Статті в журналах з теми "Quinazoline-4(3H)-ones"
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Ознайомтеся з топ-48 статей у журналах для дослідження на тему "Quinazoline-4(3H)-ones".
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Widiyana, Anita Puspa. "COMPUTATION DESIGN OF QUINAZOLINE-4(3H)-ON DERIVATIVES AS CYCLOOXYGENASE-2 (COX-2) INHIBITOR." Jurnal Farmasi Sains dan Praktis 7, no. 2 (November 1, 2021): 163–70. http://dx.doi.org/10.31603/pharmacy.v7i2.4827.
Повний текст джерелаAppani, Ramgopal, Baburao Bhukya, and Kiran Gangarapu. "Synthesis and Antibacterial Activity of 3-(Substituted)-2-(4-oxo-2-phenylquinazolin-3(4H)-ylamino)quinazolin-4(3H)-one." Scientifica 2016 (2016): 1–5. http://dx.doi.org/10.1155/2016/1249201.
Повний текст джерелаŠpirková, Katarína, and Štefan Stankovský. "Annelation to the Quinazoline Ring. Preparation of Some Substituted 2H-Imidazo- and 2,3-Dihydropyrimido[1,2-c]quinazolines." Collection of Czechoslovak Chemical Communications 61, no. 6 (1996): 957–61. http://dx.doi.org/10.1135/cccc19960957.
Повний текст джерелаTiwari, Abhishek R., and Bhalchandra M. Bhanage. "Transition-metal free synthesis of quinazolinones via tandem cyclization of 2-halobenzoic acids with amidines." RSC Advances 5, no. 70 (2015): 57235–39. http://dx.doi.org/10.1039/c5ra11159e.
Повний текст джерелаPeter Osarodion Osarumwense, Mary Olire Edema, and Cyril Odianosen Usifoh. "Synthesis and antibacterial activities of quinazolin-4(3h)-one, 2-methyl-4(3h)-quinazolinone and 2–phenyl-4(3h)-quinazolinone." International Journal of Biological and Pharmaceutical Sciences Archive 1, no. 2 (April 30, 2021): 077–84. http://dx.doi.org/10.30574/ijbpsa.2021.1.2.0027.
Повний текст джерелаOluwaseye, Adedirin, A. UZAIRU, G. A. SHALLANGWA, and S. E. ABECHI. "QSAR STUDIES ON DERIVATIVES OF QUINAZOLINE-4(3H)-ONES WITH ANTICONVULSANT ACTIVITIES." Journal of Engineering and Exact Sciences 4, no. 2 (July 4, 2018): 0255–64. http://dx.doi.org/10.18540/jcecvl4iss2pp0255-0264.
Повний текст джерелаSrivastav, Manish, MD Salahuddin, and S. M. Shantakumar. "Synthesis and Anti-inflammatory Activity of Some Novel 3-(6-Substituted-1, 3-benzothiazole-2-yl)-2-[{(4-substituted phenyl) amino} methyl] quinazolines-4 (3H)-ones." E-Journal of Chemistry 6, no. 4 (2009): 1055–62. http://dx.doi.org/10.1155/2009/507052.
Повний текст джерелаWright, William B., Andrew S. Tomcufcik, Peter S. Chan, Joseph W. Marsico, and Jeffery B. Press. "Thromboxane synthetase inhibitors and antihypertensive agents. 4. N-[(1H-imidazol-1-yl)alkyl] derivatives of quinazoline-2,4(1H,3H)-diones, quinazolin-4(3H)-ones, and 1,2,3-benzotriazin-4(3H)-ones." Journal of Medicinal Chemistry 30, no. 12 (December 1987): 2277–83. http://dx.doi.org/10.1021/jm00395a016.
Повний текст джерелаBarlaam, Bernard, Craig S. Harris, Jonathan Lecoq, and Ha Thi Hoang Nguyen. "Preparation of 6-aminoquinazolin-4(3H)-ones via direct SNAr on the quinazoline ring." Tetrahedron 68, no. 2 (January 2012): 534–43. http://dx.doi.org/10.1016/j.tet.2011.11.008.
Повний текст джерелаNaidu, P. Paradesi, Akula Raghunadh, K. Raghavendra Rao, Ramamohan Mekala, J. Moses Babu, B. R. Rao, V. Siddaiah, and Manojit Pal. "Urea/Thiourea as Ammonia Surrogate: A Catalyst-Free Synthesis of 2-Substituted 2,3-Dihydroquinazolin-4(1H)-ones/Quinazoline-4(3H)-ones." Synthetic Communications 44, no. 10 (April 29, 2014): 1475–82. http://dx.doi.org/10.1080/00397911.2013.862551.
Повний текст джерелаKumar, Ashok, Pratibha Sharma, Prerna Kumari, and Bhagwan Lal Kalal. "Exploration of antimicrobial and antioxidant potential of newly synthesized 2,3-disubstituted quinazoline-4(3H)-ones." Bioorganic & Medicinal Chemistry Letters 21, no. 14 (July 2011): 4353–57. http://dx.doi.org/10.1016/j.bmcl.2011.05.031.
Повний текст джерелаTashrifi, Zahra, Mohammad Mohammadi-Khanaposhtani, Mahmood Biglar, Bagher Larijani, and Mohammad Mahdavi. "Isatoic Anhydride: A Fascinating and Basic Molecule for the Synthesis of Substituted Quinazolinones and Benzo di/triazepines." Current Organic Chemistry 23, no. 10 (August 16, 2019): 1090–130. http://dx.doi.org/10.2174/1385272823666190701142930.
Повний текст джерелаBeutner, Gregory, William Wertjes, Sloan Ayers, Qi Gao, and Eric Simmons. "A Divergent Nickel-Catalyzed Synthesis of Quinazolinediones and Benzoxazinone Imines." Synthesis 50, no. 22 (May 17, 2018): 4453–61. http://dx.doi.org/10.1055/s-0037-1610140.
Повний текст джерелаKut, D. Zh, M. M. Kut, M. Yг Onysko, and V. G. Lendel. "Electrophilic cyclization of propargyl thioethers of 3-methyl(phenyl)-2-(prop-2-yn-1-ylthio)-7-(trifluoromethyl)quinazolin-4(3H)-ones by tellurium tetrahalides." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 6 (December 2021): 40–44. http://dx.doi.org/10.32434/0321-4095-2021-139-6-40-44.
Повний текст джерелаPrabhakar, B., P. Lingaiah, and K. Laxma Reddy. "ESR and other spectral studies on copper(II) complexes with 2,3-disubstituted quinazoline-(3H)-4-ones." Polyhedron 9, no. 6 (January 1990): 805–11. http://dx.doi.org/10.1016/s0277-5387(00)81345-5.
Повний текст джерелаKalogirou, Andreas S., Andreas Kourtellaris, and Panayiotis A. Koutentis. "Synthesis and Reactivity of 3′,5′-Dichloro-1H -spiro(quinazoline-2,4′-[1,2,6]thiadiazin)-4(3H )-ones." European Journal of Organic Chemistry 2019, no. 31-32 (June 7, 2019): 5462–74. http://dx.doi.org/10.1002/ejoc.201900576.
Повний текст джерелаNaidu, P. Paradesi, Akula Raghunadh, K. Raghavendra Rao, Ramamohan Mekala, J. Moses Babu, B. R. Rao, V. Siddaiah, and Manojit Pal. "ChemInform Abstract: Urea/Thiourea as Ammonia Surrogate: A Catalyst-Free Synthesis of 2-Substituted 2,3-Dihydroquinazolin-4(1H)-ones/Quinazoline-4(3H)-ones." ChemInform 45, no. 43 (October 10, 2014): no. http://dx.doi.org/10.1002/chin.201443172.
Повний текст джерелаPrabhakar, B., P. Lingaiah, and K. Laxma Reddy. "Synthesis and spectral studies on Co (II) and Ni (II) complexes with polyfunctional quinazoline-(3H)-4-ones." Proceedings / Indian Academy of Sciences 103, no. 5 (October 1991): 599–605. http://dx.doi.org/10.1007/bf02841060.
Повний текст джерелаKulkarni, RS, NK Sathish, AA Kempwade, and SA Kavatagimath. "Synthesis and Evaluation of Novel Quinazolin-4-(3h)-one Analogues for their Anti-Inflammatory Activity." INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE 14, no. 04 (December 25, 2023): 933–41. http://dx.doi.org/10.25258/ijpqa.14.4.20.
Повний текст джерелаSingh, Shiv Dev, Arvind Kumar, Firoz Babar, Neetu Sachan, and Arun Kumar Sharma. "Synthesis of Novel 3(N,N-dialkylamino)alkyl/phenyl Substituted Thieno [2,3-d]pyrimidinones as H1-Anti-Histaminic and Antimicrobial Agents." Current Bioactive Compounds 15, no. 1 (February 6, 2019): 63–70. http://dx.doi.org/10.2174/1573407214666180226130957.
Повний текст джерелаThuy, Linh Bui Thi, Phuoc Le Thien, Hien Dang Chi, Hai Ha Pham Thi, and Cong Nguyen Tien. "Synthesis and antibacterial activities of some novel hybrid compounds based on 2‐mercapto‐3‐arylquinazolin‐4(3H)‐one scaffold bearing specific coumarin." Vietnam Journal of Chemistry 61, S2 (November 2023): 131–36. http://dx.doi.org/10.1002/vjch.202300093.
Повний текст джерелаSulthana M.T, Chitra K, and Alagarsamy V. "Synthesis of novel 4-oxo-N-(4-oxo-3-substituted-3,4-dihydroquinazolin-2-yl amino)-2-phenylquinazoline-3(4H)-carboxamidines as AntiHIV, antitubercular and antibacterial agents." International Journal of Research in Pharmaceutical Sciences 10, no. 3 (July 19, 2019): 2186–92. http://dx.doi.org/10.26452/ijrps.v10i3.1449.
Повний текст джерелаEl-Messery, Shahenda M., Ghada S. Hassan, Mahmoud N. Nagi, El-Sayed E. Habib, Sarah T. Al-Rashood, and Hussein I. El-Subbagh. "Synthesis, biological evaluation and molecular modeling study of some new methoxylated 2-benzylthio-quinazoline-4( 3H )-ones as nonclassical antifolates." Bioorganic & Medicinal Chemistry Letters 26, no. 19 (October 2016): 4815–23. http://dx.doi.org/10.1016/j.bmcl.2016.08.022.
Повний текст джерелаJatav, Varsha, Sushil Kashaw, and Pradeep Mishra. "Synthesis, antibacterial and antifungal activity of some novel 3-[5-(4-substituted phenyl) 1,3,4-thiadiazole-2-yl]-2-styryl quinazoline-4(3H)-ones." Medicinal Chemistry Research 17, no. 2-7 (December 14, 2007): 169–81. http://dx.doi.org/10.1007/s00044-007-9047-2.
Повний текст джерелаJatav, Varsha, Pradeep Mishra, Sushil Kashaw, and J. P. Stables. "Synthesis and CNS depressant activity of some novel 3-[5-substituted 1,3,4-thiadiazole-2-yl]-2-styryl quinazoline-4(3H)-ones." European Journal of Medicinal Chemistry 43, no. 1 (January 2008): 135–41. http://dx.doi.org/10.1016/j.ejmech.2007.02.004.
Повний текст джерелаJatav, Varsha, Pradeep Mishra, Sushil Kashaw, and J. P. Stables. "CNS depressant and anticonvulsant activities of some novel 3-[5-substituted 1,3,4-thiadiazole-2-yl]-2-styryl quinazoline-4(3H)-ones." European Journal of Medicinal Chemistry 43, no. 9 (September 2008): 1945–54. http://dx.doi.org/10.1016/j.ejmech.2007.12.003.
Повний текст джерелаEl-Azab, Adel S., Nasr Y. Khalil, and Alaa A. M. Abdel-Aziz. "Remarkable Conversion of 2-Thioxo-2,3-dihydroquinazolin-4(1H)-ones into the Corresponding Quinazoline-2,4(1H,3H)-diones: Spectroscopic Analysis and X-Ray Crystallography." Journal of Chemistry 2021 (April 2, 2021): 1–8. http://dx.doi.org/10.1155/2021/6612177.
Повний текст джерелаPatil, Avinash, Swastika Ganguly, and Sanjay Surana. "Synthesis and antiulcer activity of 2-[5-substituted-1-H-benzo(d) imidazol-2-yl sulfinyl]methyl-3-substituted quinazoline-4-(3H) ones." Journal of Chemical Sciences 122, no. 3 (May 2010): 443–50. http://dx.doi.org/10.1007/s12039-010-0052-5.
Повний текст джерелаKashaw, Sushil. "P2-396: Synthesis, characterization and anti-Alzheimer's screening of new bioactive 3-[5-substituted 1,3,4-thiadiazole -2 yl]-2- styryl Quinazoline-4(3H)-ones." Alzheimer's & Dementia 8, no. 4S_Part_11 (July 2012): P401—P402. http://dx.doi.org/10.1016/j.jalz.2012.05.1106.
Повний текст джерелаGheshlaghi, Saman Zare, Ali Ebrahimi, Zeinab Faghih, Zahra Faghih, Asiyeh Shahraki, and Leila Emami. "Azole-methyl-3-(4-phenoxyphenyl) quinazolin-4(3H) ones, novel quinazoline-azole hybrid scaffolds, as new potent anticancer agents: Design, synthesis, biological evaluation, molecular dynamic simulation and theoretical approach." Tetrahedron 147 (October 2023): 133650. http://dx.doi.org/10.1016/j.tet.2023.133650.
Повний текст джерелаPrasad, Malavattu G., C. Vijaya Lakshmi, Naresh K. Katari, Sreekantha B. Jonnalagadda, and Manojit Pal. "Lemon Juice Mediated Synthesis of 3-Substituted Quinazolin-4(3H)-Ones and their Pharmacological Evaluation." Anti-Cancer Agents in Medicinal Chemistry 19, no. 16 (January 23, 2020): 2001–9. http://dx.doi.org/10.2174/1871520619666190723151909.
Повний текст джерелаМаркосян, А. И., А. C. Айвазян, С. А. Габриелян, М. Ю. Дангян та А. Г. Аракелян. "Синтез и антибактериальная активность производных 3-аллил-5,5-диметил-2-тиоксо-2,3,5,6-тетрагидробензо[h]хиназолин-4(1H)-она". Chemical Journal of Armenia, 9 листопада 2023, 228–38. http://dx.doi.org/10.54503/0515-9628-2023.76.3-228.
Повний текст джерелаO'Brien, Nicholas, Jayne Gilbert, Adam McCluskey, and Jennette Sakoff. "2,3-Dihydroquinazolin-4(1H)-ones and Quinazolin-4(3H)-ones as Broad-Spectrum Cytotoxic Agents and Impact on Tubulin Polymerisation." RSC Medicinal Chemistry, 2024. http://dx.doi.org/10.1039/d3md00600j.
Повний текст джерелаMai, Jiexiong, Ziwei Huang, Shaohuan Lv, Quan Chen, Rongrong Chen, Feng Xie, Jun Wang, and Bin Li. "Visible light-induced cascade N-alkylation/amidation reaction of quinazolin-4(3H)-ones and related N-heterocycles." Organic & Biomolecular Chemistry, 2023. http://dx.doi.org/10.1039/d2ob02226e.
Повний текст джерелаKumar Tiwary, Bipransh, Kiran Pradhan, Ashis Kumar Nanda, and Ranadhir Chakraborty. "Implication of Quinazoline-4(3H)-ones in Medicinal Chemistry: A Brief Review." Journal of Chemical Biology & Therapeutics 01, no. 02 (2016). http://dx.doi.org/10.4172/2572-0406.1000104.
Повний текст джерелаStepakov, Alexander V., Alexander S. Filatov, Anna G. Larina, Mikhail L. Petrov та Vitali M. Boitsov. "Synthesis of Quinolino[1,2-c]quinazolin-6-one Derivatives via Formal (4+2)-Cycloaddition of Alkenes to Quinazolinе-Derived N-Acyliminium Cations: An Experimental and Theoretical Study". Synthesis, 31 січня 2022. http://dx.doi.org/10.1055/a-1755-2061.
Повний текст джерелаZahran, Sally S., Fatma A. Ragab, Marwa G. El-Gazzar, Aiten M. Soliman, Walaa R. Mahmoud, and Mostafa M. Ghorab. "Antiproliferative, antiangiogenic and apoptotic effect of new hybrids of quinazoline-4(3H)-ones and sulfachloropyridazine." European Journal of Medicinal Chemistry, November 2022, 114912. http://dx.doi.org/10.1016/j.ejmech.2022.114912.
Повний текст джерелаМаркосян, А. И., А. С. Багдасарян, А. С. Айвазян, С. А. Габриелян, М. Ю. Дангян та А. Г. Аракелян. "Синтез превращения 5,5-Диметил-3-пропил-2-тиоксо-2,3,5,6-тетрагидробензо[h]хиназолин-4(1H)-она и антибактериальные свойства полученых соединений". Chemical Journal of Armenia, 26 грудня 2022, 294–303. http://dx.doi.org/10.54503/0515-9628-2022.75.3-294.
Повний текст джерелаWRIGHT, W. B. JUN, A. S. TOMCUFCIK, P. S. CHAN, J. W. MARSICO, and J. B. PRESS. "ChemInform Abstract: Thromboxane Synthetase Inhibitors and Antihypertensive Agents. Part 4. N-((1H-Imidazol-1-yl)alkyl) Derivatives of Quinazoline-2,4(1H,3H)-diones (III), Quinazolin-4(3H)-ones (V), and 1,2,3-Benzotriazin-4(3H)-ones (VII)." ChemInform 19, no. 24 (June 14, 1988). http://dx.doi.org/10.1002/chin.198824237.
Повний текст джерелаMarkosyan, A. I., A. S. Ayvazyan, S. H. Gabrielyan, S. S. Mamyan, F. H. Arsenyan, A. S. Safaryan, and H. H. Arakelyan. "Synthesis and Antibacterial and Antitumor Activity of 2-Sulfanyl-Substituted 3H-Spiro[Benzo[H]Quinazoline-5,1′-Cycloheptane]-4(6H)-Ones." Pharmaceutical Chemistry Journal, December 7, 2022. http://dx.doi.org/10.1007/s11094-022-02774-0.
Повний текст джерелаSengupta, Devashish, Ranjan Kumar Das, Debdulal Sharma, and Subrata Paul. "Microwave-assisted Synthesis of 3-amino-2-phenylquinazolin-4(3H)-one (QH) and 4-oxo-2-phenylquinazoline-3(4H)-carbothioamide (QTh)." Current Microwave Chemistry 10 (May 16, 2023). http://dx.doi.org/10.2174/2213335610666230516165046.
Повний текст джерелаJatav, Varsha, Pradeep Mishra, Sushil Kashaw, and J. P. Stables. "ChemInform Abstract: Synthesis and CNS Depressant Activity of Some Novel 3-[5-Substituted 1,3,4-Thiadiazole-2-yl]-2-styryl Quinazoline-4(3H)-ones." ChemInform 39, no. 21 (May 20, 2008). http://dx.doi.org/10.1002/chin.200821160.
Повний текст джерелаEl-Subbagh, Hussein I., and Mohamed A. Sabry. "2-Substituted-mercapto-quinazolin-4(3H)-ones as DHFR inhibitors." Mini-Reviews in Medicinal Chemistry 21 (March 4, 2021). http://dx.doi.org/10.2174/1389557521666210304105736.
Повний текст джерелаDutta, Nilakshi, Bidyutjyoti Dutta, Apurba Dutta, Bipul Sarma, and Diganta Sarma. "Room temperature ligand free Cu2O-H2O2 catalyzed tandem oxidative synthesis of quinazolin-4(3H)-one and quinazoline derivatives." Organic & Biomolecular Chemistry, 2023. http://dx.doi.org/10.1039/d2ob02085h.
Повний текст джерелаDarwish, K., and O. Dakhil. "A Review on Methods of Synthesis of Quinazolines and (4H)-3,1-Quinazolin-4-ones." Libyan Journal of Science &Technology 5, no. 2 (September 18, 2022). http://dx.doi.org/10.37376/ljst.v5i2.2267.
Повний текст джерелаTOKALI, Feyzi Sinan. "Synthesis and Structural Characterization of Novel 2-Aminomethyl Quinazolin-4(3H)-ones as Organic Building Blocks." Sakarya University Journal of Science, September 29, 2022. http://dx.doi.org/10.16984/saufenbilder.1085086.
Повний текст джерелаDevidas, Amrutkar Rakesh, and Mahendra Sing Ranawat. "Microwave Assisted Synthesis And Molecular Docking Studies Of Some 4 - (3h)-Quinazolinone Derivatives As Inhibitors Of Human Gamma-Aminobutyric Acid Receptor, The Gaba (A)R-Beta3 Homopentamer." Medicinal Chemistry 16 (December 16, 2019). http://dx.doi.org/10.2174/1573406416666191216121442.
Повний текст джерелаAbdullahi, Sagiru Hamza, Adamu Uzairu, Gideon Adamu Shallangwa, Sani Uba, and Abdullahi Bello Umar. "Ligand-based drug design of quinazolin-4(3H)-ones as breast cancer inhibitors using QSAR modeling, molecular docking, and pharmacological profiling." Journal of the Egyptian National Cancer Institute 35, no. 1 (August 7, 2023). http://dx.doi.org/10.1186/s43046-023-00182-3.
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