-
1
-
-
84949008723
-
Novel insights into mammalian embryonic neural stem cell division: focus onmicrotubules
-
[1] Mora-Bermúdez, F., Huttner, W.B., Novel insights into mammalian embryonic neural stem cell division: focus onmicrotubules. Mol. Biol. Cell. 26 (2015), 4302–4306.
-
(2015)
Mol. Biol. Cell.
, vol.26
, pp. 4302-4306
-
-
Mora-Bermúdez, F.1
Huttner, W.B.2
-
2
-
-
84907535079
-
Recent developments in tubulin polymerization inhibitors: an overview
-
[2] Kaur, R., Kaur, G., Gill, R.K., Soni, R., Bariwal, J., Recent developments in tubulin polymerization inhibitors: an overview. Eur. J. Med. Chem. 87 (2014), 89–124.
-
(2014)
Eur. J. Med. Chem.
, vol.87
, pp. 89-124
-
-
Kaur, R.1
Kaur, G.2
Gill, R.K.3
Soni, R.4
Bariwal, J.5
-
3
-
-
84961933284
-
Synthesis of triazoloquinazolinone based compounds as tubulin polymerizationinhibitors and vascular disrupting agents
-
[3] Driowya, M., Leclercq, M.J., Verones, V., Barczyk, A., Lecoeur, M., Renault, N., Flouquet, N., Ghinet, A., Berthelot, P., Lebegue, N., Synthesis of triazoloquinazolinone based compounds as tubulin polymerizationinhibitors and vascular disrupting agents. Eur. J. Med. Chem. 115 (2016), 393–405.
-
(2016)
Eur. J. Med. Chem.
, vol.115
, pp. 393-405
-
-
Driowya, M.1
Leclercq, M.J.2
Verones, V.3
Barczyk, A.4
Lecoeur, M.5
Renault, N.6
Flouquet, N.7
Ghinet, A.8
Berthelot, P.9
Lebegue, N.10
-
4
-
-
84995582050
-
Dynamics of microtubules and their associated proteins: recent insights and clinical implications
-
[4] Gan-Or, Z., Rouleau, G.A., Benarroch, E.E., Dynamics of microtubules and their associated proteins: recent insights and clinical implications. Neurology, 87, 2016, 2173.
-
(2016)
Neurology
, vol.87
, pp. 2173
-
-
Gan-Or, Z.1
Rouleau, G.A.2
Benarroch, E.E.3
-
5
-
-
84872113095
-
Design and synthesis of biaryl aryl stilbenes/ethylenes as antimicrotubule agents
-
[5] Kumar, A.S., Reddy, M.A., Jain, N., Kishor, C., Murthy, T.R., Ramesh, D., Supriya, B., Addlagatta, A., Kalivendi, S.V., Sreedhar, B., Design and synthesis of biaryl aryl stilbenes/ethylenes as antimicrotubule agents. Eur. J. Med. Chem. 60 (2013), 305–324.
-
(2013)
Eur. J. Med. Chem.
, vol.60
, pp. 305-324
-
-
Kumar, A.S.1
Reddy, M.A.2
Jain, N.3
Kishor, C.4
Murthy, T.R.5
Ramesh, D.6
Supriya, B.7
Addlagatta, A.8
Kalivendi, S.V.9
Sreedhar, B.10
-
6
-
-
84966666523
-
Cytoskeleton: microtubules set the beat
-
[6] Strzyz, P., Cytoskeleton: microtubules set the beat. Nat. Rev. Mol. Cell Biol., 17, 2016, 333.
-
(2016)
Nat. Rev. Mol. Cell Biol.
, vol.17
, pp. 333
-
-
Strzyz, P.1
-
7
-
-
77957374075
-
Microtubule-binding agents: a dynamic field of cancer therapeutics
-
[7] Dumontet, C., Jordan, M.A., Microtubule-binding agents: a dynamic field of cancer therapeutics. Nat. Rev. Drug Discov. 9 (2010), 790–803.
-
(2010)
Nat. Rev. Drug Discov.
, vol.9
, pp. 790-803
-
-
Dumontet, C.1
Jordan, M.A.2
-
8
-
-
84956594266
-
Design, synthesis and molecular docking studies of novel indole-pyrimidine hybrids as tubulin polymerization inhibitors
-
[8] Hu, M.J., Zhang, B., Yang, H.K., Liu, Y., Chen, Y.R., Ma, T.Z., Lu, L., You, W.W., Zhao, P.L., Design, synthesis and molecular docking studies of novel indole-pyrimidine hybrids as tubulin polymerization inhibitors. Chem. Biol. Drug Des. 86 (2015), 1491–1500.
-
(2015)
Chem. Biol. Drug Des.
, vol.86
, pp. 1491-1500
-
-
Hu, M.J.1
Zhang, B.2
Yang, H.K.3
Liu, Y.4
Chen, Y.R.5
Ma, T.Z.6
Lu, L.7
You, W.W.8
Zhao, P.L.9
-
9
-
-
84920842452
-
Discovery of (2S)-8-[(3R)-3-methylmorpholin-4-yl]-1-(3-methyl-2-oxobutyl)-2-(trifluoromethyl)-3,4-dihydro-2H-pyrimido[1,2-a]pyrimidin-6-one: a novel potent andselective inhibitor of Vps34 for the treatment of solid tumors
-
[9] Pasquier, B., El-Ahmad, Y., Filoche-Rommé, B., Dureuil, C., Fassy, F., Abecassis, P.Y., Mathieu, M., Bertrand, T., Benard, T., Barrière, C., El Batti, S., Letallec, J.P., Sonnefraud, V., Brollo, M., Delbarre, L., Loyau, V., Pilorge, F., Bertin, L., Richepin, P., Arigon, J., Labrosse, J.R., Clément, J., Durand, F., Combet, R., Perraut, P., Leroy, V., Gay, F., Lefrançois, D., Bretin, F., Marquette, J.P., Michot, N., Caron, A., Castell, C., Schio, L., McCort, G., Goulaouic, H., Garcia- Echeverria, C., Ronan, B., Discovery of (2S)-8-[(3R)-3-methylmorpholin-4-yl]-1-(3-methyl-2-oxobutyl)-2-(trifluoromethyl)-3,4-dihydro-2H-pyrimido[1,2-a]pyrimidin-6-one: a novel potent andselective inhibitor of Vps34 for the treatment of solid tumors. J. Med. Chem. 58 (2015), 376–400.
-
(2015)
J. Med. Chem.
, vol.58
, pp. 376-400
-
-
Pasquier, B.1
El-Ahmad, Y.2
Filoche-Rommé, B.3
Dureuil, C.4
Fassy, F.5
Abecassis, P.Y.6
Mathieu, M.7
Bertrand, T.8
Benard, T.9
Barrière, C.10
El Batti, S.11
Letallec, J.P.12
Sonnefraud, V.13
Brollo, M.14
Delbarre, L.15
Loyau, V.16
Pilorge, F.17
Bertin, L.18
Richepin, P.19
Arigon, J.20
Labrosse, J.R.21
Clément, J.22
Durand, F.23
Combet, R.24
Perraut, P.25
Leroy, V.26
Gay, F.27
Lefrançois, D.28
Bretin, F.29
Marquette, J.P.30
Michot, N.31
Caron, A.32
Castell, C.33
Schio, L.34
McCort, G.35
Goulaouic, H.36
Garcia- Echeverria, C.37
Ronan, B.38
more..
-
10
-
-
84951789086
-
Discovery of 2-(2-aminopyrimidin-5-yl)-4- morpholino-N-(pyridin-3-yl)quinazolin-7-amines as novel PI3K/mTOR inhibitors and anticancer agents
-
[10] Peng, W., Tu, Z.C., Long, Z.J., Liu, Q.T., Lu, G., Discovery of 2-(2-aminopyrimidin-5-yl)-4- morpholino-N-(pyridin-3-yl)quinazolin-7-amines as novel PI3K/mTOR inhibitors and anticancer agents. Eur. J. Med. Chem. 108 (2016), 644–654.
-
(2016)
Eur. J. Med. Chem.
, vol.108
, pp. 644-654
-
-
Peng, W.1
Tu, Z.C.2
Long, Z.J.3
Liu, Q.T.4
Lu, G.5
-
11
-
-
80455140538
-
Discovery of a potent, selective, and orally available class I phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) kinase inhibitor (GDC-0980) for the treatment of cancer
-
[11] Sutherlin, D.P., Bao, L., Berry, M., Castanedo, G., Chuckowree, I., Dotson, J., Folks, A., Friedman, L., Goldsmith, R., Gunzner, J., Heffron, T., Lesnick, J., Lewis, C., Mathieu, S., Murray, J., Nonomiya, J., Pang, J., Pegg, N., Prior, W.W., Rouge, L., Salphati, L., Sampath, D., Tian, Q., Tsui, V., Wan, N.C., Wang, S., Wei, B., Wiesmann, C., Wu, P., Zhu, B.Y., Olivero, A., Discovery of a potent, selective, and orally available class I phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) kinase inhibitor (GDC-0980) for the treatment of cancer. J. Med. Chem. 54 (2011), 7579–7587.
-
(2011)
J. Med. Chem.
, vol.54
, pp. 7579-7587
-
-
Sutherlin, D.P.1
Bao, L.2
Berry, M.3
Castanedo, G.4
Chuckowree, I.5
Dotson, J.6
Folks, A.7
Friedman, L.8
Goldsmith, R.9
Gunzner, J.10
Heffron, T.11
Lesnick, J.12
Lewis, C.13
Mathieu, S.14
Murray, J.15
Nonomiya, J.16
Pang, J.17
Pegg, N.18
Prior, W.W.19
Rouge, L.20
Salphati, L.21
Sampath, D.22
Tian, Q.23
Tsui, V.24
Wan, N.C.25
Wang, S.26
Wei, B.27
Wiesmann, C.28
Wu, P.29
Zhu, B.Y.30
Olivero, A.31
more..
-
12
-
-
83355163329
-
GDC-0980 is a novel class I PI3K/mTOR kinase inhibitor with robust activity in cancer models driven by the PI3K pathway
-
[12] Wallin, J.J., Edgar, K.A., Guan, J.E., Berry, M., Prior, W.W., Lee, L., Lesnick, J.D., Lewis, C., Nonomiya, J., Pang, J.D., Salphati, L., Olivero, A.G., Sutherlin, D.P., O'Brien, C., Spoerke, J.M., Patel, S., Lensun, L., Kassees, R., Ross, L., Lackner, M.R., Sampath, D., Belvin, M., Friedman, L.S., GDC-0980 is a novel class I PI3K/mTOR kinase inhibitor with robust activity in cancer models driven by the PI3K pathway. Mol. Cancer Ther. 10 (2011), 2426–2436.
-
(2011)
Mol. Cancer Ther.
, vol.10
, pp. 2426-2436
-
-
Wallin, J.J.1
Edgar, K.A.2
Guan, J.E.3
Berry, M.4
Prior, W.W.5
Lee, L.6
Lesnick, J.D.7
Lewis, C.8
Nonomiya, J.9
Pang, J.D.10
Salphati, L.11
Olivero, A.G.12
Sutherlin, D.P.13
O'Brien, C.14
Spoerke, J.M.15
Patel, S.16
Lensun, L.17
Kassees, R.18
Ross, L.19
Lackner, M.R.20
Sampath, D.21
Belvin, M.22
Friedman, L.S.23
more..
-
13
-
-
34250823572
-
Pharmacologic characterization of a potent inhibitor of class I phosphatidylinositide 3-kinases
-
[13] Raynaud, F.I., Eccles, S., Clarke, P.A., Hayes, A., Nutley, B., Alix, S., Henley, A., Di-Stefano, F., Ahmad, Z., Guillard, S., Bjerke, L.M., Kelland, L., Valenti, M., Patterson, L., Gowan, S., de Haven Brandon, A., Hayakawa, M., Kaizawa, H., Koizumi, T., Ohishi, T., Patel, S., Saghir, N., Parker, P., Waterfield, M., Workman, P., Pharmacologic characterization of a potent inhibitor of class I phosphatidylinositide 3-kinases. Cancer Res. 67 (2007), 5840–5850.
-
(2007)
Cancer Res.
, vol.67
, pp. 5840-5850
-
-
Raynaud, F.I.1
Eccles, S.2
Clarke, P.A.3
Hayes, A.4
Nutley, B.5
Alix, S.6
Henley, A.7
Di-Stefano, F.8
Ahmad, Z.9
Guillard, S.10
Bjerke, L.M.11
Kelland, L.12
Valenti, M.13
Patterson, L.14
Gowan, S.15
de Haven Brandon, A.16
Hayakawa, M.17
Kaizawa, H.18
Koizumi, T.19
Ohishi, T.20
Patel, S.21
Saghir, N.22
Parker, P.23
Waterfield, M.24
Workman, P.25
more..
-
14
-
-
51649088622
-
PI-103, a dual inhibitor of class IA phosphatidylinositide 3-kinase and mTOR, has antileukemic activity in AML
-
[14] Park, S., Chapuis, N., Bardet, V., Tamburini, J., Gallay, N., Willems, L., Knight, Z.A., Shokat, K.M., Azar, N., Viguie, F., Ifrah, N., Dreyfus, F., Mayeux, P., Lacombe, C., Bouscary, D., PI-103, a dual inhibitor of class IA phosphatidylinositide 3-kinase and mTOR, has antileukemic activity in AML. Leukemia 22 (2008), 1698–1706.
-
(2008)
Leukemia
, vol.22
, pp. 1698-1706
-
-
Park, S.1
Chapuis, N.2
Bardet, V.3
Tamburini, J.4
Gallay, N.5
Willems, L.6
Knight, Z.A.7
Shokat, K.M.8
Azar, N.9
Viguie, F.10
Ifrah, N.11
Dreyfus, F.12
Mayeux, P.13
Lacombe, C.14
Bouscary, D.15
-
15
-
-
80054737055
-
Identification of NVP-BKM120 as a potent, selective, orally bioavailable class I PI3 kinase inhibitor for treating cancer
-
[15] Burger, M.T., Pecchi, S., Wagman, A., Ni, Z.J., Knapp, M., Hendrickson, T., Atallah, G., Pfister, K., Zhang, Y., Bartulis, S., Frazier, K., Ng, S., Smith, A., Verhagen, J., Haznedar, J., Huh, K., Iwanowicz, E., Xin, X., Menezes, D., Merritt, H., Lee, I., Wiesmann, M., Kaufman, S., Crawford, K., Chin, M., Bussiere, D., Shoemaker, K., Zaror, I., Maira, S.M., Voliva, C.F., Identification of NVP-BKM120 as a potent, selective, orally bioavailable class I PI3 kinase inhibitor for treating cancer. ACS Med. Chem. Lett. 2 (2011), 774–779.
-
(2011)
ACS Med. Chem. Lett.
, vol.2
, pp. 774-779
-
-
Burger, M.T.1
Pecchi, S.2
Wagman, A.3
Ni, Z.J.4
Knapp, M.5
Hendrickson, T.6
Atallah, G.7
Pfister, K.8
Zhang, Y.9
Bartulis, S.10
Frazier, K.11
Ng, S.12
Smith, A.13
Verhagen, J.14
Haznedar, J.15
Huh, K.16
Iwanowicz, E.17
Xin, X.18
Menezes, D.19
Merritt, H.20
Lee, I.21
Wiesmann, M.22
Kaufman, S.23
Crawford, K.24
Chin, M.25
Bussiere, D.26
Shoemaker, K.27
Zaror, I.28
Maira, S.M.29
Voliva, C.F.30
more..
-
16
-
-
84904555503
-
Phase I doseescalation and -expansion study of buparlisib (BKM120), an oral pan-class I PI3K inhibitor, in patients with advanced solid tumors
-
[16] Rodon, J., Brana, I., Siu, L.L., De Jonge, M.J., Homji, N., Mills, D., Di Tomaso, E., Sarr, C., Trandafir, L., Massacesi, C., Eskens, F., Bendell, J.C., Phase I doseescalation and -expansion study of buparlisib (BKM120), an oral pan-class I PI3K inhibitor, in patients with advanced solid tumors. Invest. New. Drugs 32 (2014), 670–681.
-
(2014)
Invest. New. Drugs
, vol.32
, pp. 670-681
-
-
Rodon, J.1
Brana, I.2
Siu, L.L.3
De Jonge, M.J.4
Homji, N.5
Mills, D.6
Di Tomaso, E.7
Sarr, C.8
Trandafir, L.9
Massacesi, C.10
Eskens, F.11
Bendell, J.C.12
-
17
-
-
85017280396
-
5-Substituted 3-isopropyl-7-[4-(2-pyridyl)benzyl]amino-1(2)Hpyrazolo[4,3-d]pyrimidines with anti-proliferative activity as potent and selective inhibitors of cyclin-dependent kinases
-
[17] Vymětalová, L., Havlíček, L., Šturc, A., Skrášková, Z., Jorda, R., Pospíšil, T., Strnad, M., Kryštof, V., 5-Substituted 3-isopropyl-7-[4-(2-pyridyl)benzyl]amino-1(2)Hpyrazolo[4,3-d]pyrimidines with anti-proliferative activity as potent and selective inhibitors of cyclin-dependent kinases. Eur. J. Med. Chem. 110 (2016), 291–301.
-
(2016)
Eur. J. Med. Chem.
, vol.110
, pp. 291-301
-
-
Vymětalová, L.1
Havlíček, L.2
Šturc, A.3
Skrášková, Z.4
Jorda, R.5
Pospíšil, T.6
Strnad, M.7
Kryštof, V.8
-
18
-
-
85051917622
-
Preparation of Bicyclic Indolylpyrimidine Derivatives for Use as PI3K-p110d Inhibitors and Useful in Treatment of PI3 Kinase Mediated Disorders
-
WO 2010136491.
-
[18] G. Castanedo, D.M. Goldstein, R. K. Kondru, M.C. Lucas, W.S. Palmer, S. Price, B. Safina, P.P.A. Savy, E.M. Seward, D.P. Sutherlin. et al., Preparation of Bicyclic Indolylpyrimidine Derivatives for Use as PI3K-p110d Inhibitors and Useful in Treatment of PI3 Kinase Mediated Disorders, WO 2010136491.
-
-
-
Castanedo, G.1
Goldstein, D.M.2
Kondru, R.K.3
Lucas, M.C.4
Palmer, W.S.5
Price, S.6
Safina, B.7
Savy, P.P.A.8
Seward, E.M.9
Sutherlin, D.P.10
-
19
-
-
84885437427
-
Synthesis and evaluation of novel 4-nitropyrrole-based 1,3,4-oxadiazole derivatives as antimicrobial and anti-tubercular agents
-
[19] Rane, R.A., Bangalore, P., Borhade, S.D., Khandare, P.K., Synthesis and evaluation of novel 4-nitropyrrole-based 1,3,4-oxadiazole derivatives as antimicrobial and anti-tubercular agents. Eur. J. Med. Chem. 70 (2013), 49–58.
-
(2013)
Eur. J. Med. Chem.
, vol.70
, pp. 49-58
-
-
Rane, R.A.1
Bangalore, P.2
Borhade, S.D.3
Khandare, P.K.4
-
20
-
-
84995804525
-
Raić-Malić. Novel pyrimidine-2,4-dione-1,2,3-triazole and furo[2,3-d]pyrimidine-2-one-1,2,3-triazole hybrids as potential anti-cancer agents: synthesis, computational and X-ray analysis and biological evaluation
-
[20] Gregorić, M., Sedić, P.A., Grbčić, K.P.S., Tomljenović, M., Cetina, R., Vianello, S., Raić-Malić. Novel pyrimidine-2,4-dione-1,2,3-triazole and furo[2,3-d]pyrimidine-2-one-1,2,3-triazole hybrids as potential anti-cancer agents: synthesis, computational and X-ray analysis and biological evaluation. Eur. J. Med. Chem. 125 (2016), 1247–1267.
-
(2016)
Eur. J. Med. Chem.
, vol.125
, pp. 1247-1267
-
-
Gregorić, M.1
Sedić, P.A.2
Grbčić, K.P.S.3
Tomljenović, M.4
Cetina, R.5
Vianello, S.6
-
21
-
-
84924023636
-
Design, synthesis, and structure-activity relationship of novel LSD1 inhibitors based on pyrimidine-thiourea hybrids as potent, orally active antitumor agents
-
[21] Ma, L.Y., Zheng, Y.C., Wang, S.Q., Wang, B., Wang, Z.R., Pang, L.P., Zhang, M., Wang, J.W., Ding, L., Li, J., Wang, C., Hu, B., Liu, Y., Zhang, X.D., Wang, J.J., Wang, Z.J., Zhao, W., Liu, H.M., Design, synthesis, and structure-activity relationship of novel LSD1 inhibitors based on pyrimidine-thiourea hybrids as potent, orally active antitumor agents. J. Med. Chem. 58 (2015), 1705–1716.
-
(2015)
J. Med. Chem.
, vol.58
, pp. 1705-1716
-
-
Ma, L.Y.1
Zheng, Y.C.2
Wang, S.Q.3
Wang, B.4
Wang, Z.R.5
Pang, L.P.6
Zhang, M.7
Wang, J.W.8
Ding, L.9
Li, J.10
Wang, C.11
Hu, B.12
Liu, Y.13
Zhang, X.D.14
Wang, J.J.15
Wang, Z.J.16
Zhao, W.17
Liu, H.M.18
-
22
-
-
84996487021
-
Multiple biological activities and molecular docking studies of newly synthesized 3-(pyridin-4-yl)-1H-pyrazole-5-carboxamide chalcone hybrids
-
[22] Sribalan, R., Banuppriya, G., Kirubavathi, M., Jayachitra, A., Padmini, V., Multiple biological activities and molecular docking studies of newly synthesized 3-(pyridin-4-yl)-1H-pyrazole-5-carboxamide chalcone hybrids. Bioorg Med. Chem. Lett. 26 (2016), 5624–5630.
-
(2016)
Bioorg Med. Chem. Lett.
, vol.26
, pp. 5624-5630
-
-
Sribalan, R.1
Banuppriya, G.2
Kirubavathi, M.3
Jayachitra, A.4
Padmini, V.5
-
23
-
-
84962204060
-
Design and synthesis of 1-((1,5-Bis(4-chlorophenyl)-2-methyl-1H-pyrrol-3-yl)methyl)-4-methylpiperazine (BM212) and N-Adamantan-2-yl-N'-((E)-3,7-dimethylocta-2,6-dienyl)ethane-1,2-diamine (SQ109) pyrrole hybrid derivatives: discovery of potent antitubercular agents effective against multidrug-resistant mycobacteria
-
[23] Bhakta, S., Scalacci, N., Maitra, A., Brown, A.K., Dasugari, S., Evangelopoulos, D., McHugh, T.D., Mortazavi, P.N., Twist, A., Petricci, E., Manetti, F., Castagnolo, D., Design and synthesis of 1-((1,5-Bis(4-chlorophenyl)-2-methyl-1H-pyrrol-3-yl)methyl)-4-methylpiperazine (BM212) and N-Adamantan-2-yl-N'-((E)-3,7-dimethylocta-2,6-dienyl)ethane-1,2-diamine (SQ109) pyrrole hybrid derivatives: discovery of potent antitubercular agents effective against multidrug-resistant mycobacteria. J. Med. Chem. 59 (2016), 2780–2793.
-
(2016)
J. Med. Chem.
, vol.59
, pp. 2780-2793
-
-
Bhakta, S.1
Scalacci, N.2
Maitra, A.3
Brown, A.K.4
Dasugari, S.5
Evangelopoulos, D.6
McHugh, T.D.7
Mortazavi, P.N.8
Twist, A.9
Petricci, E.10
Manetti, F.11
Castagnolo, D.12
-
24
-
-
84897850835
-
Efficient one-pot synthesis of 3-amino-7-azaindoles under microwave irradiation
-
[24] Yang, H.K., You, W.W., Yan, G.H., Jiang, Z.H., Zhao, P.L., Zhou, Z.Z., Efficient one-pot synthesis of 3-amino-7-azaindoles under microwave irradiation. Synth. Commun. 44 (2014), 1165–1171.
-
(2014)
Synth. Commun.
, vol.44
, pp. 1165-1171
-
-
Yang, H.K.1
You, W.W.2
Yan, G.H.3
Jiang, Z.H.4
Zhao, P.L.5
Zhou, Z.Z.6
-
25
-
-
84864407684
-
One-pot synthesis of novel isoindoline-1,3-dione derivatives bearing 1,2,4-triazole moiety and their preliminary biological evaluation
-
[25] Zhao, P.L., Ma, W.F., Duan, A.N., Zou, M., Yan, Y.C., You, W.W., Wu, S.G., One-pot synthesis of novel isoindoline-1,3-dione derivatives bearing 1,2,4-triazole moiety and their preliminary biological evaluation. Eur. J. Med. Chem. 54 (2012), 813–822.
-
(2012)
Eur. J. Med. Chem.
, vol.54
, pp. 813-822
-
-
Zhao, P.L.1
Ma, W.F.2
Duan, A.N.3
Zou, M.4
Yan, Y.C.5
You, W.W.6
Wu, S.G.7
-
26
-
-
1642401199
-
Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain
-
[26] Ravelli, R.B., Gigant, B., Curmi, P.A., Jourdain, I., Lachkar, S., Sobel, A., Knossow, M., Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain. Nature 428 (2004), 198–202.
-
(2004)
Nature
, vol.428
, pp. 198-202
-
-
Ravelli, R.B.1
Gigant, B.2
Curmi, P.A.3
Jourdain, I.4
Lachkar, S.5
Sobel, A.6
Knossow, M.7
-
27
-
-
0015595694
-
Microtubule assembly in the absence of added nucleotides
-
[27] Shelanski, M.L., Gaskin, F., Cantor, C.R., Microtubule assembly in the absence of added nucleotides. Proc. Natl. Acad. Sci. U.S.A. 70 (1973), 765–768.
-
(1973)
Proc. Natl. Acad. Sci. U.S.A.
, vol.70
, pp. 765-768
-
-
Shelanski, M.L.1
Gaskin, F.2
Cantor, C.R.3
-
28
-
-
0037380829
-
A fluorescence-based high-throughput assay for antimicrotubule drugs
-
[28] Barron, D.M., Chatterjee, S.K., Ravindra, R., Roof, R., Baloglu, E., Kingston, D.G.I., Bane, S., A fluorescence-based high-throughput assay for antimicrotubule drugs. Anal. Biochem. 315 (2003), 49–56.
-
(2003)
Anal. Biochem.
, vol.315
, pp. 49-56
-
-
Barron, D.M.1
Chatterjee, S.K.2
Ravindra, R.3
Roof, R.4
Baloglu, E.5
Kingston, D.G.I.6
Bane, S.7
-
29
-
-
79951476387
-
PROPKA3: consistent treatment of internal and surface residues in empirical pKa predictions
-
[29] Olsson, M.H.M., Søndergard, C.R., Rostkowski, M., Jensen, J.H., PROPKA3: consistent treatment of internal and surface residues in empirical pKa predictions. J. Chem. Theor. Comput. 7 (2011), 525–537.
-
(2011)
J. Chem. Theor. Comput.
, vol.7
, pp. 525-537
-
-
Olsson, M.H.M.1
Søndergard, C.R.2
Rostkowski, M.3
Jensen, J.H.4
|