-
1
-
-
27844474247
-
Drug discovery from medicinal plants
-
DOI 10.1016/j.lfs.2005.09.012, PII S0024320505008799
-
Balunas, M.J.; Kinghorn, A.D. Drug Discovery from medicinal plants. Life Sci. 2005, 78, 431-441. (Pubitemid 41653493)
-
(2005)
Life Sciences
, vol.78
, Issue.5
, pp. 431-441
-
-
Balunas, M.J.1
Kinghorn, A.D.2
-
2
-
-
0035467993
-
Global cancer statistics in the year 2000
-
DOI 10.1016/S1470-2045(01)00486-7, PII S1470204501004867
-
Parkin, D.M. Global cancer statistics in the year 2000. Lancet Oncol. 2001, 2, 533-543. (Pubitemid 33586866)
-
(2001)
Lancet Oncology
, vol.2
, Issue.9
, pp. 533-543
-
-
Parkin, D.M.1
-
4
-
-
0029128195
-
Cloning of an organic solvent-resistance gene in Escherichia coli: The unexpected role of alkylhydroperoxide reductase
-
USA
-
Ferrante, A.; Augliera J.; Lewis, K. Cloning of an organic solvent-resistance gene in Escherichia coli: The unexpected role of alkylhydroperoxide reductase. Proc. Natl. Acad. Sci. USA 1995, 92, 7617-7621.
-
(1995)
Proc. Natl. Acad. Sci.
, vol.92
, pp. 7617-7621
-
-
Augliera, J.1
Ferrante, A.2
Lewis, K.3
-
5
-
-
0030992580
-
Tetrahydronaphthalene lignan compounds as potent anti-HIV type 1 agents
-
Hara, H.; Fujihashi, T.; Sakata, T. Tetrahydronaphthalene lignan compounds as potent anti-HIV type 1 agents. AIDS Res. Hum. Retroviruses 1997, 13, 695-705. (Pubitemid 27210458)
-
(1997)
AIDS Research and Human Retroviruses
, vol.13
, Issue.8
, pp. 695-705
-
-
Hara, H.1
Fujihashi, T.2
Sakata, T.3
Kaji, A.4
Kaji, H.5
-
6
-
-
33645384005
-
Novel 5, 6, 7, 8- tetrahydronaphth-2-ylheterocycles of possible biological activity
-
Ebeid, M.Y.; El-Zahar, M.I.; Kamel, M.M.; Omar, M.T.; Anwar, M.M. Novel 5, 6, 7, 8- tetrahydronaphth-2-ylheterocycles of possible biological activity. Egypt. Pharm. J. NRC 2004, 3, 49-65.
-
(2004)
Egypt. Pharm. J. NRC
, vol.3
, pp. 49-65
-
-
Ebeid, M.Y.1
El-Zahar, M.I.2
Kamel, M.M.3
Omar, M.T.4
Anwar, M.M.5
-
7
-
-
20544456935
-
Synthesis of new tetrahydronaphthyl-1, 2, 4- triazines of potensial antimicrobial activity
-
Nabih, I.; Zayed, A.; Kamel, M.M.; Motawie, M.S. Synthesis of new tetrahydronaphthyl-1, 2, 4- triazines of potensial antimicrobial activity. Egypt. J. Chem. 1986, 29, 101-106.
-
(1986)
Egypt. J. Chem.
, vol.29
, pp. 101-106
-
-
Nabih, I.1
Zayed, A.2
Kamel, M.M.3
Motawie, M.S.4
-
8
-
-
0029590037
-
A novel class of non-peptidic endothelin antagonists isolated from the medicinal herb Phyllanthus niruri
-
DOI 10.1021/np50124a006
-
Hussain, R.A.; Dickey, J.K.; Rosser, M.P.; Matson, J.A.; Kozlowski, M.R.; Brittain, R.J.; Webb, M.L.; Rose, P.M.; Fernandes, P.A. Novel class of non-peptidic endothelin antagonists isolated from the medicinal herb phyllanthus niruri. J. Nat. Prod. 1995, 58, 1515-1520. (Pubitemid 26006882)
-
(1995)
Journal of Natural Products
, vol.58
, Issue.10
, pp. 1515-1520
-
-
Hussain, R.A.1
Dickey, J.K.2
Rosser, M.P.3
Matson, J.A.4
Kozlowski, M.R.5
Brittain, R.J.6
Webb, M.L.7
Rose, P.M.8
Fernandes, P.9
-
9
-
-
0032287025
-
Synthesis, hypotensive and antiarrhythmic activities of 3-alkyl-1-(2- hydroxy-5, 8-dimethoxy-1, 2, 3, 4-tetrahydro-3-naphthalenyl)ureas or thioureas and their guanidine analogues
-
Chalina, E.G.; Chakarova, L. Synthesis, hypotensive and antiarrhythmic activities of 3-alkyl-1-(2- hydroxy-5, 8-dimethoxy-1, 2, 3, 4-tetrahydro-3- naphthalenyl)ureas or thioureas and their guanidine analogues. Eur. J. Med. Chem. 1998, 33, 975-983.
-
(1998)
Eur. J. Med. Chem.
, vol.33
, pp. 975-983
-
-
Chalina, E.G.1
Chakarova, L.2
-
10
-
-
33748249336
-
Synthesis and moulscicidal activity of some salicylamido tetralins
-
Kamel, M.M.; Michael, J.M. Synthesis and moulscicidal activity of some salicylamido tetralins. Egypt. J. Bilharziasis 1988, 10, 121-125.
-
(1988)
Egypt. J. Bilharziasis
, vol.10
, pp. 121-125
-
-
Kamel, M.M.1
Michael, J.M.2
-
11
-
-
0032474483
-
Synthesis and biological evaluation of new tetrahydronaphthalene derivatives as thromboxane receptor antagonists
-
Cimetière, B.; Dubuffet, T.; Muller, O.; Descombes, J.; Simonet, S.; Laubie, M.; Verbeuren, T.J.; Lavielle, G. Synthesis and biological evaluation of new tetrahydronaphthalene derivatives as thromboxane receptor antagonists. Bioorg. Med. Chem. Lett. 1998, 8, 1375-1340.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1340-1375
-
-
Cimetière, B.1
Dubuffet, T.2
Muller, O.3
Descombes, J.4
Simonet, S.5
Laubie, M.6
Verbeuren, T.J.7
Lavielle, G.8
-
12
-
-
0033054772
-
Effect of DP-1904, a thromboxane synthetase inhibitor, on antigen- and spasmogen-induced bronchoconstriction in rodents
-
DOI 10.1016/S0014-2999(98)00931-5, PII S0014299998009315
-
Takami, M.; Tsukada, W. Effect of DP-1904, a thromboxane synthetase inhibitor, on antigen- and spasmogen-induced bronchoconstriction in rodents. Eur. J. Pharmacol. 1999, 366, 253-259. (Pubitemid 29080790)
-
(1999)
European Journal of Pharmacology
, vol.366
, Issue.2-3
, pp. 253-259
-
-
Takami, M.1
Tsukada, W.2
-
13
-
-
12344275295
-
Anxiolytic-and antidepressant-like effects of 7-OH DPAT, preferential dopamine D3 receptor agonist in rats
-
Rogóz, Z.; Skuza, G.; Kodziñska, A. Anxiolytic-and antidepressant-like effects of 7-OH DPAT, preferential dopamine D3 receptor agonist in rats. Pol. J. Pharmacol. 2004, 56, 519-529.
-
(2004)
Pol. J. Pharmacol.
, vol.56
, pp. 519-529
-
-
Rogóz, Z.1
Skuza, G.2
Kodziñska, A.3
-
14
-
-
0344153885
-
1A receptor full agonist, 8-OH-DPAT, exerts antidepressant-like effects in the forced swim test in ACTH-treated rats
-
DOI 10.1016/j.ejphar.2003.09.008
-
1A receptor full agonist, 8-OH-DPAT, exerts antidepressant-like effects in the forced swim test in ACTH-treated rats. Eur. J. Pharmacol. 2003, 481, 75-77. (Pubitemid 37456789)
-
(2003)
European Journal of Pharmacology
, vol.481
, Issue.1
, pp. 75-77
-
-
Kitamura, Y.1
Araki, H.2
Shibata, K.3
Gomita, Y.4
Tanizaki, Y.5
-
15
-
-
68949204204
-
Synthesis and anticancer activity of novel tetralin-6-yl pyridine and tetralin-6-yl pyrimidine derivatives
-
Amin, K.M.; El-Zahar, M.I.; Anwar, M.; Kamel, M.; Mohamad, M. Synthesis and anticancer activity of novel tetralin-6-yl pyridine and tetralin-6-yl pyrimidine derivatives. Acta Pol. Pharm. 2009, 66, 279-291.
-
(2009)
Acta Pol. Pharm.
, vol.66
, pp. 279-291
-
-
Amin, K.M.1
El-Zahar, M.I.2
Anwar, M.3
Kamel, M.4
Mohamad, M.5
-
16
-
-
71149104734
-
Antitumor agents 269. Non-aromatic ring-A neotanshinlactone analog, TNO, as a new class of potent antitumor agents
-
Dong, Y.Z.; Shi, Q.; Nakagawa-Goto, K.; Wu, P.C.; Bastow, K.F.; Morris-Natschke, S.L.; Lee, K.H. Antitumor agents 269. Non-aromatic ring-A neotanshinlactone analog, TNO, as a new class of potent antitumor agents. Bioorg. Med. Chem. Lett. 2009, 19, 6289-6292.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6289-6292
-
-
Dong, Y.Z.1
Shi, Q.2
Nakagawa-Goto, K.3
Wu, P.C.4
Bastow, K.F.5
Morris-Natschke, S.L.6
Lee, K.H.7
-
17
-
-
0342961004
-
Synthesis of 4(1H)-pyridinone derivatives and investigation of analgesic and antiinflammatory activities
-
DOI 10.1016/S0014-827X(01)01083-7, PII S0014827X01010837
-
Öztürk, G.; Erol, D.D.; Uzbay, T.; Aytemir, M.D. Synthesis of 4(1H)-pyridinone derivatives and investigation of analgesic and antiinflammatory activities. Farmaco 2001, 56, 251-256. (Pubitemid 32463307)
-
(2001)
Farmaco
, vol.56
, Issue.4
, pp. 251-256
-
-
Ozturk, G.1
Erol, D.D.2
Uzbay, T.3
Aytemir, M.D.4
-
18
-
-
73849143009
-
The chemistry of some 6-methyl-4-hydroxy-2-pyridones
-
Findlay, J.A.; Tam, W.H.J.; Krepinsky, J. The chemistry of some 6-methyl-4-hydroxy-2-pyridones. Can. J. Chem. 1978, 56, 613-616.
-
(1978)
Can. J. Chem.
, vol.56
, pp. 613-616
-
-
Findlay, J.A.1
Tam, W.H.J.2
Krepinsky, J.3
-
19
-
-
0033617593
-
Synthesis of 4-alkyl (aryl)-6-aryl-3-cyano-2(1H)-pyridinones and their 2-imino isosteres as nonsteroidal cardiotonic agents
-
DOI 10.1016/S0014-827X(99)00004-X, PII S0014827X9900004X
-
Abadi, A.; Al-Deeb, O.; Al-Afify, A.; El-Kashef, H. Synthesis of 4-alkyl (aryl)-6-aryl-3-cyano- 2(1H)-pyridinones and their 2-imino isosteres as nonsteroidal cardiotonic agents. Farmaco 1999, 54, 195-201. (Pubitemid 29259821)
-
(1999)
Farmaco
, vol.54
, Issue.4
, pp. 195-201
-
-
Abadi, A.1
Al-Deeb, O.2
Al-Afify, A.3
El-Kashef, H.4
-
20
-
-
15944395546
-
Tosylation/mesylation of 4-hydroxy-3-nitro-2-pyridinones as an activation step in the construction of dihydropyrido[3,4-b] benzo[f][1,4]thiazepin-1-one based anti-HIV agents
-
DOI 10.1016/j.tetlet.2005.02.128
-
Storck, P.; Aubertin, A.; Grierson, D.S. Tosylation/mesylation of 4-hydroxy-3-nitro-2-pyridinones as an activation step in the construction of dihydropyrido[3, 4-b] benzo[f][1, 4]thiazepin-1-one based anti-HIV agents. Tetrahedron Lett. 2005, 46, 2919-2922. (Pubitemid 40431768)
-
(2005)
Tetrahedron Letters
, vol.46
, Issue.16
, pp. 2919-2922
-
-
Storck, P.1
Aubertin, A.-M.2
Grierson, D.S.3
-
21
-
-
41149119614
-
Interactive effect of photoperiod and fluridone on growth, reproduction, and biochemistry of dioecious hydrilla (Hydrilla verticillata)
-
DOI 10.1614/WS-07-109.1
-
Macdonald, G.E.; Puri, A.; Shilling, D.G. Interactive effect of photoperiod and fluridone on growth, reproduction, and biochemistry of dioecious hydrilla (Hydrilla Verticillata). Weed Sci. 2008, 56, 189-195. (Pubitemid 351438999)
-
(2008)
Weed Science
, vol.56
, Issue.2
, pp. 189-195
-
-
MacDonald, G.E.1
Puri, A.2
Shilling, D.G.3
-
22
-
-
33646940120
-
Chemical and biological characterisation of sapinopyridione, a phytotoxic 3,3,6-trisubstituted-2,4-pyridione produced by Sphaeropsis sapinea, a toxigenic pathogen of native and exotic conifers, and its derivatives
-
DOI 10.1016/j.phytochem.2006.03.017, PII S0031942206001658
-
Evidente, A.; Fiore, M.; Bruno, G.; Sparapano, L.; Motta, A. Chemical and biological characterisation of sapinopyridione, a phytotoxic 3, 3, 6-trisubstituted-2, 4-pyridione produced by Sphaeropsis sapinea, a toxigenic pathogen of native and exotic conifers, and its derivatives. Phytochemistry 2006, 67, 1019-1028. (Pubitemid 43792324)
-
(2006)
Phytochemistry
, vol.67
, Issue.10
, pp. 1019-1028
-
-
Evidente, A.1
Fiore, M.2
Bruno, G.3
Sparapano, L.4
Motta, A.5
-
23
-
-
0034119906
-
Synthesis and antitumour activity of 4-hydroxy-2-pyridone derivatives
-
DOI 10.1016/S0223-5234(00)00149-5
-
Cocco, M.T.; Congiu, C.; Onnis, V. Synthesis and antitumour activity of 4-hydroxy-2-pyridone derivatives. Eur. J. Med. Chem. 2000, 35, 545-552. (Pubitemid 30395103)
-
(2000)
European Journal of Medicinal Chemistry
, vol.35
, Issue.5
, pp. 545-552
-
-
Cocco, M.T.1
Congiu, C.2
Onnis, V.3
-
24
-
-
0037368423
-
New bis(pyridyl)methane derivatives from 4-hydroxy-2-pyridones: Synthesis and antitumoral activity
-
DOI 10.1016/S0223-5234(02)00002-8, PII S0223523402000028
-
Cocco, M.T.; Congiu, C.; Onnis, V. New bis(pyridyl)methane derivatives from 4-hydroxy-2- pyridones: synthesis and antitumoral activity. Eur. J. Med. Chem. 2003, 38, 37-47. (Pubitemid 36197853)
-
(2003)
European Journal of Medicinal Chemistry
, vol.38
, Issue.1
, pp. 37-47
-
-
Cocco, M.T.1
Congiu, C.2
Onnis, V.3
-
25
-
-
0001893755
-
Synthesis of some functionally substituted benzocyclanones
-
Allinger, N.L.; Jones, E.S. Synthesis of some functionally substituted benzocyclanones. J. Org. Chem. 1962, 27, 70-76.
-
(1962)
J. Org. Chem.
, vol.27
, pp. 70-76
-
-
Allinger, N.L.1
Jones, E.S.2
-
26
-
-
0025341331
-
Anticancer-drug screening
-
Storeng, P.; Ritsa, S.; Scudiero, D.; Monks, A.; McMahon, J.; Vistica, D.; Warren, J.T.; Bokesch, H.; Kenney, S.; Boyd, M.R. Anticancer-drug screening. J. Natl. Cancer Inst. 1990, 82, 1107-1112.
-
(1990)
J. Natl. Cancer Inst.
, vol.82
, pp. 1107-1112
-
-
Storeng, P.1
Ritsa, S.2
Scudiero, D.3
Monks, A.4
McMahon, J.5
Vistica, D.6
Warren, J.T.7
Bokesch, H.8
Kenney, S.9
Boyd, M.R.10
-
27
-
-
0030739913
-
An alternative molecular mechanism of action of 5-fluorouracil, a potent anticancer drug
-
DOI 10.1016/S0006-2952(97)00040-3, PII S0006295297000403
-
Ghoshal, K.; Jacob, S.T. An alternative molecular mechanism of action of 5-fluorouracil, a potent anticancer drug. Biochem. Pharmacol. 1997, 53, 1569-1575. (Pubitemid 27356085)
-
(1997)
Biochemical Pharmacology
, vol.53
, Issue.11
, pp. 1569-1575
-
-
Ghoshal, K.1
Jacob, S.T.2
|