-
2
-
-
77949363118
-
Novel irreversible epidermal growth factor receptor inhibitors by chemical modulation of the cysteine-trap portion
-
C. Carmi, A. Cavazzoni, S. Vezzosi, F. Bordi, F. Vacondio, G. Silva, S. Rivara, A. Lodola, R.R. Alfieri, S.L. Monica, M. Galetti, A. Ardizzoni, P.G. Petronini, and M. Mor Novel irreversible epidermal growth factor receptor inhibitors by chemical modulation of the cysteine-trap portion J. Med. Chem. 53 5 2010 2038 2050
-
(2010)
J. Med. Chem.
, vol.53
, Issue.5
, pp. 2038-2050
-
-
Carmi, C.1
Cavazzoni, A.2
Vezzosi, S.3
Bordi, F.4
Vacondio, F.5
Silva, G.6
Rivara, S.7
Lodola, A.8
Alfieri, R.R.9
Monica, S.L.10
Galetti, M.11
Ardizzoni, A.12
Petronini, P.G.13
Mor, M.14
-
3
-
-
77950589013
-
Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor
-
V.G. Pawar, M.L. Sos, H.B. Rode, M. Rabiller, S. Heynck, W.A.L. van Otterlo, R.K. Thomas, and D. Rauh Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor J. Med. Chem. 53 7 2010 2892 2901
-
(2010)
J. Med. Chem.
, vol.53
, Issue.7
, pp. 2892-2901
-
-
Pawar, V.G.1
Sos, M.L.2
Rode, H.B.3
Rabiller, M.4
Heynck, S.5
Van Otterlo, W.A.L.6
Thomas, R.K.7
Rauh, D.8
-
4
-
-
33751005304
-
Multitarget-directed drug design strategy: A novel molecule designed to block epidermal growth factor receptor (EGFR) and to exert proapoptotic effects
-
DOI 10.1021/jm0608762
-
A. Antonello, A. Tarozzi, F. Morroni, A. Cavalli, M. Rosini, P. Hrelia, M.L. Bolognesi, and C. Melchiorre Multitarget-directed drug design strategy: a novel molecule designed to block epidermal growth factor receptor (EGFR) and to exert proapoptotic effects J. Med. Chem. 49 23 2006 6642 6645 (Pubitemid 44749729)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.23
, pp. 6642-6645
-
-
Antonello, A.1
Tarozzi, A.2
Morroni, F.3
Cavalli, A.4
Rosini, M.5
Hrelia, P.6
Bolognesi, M.L.7
Melchiorre, C.8
-
5
-
-
33144456903
-
Tyrosine kinase inhibitors. 19. 6-alkynamides of 4-anilinoquinazolines and 4-anilinopyrido[3,4-d]pyrimidines as irreversible inhibitors of the erbB family of tyrosine kinase receptors
-
DOI 10.1021/jm050936o
-
S.R. Klutchko, Hairong Zhou, R.T. Winters, P. Tran Tuan, A.J. Bridges, I.W. Althaus, D.M. Amato, W.L. Elliott, P.A. Ellis, M.A. Meade, B.J. Roberts, D.W. Fry, A.J. Gonzales, P.J. Harvey, J.M. Nelson, V. Sherwood, Hyo-Kyung Han, G. Pace, J.B. Smaill, W.A. Denny, and H.D. Hollis Showalter Tyrosine kinase inhibitors. 19. 6-Alkynamides of 4-anilinoquinazolines and 4-anilinopyrido[3,4- d]pyrimidines as irreversible inhibitors of the erbB family of tyrosine kinase receptors J. Med. Chem. 49 4 2006 1475 1485 (Pubitemid 43271900)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.4
, pp. 1475-1485
-
-
Klutchko, S.R.1
Zhou, H.2
Winters, R.T.3
Tran, T.P.4
Bridges, A.J.5
Althaus, I.W.6
Amato, D.M.7
Elliott, W.L.8
Ellis, P.A.9
Meade, M.A.10
Roberts, B.J.11
Fry, D.W.12
Gonzales, A.J.13
Harvey, P.J.14
Nelson, J.M.15
Sherwood, V.16
Han, H.-K.17
Pace, G.18
Smaill, J.B.19
Denny, W.A.20
Showalter, H.D.H.21
more..
-
6
-
-
0346887172
-
Synthesis and biological evaluation of [4-(2-phenylethenesulfonylmethyl) phenyl]-quinazolin-4-yl-amines as orally active anti-cancer agents
-
DOI 10.1016/j.bmcl.2003.10.020
-
V.M. Sharma, K.V.A. Seshu, V.C. Sekhar, S. Madan, B. Vishnu, P.A. Babu, C.V. Krishna, J. Sreenu, V.R. Krishna, A. Venkateswarlu, S. Rajagopal, R. Ajaykumar, and T.S. Kumar Synthesis and biological evaluation of [4-(2-phenylethenesulfonylmethyl)phenyl]-quinazolin-4-yl-amines as orally active anti-cancer agents Bioorg. Med. Chem. Lett. 14 2004 67 71 (Pubitemid 38010196)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.1
, pp. 67-71
-
-
Sharma, V.M.1
Seshu, K.V.A.2
Sekhar, V.C.3
Madan, S.4
Vishnu, B.5
Babu, P.A.6
Krishna, C.V.7
Sreenu, J.8
Krishna, V.R.9
Venkateswarlu, A.10
Rajagopal, S.11
Ajaykumar, R.12
Kumar, T.S.13
-
7
-
-
0141727550
-
Design of EGFR kinase inhibitors: A ligand-based approach and its confirmation with structure-based studies
-
DOI 10.1016/S0968-0896(03)00482-6
-
A. Vema, S.K. Panigrahi, G. Rambabu, B. Gopalakrishnan, J.A.R.P. Sarma, and G.R. Desiraju Design of EGFR kinase inhibitors: a ligand-based approach and its confirmation with structure-based studies Bioorg. Med. Chem. 11 2003 4643 4653 (Pubitemid 37194269)
-
(2003)
Bioorganic and Medicinal Chemistry
, vol.11
, Issue.21
, pp. 4643-4653
-
-
Vema, A.1
Panigrahi, S.K.2
Rambabu, G.3
Gopalakrishnan, B.4
Sarma, J.A.R.P.5
Desiraju, G.R.6
-
8
-
-
0035253847
-
Tyrosine kinase inhibitors. 18. 6-Substituted 4-anilinoquinazolines and 4-anilinopyrido[3,4-d]pyrimidines as soluble, irreversible inhibitors of the epidermal growth factor receptor
-
DOI 10.1021/jm000372i
-
J.B. Smaill, H.D. Hollis Showalter, H. Zhou, A.J. Bridges, D.J. McNamara, D.W. Fry, J.M. Nelson, V. Sherwood, P.W. Vincent, B.J. Roberts, W.L. Elliott, and W.A. Denny Tyrosine kinase inhibitors. 18. 6-Substituted 4-anilinoquinazolines and 4-anilinopyrido[3,4-d]pyrimidines as soluble, irreversible inhibitors of the epidermal growth factor receptor J. Med. Chem. 44 3 2001 429 440 (Pubitemid 32113588)
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, Issue.3
, pp. 429-440
-
-
Smaill, J.B.1
Hollis Showalter, H.D.2
Zhou, H.3
Bridges, A.J.4
McNamara, D.J.5
Fry, D.W.6
Nelson, J.M.7
Sherwood, V.8
Vincent, P.W.9
Roberts, B.J.10
Elliott, W.L.11
Denny, W.A.12
-
9
-
-
0035272930
-
The 4-anilinoquinazoline class of inhibitors of the erbB family of receptor tyrosine kinases
-
DOI 10.1016/S0014-827X(01)01026-6, PII S0014827X01010266
-
W.A. Denny The 4-anilinoquinazoline class of inhibitors of the erbB famyli of receptors tyrosine kinases IL. Farmaco. 56 2001 51 56 (Pubitemid 32372583)
-
(2001)
Farmaco
, vol.56
, Issue.1-2
, pp. 51-56
-
-
Denny, W.A.1
-
10
-
-
0035899182
-
6-Substituted-4-(3-bromophenylamino)quinazolines as putative irreversible inhibitors of the epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases with enhanced antitumor activity
-
DOI 10.1021/jm0005555
-
T. Hwei-Ru, N. Mamuya, B.D. Johnson, M.F. Reich, B.C. Gruber, Fei Ye, R. Nilakantan, Ru Shen, C. Discafani, R. DeBlanc, R. Davis, F.E. Koehn, L.M. Greenberger, Yu-Fen Wang, and A. Wissner 6-Substituted-4-(3-bromophenylamino) quinazolines as putative irreversible inhibitors of the epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases with enhanced antitumor activity J. Med. Chem. 44 17 2001 2719 2734 (Pubitemid 32879714)
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, Issue.17
, pp. 2719-2734
-
-
Tsou, H.R.1
Mamuya, N.2
Johnson, B.D.3
Reich, M.F.4
Gruber, B.C.5
Ye, F.6
Nilakantan, R.7
Shen, R.8
Discafani, C.9
DeBlanc, R.10
Davis, R.11
Koehn, F.E.12
Greenberger, L.M.13
Wang, Y.-F.14
Wissner, A.15
-
11
-
-
0033852253
-
Synthesis of 4-(phenylamino)pyrimidine derivatives as ATP-competitive protein kinase inhibitors with potential for cancer chemotherapy
-
G.W. Rewcastle, W.A. Denny, and H.D.H. Showalter Synthesis of 4-(phenylamino)-pyrimidine derivatives as ATP-competitive protein kinase inhibitors with potential for cancer chemotherapy Curr. Org. Chem. 4 2000 679 706 (Pubitemid 30611645)
-
(2000)
Current Organic Chemistry
, vol.4
, Issue.7
, pp. 679-706
-
-
Rewcastle, G.W.1
Denny, W.A.2
Showalter, H.D.H.3
-
12
-
-
0034611617
-
Tyrosine kinase inhibitors. 17. Irreversible inhibitors of the epidermal growth factor receptor: 4-(phenylamino)quinazoline- and 4- (phenylamino) pyrido[3,2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions
-
DOI 10.1021/jm990482t
-
J.B. Smaill, G.W. Rewcastle, J.A. Loo, K.D. Greis, O.H. Chan, E.L. Reyner, E. Lipka, H.D. Hollis Showalter, P.W. Vincent, W.L. Elliott, and W.A. Denny Tyrosine kinase inhibitors. 17. Irreversible inhibitors of the epidermal growth factor receptor: 4-(phenylamino)quinazoline- and 4-(phenylamino)pyrido[3, 2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions J. Med. Chem. 43 7 2000 1380 1397 (Pubitemid 30212579)
-
(2000)
Journal of Medicinal Chemistry
, vol.43
, Issue.7
, pp. 1380-1397
-
-
Smaill, J.B.1
Rewcastle, G.W.2
Loo, J.A.3
Greis, K.D.4
Chan, O.H.5
Reyner, E.L.6
Lipka, E.7
Showalter, H.D.H.8
Vincent, P.W.9
Elliott, W.L.10
Denny, W.A.11
-
13
-
-
0034613645
-
Inhibitors of Src tyrosine kinase: The preparation and structure-activity relationship of 4-anilino-3-cyanoquinolines and 4-anilinoquinazolines
-
Y.D. Wang, K. Miller, D.H. Boschelli, F. Ye, B. Wu, M.B. Floyd, D.W. Powell, A. Wissner, J.M. Weber, and F. Boschelli Inhibitors of Src tyrosine kinase: the preparation and structure-activity relationship of 4-anilino-3-cyanoquinolines and 4-anilinoquinazolines Bioorg. Med. Chem. Lett. 10 2000 2477 2480
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2477-2480
-
-
Wang, Y.D.1
Miller, K.2
Boschelli, D.H.3
Ye, F.4
Wu, B.5
Floyd, M.B.6
Powell, D.W.7
Wissner, A.8
Weber, J.M.9
Boschelli, F.10
-
14
-
-
36049042252
-
Cytotoxicity and detection of damage to DNA by 3-(5-nitro-2-thienyl)-9- chloro-5-mopholin-4-yl-[1,2,4]triazolo[4,3-c]quinazoline on human cancer cell line HeLa
-
Univ. Palacky Olomouc Czech. Repub.
-
R. Ovadekova, S. Jantova, V. Theiszova, and J. Labuda Cytotoxicity and detection of damage to DNA by 3-(5-nitro-2-thienyl)-9-chloro-5-mopholin-4-yl-[1, 2,4]triazolo[4,3-c]quinazoline on human cancer cell line HeLa Biomed. Pap. Med. Fac. 149 2 2005 455 459 Univ. Palacky Olomouc Czech. Repub.
-
(2005)
Biomed. Pap. Med. Fac.
, vol.149
, Issue.2
, pp. 455-459
-
-
Ovadekova, R.1
Jantova, S.2
Theiszova, V.3
Labuda, J.4
-
15
-
-
0034597121
-
Expeditious synthesis and cytotoxic activity of new cyanoindolo[3,2-c] quinolines and benzimidazolo[1,2-c]quinazolines
-
C. Lamazzi, S. Leonce, B. Pfeiffer, P. Renard, G. Guillaumet, C.W. Rees, and T. Besson Expeditious synthesis and cytotoxic activity of new cyanoindolo[3,2-c]quinolines and benzimidazolo[1,2-c]quinazolines Bioorg. Med. Chem. Lett. 10 2000 2183 2185
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2183-2185
-
-
Lamazzi, C.1
Leonce, S.2
Pfeiffer, B.3
Renard, P.4
Guillaumet, G.5
Rees, C.W.6
Besson, T.7
-
16
-
-
1842686942
-
Synthesis and cytotoxic activity of novel quinazolino-carboline-5- one derivatives
-
DOI 10.1016/j.bmc.2004.03.005, PII S0968089604001786
-
R. Baruah, K. Dasu, B. Vaitilingam, P. Mamnoor, P.P. Venkata, S. Rajagopal, and K.R. Yeleswarapu Synthesis and cytotoxic activity of novel quinazolino-β-carboline-5-ones derivatives Bioorg. Med. Chem. 12 2004 1991 1994 (Pubitemid 38471692)
-
(2004)
Bioorganic and Medicinal Chemistry
, vol.12
, Issue.9
, pp. 1991-1994
-
-
Baruah, B.1
Dasu, K.2
Vaitilingam, B.3
Mamnoor, P.4
Venkata, P.P.5
Rajagopal, S.6
Yeleswarapu, K.R.7
-
17
-
-
0032271718
-
Synthesis of 1,2,4-triazino[4,3-c]quinazolines and 4-(pyrazol-1-yl) quinazolines
-
M.A.E. Shaban, M.A.M. Taha, and A.Z. Nasr Synthesis of 1,2,4-triazino[4,3-c]quinazolines and 4-(pyrazol-1-yl)quinazolines Heterocycl. Commun. 4 5 1998 473 478
-
(1998)
Heterocycl. Commun.
, vol.4
, Issue.5
, pp. 473-478
-
-
Shaban, M.A.E.1
Taha, M.A.M.2
Nasr, A.Z.3
-
18
-
-
0038189029
-
Condensed 1,2,4-Triazines: II. Fused to heterocycles with six- and seven-membered rings and fused to two heterocyclic rings
-
E.S.H. El Ashry, N. Rashed, A. Mousaad, and E. Ramadan Condensed 1,2,4-Triazines: II. Fused to heterocycles with six- and seven-membered rings and fused to two heterocyclic rings Adv. Heterocycl. Chem. 61 1994 267 270
-
(1994)
Adv. Heterocycl. Chem.
, vol.61
, pp. 267-270
-
-
El Ashry, E.S.H.1
Rashed, N.2
Mousaad, A.3
Ramadan, E.4
-
19
-
-
77951532099
-
Synthesis of 2-(3,4-dihydro-3-oxo-2H-[1,2,4]triazino[4,3-c]quinazolin-4- yl)acetic acid derivatives as potential antioxidants in nitrosative stress model
-
S.I. Kovalenko, I.F. Belenichev, V.V. Galitsa, and O.V. Krivoshey Synthesis of 2-(3,4-dihydro-3-oxo-2H-[1,2,4]triazino[4,3-c]quinazolin-4-yl) acetic acid derivatives as potential antioxidants in nitrosative stress model Pharmacia 58 2 2010 145 157
-
(2010)
Pharmacia
, vol.58
, Issue.2
, pp. 145-157
-
-
Kovalenko, S.I.1
Belenichev, I.F.2
Galitsa, V.V.3
Krivoshey, O.V.4
-
20
-
-
0000588368
-
Synthesis of some New Heterocyclic Systems bearing 2-Phenyl-6-iodo-4(3H)- quinazolinon-3-yl Moiety as Antibacterial Agents
-
S.G. Abdel-Hamide Synthesis of some new heterocyclic systems bearing 2-phenyl-6-iodo-4(3H)-quinazolinon-3-yl moiety as antibacteral agents J. Indian Chem. Soc. 74 1997 613 618 (Pubitemid 127488769)
-
(1997)
Journal of the Indian Chemical Society
, vol.74
, Issue.8
, pp. 613-618
-
-
Abdel-Hamide, S.G.1
-
21
-
-
0037931032
-
Thiazolydinyl-triazinoquinazolines as potent anti-inflammatory agents
-
E. Bansal, T. Ram, S. Sharma, M. Tyagi, A.P. Rani, K. Bajaj, R. Tyagi, B. Goel, V.K. Srivastava, J.N. Guru, and A. Kumar Thiazolydinyl- triazinoquinazolines as potent anti-inflammatory agents Indian J. Chem. Sect. B. 40 4 2001 307 312
-
(2001)
Indian J. Chem. Sect. B.
, vol.40
, Issue.4
, pp. 307-312
-
-
Bansal, E.1
Ram, T.2
Sharma, S.3
Tyagi, M.4
Rani, A.P.5
Bajaj, K.6
Tyagi, R.7
Goel, B.8
Srivastava, V.K.9
Guru, J.N.10
Kumar, A.11
-
22
-
-
84987313814
-
1,2,4-Triazino[4,3-c]- and [2,3-c]quinazolines
-
D.L. Trepanier, S. Sunder, and W.H. Braun 1,2,4-Triazino[4,3-c]- and [2,3-c]quinazolines J. Heterocycl. Chem. 11 5 1974 747 750
-
(1974)
J. Heterocycl. Chem.
, vol.11
, Issue.5
, pp. 747-750
-
-
Trepanier, D.L.1
Sunder, S.2
Braun, W.H.3
-
23
-
-
0016721915
-
1,2,4-Triazino[4,3-c]- and [2,3-cquinazolines
-
D.L. Trepanier, and S. Sunder 1,2,4-Triazino[4,3-c]- and [2,3-cquinazolines J. Heterocycl. Chem. 12 2 1975 321 326
-
(1975)
J. Heterocycl. Chem.
, vol.12
, Issue.2
, pp. 321-326
-
-
Trepanier, D.L.1
Sunder, S.2
-
24
-
-
49349128974
-
1,2,4-triazines and condensed derivatives - XVI: 1-oxo-1,2-dihydro- and 1-oxo-1,2,6,7-tetrahydro[1,2,4]triazino[1,6-c]-quinazolin-5-ium salts. Synthesis and some reactions
-
G. Doleschall, and K. Lempert 1,2,4-triazines and condensed derivatives - XVI: 1-oxo-1,2-dihydro- and 1-oxo-1,2,6,7-tetrahydro[1,2,4]triazino[1,6-c]- quinazolin-5-ium salts. Synthesis and some reactions Tetrahedron 32 1976 1735 1740
-
(1976)
Tetrahedron
, vol.32
, pp. 1735-1740
-
-
Doleschall, G.1
Lempert, K.2
-
25
-
-
2742583795
-
Synthesis and reactions of some new 1, 2, 4-triazinoquinazolinone derivatives
-
H.A. llimony, H.M. El-Shaaer, S.G. Abdel-Hamide, S.A. Abdel-Aziz, and R.M. Abdel-Rahman Synthesis and reactions of some new 1,2,4- triazinoquinazolinone derivatives Indian J. Chem. Sect. B. 35 10 1996 1026 1030 (Pubitemid 126463393)
-
(1996)
Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry
, vol.35
, Issue.10
, pp. 1026-1030
-
-
Allimony, H.A.1
El-Shaaer, H.M.2
Abdel-Hamide, S.G.3
Abdel-Aziz, S.A.4
Abdel-Rahman, R.M.5
-
26
-
-
0343827624
-
Synthesis and biological evaluation of some new fused quinazoline derivatives
-
S.S. Ibrahim, A.M. Abdel-Halim, Y. Gabr, S. El-Edfawy, and R.M. Abdel-Rahman Synthesis and biological evaluation of some new fused quinazoline derivatives J. Chem. Res. (M) 5 1997 1041 1063
-
(1997)
J. Chem. Res. (M)
, vol.5
, pp. 1041-1063
-
-
Ibrahim, S.S.1
Abdel-Halim, A.M.2
Gabr, Y.3
El-Edfawy, S.4
Abdel-Rahman, R.M.5
-
27
-
-
2942679380
-
Reactivity of 4H-3,1-benzoxazin-4-ones towards nitrogen and carbon nucleophilic reagents: Applications to the synthesis of new heterocycles
-
General Papers
-
H.M.F. Madkour Reactivity of 4H-3,1-benzoxazin-4-ones towards nitrogen and carbon nucleophilic reagents: applications to the synthesis of new heterocycles ARKIVOC i 2004 36 54 (Pubitemid 38783185)
-
(2004)
Arkivoc
, vol.2004
, Issue.1
, pp. 36-54
-
-
Madkour, H.M.F.1
-
28
-
-
35348997901
-
Novel method for the synthesis of [1,2,4]triazino[4,3-c]quinazoline system
-
DOI 10.1080/00397910701569460, PII 783265277
-
S.I. Kovalenko, A.V. Karpenko, O.V. Krivoshey, S.V. Shishkina, and O.V. Shishkin Novel method for the synthesis of [1,2,4]triazino[4,3-c]quinazoline system Synth. Commun. 37 2007 3719 3727 (Pubitemid 47613515)
-
(2007)
Synthetic Communications
, vol.37
, Issue.21
, pp. 3719-3727
-
-
Kovalenko, S.I.1
Karpenko, A.V.2
Krivoshey, O.V.3
Shishkina, S.V.4
Shishkin, O.V.5
-
29
-
-
34547102218
-
A new one-step synthesis of [1,2,4]triazino[2,3-c]quinazolines
-
O.V. Karpenko, S.I. Kovalenko, O.O. Chekotylo, and S.V. Shyshkyna A new one-step synthesis of [1,2,4]triazino[2,3-c]quinazolines HETEROCYCLES 71 3 2007 619 626
-
(2007)
HETEROCYCLES
, vol.71
, Issue.3
, pp. 619-626
-
-
Karpenko, O.V.1
Kovalenko, S.I.2
Chekotylo, O.O.3
Shyshkyna, S.V.4
-
30
-
-
67649336589
-
Synthesis of spiro-fused (C5)-pyrazolino-(C6)-triazinones, a new heterocyclic system
-
A.V. Karpenko, S.I. Kovalenko, and O.V. Shishkin Synthesis of spiro-fused (C5)-pyrazolino-(C6)-triazinones, a new heterocyclic system Tetrahedron 65 31 2009 5964 5972
-
(2009)
Tetrahedron
, vol.65
, Issue.31
, pp. 5964-5972
-
-
Karpenko, A.V.1
Kovalenko, S.I.2
Shishkin, O.V.3
-
31
-
-
80955124793
-
An Efficient Synthesis of 3-R-6-thio-6,7-dihydro-2-[1,2,4]triazino[2,3-c] -quinazoline-2-ones and its Derivatives, Antimicrobial and Antifungal Activity
-
G.G. Berest, A. Yu. Voskoboynic, S.I. Kovalenko, R.S. Sinyak, I.V. Omelchenko, O.V. Shishkin, E.Z. Komarovska-Porokhnyavets, and V.P. Novikov An Efficient Synthesis of 3-R-6-thio-6,7-dihydro-2-[1,2,4]triazino[2,3-c]- quinazoline-2-ones and its Derivatives, Antimicrobial and Antifungal Activity J. Org. Pharm. Chem. 8 3 2010 42 52 http://www.pharm.kharkiv.edu/files/ %D0%96%D0%9E%D0%A4%D0%A5-%E2%84%963-2010-%D1%81.42-51.pdf
-
(2010)
J. Org. Pharm. Chem.
, vol.8
, Issue.3
, pp. 42-52
-
-
Berest, G.G.1
Voskoboynic, A.Yu.2
Kovalenko, S.I.3
Sinyak, R.S.4
Omelchenko, I.V.5
Shishkin, O.V.6
Komarovska-Porokhnyavets, E.Z.7
Novikov, V.P.8
-
32
-
-
80955124782
-
1-thio-6,7-dihydro-2-[1,2,4]triazino[2,3- ]quinazolin-2-nes and their derivatives
-
1-thio-6,7-dihydro-2-[1,2,4]triazino[2,3-] quinazolin-2-nes and their derivatives Official Bulletin "Promyslova Vlasnist" (Industrial Property) 11 2010 3.56 3.57
-
(2010)
Official Bulletin "promyslova Vlasnist" (Industrial Property)
, vol.11
, pp. 356-357
-
-
Kovalenko, S.I.1
Stepanyuk, G.I.2
Berest, G.G.3
Voskoboynik, O.Yu.4
Sinyak, R.S.5
Hodakivskiy, O.A.6
Marinich, L.I.7
Babiy, V.Yu.8
Chornoivan, N.I.9
-
33
-
-
79955637311
-
The many faces of the adamantyl group in drug design
-
J. Liu, D. Obando, V. Liao, T. Lifa, and R. Codd The many faces of the adamantyl group in drug design Eur. J. Med. Chem. 46 2011 1949 1963
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 1949-1963
-
-
Liu, J.1
Obando, D.2
Liao, V.3
Lifa, T.4
Codd, R.5
-
34
-
-
80955124792
-
Features of structure and properties of adamantans
-
oscow
-
E.I. Bagriy Features of structure and properties of adamantans Science 1989 5 57 oscow
-
(1989)
Science
, pp. 5-57
-
-
Bagriy, E.I.1
-
35
-
-
0000220205
-
Some reactions of adamantane and adamantane derivatives
-
10.1021/jo01351a011
-
G.W. Smith, and H.D. Williams Some reactions of adamantane and adamantane derivatives J. Org. Chem. 26 7 1961 2207 2212 10.1021/jo01351a011
-
(1961)
J. Org. Chem.
, vol.26
, Issue.7
, pp. 2207-2212
-
-
Smith, G.W.1
Williams, H.D.2
-
36
-
-
66949129986
-
Synthesis of new 2-thio-[1,2,4]triazolo[1,5-c]quinazoline derivatives and its antimicrobial activity
-
L.N. Antipenko, A.V. Karpenko, S.I. Kovalenko, A.M. Katsev, E. Komarovska-Porokhnyavets, V. Novikov, and A. Chekotilo Synthesis of new 2-thio-[1,2,4]triazolo[1,5-c]quinazoline derivatives and its antimicrobial activity Chem. Pharm. Bull. 57 2009 580 585
-
(2009)
Chem. Pharm. Bull.
, vol.57
, pp. 580-585
-
-
Antipenko, L.N.1
Karpenko, A.V.2
Kovalenko, S.I.3
Katsev, A.M.4
Komarovska-Porokhnyavets, E.5
Novikov, V.6
Chekotilo, A.7
-
37
-
-
84872275587
-
-
Approved Standard - 9th Edition, Wayne, PA, Clinical and Laboratory Standards Institute, CLSI M2-A9
-
Performance Standards for Antimicrobial Disk Susceptibility Tests; Approved Standard - 9th Edition, Wayne, PA, Clinical and Laboratory Standards Institute, CLSI M2-A9.
-
Performance Standards for Antimicrobial Disk Susceptibility Tests
-
-
-
38
-
-
84873082614
-
-
http://dtp.nci.nih.gov.
-
-
-
-
39
-
-
0025775062
-
Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines
-
A. Monks, D. Scudiero, P. Skehan, R. Shoemaker, K. Paull, D. Vistica, C. Hose, J. Langley, P. Cronise, and A. Vaigro-Wolff Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines J. Nat. Cancer Inst. 83 11 1991 757 766
-
(1991)
J. Nat. Cancer Inst.
, vol.83
, Issue.11
, pp. 757-766
-
-
Monks, A.1
Scudiero, D.2
Skehan, P.3
Shoemaker, R.4
Paull, K.5
Vistica, D.6
Hose, C.7
Langley, J.8
Cronise, P.9
Vaigro-Wolff, A.10
-
40
-
-
0028906786
-
Some practical considerations and applications of the National Cancer Institute in vitro anticancer drug discovery screen
-
M.R. Boyd, and K.D. Paull Some practical considerations and applications of the National Cancer Institute in vitro anticancer drug discovery screen Drug Dev. Res. 34 1995 91 109
-
(1995)
Drug Dev. Res.
, vol.34
, pp. 91-109
-
-
Boyd, M.R.1
Paull, K.D.2
-
41
-
-
0003155576
-
The NCI in vitro anticancer drug discovery screen; Concept, implementation and operation
-
B.A. Teicher, Humana Press
-
M.R. Boyd The NCI in vitro anticancer drug discovery screen; concept, implementation and operation B.A. Teicher, Cancer Drug Discovery and Development vol. 2 1997 Humana Press 23 43
-
(1997)
Cancer Drug Discovery and Development
, vol.2
, pp. 23-43
-
-
Boyd, M.R.1
-
42
-
-
0036511069
-
Application of high-throughput, molecular-targeted screening to anticancer drug discovery
-
R.H. Shoemaker, D.A. Scudiero, and G. Melillo Application of high-throughput, molecular-targeted screening to anticancer drug discovery Curr. Top. Med. Chem. 2 3 2002 229 246
-
(2002)
Curr. Top. Med. Chem.
, vol.2
, Issue.3
, pp. 229-246
-
-
Shoemaker, R.H.1
Scudiero, D.A.2
Melillo, G.3
|