DCK) analogues
-
Xie, L.; Takeuchi, Y.; Cosentino, L. M.; Lee K. H. Anti-AIDS agents 33. Synthesis and anti-HIV activity of monomethyl substituted 3′,4′-di-O-(-)-camphanoyl-(+)-cis-khellactone (DCK) analogues. Bioorg. Med. Chem. Lett. 1998, 8, 2151-2156.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 2151-2156
-
-
Xie, L.1
Takeuchi, Y.2
Cosentino, L.M.3
Lee K, H.4
-
22
-
-
0013541108
-
Mushroom tyrosinase catalyzed synthesis of coumestans, benzofuran derivatives and related heterocyclic compounds
-
Pandey, G.; Muralikrishna, C.; Bhalerao, U. T. Mushroom tyrosinase catalyzed synthesis of coumestans, benzofuran derivatives and related heterocyclic compounds. Tetrahedron 1989, 45, 6867-6874.
-
(1989)
Tetrahedron
, vol.45
, pp. 6867-6874
-
-
Pandey, G.1
Muralikrishna, C.2
Bhalerao, U.T.3
-
23
-
-
0001735188
-
Partial methylation of 4-hydroxyl group in coumarins
-
Ahlumalia, Y. K.; Kumar, D. Partial methylation of 4-hydroxyl group in coumarins. Indian J. Chem. 1977, 15B, 945-946.
-
(1977)
Indian J. Chem.
, vol.15 B
, pp. 945-946
-
-
Ahlumalia, Y.K.1
Kumar, D.2
-
24
-
-
0001138103
-
A convenient synthesis of a simple coumarin from salicylaldehyde and Wittig reagent (I). A synthesis of methoxycoumarin and hydroxycoumarin
-
Harayama, T.; Katsuno, K.; Nishioka, H.; Fujii, M.; Nishita, Y.; Ishii, H.; Kaneko, Y. A convenient synthesis of a simple coumarin from salicylaldehyde and Wittig reagent (I). A synthesis of methoxycoumarin and hydroxycoumarin. Heterocydes 1994, 39, 613-622.
-
(1994)
Heterocydes
, vol.39
, pp. 613-622
-
-
Harayama, T.1
Katsuno, K.2
Nishioka, H.3
Fujii, M.4
Nishita, Y.5
Ishii, H.6
Kaneko, Y.7
-
25
-
-
0001030405
-
Convenient synthesis of a simple coumarin from salocyaldehyde and Wittig reagent (III). Synthesis of nitrocoumarins
-
Harayama, T.; Nakatsuka, K.; Nishioka, H.; Murakami, K.; Ohmori, Y.; Takeuchi, Y.; Ishii, H.; Kenmotsu, K. Convenient synthesis of a simple coumarin from salocyaldehyde and Wittig reagent (III). Synthesis of nitrocoumarins. Heterocycles 1994, 38, 2729-2738.
-
(1994)
Heterocycles
, vol.38
, pp. 2729-2738
-
-
Harayama, T.1
Nakatsuka, K.2
Nishioka, H.3
Murakami, K.4
Ohmori, Y.5
Takeuchi, Y.6
Ishii, H.7
Kenmotsu, K.8
-
26
-
-
37049172229
-
Indoles. Part I. The formylation of indole and some reactions of 3-formylindole
-
Smith, G. F. Indoles. Part I. The formylation of indole and some reactions of 3-formylindole. J. Chem. Soc. 1954, 3842-3846.
-
(1954)
J. Chem. Soc.
, pp. 3842-3846
-
-
Smith, G.F.1
-
27
-
-
0026463461
-
Synthetic studies on naturally occurring coumarins. II. Synthesis of 6,7-dimethoxy-and 7,8-dimethoxy-5-[(E)-3-oxo-1-butenyl]coumarins
-
Ishii, H.; Ishikawa, T.; Wada, H.; Miyazaki, H.; Kaneko, Y.; Harayama, T. Synthetic studies on naturally occurring coumarins. II. Synthesis of 6,7-dimethoxy-and 7,8-dimethoxy-5-[(E)-3-oxo-1-butenyl]coumarins. Chem. Pharm. Bull. 1992, 40, 2614-2619.
-
(1992)
Chem. Pharm. Bull.
, vol.40
, pp. 2614-2619
-
-
Ishii, H.1
Ishikawa, T.2
Wada, H.3
Miyazaki, H.4
Kaneko, Y.5
Harayama, T.6
-
28
-
-
0000475990
-
Deoxygenation of aldehydes and ketones with sodium cyanoborohydride
-
Elliger, C. A. Deoxygenation of aldehydes and ketones with sodium cyanoborohydride. Synth. Commun. 1985, 15, 1315-1324.
-
(1985)
Synth. Commun.
, vol.15
, pp. 1315-1324
-
-
Elliger, C.A.1
-
29
-
-
0001464941
-
A convenient synthesis of benzofuran-3-acetic acids
-
Fall, Y.; Santana, L.; Teijeira, M.; Uriarte, E. A convenient synthesis of benzofuran-3-acetic acids. Heterocycles 1995, 41, 647-650.
-
(1995)
Heterocycles
, vol.41
, pp. 647-650
-
-
Fall, Y.1
Santana, L.2
Teijeira, M.3
Uriarte, E.4
-
30
-
-
38049185326
-
Synthesis of 2,2-dimethylchromenes
-
Hlubucek, J.; Ritchie, E.; Taylor, W. C. Synthesis of 2,2-dimethylchromenes. Aust. J. Chem. 1971, 24, 2347-2354.
-
(1971)
Aust. J. Chem.
, vol.24
, pp. 2347-2354
-
-
Hlubucek, J.1
Ritchie, E.2
Taylor, W.C.3
-
31
-
-
0000467894
-
Claisen rearrangements III. Convenient synthesis of the coumarins, osthenol, demethylsuberosin and coumurrayin
-
Murray, R. D. H.; Ballantyne, M. M.; Mathai, K. P. Claisen rearrangements III. Convenient synthesis of the coumarins, osthenol, demethylsuberosin and coumurrayin. Tetrahedron 1971, 27, 1247-1251.
-
(1971)
Tetrahedron
, vol.27
, pp. 1247-1251
-
-
Murray, R.D.H.1
Ballantyne, M.M.2
Mathai, K.P.3
-
32
-
-
0029055026
-
Asymmetric synthesis of 3′,4′-di-O-(-)-camphanoyl-(+)-cis-khellactone (DCK), a potent anti-HIV agent
-
Xie, L.; Crimmins, M. T.; Lee, K. H. Asymmetric synthesis of 3′,4′-di-O-(-)-camphanoyl-(+)-cis-khellactone (DCK), a potent anti-HIV agent. Tetrahedron Lett. 1995, 36, 4529-4532.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 4529-4532
-
-
Xie, L.1
Crimmins, M.T.2
Lee, K.H.3
-
33
-
-
33751385752
-
Improved enantioselectivity in asymmetric dihydroxylations of terminal olefins using pyrimidine ligands
-
Crispino, G. A.; Jeong, K. S.; Kolb, H. C.; Wang, Z. M.; Xu, D. Q.; Sharpless, K. B. Improved enantioselectivity in asymmetric dihydroxylations of terminal olefins using pyrimidine ligands. J. Org. Chem. 1993, 58, 3785-3786.
-
(1993)
J. Org. Chem.
, vol.58
, pp. 3785-3786
-
-
Crispino, G.A.1
Jeong, K.S.2
Kolb, H.C.3
Wang, Z.M.4
Xu, D.Q.5
Sharpless, K.B.6
-
34
-
-
0000797769
-
Catalytic asymmetric dihydroxylation of cis-disubstituted olefins
-
Wang, L.; Sharpless, K B. Catalytic asymmetric dihydroxylation of cis-disubstituted olefins. J. Am. Chem. Soc. 1992, 114, 7568-7570.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 7568-7570
-
-
Wang, L.1
Sharpless, K.B.2
-
35
-
-
0003084653
-
Toward an understanding of the high enantioselectivity in the osmium-catalyzed asymmetric dihydroxylation 3. New insights into isomeric forms of the putative osmaoxetane intermediate
-
Norrby, P. O.; Becker, H.; Sharpless, K. B. Toward an understanding of the high enantioselectivity in the osmium-catalyzed asymmetric dihydroxylation 3. New insights into isomeric forms of the putative osmaoxetane intermediate. J. Am. Chem. Soc. 1996, 118, 35-42.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 35-42
-
-
Norrby, P.O.1
Becker, H.2
Sharpless, K.B.3
-
36
-
-
0000770498
-
Asymmetric dihydroxylation 2. A qualitative molecular mechanics approach
-
Norrby, P. O.; Kolb, H. C.; Sharpless, K. B. Asymmetric dihydroxylation 2. A qualitative molecular mechanics approach. J. Am. Chem. Soc. 1994, 116, 8470-8478.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 8470-8478
-
-
Norrby, P.O.1
Kolb, H.C.2
Sharpless, K.B.3
-
37
-
-
0344669344
-
-
This assay was performed by the National Cancer Institute, Bethesda, Maryland
-
This assay was performed by the National Cancer Institute, Bethesda, Maryland.
-
-
-
-
38
-
-
0024578841
-
New soluble-formazan assay for HIV-1 cytopathic effects: Application to high-flux screening of synthetic and natural products for AIDS-antiviral activity
-
Weislow, O. W.; Kiser, R.; Fine, D.; Bader, J.; Shoemaker, R. H.; Boyd, M. R. New soluble-formazan assay for HIV-1 cytopathic effects: application to high-flux screening of synthetic and natural products for AIDS-antiviral activity. J. Natl. Cancer Inst. 1989, 81, 577-586.
-
(1989)
J. Natl. Cancer Inst.
, vol.81
, pp. 577-586
-
-
Weislow, O.W.1
Kiser, R.2
Fine, D.3
Bader, J.4
Shoemaker, R.H.5
Boyd, M.R.6
|