-
1
-
-
78649326709
-
2-Azetidinone: A new profile of various pharmacological activities
-
(a) Mehta, P.D.; Sengar, N.P.S.; Pathak, A.K. 2-Azetidinone: A new profile of various pharmacological activities. Eur. J. Med. Chem., 2010, 45, 5541-5560
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 5541-5560
-
-
Mehta, P.D.1
Sengar, N.P.S.2
Pathak, A.K.3
-
2
-
-
78650162473
-
Highly reactive 4-membered ring nitrogen-containing heterocycles: Synthesis and properties
-
(b) Alcaide, B.; Almendros, P.; Aragoncillo, C. Highly reactive 4-membered ring nitrogen-containing heterocycles: Synthesis and properties. Curr. Opin. Drug Disc., 2010, 13, 685-697
-
(2010)
Curr. Opin. Drug Disc.
, vol.13
, pp. 685-697
-
-
Alcaide, B.1
Almendros, P.2
Aragoncillo, C.3
-
3
-
-
54049106971
-
Drug delivery approaches to overcome bacterial resistance to beta-lactam antibiotics
-
(c) Abeylath, S.C.; Turos, E. Drug delivery approaches to overcome bacterial resistance to beta-lactam antibiotics. Expert Opin. Drug Del., 2008, 5, 931-949
-
(2008)
Expert Opin. Drug Del.
, vol.5
, pp. 931-949
-
-
Abeylath, S.C.1
Turos, E.2
-
4
-
-
4444380663
-
Recent developments in the design of mechanism-based and alternate substrate inhibitors of serine proteases
-
DOI 10.2174/1568026043387971
-
(d) Zhong, J.Y.; Groutas, W.C. Recent developments in the design of mechanism-based and alternate substrate inhibitors of serine proteases. Curr. Top. Med. Chem., 2004, 4, 1203-1216. (Pubitemid 39172332)
-
(2004)
Current Topics in Medicinal Chemistry
, vol.4
, Issue.12
, pp. 1203-1216
-
-
Zhong, J.1
Groutas, W.C.2
-
6
-
-
0042423395
-
Design of β-lactams with mechanism based nonantibacterial activities
-
DOI 10.2174/0929867033457089
-
Veinberg, G.; Vorona, M.; Shestakova, I.; Kanepe, I.; Lukevics, E. Design of β-Lactams with Mechanism Based Nonantibacterial Activities. Curr. Med. Chem., 2003, 10, 1741-1757. (Pubitemid 37038597)
-
(2003)
Current Medicinal Chemistry
, vol.10
, Issue.17
, pp. 1741-1757
-
-
Veinberg, G.1
Vorona, M.2
Shestakova, I.3
Kanepe, I.4
Lukevics, E.5
-
7
-
-
3042621839
-
β-Lactam cholesterol absorption inhibitors
-
Burnett, D.A. β-Lactam Cholesterol Absorption Inhibitors. Curr.Med.Chem., 2004, 11, 1873-1887.
-
(2004)
Curr.Med.Chem.
, vol.11
, pp. 1873-1887
-
-
Burnett, D.A.1
-
8
-
-
70450211715
-
β-Lactamase inhibitors: The story so far
-
Perez-Llarena, F.J.; Bou, G. β-Lactamase Inhibitors: The Story so Far. Curr. Med. Chem., 2009, 16, 3740-3765.
-
(2009)
Curr. Med. Chem.
, vol.16
, pp. 3740-3765
-
-
Perez-Llarena, F.J.1
Bou, G.2
-
9
-
-
67651114152
-
β-Lactams as neuroprotective agents
-
Konaklieva, M.I.; Plotkin, B.J.; Herbert, T. β-Lactams as Neuroprotective Agents. Anti-Infective Agents Med. Chem., 2009, 8, 28-35.
-
(2009)
Anti-Infective Agents Med. Chem.
, vol.8
, pp. 28-35
-
-
Konaklieva, M.I.1
Plotkin, B.J.2
Herbert, T.3
-
10
-
-
63149127459
-
Current status of newer carbapenems
-
Bassetti, M.; Nicolini, L.; Esposito, S.; Righi, E.; Viscoli, C. Current Status of Newer Carbapenems. Curr. Med. Chem., 2009, 16, 564-575.
-
(2009)
Curr. Med. Chem.
, vol.16
, pp. 564-575
-
-
Bassetti, M.1
Nicolini, L.2
Esposito, S.3
Righi, E.4
Viscoli, C.5
-
11
-
-
0019462457
-
Monocyclic β-lactam antibiotics produced by bacteria
-
DOI 10.1038/291489a0
-
Sykes, R.B.; Cimarusti, C.M.; Bonner, D.P.; Bush, K.; Floyd, D.M.; Georgopapadakou, N.H.; Koster, W.H.; Liu, W.C.; Parker, W.L.; Prindpe, P.A.; Rathnum, M.L.; Slusarchyk, W.A.; Trejo, W.H.; Wells, J.S. Monocyclic β-lactam antibiotics produced by bacteria. Nature, 1981, 291, 489-491. (Pubitemid 11093664)
-
(1981)
Nature
, vol.291
, Issue.5815
, pp. 489-491
-
-
Sykes, R.B.1
Cimarusti, C.M.2
Bonner, D.P.3
-
12
-
-
0023678710
-
A Highly Efficient Practical approach to natural Taxol
-
Denis, J-N.; Greene, A.E.; Guenard, D.; Gueritte-Voegelein, F.; Mangatal, L.; Potier, P. A Highly Efficient, Practical approach to natural Taxol. J. Am. Chem. Soc., 1988, 110, 5917-5919.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 5917-5919
-
-
Denis, J.-N.1
Greene, A.E.2
Guenard, D.3
Gueritte-Voegelein, F.4
Mangatal, L.5
Potier, P.6
-
14
-
-
38849098435
-
Hugo (Ugo) Schiff, Schiff bases, and a century of β-lactam synthesis
-
DOI 10.1002/anie.200702965
-
(a) For reviews on the Staudinger reaction, see: (a) Tidwell, T.T. Hugo (Ugo) Schiff, Schiff Bases, and a Century of β-Lactam Synthesis. Angew. Chem. Int. Ed., 2008, 47, 1016-1020 (Pubitemid 351204394)
-
(2008)
Angewandte Chemie - International Edition
, vol.47
, Issue.6
, pp. 1016-1020
-
-
Tidwell, T.T.1
-
15
-
-
53049101572
-
Preparation of betalactams by [2+2] cycloaddition of ketenes and imines
-
(b) Fu, N.; Tidwell, T.T. Preparation of betalactams by [2+2] cycloaddition of ketenes and imines. Tetrahedron, 2008, 64, 10465-10496
-
(2008)
Tetrahedron
, vol.64
, pp. 10465-10496
-
-
Fu, N.1
Tidwell, T.T.2
-
16
-
-
3042663164
-
Asymmetric synthesis of β-lactams through the Staudinger reaction and their use as building blocks of natural and nonnatural products
-
(c) Palomo, C.; Aizpurua, J.M.; Ganboa, I.; Oiarbide, M. Asymmetric synthesis of beta-lactams through the Staudinger reaction and their use as building blocks of natural and nonnatural products. Curr. Med. Chem., 2004, 11, 1837-1872 (Pubitemid 38828202)
-
(2004)
Current Medicinal Chemistry
, vol.11
, Issue.14
, pp. 1837-1872
-
-
Palomo, C.1
Aizpurua, J.M.2
Ganboa, I.3
Oiarbide, M.4
-
17
-
-
0032707721
-
Asymmetric synthesis of β-Lactams by Staudinger ketene-imine cycloaddition reaction
-
(d) Palomo, C.; Aizpurua, J.M.; Ganboa, I.; Oiarbide, M. Asymmetric synthesis of β-Lactams by Staudinger ketene-imine cycloaddition reaction. Eur. J. Org. Chem., 1999, 12, 3223-3235
-
(1999)
Eur. J. Org. Chem.
, vol.12
, pp. 3223-3235
-
-
Palomo, C.1
Aizpurua, J.M.2
Ganboa, I.3
Oiarbide, M.4
-
18
-
-
0000869493
-
Chiral control of the Staudinger reaction
-
(e) Cooper, R.G.D.; Daugherty, B.W.; Boyd, D.B. Chiral control of the Staudinger reaction. Pure Appl. Chem., 1987, 59, 485-492.
-
(1987)
Pure Appl. Chem.
, vol.59
, pp. 485-492
-
-
Cooper, R.G.D.1
Daugherty, B.W.2
Boyd, D.B.3
-
19
-
-
67650694508
-
Catalytic, asymmetric reactions of ketenes and ketene enolates
-
For the catalytic asymmetric Staudinger reaction to give β-Lactams see for instance: Paull, D.H.; Weatherwax, A.; Lectka, T. Catalytic, asymmetric reactions of ketenes and ketene enolates. Tetrahedron, 2009, 65, 6771-6803, and references cited therein.
-
(2009)
Tetrahedron
, vol.65
, pp. 6771-6803
-
-
Paull, D.H.1
Weatherwax, A.2
Lectka, T.3
-
20
-
-
80052950929
-
Synthesis and antimicrobial activities of 2-azetidinone and its derivatives
-
Murhekar, M.M.; Khadsan R.E. Synthesis and antimicrobial activities of 2-azetidinone and its derivatives. Pharma Chemica, 2010, 2(4), 219-223.
-
(2010)
Pharma Chemica
, vol.2
, Issue.4
, pp. 219-223
-
-
Murhekar, M.M.1
Khadsan, R.E.2
-
21
-
-
80052920529
-
Synthesis, characterisation of some 2-azetidinone derivatives from 2-aminopyridine and evaluation of their antimicrobial activity
-
Mathew, B.; Mathew, G.E.; Mathew, N.; Vijayabaskaran M. Synthesis, characterisation of some 2-azetidinone derivatives from 2-aminopyridine and evaluation of their antimicrobial activity. Pharma Chemica, 2010, 2(6), 238-242.
-
(2010)
Pharma Chemica
, vol.2
, Issue.6
, pp. 238-242
-
-
Mathew, B.1
Mathew, G.E.2
Mathew, N.3
Vijayabaskaran, M.4
-
22
-
-
70350095135
-
Synthesis and antimicrobial evaluation of some 2-azetidinone derivatives
-
Jubie, S.; Gowramma, B.; Muthal, N.K.; Kalirajan, R.; Gomathi, S.; Elango, K. Synthesis and antimicrobial evaluation of some 2-azetidinone derivatives. Int. J. Chem. Tech Res., 2009, 1(2), 153-157.
-
(2009)
Int. J. Chem. Tech Res.
, vol.1
, Issue.2
, pp. 153-157
-
-
Jubie, S.1
Gowramma, B.2
Muthal, N.K.3
Kalirajan, R.4
Gomathi, S.5
Elango, K.6
-
23
-
-
78649665333
-
An efficient synthesis and biological testing of novel 3-chloro-4-aryl-1-(4-(phenyldiazenyl) phenyl)azetidin-2-ones
-
Chopde, H.N.; Pagadala, R.; Meshram, J.S.; Jetti V. An efficient synthesis and biological testing of novel 3-chloro-4-aryl-1-(4-(phenyldiazenyl) phenyl)azetidin-2-ones. J. Heterocyclic Chem., 2010, 47, 1361-1366.
-
(2010)
J. Heterocyclic Chem.
, vol.47
, pp. 1361-1366
-
-
Chopde, H.N.1
Pagadala, R.2
Meshram, J.S.3
Jetti, V.4
-
24
-
-
79952566391
-
Synthesis of novel benzimidazole derivatives as potent antimicrobial agent
-
Baviskar, B.; Baviskar, B.; Chuadhary, S.; Parwani, K.; Balani, P.; Salode, V.; Patil, S.; Khadabadi, S.S. Synthesis of novel benzimidazole derivatives as potent antimicrobial agent. Rasayan J. Chem., 2009, 2(1), 186-190.
-
(2009)
Rasayan J. Chem.
, vol.2
, Issue.1
, pp. 186-190
-
-
Baviskar, B.1
Baviskar, B.2
Chuadhary, S.3
Parwani, K.4
Balani, P.5
Salode, V.6
Patil, S.7
Khadabadi, S.S.8
-
25
-
-
77950212862
-
Synthesis invitro antimicrobial and cytotoxic studies of novel azetidinone derivatives
-
Keri, R.S.; Hosamani, K.M.; Reddy, H.R.S.; Shingalapur, R.V. Synthesis, invitro antimicrobial and cytotoxic studies of novel azetidinone derivatives. Arch. Pharm. Chem. Life Sci., 2010, 343, 237-247.
-
(2010)
Arch. Pharm. Chem. Life Sci.
, vol.343
, pp. 237-247
-
-
Keri, R.S.1
Hosamani, K.M.2
Reddy, H.R.S.3
Shingalapur, R.V.4
-
26
-
-
79955535278
-
Synthesis characterization and antimicrobial activity of new N-substituted-3-chloro-2-azetidinones
-
Vijay Kumar, M.M.J.; Jayadevaiah, K.V.; Nagaraja, T.S.; Bharathi, D.R.; Shameer, H.; Jayachandran, E.; Sreenivasa, G.M. Synthesis, characterization and antimicrobial activity of new N-substituted-3-chloro-2-azetidinones. Arch. Pharm. Sci. & Res., 2009, 1, 31-39.
-
(2009)
Arch. Pharm. Sci. & Res.
, vol.1
, pp. 31-39
-
-
Vijay Kumar, M.M.J.1
Jayadevaiah, K.V.2
Nagaraja, T.S.3
Bharathi, D.R.4
Shameer, H.5
Jayachandran, E.6
Sreenivasa, G.M.7
-
27
-
-
77953440194
-
Synthesis and biological evaluation of schiff base and 4-thiazolidinones of amino salicylic acid and their derivatives as an antimicrobial agent
-
Wadher, S.J.; Karande, N.A.; Sonawane, S.D.; Yeole, P.G. synthesis and biological evaluation of schiff base and 4-thiazolidinones of amino salicylic acid and their derivatives as an antimicrobial agent. Int. J. ChemTech. Res., 2009, 1(4), 1303-1307
-
(2009)
Int. J. ChemTech. Res.
, vol.1
, Issue.4
, pp. 1303-1307
-
-
Wadher, S.J.1
Karande, N.A.2
Sonawane, S.D.3
Yeole, P.G.4
-
28
-
-
10244240685
-
Synthesis spectral, and antimicrobial studies of 1-butyl-3-substituted-4- (2-aryl-1H-indol-3-yl)-2-azetidinones
-
Pathak, V.N.; Gupta, R.; Garg, M. Synthesis, spectral, and antimicrobial studies of 1-butyl-3-substituted-4-(2-aryl-1H-indol-3-yl)-2-azetidinones. Heteroatom Chem., 2004, 15, 494-501.
-
(2004)
Heteroatom Chem.
, vol.15
, pp. 494-501
-
-
Pathak, V.N.1
Gupta, R.2
Garg, M.3
-
29
-
-
54049152860
-
Synthesis of new substituted azetidinoyl and thiazolidinoyl-1, 3,4-thiadiazino (6,5-b) indoles as promising anti-inflammatory agents
-
Bhati, S.K.; Kumar, A. Synthesis of new substituted azetidinoyl and thiazolidinoyl-1, 3,4-thiadiazino (6,5-b) indoles as promising anti-inflammatory agents. Eu. J. Med. Chem., 2008, 43, 2323-2330.
-
(2008)
Eu. J. Med. Chem.
, vol.43
, pp. 2323-2330
-
-
Bhati, S.K.1
Kumar, A.2
-
30
-
-
62549104303
-
Synthesisand evaluation of some new benzimidazole derivatives as potential antimicrobial agents
-
Ansari, K.F.; Lal, C. Synthesis and evaluation of some new benzimidazole derivatives as potential antimicrobial agents. Eur. J. Med. Chem., 2009, 44, 2294-2299.
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 2294-2299
-
-
Ansari, K.F.1
Lal, C.2
-
31
-
-
80052027025
-
Synthesis and in vitro antibacterial and antifungal activities of some novel spiro[azetidine-2,3′-indole]-2,4(1′H)-dione
-
DOI: 10.1007/s00044-010-9354-x
-
Shah, R.J.; Modi, N.R.; Patel, M.J.; Patel, J.L.; Chauhan, B.F.; Patel, M.M. Design, synthesis and in vitro antibacterial and antifungal activities of some novel spiro[azetidine-2,3′-indole]-2,4(1′H)-dione. Med. Chem. Res., 2010, DOI: 10.1007/s00044-010-9354-x.
-
(2010)
Med. Chem. Res.
-
-
Shah, R.J.1
Modi, N.R.2
Patel, M.J.3
Patel, J.L.4
Chauhan, B.F.5
Design, M.P.M.6
-
32
-
-
77954214113
-
Synthesis and molecular modeling studies of 3-chloro-4-substituted-1-(8- hydroxy-quinolin-5-yl)-azetidin-2-ones as novel anti-filarial agents
-
Chhajed, S.S.; Manisha, P.; Bastikar, V.A.; Animeshchandra, H.; Ingle, V.N.; Upasani, C.D.; Wazalwar, S.S. Synthesis and molecular modeling studies of 3-chloro-4-substituted-1-(8-hydroxy-quinolin-5-yl)-azetidin-2-ones as novel anti-filarial agents. Bioorg. Med.Chem. Lett., 2010, 20, 3640-3644.
-
(2010)
Bioorg. Med.Chem. Lett.
, vol.20
, pp. 3640-3644
-
-
Chhajed, S.S.1
Manisha, P.2
Bastikar, V.A.3
Animeshchandra, H.4
Ingle, V.N.5
Upasani, C.D.6
Wazalwar, S.S.7
-
33
-
-
34250351528
-
Poly fused isolated spiro sulphur compounds of quinone and their biological activity
-
El-Kanzi, N.A.A.;. Soleiman, H.A; Khalafallah, A.K.; Poly fused isolated spiro sulphur compounds of quinone and their biological activity. Phosphorous, Sulfur and Silicon, 2007, 182, 1459-1473.
-
(2007)
Phosphorous, Sulfur and Silicon
, vol.182
, pp. 1459-1473
-
-
El-Kanzi, N.A.A.1
Soleiman, H.A.2
Khalafallah, A.K.3
-
34
-
-
78650515328
-
Conventional and microwave assisted synthesis of 2-oxo-4-substituted aryl-azetidine derivatives of benzotriazole: A new class of biological compounds
-
Dubey, A.; Srivastava, S.K.; Srivastava S.D. Conventional and microwave assisted synthesis of 2-oxo-4-substituted aryl-azetidine derivatives of benzotriazole: A new class of biological compounds. Bioorg. Med. Chem. Lett., 2011, 21, 569-573.
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 569-573
-
-
Dubey, A.1
Srivastava, S.K.2
Srivastava, S.D.3
-
35
-
-
80052926008
-
Synthesis characterization and biological evaluation of some azetidinone derivatives with naphathalamine moiety
-
Mishra, S. K.; Mishra, P.; Gupta, C.P.; Kannojia, P.; Garud, N.; Tomar, V. Synthesis, characterization and biological evaluation of some azetidinone derivatives with naphathalamine moiety. J. Pharm. Res., 2010, 3(4), 900-905.
-
(2010)
J. Pharm. Res.
, vol.3
, Issue.4
, pp. 900-905
-
-
Mishra, S.K.1
Mishra, P.2
Gupta, C.P.3
Kannojia, P.4
Garud, N.5
Tomar, V.6
-
36
-
-
33846036891
-
N/C-4 substituted azetidin-2-ones: Synthesis and preliminary evaluation as new class of antimicrobial agents
-
DOI 10.1016/j.bmcl.2006.10.064, PII S0960894X06012443
-
Halve, A.K.; Bhadauria, D.; Dubey R. N/C-4 substituted azetidin-2-ones: synthesis and preliminary evaluation as new class of antimicrobial agents. Bioorg. Med. Chem. Lett., 2007, 17, 341-345. (Pubitemid 46073767)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.2
, pp. 341-345
-
-
Halve, A.K.1
Bhadauria, D.2
Dubey, R.3
-
37
-
-
77949415780
-
2-Acetylbenzofurans: Synthesis, reactions and applications
-
For a recent review on biologically active benzofurans see for instance: Metwally, M.A.; Abdel-Wahab, B.F.; El-Hiti G.A. 2-Acetylbenzofurans: synthesis, reactions and applications. Curr. Org. Chem., 2010, 14, 48-64.
-
(2010)
Curr. Org. Chem.
, vol.14
, pp. 48-64
-
-
Metwally, M.A.1
Abdel-Wahab, B.F.2
El-Hiti, G.A.3
-
38
-
-
77957336333
-
Synthesis and antitubercular activities of azetidinone and thiazolidinone derivatives from 5-chloro-3-methylbenzofuran
-
Raga, B.; Amith, L.; VijayKumar, T.; Havangirao, M.; Upendra, C.H. Synthesis and antitubercular activities of azetidinone and thiazolidinone derivatives from 5-chloro-3-methylbenzofuran. Int. J. Chem. Tech. Res., 2010, 2(3), 1764-1770.
-
(2010)
Int. J. Chem. Tech. Res.
, vol.2
, Issue.3
, pp. 1764-1770
-
-
Raga, B.1
Amith, L.2
Vijaykumar, T.3
Havangirao, M.4
Upendra, C.H.5
-
39
-
-
33750525295
-
Green route for the heterocyclization of 2-mercaptobenzimidazole into β-lactum segment derivatives containing -CONH- bridge with benzimidazole: Screening in vitro antimicrobial activity with various microorganisms
-
DOI 10.1016/j.bmc.2006.09.017, PII S0968089606007346
-
Desai, K.G.; Desai, K.R. Green route for the heterocyclization of 2-mercaptobenzimidazole into beta-lactam segment derivatives containing - CONH-bridge with benzimidazole: Screening in vitro antimicrobial activity with various microorganisms. Bioorg. Med. Chem., 2006, 14, 8271-8279. (Pubitemid 44667558)
-
(2006)
Bioorganic and Medicinal Chemistry
, vol.14
, Issue.24
, pp. 8271-8279
-
-
Desai, K.G.1
Desai, K.R.2
-
40
-
-
3342965239
-
Synthesis of some biologically active pyrazole, thiazolidinone, and azetidinone derivatives
-
Pawar, R.B.; Mulwad, V.V. Synthesis of some biologically active pyrazole, thiazolidinone, and azetidinone derivatives. Chem. Heterocycl. Compd., 2004, 40, 219-226.
-
(2004)
Chem. Heterocycl. Compd.
, vol.40
, pp. 219-226
-
-
Pawar, R.B.1
Mulwad, V.V.2
-
41
-
-
36849056102
-
Synthesisand biological activity of N-substituted-3-chloro-2-azetidinones
-
Chavan, A.A.; Pai, N.R. Synthesis and biological activity of N-substituted-3-chloro-2-azetidinones. Molecules, 2007, 12, 2467-2477.
-
(2007)
Molecules
, vol.12
, pp. 2467-2477
-
-
Chavan, A.A.1
Pai, N.R.2
-
42
-
-
57949096601
-
Synthesisand anti-inflammatory activity of newer quinazolin-4-one derivatives
-
Kumar, A.; Rajput, C.S. Synthesis and anti-inflammatory activity of newer quinazolin-4-one derivatives. Eur. J. Med. Chem., 2009, 44 , 83-90.
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 83-90
-
-
Kumar, A.1
Rajput, C.S.2
-
43
-
-
77951299188
-
Stereoselective synthesis and antibacterial evaluation of new monocyclic beta-lactams
-
Cerić, H.; Šindler-Kulyk, M.; Kovaĉeví, M.; Perí, M.; Živković, A. Azetidinone-isothiazolidinones: stereoselective synthesis and antibacterial evaluation of new monocyclic beta-lactams. Bioorg. Med. Chem. 2010, 18, 3053-3058.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 3053-3058
-
-
Cerić, H.1
Šindler-Kulyk, M.2
Kovaĉeví, M.3
Perí, M.4
Živković, A.5
-
44
-
-
0037763894
-
3,4-Disubstituted azetidinones as selective inhibitors of the cysteine protease cathepsin K. exploring P2 elements for selectivity
-
DOI 10.1016/S0960-894X(03)00304-4
-
Setti, E.L.; Davis, D.; Chung, T.; Mc Carter, J. 3,4-Disubstituted azetidinones as selective inhibitors of the cysteine protease cathepsin K. Exploring P2 elements for selectivity. Bioorg. Med. Chem. Lett., 2003, 13, 2051-2053. (Pubitemid 36638408)
-
(2003)
Bioorganic and Medicinal Chemistry Letters
, vol.13
, Issue.12
, pp. 2051-2053
-
-
Setti, E.L.1
Davis, D.2
Chung, T.3
McCarter, J.4
-
45
-
-
13944257671
-
3,4-Disubstituted azetidinones as selective inhibitors of the cysteine protease cathepsin K. Exploring P3 elements for potency and selectivity
-
DOI 10.1016/j.bmcl.2004.12.088
-
Setti, E.L.; Davis, D.; Janc, J.W.; Jeffery, D.A.; Cheung, H.; Yu, W. 3,4-Disubstituted azetidinones as selective inhibitors of the cysteine protease cathepsin K. Exploring P3 elements for potency and selectivity. Bioorg. Med. Chem. Lett., 2005, 15, 1529-1534. (Pubitemid 40269026)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.5
, pp. 1529-1534
-
-
Setti, E.L.1
Davis, D.2
Janc, J.W.3
Jeffery, D.A.4
Cheung, H.5
Yu, W.6
-
46
-
-
0037421033
-
3-Acylamino-azetidin-2-one as a novel class of cysteine proteases inhibitors
-
DOI 10.1016/S0960-894X(02)00831-4, PII S0960894X02008314
-
Zhou, N.E.; Guo, D.; Thomas, G.; Reddy, A.V.N.; Kaleta, J.; Purisima, E.; Menard, R.; Micetich, R.G.; Singh, R. 3-Acylamino-azetidin-2-one as a Novel Class of Cysteine Proteases Inhibitors. Bioorg. Med. Chem. Lett., 2003, 13, 139-141. (Pubitemid 35447701)
-
(2003)
Bioorganic and Medicinal Chemistry Letters
, vol.13
, Issue.1
, pp. 139-141
-
-
Zhou, N.E.1
Guo, D.2
Thomas, G.3
Reddy, A.V.N.4
Kaleta, J.5
Purisima, E.6
Menard, R.7
Micetich, R.G.8
Singh, R.9
-
47
-
-
33846590535
-
Azetidinones as vasopressin V1a antagonists
-
DOI 10.1016/j.bmc.2006.12.031, PII S0968089606010388
-
Guillon, C.D.; Koppel, G.A.; Brownstein, M.J.; Chaney, M.O.; Ferris, C.F.; Lu, S.; Fabio, K.M.; Miller, M.J.; Heindel, N.D.; Hunden, D.C.; Cooper, R.D.G.; Kaldor, S.W.; Skelton, J.J.; Dressman, B.A.; Clay, M.P.; Steinberg, M.I.; Bruns, R.F.; Simon, N.G. Azetidinones as vasopressin V1a antagonists. Bioorg. Med. Chem., 2007, 15, 2054-2080. (Pubitemid 46176627)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.5
, pp. 2054-2080
-
-
Guillon, C.D.1
Koppel, G.A.2
Brownstein, M.J.3
Chaney, M.O.4
Ferris, C.F.5
Lu, S.-f.6
Fabio, K.M.7
Miller, M.J.8
Heindel, N.D.9
Hunden, D.C.10
Cooper, R.D.G.11
Kaldor, S.W.12
Skelton, J.J.13
Dressman, B.A.14
Clay, M.P.15
Steinberg, M.I.16
Bruns, R.F.17
Simon, N.G.18
-
48
-
-
0031887332
-
Proteasomes: Structure and biology
-
Tanaka, K.J. Proteasomes: Structure and biology. J. Biochem., 1998, 123, 195-204.
-
(1998)
J. Biochem.
, vol.123
, pp. 195-204
-
-
Tanaka, K.J.1
-
49
-
-
33846062934
-
Novel β-lactam derivatives: Potent and selective inhibitors of the chymotrypsin-like activity of the human 20S proteasome
-
DOI 10.1016/j.bmcl.2006.10.047, PII S0960894X06012248
-
Imbach, P.; Lang, M.; García-Echeverría, C.; Guagnano, V.; Noorani, M.; Roesel, J.; Bitsch, F.; Rihs G.; Furet, P. Novel β-lactam derivatives: potent and selective inhibitors of the chymotrypsin-like activity of the human 20S proteasome. Bioorg. Med. Chem. Lett. , 2007, 17, 358-362. (Pubitemid 46073758)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.2
, pp. 358-362
-
-
Imbach, P.1
Lang, M.2
Garcia-Echeverria, C.3
Guagnano, V.4
Noorani, M.5
Roesel, J.6
Bitsch, F.7
Rihs, G.8
Furet, P.9
-
50
-
-
77957165689
-
Design, synthesis, and crystal structures of 6-alkylidene-2′- substituted penicillanic acid sulfones as potent inhibitors of acinetobacter baumannii OXA-24 carbapenemase
-
For a recent paper see for instance: Bou, G.; Santillana, E.; Sheri, A.; Beceiro, A.; Sampson, J.M.; Kalp, M.; Bethel, C.R.; Distler, A.M.; Drawz, S.M.; Pagadala, S.R.R.; van den Akker, F.; Bonomo, R.A.; Romero, A.; Buynak, J.D. Design, synthesis, and crystal structures of 6-alkylidene-2′-substituted penicillanic acid sulfones as potent inhibitors of acinetobacter baumannii OXA-24 carbapenemase. J. Am. Chem. Soc., 2010, 132, 13320-13331, and references cited therein.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 13320-13331
-
-
Bou, G.1
Santillana, E.2
Sheri, A.3
Beceiro, A.4
Sampson, J.M.5
Kalp, M.6
Bethel, C.R.7
Distler, A.M.8
Drawz, S.M.9
Pagadala, S.R.R.10
Van Den Akker, F.11
Bonomo, R.A.12
Romero, A.13
Buynak, J.D.14
-
51
-
-
0346882933
-
Synthesis of antitumor 6-alkylidenepenicillanate sulfones and related 3-alkylidene-2-azetidinones
-
DOI 10.1016/j.bmcl.2003.09.078
-
Veinberg, G.; Shestakova, I.; Vorona, M.; Kanepe, I.; Lukevics, E. Synthesis of antitumor 6-alkylidenepenicillanate sulfones and related 3-alkylidene-2-azetidinones. Bioorg. Med. Chem. Lett., 2004, 14, 147-150. (Pubitemid 38016211)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.1
, pp. 147-150
-
-
Veinberg, G.1
Shestakova, I.2
Vorona, M.3
Kanepe, I.4
Lukevics, E.5
-
52
-
-
0037989827
-
Synthesis of novel 4-(2-oxoethylidene)azetidin-2-ones by a Lewis acid mediated reaction of acyldiazo compounds
-
Cainelli, G.; Giacomini, D.; Galletti, P.; Quintavalla, A. Synthesis of novel 4-(2-oxoethylidene)azetidin-2-ones by a Lewis acid mediated reaction of acyldiazo compounds. Eur. J. Org. Chem., 2003, 1765-1774
-
(2003)
Eur. J. Org. Chem.
, pp. 1765-1774
-
-
Cainelli, G.1
Giacomini, D.2
Galletti, P.3
Quintavalla, A.4
-
53
-
-
0037033218
-
Synthesis of novel 4-(1-ethoxycarbonyl-methylidene)-azetidin-2-ones via a Lewis acid-catalyzed reaction of ethyl diazoacetate
-
PII S0040403901021086
-
Cainelli, G.; Galletti, P.; Gazzano, M.; Giacomini, D.; Quintavalla, A. Synthesis of novel 4-(1-ethoxycarbonyl-methylidene)-azetidin-2-ones via a Lewis acidcatalyzed reaction of ethyl diazoacetate. Tetrahedron Lett., 2002, 43, 233-235. (Pubitemid 34024867)
-
(2002)
Tetrahedron Letters
, vol.43
, Issue.2
, pp. 233-235
-
-
Cainelli, G.1
Galletti, P.2
Gazzano, M.3
Giacomini, D.4
Quintavalla, A.5
-
54
-
-
33646456009
-
Synthesis, and Biological Evaluation of 4-Alkyliden-beta Lactams: New Products with Promising Antibiotic Activity Against Resistant Bacteria
-
Broccolo, F.; Cainelli, G.; Caltabiano, G.; Cocuzza, C.E.A.; Fortuna, C.G.; Galletti, P.; Giacomini, D.; Musumarra, G.; Musumeci, R.; Quintavalla, A. Design, Synthesis, and Biological Evaluation of 4-Alkyliden-beta Lactams: New Products with Promising Antibiotic Activity Against Resistant Bacteria. J. Med. Chem., 2006, 49, 2804-2811.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 2804-2811
-
-
Broccolo, F.1
Cainelli, G.2
Caltabiano, G.3
Cocuzza, C.E.A.4
Fortuna, C.G.5
Galletti, P.6
Giacomini, D.7
Musumarra, G.8
Musumeci, R.9
Design, Q.A.10
-
55
-
-
0344420063
-
4-Alkylidene-azetidin-2-ones: Novel inhibitors of leukocyte elastase and gelatinase
-
DOI 10.1016/j.bmc.2003.09.035
-
(a) Cainelli, G.; Galletti, P.; Garbisa, S.; Giacomini, D.; Sartor, L.; Quintavalla, A. 4-Alkylidene-azetidin-2-ones: Novel Inhibitors of Leukocyte Elastase and Gelatinase. Bioorg. Med. Chem. 2003, 11, 5391-5399 (Pubitemid 37464666)
-
(2003)
Bioorganic and Medicinal Chemistry
, vol.11
, Issue.24
, pp. 5391-5399
-
-
Cainelli, G.1
Galletti, P.2
Garbisa, S.3
Giacomini, D.4
Sartor, L.5
Quintavalla, A.6
-
56
-
-
25844476174
-
4-Alkyliden-β-lactams conjugated to polyphenols: Synthesis and inhibitory activity
-
DOI 10.1016/j.bmc.2005.06.041, PII S0968089605005547
-
(b) Cainelli, G.; Galletti, P.; Garbisa, S.; Giacomini, D.; Sartor, L.; Quintavalla, A. 4-Alkyliden-β-Lactams conjugated to polyphenols: synthesis and inhibitory activity. Bioorg. Med. Chem. 2005, 13, 6120-6132. (Pubitemid 41400133)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.22
, pp. 6120-6132
-
-
Cainelli, G.1
Galletti, P.2
Garbisa, S.3
Giacomini, D.4
Sartor, L.5
Quintavalla, A.6
-
57
-
-
38849143983
-
Neutrophil elastase, proteinase 3 and cathepsin G: Physicochemical properties, activity and physiopathological functions
-
DOI 10.1016/j.biochi.2007.10.009, PII S0300908407003033
-
Korkmaz, B.; Moreau, T.; Gauthier, F. Neutrophil elastase, proteinase 3 and cathepsin G: physicochemical properties, activity and physiopathological functions. Biochimie, 2008, 90, 227-242. (Pubitemid 351187763)
-
(2008)
Biochimie
, vol.90
, Issue.2
, pp. 227-242
-
-
Korkmaz, B.1
Moreau, T.2
Gauthier, F.3
-
58
-
-
49649117771
-
New polyphenolic β-Lactams with antioxidant activity
-
Cainelli, G.; Angeloni, C.; Cervellati, R.; Galletti, P.; Giacomini, D.; Hrelia, S.; Sinisi, R. New polyphenolic β-Lactams with antioxidant activity. Chem. Biodivers., 2008, 5, 811-829.
-
(2008)
Chem. Biodivers.
, vol.5
, pp. 811-829
-
-
Cainelli, G.1
Angeloni, C.2
Cervellati, R.3
Galletti, P.4
Giacomini, D.5
Hrelia, S.6
Sinisi, R.7
-
59
-
-
0033550261
-
Synthesis, reactivity and biochemical evaluation of 1,3- substituted azetidin-2-ones as enzyme inhibitors
-
DOI 10.1016/S0040-4020(99)00819-4, PII S0040402099008194
-
Beauve, C; Bouchet, M.; Touillaux, R.; Fastrez, J.; Marchand-Brynaert, J. Synthesis, Reactivity and Biochemical Evaluation of 1,343ubstituted Azetidin-2-ones as Enzyme Inhibitors. Tetrahedron 1999, 55, 13301-13320. (Pubitemid 29502278)
-
(1999)
Tetrahedron
, vol.55
, Issue.46
, pp. 13301-13320
-
-
Beauve, C.1
Bouchet, M.2
Touillaux, R.3
Fastrez, J.4
Marchand-Brynaert, J.5
-
60
-
-
0028899156
-
β-Lactam compounds. Inhibitors of transpeptidases, β-lactamases and elastases: A review
-
Mascaretti, O.A.; Boschetti, C.E.; Danelon, G.O.; Mata, E.G.; Roveri, O.A. β-Lactam compounds. Inhibitors of transpeptidases, β-lactamases and elastases: a review. Curr. Med. Chem., 1995 ,1 , 441-470.
-
(1995)
Curr. Med. Chem.
, vol.1
, pp. 441-470
-
-
Mascaretti, O.A.1
Boschetti, C.E.2
Danelon, G.O.3
Mata, E.G.4
Roveri, O.A.5
-
61
-
-
0024987599
-
Monocyclic β-lactam inhibitors of human leukocyte elastase
-
DOI 10.1016/S0040-4020(01)82006-8
-
(a) Firestone, R.A.; Barker, P.L.; Pirano, J.M.; Ashe, B.M.; Dahlgren. M.E. Monocyclic β-lactam inhibitors of human leukocyte elastase. Tetrahedron, 1990, 46, 2255-2262 (Pubitemid 20266885)
-
(1990)
Tetrahedron
, vol.46
, Issue.7
, pp. 2255-2262
-
-
Firestone, R.A.1
Barker, P.L.2
Pisano, J.M.3
Ashe, B.M.4
Dahlgren, M.E.5
-
62
-
-
0029839451
-
An asymmetric synthesis of L-694,458, a human leukocyte elastase inhibitor, via novel enzyme resolution of β-lactam esters
-
DOI 10.1021/jo960618k
-
(b) Cvetovich, R.J.; Chartrain, M.; Hartner, F. W. Jr.; Roberge, C.; Amato, J. S.; Grabowski, E. J. An asymmetric synthesis of L-694,458, a Human Leukocyte Elastase Inhibitor, via novel enzyme resolution of β-Lactam Esters. J. Org. Chem., 1996, 61, 6575-6580. (Pubitemid 26328642)
-
(1996)
Journal of Organic Chemistry
, vol.61
, Issue.19
, pp. 6575-6580
-
-
Cvetovich, R.J.1
Chartrain, M.2
Hartner Jr., F.W.3
Roberge, C.4
Amato, J.S.5
Grabowski, E.J.J.6
-
63
-
-
34547602336
-
The efficiency of C-4 substituents in activating the β-lactam scaffold towards serine proteases and hydroxide ion
-
DOI 10.1039/b706622h
-
Mulchande, J.; Martins, L.; Moreira, R.; Archer, M.; Oliveira, T.F.; Iley, J. The efficiency of C-4 substituents in activating the β-lactam scaffold towards serine proteases and hydroxide ion. Org. Biomol. Chem., 2007, 5, 2617-2626. (Pubitemid 47192315)
-
(2007)
Organic and Biomolecular Chemistry
, vol.5
, Issue.16
, pp. 2617-2626
-
-
Mulchande, J.1
Martins, L.2
Moreira, R.3
Archer, M.4
Oliveira, T.F.5
Iley, J.6
-
64
-
-
0037128464
-
Synthesis, hydrolysis, biochemical and theoretical evaluation of 1,4-bis(alkoxycarbonyl)azetidin-2-ones as potential elastase inhibitors
-
DOI 10.1016/S0040-4020(02)00112-6, PII S0040402002001126
-
(a) Gerard, S.; Dive, G.; Clamot, B.; Touillaux, R.; Marchand-Brynaert, J. Synthesis, hydrolysis, biochemical and theoretical evaluation of 1,4-bis(alkoxycarbonyl)azetidin-2-ones as potential elastase inhibitors. Tetrahedron, 2002, 58, 2423-2433 (Pubitemid 34215052)
-
(2002)
Tetrahedron
, vol.58
, Issue.12
, pp. 2423-2433
-
-
Gerard, S.1
Dive, G.2
Clamot, B.3
Touillaux, R.4
Marchand-Brynaert, J.5
-
65
-
-
0036976190
-
1-Alkoxycarbonyl-3-halogenoazetidin-2-ones as elastase (PPE) inhibitors
-
DOI 10.1016/S0968-0896(02)00304-8, PII S0968089602003048
-
(b) Gerard, S.; Nollet, G.; Put, J.V.; Marchand-Brynaert, J. 1-Alkoxycarbonyl-3-halogenoazetidin-2-ones as Elastase (PPE) Inhibitors. Bioorg. Med. Chem., 2002, 10, 3955-3964 (Pubitemid 36164694)
-
(2002)
Bioorganic and Medicinal Chemistry
, vol.10
, Issue.12
, pp. 3955-3964
-
-
Gerard, S.1
Nollet, G.2
Vande Put, J.3
Marchand-Brynaert, J.4
-
66
-
-
0347301852
-
Synthesis and evaluation of N1/C4-substituted β-lactams as PPE and HLE inhibitors
-
DOI 10.1016/j.bmc.2003.10.009
-
(c) Gerard, S.; Galleni, M.; Dive, G.; Marchand-Brynaert, J. Synthesis and evaluation of N1/C4-substituted β-Lactams as PPE and HLE inhibitors. Bioorg. Med. Chem., 2004, 12, 129-138. (Pubitemid 38096225)
-
(2004)
Bioorganic and Medicinal Chemistry
, vol.12
, Issue.1
, pp. 129-138
-
-
Gerard, S.1
Galleni, M.2
Dive, G.3
Marchand-Brynaert, J.4
-
67
-
-
0041346136
-
NAcylation of 4-alkyliden-β-Lactams: Unexpected results
-
Cainelli, G.; Giacomini, D.; Gazzano, M.; Galletti, P.; Quintavalla, A. NAcylation of 4-alkyliden-β-Lactams: unexpected results. Tetrahedron Lett., 2003, 44; 6269-6272.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 6269-6272
-
-
Cainelli, G.1
Giacomini, D.2
Gazzano, M.3
Galletti, P.4
Quintavalla, A.5
-
68
-
-
31144450693
-
Inhibition of leukocyte elastase, polymorphonuclear chemoinvasion, and inflammation-triggered pulmonary fibrosis by a 4-alkyliden-β-lactam with a galloyl moiety
-
DOI 10.1124/jpet.105.096248
-
Dell'Aica, I; Sartor, L.; Galletti, P.; Giacomini, D.; Quintavalla, A.; Calabrese, F.; Brunetta, E.; Piazza, F.; Agostini, C.; Garbisa, S. Inhibition of leukocyte elastase, PMN chemoinvasion, and inflammation-triggered pulmonary fibrosis by a 4-alkyliden-β-lactam with a galloyl moiety. J. Pharmacol. Exp. Therap., 2006, 316, 539-546. (Pubitemid 43130979)
-
(2006)
Journal of Pharmacology and Experimental Therapeutics
, vol.316
, Issue.2
, pp. 539-546
-
-
Dell'Aica, I.1
Sartor, L.2
Galletti, P.3
Giacomini, D.4
Quintavalla, A.5
Calabrese, F.6
Giacometti, C.7
Brunetta, E.8
Piazza, F.9
Agostini, C.10
Garbisa, S.11
-
69
-
-
34547235253
-
Inhibitory effect by new monocyclic 4-alkyliden-beta-lactam compounds on human platelet activation
-
DOI 10.1080/09537100601100796, PII 780574149
-
Cainelli, G.; Folda, A.; Scutari, G.; Deana, R.; Pavanetto, M.; Zarpellon, A.; Giacomini, D.; Galletti, P.; Quintavalla, A. Inhibitory effect by new monocyclic 4-alkyliden-β-lactam compounds on human platelet activation. Platelets, 2007,18, 357-364. (Pubitemid 47123836)
-
(2007)
Platelets
, vol.18
, Issue.5
, pp. 357-364
-
-
Pavanetto, M.1
Zarpellon, A.2
Giacomini, D.3
Galletti, P.4
Quintavalla, A.5
Cainelli, G.6
Folda, A.7
Scutari, G.8
Deana, R.9
-
70
-
-
34547828204
-
Antithrombotic and hemostatic effects of a small molecule factor XIa inhibitor in rats
-
DOI 10.1016/j.ejphar.2007.05.043, PII S0014299907006462
-
Schumacher, W.A.; Seiler, S.E.; Steinbacher, T.E; Stewart, B.; Bostwick, J.S.; Hartl, K.S.; Liu, E.C.; Ogletree, M.L. Antithrombotic and hemostatic effects of a small molecule factor XIa inhibitor in rats. Eur. J. Pharmacol., 2007, 570, 167-174. (Pubitemid 47247686)
-
(2007)
European Journal of Pharmacology
, vol.570
, Issue.1-3
, pp. 167-174
-
-
Schumacher, W.A.1
Seiler, S.E.2
Steinbacher, T.E.3
Stewart, A.B.4
Bostwick, J.S.5
Hartl, K.S.6
Liu, E.C.7
Ogletree, M.L.8
-
71
-
-
11144355065
-
Synthesis of potent and highly selective nonguanidine azetidinone inhibitors of human tryptase
-
DOI 10.1016/j.bmcl.2004.02.011, PII S0960894X04002161
-
(a) Bisacchi, G. S.; Slusarchyk, W. A.; Bolton, S. A.; Hartl, K. S.; Jacobs, M.L.; Pi, Z.; Sutton, J.C.; Treuner, U. Synthesis of potent and highly selective nonguanidine azetidinone inhibitors of human tryptase. Bioorg. Med. Chem Lett.; 2004, 14; 2227-2231 (Pubitemid 38481395)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.9
, pp. 2227-2231
-
-
Bisacchi, G.S.1
Slusarchyk, W.A.2
Bolton, S.A.3
Hartl, K.S.4
Jacobs, G.5
Mathur, A.6
Meng, W.7
Ogletree, M.L.8
Pi, Z.9
Sutton, J.C.10
Treuner, U.11
Zahler, R.12
Zhao, G.13
Seiler, S.M.14
-
72
-
-
11144356290
-
Solid-phase synthesis and SAR of 4-carboxy-2-azetidinone mechanism-based tryptase inhibitors
-
DOI 10.1016/j.bmcl.2004.02.012, PII S0960894X04002173
-
(b) Sutton, J.C.; Bolton, S.A.; Davis, M.E.; Hartl, K.S.; Jacobson, B. Solid-phase synthesis and SAR of 4-carboxy-2-azetidinone mechanism-based tryptase inhibitors. Bioorg. Med. Chem Lett., 2004, 14; 2233-2239. (Pubitemid 38481396)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.9
, pp. 2233-2239
-
-
Sutton, J.C.1
Bolton, S.A.2
Davis, M.E.3
Hartl, K.S.4
Jacobson, B.5
Mathur, A.6
Ogletree, M.L.7
Slusarchyk, W.A.8
Zahler, R.9
Seiler, S.M.10
Bisacchi, G.S.11
-
73
-
-
80052467986
-
A small-molecule factor XIa inhibitor produces antithrombotic efficacy with minimal bleeding time prolongation in rabbits
-
DOI 10.1007/s11239-011-0599-0
-
Wong, P.C.; Crain, E.J.; Watson, C.A.; Schumacher, W.A. A small-molecule factor XIa inhibitor produces antithrombotic efficacy with minimal bleeding time prolongation in rabbits. J. Thromb. Thrombolysis, 2011, DOI 10.1007/s11239-011-0599-0.
-
(2011)
J. Thromb. Thrombolysis
-
-
Wong, P.C.1
Crain, E.J.2
Watson, C.A.3
Schumacher, W.A.4
-
74
-
-
79551711217
-
New parenteral anticoagulants in development
-
Gomez-Outes, A.; Suarez-Gea, M.L.; Lecumberri, R.; Rocha, E.; Pozo-Hernandez, C.; Vargas-Castrillon, E. New parenteral anticoagulants in development. Ther. Adv. Cardiovasc. Dis., 2011, 5, 33-59.
-
(2011)
Ther. Adv. Cardiovasc. Dis.
, vol.5
, pp. 33-59
-
-
Gomez-Outes, A.1
Suarez-Gea, M.L.2
Lecumberri, R.3
Rocha, E.4
Pozo-Hernandez, C.5
Vargas-Castrillon, E.6
-
75
-
-
39749093736
-
Mechanistic insights into the inhibition of prostate specific antigen by β-lactam class compounds
-
DOI 10.1002/prot.21676
-
Singh, P.; Williams, S.A.;. Shah, M.H.; Lectka, T.; Pritchard, G.J.; Isaacs, J.T.; Denmead, S.R. Mechanistic Insights into the Inhibition of Prostate Specific Antigen by β-Lactam Class Compounds. Proteins: Struct., Funct., Bioinfo., 2008, 70, 1416-1428. (Pubitemid 351304100)
-
(2008)
Proteins: Structure, Function and Genetics
, vol.70
, Issue.4
, pp. 1416-1428
-
-
Singh, P.1
Williams, S.A.2
Shah, M.H.3
Lectka, T.4
Pritchard, G.J.5
Isaacs, J.T.6
Denmeade, S.R.7
-
76
-
-
63849228551
-
Novel large-ring 1,3-bridged 2-azetidinones as potential inhibitors of penicillin-binding proteins
-
(a) Urbach, A.; Dive, G.; Marchand-Brynaert, J. Novel large-ring 1,3-bridged 2-azetidinones as potential inhibitors of penicillin-binding proteins. Eur. J. Org. Chem., 2009, 1757-1770
-
(2009)
Eur. J. Org. Chem.
, pp. 1757-1770
-
-
Urbach, A.1
Dive, G.2
Marchand-Brynaert, J.3
-
77
-
-
62549090567
-
Large ring 1,3-bridged 2-azetidinones: Experimental and theoretical studies
-
(b) Urbach, A.; Dive, G.; Tinant, B.; Duval, V, Marchand-Brynaert, J. Large ring 1,3-bridged 2-azetidinones: experimental and theoretical studies. Eur. J. Med. Chem., 2009, 44, 2071-2080.
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 2071-2080
-
-
Urbach, A.1
Dive, G.2
Tinant, B.3
Duval, V.4
Marchand-Brynaert, J.5
-
78
-
-
70149092317
-
β-Lactam probes as selective chemical-proteomic tools for the identification and functional characterization of resistance associated enzymes in MRSA
-
Staub, I.; Sieber, S.A.; β-Lactam probes as selective chemical-proteomic tools for the identification and functional characterization of resistance associated enzymes in MRSA. J. Am. Chem. Soc., 2009, 131, 6271-6276
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 6271-6276
-
-
Staub, I.1
Sieber, S.A.2
-
79
-
-
53549118638
-
β-Lactams as selective chemical probes for the in vivo labeling of bacterial enzymes involved in cell wall biosynthesis, antibiotic resistance, and virulence
-
(b) Staub, I.; Sieber, S.A. β-Lactams as selective chemical probes for the in vivo labeling of bacterial enzymes involved in cell wall biosynthesis, antibiotic resistance, and virulence. J. Am. Chem. Soc., 2008, 130, 13400-13409.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 13400-13409
-
-
Staub, I.1
Sieber, S.A.2
-
80
-
-
70949088924
-
β-Lactams derived from a carbapenem Chiron are selective inhibitors of human fatty acid amide hydrolase versus human monoacylglycerol Lipase
-
Feledziak, M.; Urbach, A.; Muccioli, G.G.; Marchand-Brynaert, J.; Labar, G.; Didier M.L.; Michaux, C. β-Lactams derived from a carbapenem Chiron are selective inhibitors of human fatty acid amide hydrolase versus human monoacylglycerol Lipase. J. Med. Chem.,2009; 52; 7054-7068.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7054-7068
-
-
Feledziak, M.1
Urbach, A.2
Muccioli, G.G.3
Marchand-Brynaert, J.4
Labar, G.5
Didier, M.L.6
Michaux, C.7
-
81
-
-
1842740407
-
Synthesis and anti-HCMV activity of 1-acyl-β-lactams and 1-acylazetidines derived from phenylalanine
-
DOI 10.1016/j.bmcl.2004.02.010, PII S0960894X0400215X
-
(a) Gerona-Navarro, G.; Vega, M.;Garcia-Lopez, M.T.; Andrei, G.; Snoeck, R.; Balzarini, J.; De Clercq, E.; Gonzalez-Muniz, R. Synthesis and anti-HCMV activity of 1-acyl-β-Lactams and 1-acylazetidines derived from phenylalanine. Bioorg. Med. Chem. Lett., 2004, 14; 2253-2256 (Pubitemid 38481400)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.9
, pp. 2253-2256
-
-
Gerona-Navarro, G.1
Perez De Vega, Ma.J.2
Garcia-Lopez, Ma.T.3
Andrei, G.4
Snoeck, R.5
Balzarini, J.6
De Clercq, E.7
Gonzalez-Muniz, R.8
-
82
-
-
17144408696
-
From 1-acyl-β-lactam human cytomegalovirus protease inhibitors to 1-benzyloxycarbonylazetidines with improved antiviral activity. A straightforward approach to convert covalent to noncovalent inhibitors
-
DOI 10.1021/jm0492812
-
(b) Gerona-Navarro, G.; Vega, M.; Garcia-Lopez, M.T.; Andrei, G.; Snoeck, R.; De Clercq, E.; Balzarini, J.; Gonzalez-Muniz, R. From 1-Acyl-β-lactam Human Cytomegalovirus Protease inhibitors to 1-benzyloxycarbonylazetidines with improved antiviral activity. A straightforward approach to convert covalent to noncovalent inhibitors. J. Med. Chem., 2005, 48; 2612-2621. (Pubitemid 40516450)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.7
, pp. 2612-2621
-
-
Gerona-Navarro, G.1
Perez De Vega, M.J.2
Garcia-Lopez, M.T.3
Andrei, G.4
Snoeck, R.5
De Clercq, E.6
Balzarini, J.7
Gonzalez-Muniz, R.8
-
83
-
-
41849149998
-
Synthesisand DNA-cleaving activity of lactenediynes conjugated with DNA-complexing moieties
-
Banfi, L.; Basso, A.; Bevilacqua, E.; Gandolfo, V.; Giannini, G.; Guanti, G.; Musso, L.; Paravidino, M.; Riva, R. Synthesis and DNA-cleaving activity of lactenediynes conjugated with DNA-complexing moieties. Bioorg. Med. Chem., 2008, 16; 3501-3518.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 3501-3518
-
-
Banfi, L.1
Basso, A.2
Bevilacqua, E.3
Gandolfo, V.4
Giannini, G.5
Guanti, G.6
Musso, L.7
Paravidino, M.8
Riva, R.9
-
84
-
-
0020315340
-
Mode of action of azthreonam
-
Georgopapadakou, N.H.; Smith, S.A.; Sykes, R.B. Mode of Action of Azthreonam. Antimicrob. Ag. Chemother., 1982, 950-956. (Pubitemid 12012613)
-
(1982)
Antimicrobial Agents and Chemotherapy
, vol.21
, Issue.6
, pp. 950-956
-
-
Georgopapadakou, N.H.1
Smith, S.A.2
Sykes, R.B.3
-
85
-
-
69249114845
-
New molecules from old classes: Revisiting the development of β-lactams
-
Page, M.G.P.; Heim, J. New molecules from old classes: Revisiting the development of β-lactams. IDrugs, 2009, 12, 561-565.
-
(2009)
IDrugs
, vol.12
, pp. 561-565
-
-
Page, M.G.P.1
Heim, J.2
-
86
-
-
0034725812
-
N-Thiolated bicyclic and monocyclic β-Lactams
-
Turos, E.; Konaklieva, M.I.; Ren, R.X.F.; Shi, H.; Gonzalez, J.; Dickey, S.; Lim, D. N-Thiolated bicyclic and monocyclic β-Lactams. Tetrahedron, 2000, 56, 5571-5578.
-
(2000)
Tetrahedron
, vol.56
, pp. 5571-5578
-
-
Turos, E.1
Konaklieva, M.I.2
Ren, R.X.F.3
Shi, H.4
Gonzalez, J.5
Dickey, S.6
Lim, D.7
-
87
-
-
27544491790
-
4 ring substituents on anti-MRSA activity
-
DOI 10.1016/j.bmc.2005.08.011, PII S0968089605007790
-
Turos, E.; Coates, C.; Shim, J.-Y.; Wang, Y.; Leslie, J.M.; Long, T.E.; Reddy, G.S.K.; Ortiz, A.; Culbreath, M.; Dickey, S.; Lim, D.V.; Alonso, E.; Gonzalez, J. N-Methylthio β-lactam antibacterials: Effects of the C3/C4 ring substituents on anti-MRSA activity. Bioorg. Med. Chem., 2005, 13, 6289-308. (Pubitemid 41541920)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.23
, pp. 6289-6308
-
-
Turos, E.1
Coates, C.2
Shim, J.-Y.3
Wang, Y.4
Leslie, J.M.5
Long, T.E.6
Reddy, G.S.K.7
Ortiz, A.8
Culbreath, M.9
Dickey, S.10
Lim, D.V.11
Alonso, E.12
Gonzalez, J.13
-
88
-
-
33644796914
-
N-Thiolated β-lactams: A new family of anti-Bacillus agents
-
DOI 10.1016/j.bmcl.2006.01.070, PII S0960894X06001089
-
Turos, E.; Long, T.E.; Heldreth, B.; Leslie, J.M.; Reddy, G.S.K.; Wang, Y.; Coates, C.; Konaklieva, M.; Dickey, S.; Lim, D.V.; Alonso, E.; Gonzalez, J. N-Thiolated β-Lactams: A new family of anti-Bacillus agents. Bioorg. Med. Chem. Lett., 2006, 16, 2084-2090. (Pubitemid 43351055)
-
(2006)
Bioorganic and Medicinal Chemistry Letters
, vol.16
, Issue.8
, pp. 2084-2090
-
-
Turos, E.1
Long, T.E.2
Heldreth, B.3
Leslie, J.M.4
Reddy, G.S.K.5
Wang, Y.6
Coates, C.7
Konaklieva, M.8
Dickey, S.9
Lim, D.V.10
Alonso, E.11
Gonzalez, J.12
-
89
-
-
33846955422
-
N-thiolated β-lactams: Studies on the mode of action and identification of a primary cellular target in Staphylococcus aureus
-
Revell, K.D.; Heldreth, B.; Long, T.E.; Jang, S.; Turos, E. N-thiolated β-lactams: Studies on the mode of action and identification of a primary cellular target in Staphylococcus aureus. Bioorg. Med. Chem., 2007, 15, 2453-2467.
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 2453-2467
-
-
Revell, K.D.1
Heldreth, B.2
Long, T.E.3
Jang, S.4
Turos, E.5
-
90
-
-
44949097209
-
Unsymmetric aryl-alkyl disulfide growth inhibitors of methicillin-resistant Staphylococcus aureus and Bacillus anthracis
-
DOI 10.1016/j.bmc.2008.05.032, PII S096808960800463X
-
Turos, E.; Revell, K.D.; Ramaraju, P.; Gergeres, D.A.; Greenhalgh, K.; Young, A.; Sathyanarayan, N.; Dickey, S.; Lim, D.; Alhamadsheh, M.M.; Reynolds, K. Unsymmetric aryl-alkyl disulfide growth inhibitors of methicillin-resistant Staphylococcus aureus and Bacillus anthracis. Bioorg. Med. Chem., 2008, 16, 6501-6508. (Pubitemid 351802214)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.13
, pp. 6501-6508
-
-
Turos, E.1
Revell, K.D.2
Ramaraju, P.3
Gergeres, D.A.4
Greenhalgh, K.5
Young, A.6
Sathyanarayan, N.7
Dickey, S.8
Lim, D.9
Alhamadsheh, M.M.10
Reynolds, K.11
-
91
-
-
1642579531
-
Novel N-thiolated β-lactam antibiotics selectively induce apoptosis in human tumor and transformed, but not normal or nontransformed, cells
-
DOI 10.1016/j.bcp.2003.09.017
-
Kazi, A.; Hill, R.; Long, T.E.; Kuhn, D J.; Turos, E.; Dou, Q. Novel N thiolated β-lactam antibiotics selectively induce apoptosis in human tumor and transformed, but not normal or nontransformed, cells. P Biochem. Pharmacol., 2004, 67, 365-374. (Pubitemid 38112766)
-
(2004)
Biochemical Pharmacology
, vol.67
, Issue.2
, pp. 365-374
-
-
Kazi, A.1
Hill, R.2
Long, T.E.3
Kuhn, D.J.4
Turos, E.5
Dou, Q.P.6
-
92
-
-
49349092793
-
Studies on the antifungal properties of N-thiolated β-Lactams
-
O'Driscoll, M.; Greenhalgh, K.; Young, A.; Turos, E.; Dickey, S.; Lim, D.V. Studies on the antifungal properties of N-thiolated β-Lactams. Bioorg. Med. Chem., 2008, 16, 7832-7837.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 7832-7837
-
-
O'Driscoll, M.1
Greenhalgh, K.2
Young, A.3
Turos, E.4
Dickey, S.5
Lim, D.V.6
-
93
-
-
73449085175
-
Azetidinones as Zinc-Binding Groups to Design Selective HDAC8 Inhibitors
-
Galletti, P.;Quintavalla, A.; Ventrici, C.; Giannini, G.; Cabri, W; Penco, S.; Gallo, G.; Vincenti, S.; Giacomini, D. Azetidinones as Zinc-Binding Groups to Design Selective HDAC8 Inhibitors. ChemMedChem, 2009, 4, 1-12.
-
(2009)
ChemMedChem
, vol.4
, pp. 1-12
-
-
Galletti, P.1
Quintavalla, A.2
Ventrici, C.3
Giannini, G.4
Cabri, W.5
Penco, S.6
Gallo, G.7
Vincenti, S.8
Giacomini, D.9
-
94
-
-
0028341682
-
2-Azetidinones as inhibitors of cholesterol absorption
-
DOI 10.1021/jm00038a001
-
(a) Burnett, D.A.; Caplen, M.A.; Davis, H.R., Jr.; Burrier, R.E.; Clader, J.W. 2-Azetidinones as inhibitors of cholesterol absorption. J. Med. Chem., 1994, 37, 1733-1736 (Pubitemid 24219762)
-
(1994)
Journal of Medicinal Chemistry
, vol.37
, Issue.12
, pp. 1733-1736
-
-
Burnett, D.A.1
Caplen, M.A.2
Davis Jr., H.R.3
Burrier, R.E.4
Clader, J.W.5
-
95
-
-
0032477601
-
Carboxy-substitutes 2-azetidinones as cholesterol absorption inhibitors
-
DOI 10.1016/S0960-894X(98)00009-2, PII S0960894X98000092
-
(b) Vaccaro, W.D.; Sher, R.; Davis, H.R. Jr Carboxysubstituted 2-azetidinones as cholesterol absorption inhibitors. Bioorg. Med. Chem. Lett., 1998, 8, 319-322 (Pubitemid 28066355)
-
(1998)
Bioorganic and Medicinal Chemistry Letters
, vol.8
, Issue.3
, pp. 319-322
-
-
Vaccaro, W.D.1
Sher, R.2
Davis Jr., H.R.3
-
96
-
-
19544371758
-
Ezetimibe: A review of its metabolism, pharmacokinetics and drug interactions
-
DOI 10.2165/00003088-200544050-00002
-
(c) Kosoglou, T.; Statkevich, P.; Johnson-Levonas, A..O.;Paolini, J.F.; Bergman, A.J.; Alton, K.B. Ezetimibe: A Review of its Metabolism, Pharmacokinetics and Drug Interactions. Clinical Pharmacokinetics, 2005, 44, 467-494. (Pubitemid 40733733)
-
(2005)
Clinical Pharmacokinetics
, vol.44
, Issue.5
, pp. 467-494
-
-
Kosoglou, T.1
Statkevich, P.2
Johnson-Levonas, A.O.3
Paolini, J.F.4
Bergman, A.J.5
Alton, K.B.6
-
97
-
-
61349183123
-
2-Azetidinone derivatives: Design, synthesis and evaluation of cholesterol absorption inhibitors
-
Wang, Y.; Zhang, H.; Huang, W.; Kong, J.; Zhou, J; Zhang, B. 2-Azetidinone derivatives: design, synthesis and evaluation of cholesterol absorption inhibitors. Eur. J. Med. Chem., 2009, 44, 1638-1643
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 1638-1643
-
-
Wang, Y.1
Zhang, H.2
Huang, W.3
Kong, J.4
Zhou, J.5
Zhang, B.6
-
98
-
-
33845600703
-
Ezetimibe analogs with a reorganized azetidinone ring: Design, syn
-
thesis, and evaluation of cholesterol absorption inhibitions
-
(b) Xu, X.; Fu, R.; Chen, J.; Chenc, S.; Bai, X. Ezetimibe analogs with a reorganized azetidinone ring: Design, synthesis, and evaluation of cholesterol absorption inhibitions. Bioorg. Med. Chem.Lett., 2007, 17, 101-104.
-
(2007)
Bioorg. Med. Chem.Lett.
, vol.17
, pp. 101-104
-
-
Xu, X.1
Fu, R.2
Chen, J.3
Chenc, S.4
Bai, X.5
-
99
-
-
3042621839
-
Beta-lactam cholesterol absorption inhibitors
-
Burnett, D.A. Beta-lactam cholesterol absorption inhibitors. Curr. Med. Chem., 2004, 11, 1873-87.
-
(2004)
Curr. Med. Chem.
, vol.11
, pp. 1873-1887
-
-
Burnett, D.A.1
-
100
-
-
0034725865
-
Synthesis of 3-arylpropenyl, 3-arylpropynyl and 3-arylpropyl 2-azetidinones as cholesterol absorption inhibitors: Application of the palladium-catalyzed arylation of alkenes and alkynes
-
PII S0040402000004294
-
Rosenblum, S.B.; Huynh, T.; Afonso, A.; Davis H.R. Jr., Synthesis of 3-Arylpropenyl, 3-Arylpropynyl and 3-Arylpropyl 2-zetidinones as Cholesterol Absorption Inhibitors: Application of the Palladium-Catalyzed Arylation of Alkenes and Alkynes. Tetrahedron, 2000, 56, 5735-5742. (Pubitemid 30619323)
-
(2000)
Tetrahedron
, vol.56
, Issue.31
, pp. 5735-5742
-
-
Rosenblum, S.B.1
Huynh, T.2
Afonso, A.3
Davis Jr., H.R.4
-
101
-
-
18144387622
-
Stereocontrolled synthesis of anticancer β-lactams via the Staudinger reaction
-
DOI 10.1016/j.bmc.2005.03.044
-
(a) Banik, B.K.; Banik, I.; Becker, F.B. Stereocontrolled synthesis of anticancer β-Lactams via the Staudinger reaction. Bioorg. Med. Chem., 2005, 13, 3611-3622 (Pubitemid 40615913)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.11
, pp. 3611-3622
-
-
Banik, B.K.1
Banik, I.2
Becker, F.F.3
-
102
-
-
2142824194
-
Synthesis of anticancer β-lactams: Mechanism of action
-
DOI 10.1016/j.bmc.2004.03.033, PII S0968089604002196
-
(b) Banik, B.K.; Becker, F.B.; Banik, I. Synthesis of anticancer β-Lactams: mechanism of action. Bioorg. Med. Chem., 2004, 12, 2523-2528. (Pubitemid 38542777)
-
(2004)
Bioorganic and Medicinal Chemistry
, vol.12
, Issue.10
, pp. 2523-2528
-
-
Banik, B.K.1
Becker, F.F.2
Banik, I.3
-
103
-
-
77950843614
-
Asymmetric synthesis of anticancer β-Lactams via Staudinger reaction
-
Banik, B.K.; Samajdar, S.; Becker F.B. Asymmetric synthesis of anticancer β-Lactams via Staudinger reaction. Mol.Med. Rep. 2010, 3, 319-321
-
(2010)
Mol.Med. Rep.
, vol.3
, pp. 319-321
-
-
Banik, B.K.1
Samajdar, S.2
Becker, F.B.3
-
104
-
-
73549100633
-
Asymmetric synthesis of anticancer β-lactams via Staudinger reaction: Utilization of chiral ketene from carbohydrate
-
(b) Banik, B.K.; Banik, I.; Becker, F.B Asymmetric synthesis of anticancer β-lactams via Staudinger reaction: Utilization of chiral ketene from carbohydrate. Eur. J. Med. Chem., 2010, 45, 846-848.
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 846-848
-
-
Banik, B.K.1
Banik, I.2
Becker, F.B.3
-
105
-
-
78649326841
-
Lead identification of conformationally restricted β-lactam type combretastatin analogues: Synthesis, antiproliferative activity and tubulin targeting effects
-
Carr, M.; Greene, L.M.; Knox, A.J.S.; Lloyd, D.G.; Zisterer, D.M.; Meegan, M.J. Lead identification of conformationally restricted β-lactam type combretastatin analogues: Synthesis, antiproliferative activity and tubulin targeting effects. Eur. J. Med. Chem., 2010, 45, 5752-5766
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 5752-5766
-
-
Carr, M.1
Greene, L.M.2
Knox, A.J.S.3
Lloyd, D.G.4
Zisterer, D.M.5
Meegan, M.J.6
-
106
-
-
78650312289
-
Synthesisand Evaluation of Azetidinone Analogues of Combretastatin A-4 as Tubulin Targeting Agents
-
(b) O'Boyle, N.M.; Carr, M.; Greene, L.M.; Bergin, O.; Nathwani, S.M.; McCabe, T.; Lloyd, D.G.; Zisterer, D.M.; Meegan, M.J. Synthesis and Evaluation of Azetidinone Analogues of Combretastatin A-4 as Tubulin Targeting Agents. J. Med. Chem. 2010, 53, 8569-8584
-
(2010)
J. Med. Chem.
, vol.53
, pp. 8569-8584
-
-
O'Boyle, N.M.1
Carr, M.2
Greene, L.M.3
Bergin, O.4
Nathwani, S.M.5
McCabe, T.6
Lloyd, D.G.7
Zisterer, D.M.8
Meegan, M.J.9
-
107
-
-
53249113228
-
β-Lactam type molecular scaffolds for antiproliferative activity: Synthesis and cytotoxic effects in breast cancer cells
-
(c) Meegan, M.J.; Carr, M.; Knox, A. J.S.; Zisterer, D.M.; Lloyd, D.G. J. β-Lactam type molecular scaffolds for antiproliferative activity: Synthesis and cytotoxic effects in breast cancer cells. Enzyme Inhib. Med. Chem., 2008, 23, 668-685.
-
(2008)
Enzyme Inhib. Med. Chem.
, vol.23
, pp. 668-685
-
-
Meegan, M.J.1
Carr, M.2
Knox, A.J.S.3
Zisterer, D.M.4
Lloyd, D.G.J.5
-
108
-
-
1842741030
-
Examination of the 1,4-disubstituted azetidinone ring system as a template for combretastatin A-4 conformationally restricted analogue design
-
DOI 10.1016/j.bmcl.2004.02.050, PII S0960894X04002574
-
Sun, L.; Vasilevich, N.I; Fuselier, J.A.; Hocart, S.J.; Coy, D.H. Examination of the 1,4-disubstituted azetidinone ring system as a template for combretastatin A-4 conformationally restricted analogue design Bioorg. Med. Chem. Lett., 2004, 14, 2041-2046. (Pubitemid 38481357)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.9
, pp. 2041-2046
-
-
Sun, L.1
Vasilevich, N.I.2
Fuselier, J.A.3
Hocart, S.J.4
Coy, D.H.5
-
109
-
-
43049151814
-
Identification of novel cannabinoid CB1 receptor antagonists by using virtual screening with a pharmacophore model
-
DOI 10.1021/jm701519h
-
Wang, H.; Duffy, R.A.; Boykow, G.C.; Chackalamannil, S.; Madison. V.S. Identification of Novel Cannabinoid CB1 Receptor Antagonists by Using Virtual Screening with a Pharmacophore Model. J. Med. Chem., 2008, 51, 2439-2446. (Pubitemid 351628505)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.8
, pp. 2439-2446
-
-
Wang, H.1
Duffy, R.A.2
Boykow, G.C.3
Chackalamannil, S.4
Madison, V.S.5
-
110
-
-
53349162101
-
PASS-assisted exploration of antidepressant activity of 1,3,4-trisubstituted-b-lactam derivatives. Bioor
-
Mittal, M.; Goel, R.K.; Bhargava, G.; Mahajan, M.P. PASS-assisted exploration of antidepressant activity of 1,3,4-trisubstituted-b-lactam derivatives. Bioor. Med. Chem. Lett., 2008, 18, 5347-5349.
-
(2008)
Med. Chem. Lett.
, vol.18
, pp. 5347-5349
-
-
Mittal, M.1
Goel, R.K.2
Bhargava, G.3
Mahajan, M.P.4
-
111
-
-
33846244711
-
Synthesis and antimicrobial activity of new 2-azetidinones from N-(salicylidene)amines and 2-diazo-1,2-diarylethanones
-
Singh, G.S.; Mbukwa E.; Pheko T. Synthesis and antimicrobial activity of new 2-azetidinones from N-(salicylidene)amines and 2-diazo-1,2-diarylethanones. ARKIVOC, 2007, ix, 80-90.
-
(2007)
ARKIVOC
, vol.9
, pp. 80-90
-
-
Singh, G.S.1
Mbukwa, E.2
Pheko, T.3
-
112
-
-
71849115961
-
Synthesis and bioactivity of catechin/epicatechin and 2-azetidinone derived chimeric molecules
-
Basab ,R.; Amit, B.; Arindam, C.; Sudip, G.K. Design, synthesis and bioactivity of catechin/epicatechin and 2-azetidinone derived chimeric molecules. Bioorg. Med. Chem. Lett., 2009, 19; 7007-7010.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 7007-7010
-
-
Basab, R.1
Amit, B.2
Arindam, C.3
Design, K.S.G.4
-
113
-
-
40749106101
-
Synthesis and antimicrobial activity of β-lactam-bile acid conjugates linked via triazole
-
DOI 10.1016/j.bmcl.2008.01.102, PII S0960894X08001303
-
Vatmurge, N.S.; Hazra, B.G.; Pore, V.S.; Shirazi, F.; Chavan, P.S.; Deshpande, M.V. Synthesis and antimicrobial activity of beta-lactam-bile acid conjugates linked via triazole. Bioorg. Med. Chem. Lett., 2008, 18, 2043-2047. (Pubitemid 351380871)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.6
, pp. 2043-2047
-
-
Vatmurge, N.S.1
Hazra, B.G.2
Pore, V.S.3
Shirazi, F.4
Chavan, P.S.5
Deshpande, M.V.6
-
114
-
-
20844446096
-
Stereoselective synthesis, reactions and antimicrobial activity of 3-vinyl-2-azetidinones
-
Sharma, S.D.; Anand, R.D.; Kaur, G. Stereoselective synthesis, reactions and antimicrobial activity of 3-vinyl-2-azetidinones. J. Chem. Res., Synopses, 2005 , 4, 248-251. (Pubitemid 40863395)
-
(2005)
Journal of Chemical Research
, Issue.4
, pp. 248-251
-
-
Sharma, S.D.1
Anand, R.D.2
Kaur, G.3
-
115
-
-
53549097892
-
Synthesisand biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-β-lactam
-
Vatmurge, N.S.; Hazra, B.G.; Pore, V.S.; Shirazi, F.; Deshpande, M.V.; Kadreppa, S.; Chattopadhyayc, S. Synthesis and biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-β-lactam. Org. Biomol. Chem., 2008, 6, 3823-3830.
-
(2008)
Org. Biomol. Chem.
, vol.6
, pp. 3823-3830
-
-
Vatmurge, N.S.1
Hazra, B.G.2
Pore, V.S.3
Shirazi, F.4
Deshpande, M.V.5
Kadreppa, S.6
Chattopadhyayc, S.7
-
116
-
-
85059441520
-
Bis-N-aryl-β-Lactams: Vilsmeier reagent as an efficient entity for the synthesis via alternate cycloaddition reaction and in vitro biology
-
Alia, P.; Meshrama, J.; Tiwaria, V.; Dongrea, R.; Sheikh, J.; Ahemad, M. Bis-N-aryl-β-Lactams: Vilsmeier reagent as an efficient entity for the synthesis via alternate cycloaddition reaction and in vitro biology. Pharma Chemica, 2010, 2 (3), 138-147.
-
(2010)
Pharma Chemica
, vol.2
, Issue.3
, pp. 138-147
-
-
Alia, P.1
Meshrama, J.2
Tiwaria, V.3
Dongrea, R.4
Sheikh, J.5
Ahemad, M.6
-
118
-
-
40149088458
-
TRPV1 antagonists as potential antitussive agents
-
DOI 10.1007/s00408-007-9032-z
-
For a recent review see: McLeod, R.L.; Correll, C.C.; Jia, Y.; Anthes, J.C. TRPV1 antagonists as potential antitussive agents. Lung, 2008, 186, S59-S65. (Pubitemid 351327286)
-
(2008)
Lung
, vol.186
, Issue.SUPPL. 1
-
-
McLeod, R.L.1
Correll, C.C.2
Jia, Y.3
Anthes, J.C.4
-
119
-
-
77955415074
-
T-type calcium channel blockers: Spiro-piperidine azetidines and azetidinones optimization, design and synthesis
-
(a) Smith, E.M.; Sorota, S.; Kim, H.M.; McKittrick, B.A.; Nechuta, T.L.; Bennett, C.; Knutson, C.;Burnett, D. A.; Kieselgof, J.; Tan, Z.; Rindgen, D.; Bridal, T.; Zhou, X.; Jia, Y-P.; Dong, Z.; Mullins, D.; Zhang, X.; Priestley, T.; Correll, C.C.; Tulshian, D.; Czarniecki, M.; Greenlee, W.J. T-type calcium channel blockers: spiro-piperidine azetidines and azetidinones optimization, design and synthesis. Bioorg. Med. Chem. Lett., 2010, 20, 4602-4606
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 4602-4606
-
-
Smith, E.M.1
Sorota, S.2
Kim, H.M.3
McKittrick, B.A.4
Nechuta, T.L.5
Bennett, C.6
Knutson, C.7
Burnett, D.A.8
Kieselgof, J.9
Tan, Z.10
Rindgen, D.11
Bridal, T.12
Zhou, X.13
Jia, Y.-P.14
Dong, Z.15
Mullins, D.16
Zhang, X.17
Priestley, T.18
Correll, C.C.19
Tulshian, D.20
Czarniecki, M.21
Greenlee, W.J.22
more..
-
120
-
-
58549085376
-
-
(b) for previously reported spiro-azetidinones as TRPV1 inhibitor see: Xiao, D.; Palani A..; Aslanian, R.; McKittrick, B.A.;. McPhail, A.T; Correll, C.; Phelps, P.T.; Anthens, J.C. Bioorg. Med. Chem., 2009, 19, 783-787.
-
(2009)
Bioorg. Med. Chem.
, vol.19
, pp. 783-787
-
-
Xiao, D.1
Palani, A.2
Aslanian, R.3
McKittrick, B.A.4
McPhail, A.T.5
Correll, C.6
Phelps, P.T.7
Anthens, J.C.8
-
121
-
-
33846429592
-
Drug insight: Mechanisms of action and therapeutic applications for agonists of peroxisome proliferator-activated receptors
-
DOI 10.1038/ncpendmet0397, PII NCPENDMET0397
-
For a recent PPARs review see for instance: Gervois, P.; Fruchart, J.-C.; Staels, B. Drug insight: mechanisms of action and therapeutic applications for agonists of peroxisome proliferator-activated receptors. Nat. Rev. Endocrinol., 2007, 3, 145-156. (Pubitemid 46146967)
-
(2007)
Nature Clinical Practice Endocrinology and Metabolism
, vol.3
, Issue.2
, pp. 145-156
-
-
Gervois, P.1
Fruchart, J.-C.2
Staels, B.3
-
122
-
-
40749086322
-
Discovery of azetidinone acids as conformationally-constrained dual PPARα/γ agonists
-
DOI 10.1016/j.bmcl.2008.01.126, PII S0960894X08001509
-
Wang, W.; Devasthale, P.; Farrelly, D.; Gu, L.; Harrity, T.; Cap, M.; Chu, C.; Kunselman, L.; Morgan, N.; Ponticiello, R.; Zebo, R.; Zhang, L.; Locke, K.; Lippy, J.; O'Malley, K.; Hosagrahara, V.; Zhang, L.; Kadiyala, P.; Chang, C.; Muckelbauer, J.; Doweyko, A.M.; Zahler, R.; Ryono, D.; Hariharanb, N.; Cheng, P.T.W. Discovery of azetidinone acids as conformationallyconstrained dual PPAR alpha/gamma agonists. Bioorg. Med. Chem.Lett., 2008, 18, 1939-1944. (Pubitemid 351380888)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.6
, pp. 1939-1944
-
-
Wang, W.1
Devasthale, P.2
Farrelly, D.3
Gu, L.4
Harrity, T.5
Cap, M.6
Chu, C.7
Kunselman, L.8
Morgan, N.9
Ponticiello, R.10
Zebo, R.11
Zhang, L.12
Locke, K.13
Lippy, J.14
O'Malley, K.15
Hosagrahara, V.16
Zhang, L.17
Kadiyala, P.18
Chang, C.19
Muckelbauer, J.20
Doweyko, A.M.21
Zahler, R.22
Ryono, D.23
Hariharan, N.24
Cheng, P.T.W.25
more..
-
123
-
-
19944402503
-
Beta-lactam compounds as apparently uncompetitive inhibitors of HIV-1 protease
-
DOI 10.1016/j.bmcl.2005.04.020, PII S0960894X05004804
-
Sperka, T.; Pitlik, J.; Bagossi, P.; Tözséra, J. Beta-lactam compounds as apparently uncompetitive inhibitors of HIV-1 protease. Bioorg. Med.Chem. Lett., 2005, 15, 3086-3090. (Pubitemid 40755201)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.12
, pp. 3086-3090
-
-
Sperka, T.1
Pitlik, J.2
Bagossi, P.3
Tozser, J.4
-
124
-
-
41149135482
-
β-Lactam congeners of orlistat as inhibitors of fatty acid synthase
-
DOI 10.1016/j.bmcl.2008.02.043, PII S0960894X08002047
-
Zhang, W.; Richardson, R.D.; Chamni, S.; Smith, J.W. ; Romo, D. β-Lactam congeners of Orlistat as inhibitors of fatty acid synthase. Bioorg. Med. Chem. Lett., 2008, 18, 2491-2494. (Pubitemid 351442878)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.7
, pp. 2491-2494
-
-
Zhang, W.1
Richardson, R.D.2
Chamni, S.3
Smith, J.W.4
Romo, D.5
-
125
-
-
33845909566
-
Pharmacological inhibitors of fatty acid synthase (FASN)-catalyzed endogenous fatty acid biogenesis: A new family of anti-cancer agents?
-
DOI 10.2174/138920106779116928
-
For a review, see: Lupu, R.; Menendez, J. A. pharmacological inhibitors of fatty acid synthase (FASN)-catalyzed endogenous fatty acid biogenesis: a new family of anti-cancer agents? Curr. Pharm. Biotech., 2006, 7, 483-494. (Pubitemid 46017540)
-
(2006)
Current Pharmaceutical Biotechnology
, vol.7
, Issue.6
, pp. 483-494
-
-
Lupu, R.1
Menendez, J.A.2
-
126
-
-
33847607994
-
Synthesis and biological evaluation of unprecedented classes of spiro-β-lactams and azido-β-lactams as acyl-CoA:cholesterol acyltransferase inhibitors
-
DOI 10.1016/j.bmcl.2007.01.027, PII S0960894X07000777
-
Benfatti, F.; Cardillo, G.; Gentilucci, L.; Tolomelli, A. Synthesis and biological evaluation of unprecedented classes of spiro-β-Lactams and azido-β-lactams as acyl-CoA:cholesterol acyltransferase inhibitors. Bioorg. Med. Chem. Lett., 2007, 1, 1946-1950. (Pubitemid 46367665)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.7
, pp. 1946-1950
-
-
Benfatti, F.1
Cardillo, G.2
Gentilucci, L.3
Tolomelli, A.4
-
127
-
-
74849100941
-
4-Oxo-β-Lactams (azetidine-2,4-diones) are potent and selective inhibitors of Human Leukocyte Elastase
-
(a) Mulchande, J.; Oliveira, R.; Carrasco, M.; Gouveia, L.; Guedes, R.C.; Iley , J.; Moreira, R. 4-Oxo-β-Lactams (azetidine-2,4-diones) are potent and selective inhibitors of Human Leukocyte Elastase. J. Med. Chem., 2010, 53, 241-253
-
(2010)
J. Med. Chem.
, vol.53
, pp. 241-253
-
-
Mulchande, J.1
Oliveira, R.2
Carrasco, M.3
Gouveia, L.4
Guedes, R.C.5
Iley, J.6
Moreira, R.7
-
128
-
-
41149169679
-
Azetidine-2,4-diones (4-oxo-β-lactams) as scaffolds for designing elastase inhibitors
-
DOI 10.1021/jm701257h
-
Mulchande, J.; Guedes, R.C.; Tsang, W.Y.; Page, M.I.; Moreira, R.; Iley, J. Azetidine-2,4-diones (4-oxo-β-Lactams) as scaffolds for designing elastase inhibitors. J. Med. Chem., 2008, 51, 1783-1790. (Pubitemid 351438860)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.6
, pp. 1783-1790
-
-
Mulchande, J.1
Guedes, R.C.2
Tsang, W.-Y.3
Page, M.I.4
Moreira, R.5
Iley, J.6
-
129
-
-
67349276713
-
Studies on the cytotoxic activity of synthetic 2H-azirine-2-azetidinone compounds
-
Maia, D.P.; Wilke, D.V.; Mafezoli, J.; da Silva, J.N. Jr.; de Moraesa, M.O.; Pessoa, C.; Costa-Lotufo, L.V. Studies on the cytotoxic activity of synthetic 2H-azirine-2-azetidinone compounds. Chem-Biol. Interact., 2009, 180, 220-225.
-
(2009)
Chem-Biol. Interact.
, vol.180
, pp. 220-225
-
-
Maia, D.P.1
Wilke, D.V.2
Mafezoli, J.3
Da Silva Jr., J.N.4
De Moraesa, M.O.5
Pessoa, C.6
Costa-Lotufo, L.V.7
|