References
- Kuethe, J. T.; Wong, A.; Qu, C.; Smitrovich, J.; Davis, I. W.; Hughes, D. L. J. Org. Chem. 2005, 70, 504.
- Varvaresou, A.; Tsantili-Kakoulidou, A.; Siatra-Papastaikoudi, T.; Tiligada, E. Arzneim Forsch 2000, 50, 48-54.
- Mohan, J.; Kataria, S. Indian Chem. J. Sect. B 1996, 35, 456-458.
- Palluotto, F.; Carotti, A.; Casini, G.; Ferappi, M.; Rosata, A.; Vitali, C.; Campagna, F. Farmaco 1999, 54(3), 191-194. https://doi.org/10.1016/S0014-827X(99)00021-X
- Dzurilla, M.; Ruzinsky, M.; Kutschy, P.; Tewari, J.; Kovacik, V. Collect. Czech. Chem. Commun. 1999, 64, 1448-1456. https://doi.org/10.1135/cccc19991448
- Kutsky, P.; Dzurilla, T. M.; Sabova, A. Collect. Czech. Chem. Commun. 1999, 64, 348-362. https://doi.org/10.1135/cccc19990348
- Kutsky, P.; Dzurilla, M.; Takasugi, M.; Toerock, M.; Achbergerova, I. Tetrahedron 1998, 54, 3549-3566. https://doi.org/10.1016/S0040-4020(98)00088-X
- Khan, M. H.; Twari, S.; Begum, K.; Nizamuddin, 0, Indian Chem. J. Sect. B 1998, 37, 1075-1077.
- Machia, M.; Mamera, C.; Nencetti, S.; Rossello, A.; Broccali, G.; Limonta, D. Farmaco 1996, 51, 75-78.
- Garuti, L.; Roberti, M.; Rossi, T.; Castelli, M.; Malagoli, M. Eur. J. Med. Chem. Chem. 1998, Ther. 33, 43-46. https://doi.org/10.1016/S0223-5234(99)80074-9
- Draheim, S. A.; Bach, N. J.; Dillard, R. D.; Berry, D. R.; Carlson, D. G. J. Med. Chem. 1996, 39, 5159-5175. https://doi.org/10.1021/jm960487f
- Battagba, S.; Boldrini, E.; Settimo, F. D.; Dondio, G.; Motta, C. L. Eur. J. Med. Chem. Chim. Ther. 1999, 34, 93-106. https://doi.org/10.1016/S0223-5234(99)80044-0
- Zotova, S. A.; Korneeva, T. M.; Shvedov, V. I.; Fadaeva, N. I.; Leneva, I. A. Pharm. Chem. J. 1995, 29, 57-59. https://doi.org/10.1007/BF02219467
- Lai, G.; Anderson, W. K. Tetrahedron 2000, 56, 2583-2590. https://doi.org/10.1016/S0040-4020(00)00177-0
- Amir, M.; Dhar, N.; Tiwari, S. K. Indian. J. Chem. Sect. B 1997, 36, 96-98.
- Grasso, S.; Molica, C.; Monforte, A. M.; Monforte, P.; Zappala, M. Farmaco 1995, 50, 113-118.
- Katayama, M.; Gautam, R. K. Biosci. Biotechnol. Biochem. 1996, 60, 755-759. https://doi.org/10.1271/bbb.60.755
- Riyadh, S. M.; Farghaly, T. A.; Gomha, S. M. Arch. Pharm. Res. 2010, 33, 1721. https://doi.org/10.1007/s12272-010-1102-8
- Gomha, S. M.; Riyadh, S. M. ARKIVOC 2009, xi, 58-68.
- Abbas, I. M.; Riyadh, S. M.; Abdallah, M. A.; Gomha, S. M. J. Het. Chem. 2006, 43, 935-942. https://doi.org/10.1002/jhet.5570430419
- Abdel-Aziz, H. A.; Saleh, T. S.; El-Zahabi, H. S. A. Arch. Pharm. 2010, 343, 24-30.
- Abdel-Aziz, H. A.; Hamdy, N. A.; Gamal-Eldeen, A. M.; Fakhr, I. M. I. Z. Naturforsch C 2011, 66, 7. https://doi.org/10.5560/ZNB.2011.66c0007
- Acheson, R. M.; Prince, R. J.; Procter, G. J. Chem. Soc., Perkin Trans. 1 1979, 3, 595-599.
- Cowper, R. M.; Davidson, L. H. Org. Syn., Coll. 1943, II, 840.
- Dieckmann, W.; Platz, O. Chem. Ber. 1906, 38, 2989.
- Hegarty, A. F.; Cashoman, M. P.; Scott, F. L. Chem. Commun. 1971, 13, 684.
- National Committee for Clinical Laboratory Standards (NCCLS), "Standard Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria, Which Grows Aerobically," Nat. Comm. Lab. Stands. Villanova, 1982; p 242.
- Habib, N. S.; Rida, S. M.; Badawey, E. A. M.; Fahmy, H. T. Y.; Ghozlan, H. A. Pharmazie 1997, 52, 346-350.
- Bondock, S.; Fadaly, W.; Metwally, M. A. Eur. J. Med. Chem. 2010, 45, 3692. https://doi.org/10.1016/j.ejmech.2010.05.018
- Rostom, S. A. F.; El-Ashmawy, I. M.; Abd El Razik, H. A.; Badr, M. H.; Ashour, H. M. A. Bioorg. Med. Chem. 2009, 17, 882. https://doi.org/10.1016/j.bmc.2008.11.035
- Farag, A. M.; Dawood, K. M.; Kandeel, Z. E. Tetrahedron 1997, 53, 161. https://doi.org/10.1016/S0040-4020(96)00959-3
- Hamdy, N. A.; Abdel-Aziz, H. A.; Farag, A. M.; Fakhr, I. M. I. Monatsh. fur Chem. 2007, 138, 1001-1010. https://doi.org/10.1007/s00706-007-0717-z
- Dawood, K. M.; Farag, A. M.; Abdel-Aziz, H. A. J. Chem. Res. 2005, 378-381.
Cited by
- 3-Amino-8-hydroxy-4-imino-6-methyl-5-phenyl-4,5-dihydro-3H-chromeno [2,3-d ]pyrimidine: An Effecient Key Precursor for Novel Synthesis of Some Interesting Triazines and Triazepines as Potential Anti-Tumor Agents vol.17, pp.12, 2012, https://doi.org/10.3390/molecules171011538
- A Convenient Ultrasound-Promoted Synthesis of Some New Thiazole Derivatives Bearing a Coumarin Nucleus and Their Cytotoxic Activity vol.17, pp.12, 2012, https://doi.org/10.3390/molecules17089335
- Novel anti-HIV-1 NNRTIs based on a pyrazolo[4,3-d]isoxazole backbone scaffold: design, synthesis and insights into the molecular basis of action vol.5, pp.11, 2014, https://doi.org/10.1039/C4MD00282B
- Synthesis and Anti-cancer Activity of 1,3,4-Thiadiazole and 1,3-Thiazole Derivatives Having 1,3,4-Oxadiazole Moiety vol.52, pp.5, 2015, https://doi.org/10.1002/jhet.2250
- Synthesis, characterization, and pharmacological evaluation of some novel thiadiazoles and thiazoles incorporating pyrazole moiety as anticancer agents vol.146, pp.1, 2015, https://doi.org/10.1007/s00706-014-1303-9
- Synthesis and Cytotoxicity Evaluation of Some Novel Thiazoles, Thiadiazoles, and Pyrido[2,3-d][1,2,4]triazolo[4,3-a]pyrimidin-5(1H)-ones Incorporating Triazole Moiety vol.20, pp.1, 2015, https://doi.org/10.3390/molecules20011357
- Synthesis and Characterization of Bisimidazoles, Bistriazoles, Bisthiadiazoles, and Bisthiazoles from Novel Bishydrazonoyl Dichlorides vol.53, pp.1, 2016, https://doi.org/10.1002/jhet.2320
- Synthesis of New 3-Heteroarylindoles as Potential Anticancer Agents vol.21, pp.7, 2016, https://doi.org/10.3390/molecules21070929
- -Heterocycles Incorporating Thienothiophene vol.54, pp.1, 2017, https://doi.org/10.1002/jhet.2636
- Hydrazonoyl Halides Precursors to Synthesis of New Thiazole, Thiadiazole, and Benzothiazepine Derivatives vol.54, pp.2, 2017, https://doi.org/10.1002/jhet.2688
- Synthesis of Pyridotriazolopyrimidines as Antitumor Agents vol.54, pp.2, 2017, https://doi.org/10.1002/jhet.2699
- A facile synthesis and anticancer activity of some novel thiazoles carrying 1,3,4-thiadiazole moiety vol.11, pp.1, 2017, https://doi.org/10.1186/s13065-017-0255-7
- Synthesis of some new pyrazolo[1,5-a]pyrimidine, pyrazolo[5,1-c]triazine, 1,3,4-thiadiazole and pyridine derivatives containing 1,2,3-triazole moiety vol.11, pp.1, 2017, https://doi.org/10.1186/s13065-017-0282-4
- A facile access and evaluation of some novel thiazole and 1,3,4-thiadiazole derivatives incorporating thiazole moiety as potent anticancer agents vol.11, pp.1, 2017, https://doi.org/10.1186/s13065-017-0335-8
- Synthesis, Antitumor Evaluation and Molecular Docking of New Morpholine Based Heterocycles vol.22, pp.7, 2017, https://doi.org/10.3390/molecules22071211
- Synthesis and characterization of new pyrazole-based thiazoles vol.47, pp.15, 2017, https://doi.org/10.1080/00397911.2017.1330961
- Synthetic Utility of Pyridinium Bromide: Synthesis and Antimicrobial Activity of Novel 2,4,6-Trisubstituted Pyridines Having Pyrazole Moiety vol.54, pp.3, 2017, https://doi.org/10.1002/jhet.2790
- Synthesis of Some Novel Heterocycles Bearing Thiadiazoles as Potent Anti-inflammatory and Analgesic Agents vol.54, pp.5, 2017, https://doi.org/10.1002/jhet.2872
- Utility of Pyrazolylchalcone Synthon to Synthesize Azolopyrimidines under Grindstone Technology vol.65, pp.1, 2017, https://doi.org/10.1248/cpb.c16-00759
- Ecofriendly one-pot synthesis and antiviral evaluation of novel pyrazolyl pyrazolines of medicinal interest vol.40, pp.13036130, 2016, https://doi.org/10.3906/kim-1510-25
- Synthesis and biological evaluation of some novel thiadiazole-benzofuran hybrids as potential antitumor agents vol.48, pp.6, 2018, https://doi.org/10.1080/00397911.2017.1416637
- Intramolecular Ring Transformation of Bis-oxadiazoles to Bis-thiadiazoles and Investigation of Their Anticancer Activities vol.55, pp.10, 2018, https://doi.org/10.1002/jhet.3300
- -Thiadiazoles as Potent Antimicrobial Agents vol.55, pp.4, 2018, https://doi.org/10.1002/jhet.3108
- ]pyrimidinones vol.55, pp.5, 2018, https://doi.org/10.1002/jhet.3146
- Synthesis and biological evaluation of an indole core-based derivative with potent antimicrobial activity vol.44, pp.9, 2018, https://doi.org/10.1007/s11164-018-3426-9
- Synthetic Utility of Ethylidenethiosemicarbazide: Synthesis and Anticancer Activity of 1,3-Thiazines and Thiazoles with Imidazole Moiety vol.87, pp.2, 2012, https://doi.org/10.3987/com-12-12625
- A Convenient Synthesis of Some New Thiazole and Pyrimidine Derivatives Incorporating a Naphthalene Moiety vol.37, pp.2, 2012, https://doi.org/10.3184/174751912x13567137687630
- An Efficient Synthesis of Functionalised 2-(heteroaryl)-3H-benzo[f] Chromen-3-ones and Antibacterial Evaluation vol.37, pp.5, 2012, https://doi.org/10.3184/174751913x13662197808100
- Synthesis and Antihypertensive α-Blocking Activity Evaluation of Thiazole Derivatives Bearing Pyrazole Moiety vol.91, pp.9, 2015, https://doi.org/10.3987/com-15-13290
- Synthesis and Characterisation of Some Novel Fused Thiazolo[3,2-A] Pyrimidinones and Pyrimido[2,1-B][1,3]Thiazinones vol.39, pp.12, 2012, https://doi.org/10.3184/174751915x14474391581067
- Heterocyclisation of 2,5-diacetyl-3,4-disubstituted-thieno[2,3-b]Thiophene Bis-Thiosemicarbazones Leading to Bis-Thiazoles and Bis-1,3,4-thiadiazoles as Anti-breast Cancer Agents vol.40, pp.2, 2016, https://doi.org/10.3184/174751916x14537182696214
- Synthesis of Some Novel Thiadiazoles and Thiazoles Linked to Pyrazole Ring vol.92, pp.4, 2016, https://doi.org/10.3987/com-15-13370
- Application of Mannich and Michael Reactions in Synthesis of Pyridopyrimido[2,1-b][1,3,5]thiadiazinones and Pyridopyrimido[2,1-b][1,3]thiazinones as Anticancer Agents vol.92, pp.4, 2012, https://doi.org/10.3987/com-16-13419
- DABCO-Catalyzed Green Synthesis of Thiazole and 1,3-Thiazine Derivatives Linked to Benzofuran vol.92, pp.8, 2012, https://doi.org/10.3987/com-16-13470
- A facile synthesis and characterization of some new thiophene based heterocycles vol.1149, pp.None, 2017, https://doi.org/10.1016/j.molstruc.2017.08.057
- Highly Efficient [3 + 2] Cycloaddition: Click Synthesis of Novel 1 H ‐indol‐3‐yl‐benzo[ d ]imidazole Bis‐triazoles vol.56, pp.9, 2012, https://doi.org/10.1002/jhet.3679
- A new series of thiazolyl pyrazoline derivatives linked to benzo[1,3]dioxole moiety: Synthesis and evaluation of antimicrobial and anti-proliferative activities vol.50, pp.3, 2012, https://doi.org/10.1080/00397911.2019.1695839
- Synthesis, crystal structure, spectroscopic, electronic and nonlinear optical properties of potent thiazole based derivatives: Joint experimental and computational insight vol.1202, pp.None, 2012, https://doi.org/10.1016/j.molstruc.2019.127354
- Methods of Synthesis for the Azolo[1,2,4]Triazines vol.56, pp.10, 2020, https://doi.org/10.1007/s10593-020-02808-z
- Novel nano-architectured carbon quantum dots (CQDs) with phosphorous acid tags as an efficient catalyst for the synthesis of multisubstituted 4H-pyran with indole moieties under mild conditions vol.11, pp.42, 2012, https://doi.org/10.1039/d1ra02515e