Log in

Relevant bibliographies by topics / Quinazolinone derivatives

Contents

Journal articles
Dissertations / Theses
Books
Book chapters
Conference papers

Academic literature on the topic 'Quinazolinone derivatives'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Quinazolinone derivatives.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Quinazolinone derivatives"

1

Deng, Zhijiang, Jieming Li, Pengbo Zhu, et al. "Quinazolinones as Potential Anticancer Agents: Synthesis and Action Mechanisms." Biomolecules 15, no. 2 (2025): 210. https://doi.org/10.3390/biom15020210.

Full text

Abstract:

Quinazolinones, essential quinazoline derivatives, exhibit diverse biological activities with applications in pharmaceuticals and insecticides. Some derivatives have already been developed as commercial drugs. Given the rising cancer incidence, there is a critical need for new anticancer agents, and quinazolinones show promising potential in this domain. The present review focuses on novel advances in the synthesis of these important scaffolds and other medicinal aspects involving drug design, the structure–activity relationship, and action mechanisms of quinazoline and quinazolinone derivativ

APA, Harvard, Vancouver, ISO, and other styles

2

Asif, Mohammad. "Chemical Characteristics, Synthetic Methods, and Biological Potential of Quinazoline and Quinazolinone Derivatives." International Journal of Medicinal Chemistry 2014 (November 13, 2014): 1–27. http://dx.doi.org/10.1155/2014/395637.

Full text

Abstract:

The heterocyclic fused rings quinazoline and quinazolinone have drawn a huge consideration owing to their expanded applications in the field of pharmaceutical chemistry. Quinazoline and quinazolinone are reported for their diversified biological activities and compounds with different substitutions bring together to knowledge of a target with understanding of the molecule types that might interact with the target receptors. Quinazolines and quinazolinones are considered as an important chemical for the synthesis of various physiological significance and pharmacological utilized molecules. Quin

APA, Harvard, Vancouver, ISO, and other styles

3

Barat, Gaman G., and Mahesh R. Solanki. "Antimicrobial Study of Novel Triazoles Synthesized from Chalcones." Oriental Journal Of Chemistry 40, no. 3 (2024): 794–98. http://dx.doi.org/10.13005/ojc/400322.

Full text

Abstract:

Heterocyclic compound such as quinazoline derivatives shows wide range of medicinal application in the area such as anticonvulsant, antitumor, antifungal, antimalaria, anti-hyperlipidemic and anti-inflammatory etc. activity because of these it shows great interest to study. In the presence study, we have synthesized triazole based quinazolinones by condensation reaction between α-methyl ketone and aromatic aldehydes under ethanol as the solvent to produced chalcones derivatives. This chalcone derivative have α, β-unsaturated part which is enhanced the reactivity of compound. Chalcone further r

APA, Harvard, Vancouver, ISO, and other styles

4

Starikova, Alla Andreevna, Alexandra Aleksandrovna Tsibizova, and Marina Aleksandrovna Samotrueva. "BIOLOGICAL ACTIVITY OF NATURAL QUINAZOLINE ALKALOIDS." Chemistry of plant raw material, no. 2 (May 4, 2025): 47–73. https://doi.org/10.14258/jcprm.20250214908.

Full text

Abstract:

To date, quinazoline alkaloids of natural origin, as well as synthetic derivatives based on them, whose structure contains an aromatic heterocyclic system including a pyrimidine cycle and a benzoin ring connected to it, are promising according to the criterion of the optimal profile of pharmacological activity. Currently, several hundred compounds of the quinazoline nature have been identified with a wide range of biological activities, including psychotropic (antidepressant, antipsychotic, sedative, hypnotic, anticonvulsant, etc.), antiplatelet, hypotensive, anti-inflammatory, antioxidant and

APA, Harvard, Vancouver, ISO, and other styles

5

Vishwakarma, Lav Kush Kumar, and Varsha Kashaw. "Nanocatalyzed Synthetic Approach for the Quinazolinone and Quinazoline Derivatives: A Review (2015 – Present)." Journal of Drug Delivery and Therapeutics 13, no. 3 (2023): 171–83. http://dx.doi.org/10.22270/jddt.v13i3.5765.

Full text

Abstract:

Due to their diverse chemical reactivities and essential range of biological action, quinazolines and their derivatives rank among the most significant heterocyclic compounds. Quinazoline and quinazolinone scaffolds pharmacological properties have sparked medicinal chemists' interest in creating original medications or drug candidates. The growth of quinazoline hybrid lead compounds and the related heterocycles is summarised in the current review of medicinal chemistry. Additionally, by shedding light on the potential significance of these hybridised pharmacophoric characteristics in the demon

APA, Harvard, Vancouver, ISO, and other styles

6

Prakash, Gaurav, Ajay Kumar Das, and V. D. Tripathi. "A Catalyst Free and Sustainable Synthesis of Quinazolinones in Glycerol as Green Solvent." Asian Journal of Chemistry 35, no. 5 (2023): 1089–94. http://dx.doi.org/10.14233/ajchem.2023.27612.

Full text

Abstract:

In this article, glycerol was employed in a quest to develop an environmentally benign and sustainable synthetic protocol for synthesis of quinazolinone and spiro-quinazolinone derivatives. These studies were performed to investigate the effect of electron-rich and electronegative groups on the synthetic route of an established protocol. Different substituted isatin and benzaldehyde derivatives have been incorporated to synthesize analogues of two series of quinazolinones in order to investigate the efficacy of the developed methodology and substrate tolerance. A total of 12 derivatives were s

APA, Harvard, Vancouver, ISO, and other styles

7

Mishra, AD. "A New Route for the Synthesis of Quinazolinones." Nepal Journal of Science and Technology 12 (July 22, 2012): 133–38. http://dx.doi.org/10.3126/njst.v12i0.6491.

Full text

Abstract:

Quinazolinone derivatives are highly bioactive heterocyclic compounds with wider range of microbial activities such as anti-malarial, anti-cancer, anti-inflammatory, anti-hypertensive, anti-convulsant, anti-HIV, etc. Solid supported microwave synthesis of some 3-substituted-4-(2H)-quinazolinones has been carried out by the reaction of anthranilic acid, formaldehyde and primary aromatic amines. The usage of hazardous reagents and organic solvents has been avoided. The reactions were conducted in presence of acidic alumina where formaldehyde entered into cycloaddition to yield the quinazolinone

APA, Harvard, Vancouver, ISO, and other styles

8

Jianghong, Man, Qi Jianbin, Jiang Jie, and Li Sha. "Microwave Reaction Improved Heterocyclization of Quinazolinone Ring in Synthesis of Erlotinib Analogues." Journal of Pharmaceutical and Biomedical Sciences 10, no. 05 (2020): 99–105. https://doi.org/10.1234/zenodo.3876.

Full text

Abstract:

Background Tinibs were a kind of important epidermal growth factor receptor (EGFR) inhibitors used as potential therapeutic agents in treating non-small cell lung cancer (NSCLC) in clinic. The drug resistance of clinical used tinibs made the development of more active tinib analogues an attractive field in research. Quinazoline ring was regarded as the key fragment in tinibs and quinazolinone was indispensible intermediate in the synthesis of quinazoline. Thus, synthesis of quinazolinone intermediates was a key step which would further limit the overall yield of final product of tinib analogue

APA, Harvard, Vancouver, ISO, and other styles

9

Yaduwanshi, Phool Singh, Sheelu Singh, Prinsi Sahapuriya, Priyanka Dubey, Jyoti Thakur, and Savita Yadav. "Synthesis of Some Noval Qunazolinone Derivatives for their Anticonvulsant Activity." Oriental Journal Of Chemistry 40, no. 2 (2024): 369–73. http://dx.doi.org/10.13005/ojc/400207.

Full text

Abstract:

The quinoline family comprises an appealing group of heterocyclic compounds, with quinazolinones and their synthetic analogs being of particular interest. To synthesize 3- amino 2-phenyl quinazolinones, anthranilic acid and its substituted derivatives were employed as initial materials. The MES method was utilized to evaluate the anticonvulsant activity of the developed substances on albino mice, with phenytoin serving as a benchmark anticonvulsant medication.The synthesized compounds demonstrated noteworthy anticonvulsant activity, comparable to that of established prescription medications. A

APA, Harvard, Vancouver, ISO, and other styles

10

Abdel-Megeed, Mohamed Farghali, and Abderrahman Teniou. "Synthesis of some 3-substituted 4(3H)-quinazolinone and 4(3H)-quinazolinethione derivatives and related fused biheterocyclic ring systems." Collection of Czechoslovak Chemical Communications 53, no. 2 (1988): 329–35. http://dx.doi.org/10.1135/cccc19880329.

Full text

Abstract:

The reactions of 2-phenyl-4(3H)-quinazoline, 2-phenyl-3-amino-4(3H)-quinazolinone, and corresponding thiones with phenyl isocyanate or phenyl isothiocyanate were investigated. The resulting urea and thiourea quinazolinone or quinazolinethione derivatives reacted with hydrazine hydrate, phenylhydrazine, and urea or thiourea to form fused biheterocyclic ring systems with potential biological activities. The products were identified by IR, 1H NMR, and mass spectroscopy.

APA, Harvard, Vancouver, ISO, and other styles

More sources

Dissertations / Theses on the topic "Quinazolinone derivatives"

1

Li, Jiyang [Verfasser]. "Investigation of Phthalazine, Quinazoline and Pyrimidine Derivatives as ABCG2 Inhibitors / Jiyang Li." Bonn : Universitäts- und Landesbibliothek Bonn, 2018. http://d-nb.info/1167857135/34.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Krapf, Michael [Verfasser]. "Investigation of Quinazoline Derivatives as Inhibitors of Breast Cancer Resistance Protein (BCRP/ABCG2) / Michael Krapf." Bonn : Universitäts- und Landesbibliothek Bonn, 2018. http://d-nb.info/1160594155/34.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Cardoso, Leandro 1979. "Utilização farmacológica de um composto inédito derivado de quinazolina como inibidor potencial da quinase de adesão focal (FAK) no processo de hipertrofia cardíaca em camundongo = Pharmacological use of a novel compound quinazoline derivative as potential inhibitor of the focal adhesion kinase in the process of cardiac hypertrophy in mice." [s.n.], 2012. http://repositorio.unicamp.br/jspui/handle/REPOSIP/310205.

Full text

Abstract:

Orientador: Kleber Gomes Franchini<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas<br>Made available in DSpace on 2018-08-20T23:08:02Z (GMT). No. of bitstreams: 1 Cardoso_Leandro_M.pdf: 3831901 bytes, checksum: 40e5df211d7e6fd923f654bd8d3a1ec1 (MD5) Previous issue date: 2012<br>Resumo: Nas doenças do coração ocorre hipertrofia e remodelamento do ventrículo esquerdo com impacto negativo na evolução clínica. Esses fatores influenciam independentemente o risco cardiovascular por elevarem a predisposição a infartos do miocárdio, ao desenvolvimento de

APA, Harvard, Vancouver, ISO, and other styles

4

LIN, CHUN-HUNG, and 林俊宏. "Study of Quinazolinone Derivatives on Enhancement of Anticancer Drugs Activity." Thesis, 1998. http://ndltd.ncl.edu.tw/handle/30968119740447194201.

Full text

Abstract:

碩士<br>國立臺灣大學<br>藥學系研究所<br>86<br>ABSTRACT We have evaluated the effect of the quinazolinone derivatives on P-glycoprotein-mediated MDR in breast cancer by performing an in vitro cytotoxicity assay and flow cytometry. The cell lines employed for this study were human breast cancer cells selected for resistance to adriamycin, MCF7/adr, and its counterpart, wildtype MCF7. Compared with the sensitivity of the wildtype and adr-resistant cells, the MCF7/adr subline showed more th

APA, Harvard, Vancouver, ISO, and other styles

5

Lo, Chi-Chun, and 羅吉鈞. "Synthesis and pharmacological evaluation of 4(3H)quinazolinone derivatives as potencial angiotensin II antagonists." Thesis, 1996. http://ndltd.ncl.edu.tw/handle/58461088283823970919.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Hour, Mann-Jen, and 侯曼貞. "Synthesis, Cytotoxicity and Antiplatelet Activity of 6,7,2',3',4',5'-Substituted 2-phenyl-4-quinazolinone Derivatives." Thesis, 2000. http://ndltd.ncl.edu.tw/handle/66215076548891573814.

Full text

Abstract:

博士<br>中國醫藥學院<br>藥物化學研究所<br>88<br>As part of our continuing search for potential anticancer candidates of 2-phenyl-4-quinazolinones and 2-phenyl-4-quinolones, two series of 6,7,2',3',4',5'-substituted 2-phenyl-4-quinazolinones and 6,2',3',4',5'-substituted 2,3-dihydro-2-phenyl-4-quinazolinones have been synthesized and evaluated for cytotoxicity and inhibition of tubulin polymerization. Through these biological screening, a preliminary structure-activity relationship has been established. On the whole, a good correlation was found between the two activities. Among them, 6-N,N-dimethylamino and

APA, Harvard, Vancouver, ISO, and other styles

7

Liu, Chih-Fa, та 劉誌發. "design and synthesis of quinazolinone and 1,2-benzothiazine 1,1-dioxide derivatives as potential selective α1A-adrenoceptor antagonists". Thesis, 2000. http://ndltd.ncl.edu.tw/handle/59531007520783388600.

Full text

Abstract:

碩士<br>國立臺灣大學<br>藥學研究所<br>88<br>This study is aimed to synthesize two series of compounds, namely, substituted arylpiperazinyl benzothiazinone 1,1-dioxide (A) and substituted arylpiperazinyl quinazolinone (B) derivatives for evaluation of α1A adrenoceptor selectivity and are considered to be potential for treatment of benign prostatic hyperplasia (BPH). The synthesis of compounds in A series started from esterification of 3,4-dimethoxyphenyl acetic acid (25) in methanol with a catalytic amount of concentrated sulfuric acid to give 3,4-dimethoxy-1-(carbomethoxymethyl)benzene (26). T

APA, Harvard, Vancouver, ISO, and other styles

8

Lu, Chi-Cheng, and 呂啟誠. "Investigations for targeting signaling pathways in the apoptosis induction and anti-metastasis of the novel quinazolinone derivatives in leukemia and oral cancer cells in vitro and anti-tumor activity in vivo." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/69439994355722115199.

Full text

Abstract:

博士<br>國立中興大學<br>生命科學系所<br>100<br>The previous studies have demonstrated that 2-phenyl 6-pyrrolidinyl-4-quinazolinone derivatives exhibited antitumor actions and biological responses. Among them, both of the most potent newly synthesized compounds, 6-pyrrolidinyl-2-(2-hydroxyphenyl)-4-quinazolinone (MJ-29) and 6-pyrrolidinyl- 2-(3-Methoxyphenyl)-4-quinazolinone (HMJ-38) for their mechanisms underlying anticancer activities remain unclear and have not been well clarified. In this dissertation, we attempt to investigate anti-leukemia and anti-oral cancer effects in vitro and in vivo. In the chapt

APA, Harvard, Vancouver, ISO, and other styles

9

Li, Hong-Bin, and 李鴻斌. "Study of 4-(Substitutedphenylamino)Quinazoline Derivatives." Thesis, 1997. http://ndltd.ncl.edu.tw/handle/12061863258573308290.

Full text

Abstract:

碩士<br>文化大學<br>應用化學系<br>85<br>The objective of this thesis is to investigate the synthesis of 4-(substitutedphenylamino)quinazoline derivatives. Because the C4-C8 sites of the compound with different substituents are able to be used as tyrosine kinase inhibitors.In the study,it consist of three synthetic processes.Firstly,the starting material, monochloroanthranilic acid and dichloroanthranilic acid reacted with formamide in high temperature and refluxed to give mono- and di-chloro substitut

APA, Harvard, Vancouver, ISO, and other styles

10

Huang, Ya-Ping, and 黃雅蘋. "Synthesis and Antiproliferative Evaluation of Substituted Quinazoline Derivatives." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/29298330647027420014.

Full text

Abstract:

碩士<br>高雄醫學大學<br>醫藥暨應用化學研究所<br>100<br>Quinazoline derivatives have been found to possess a wide variety of biological activities. The aims of this thesis are to synthesize and evaluate a series of 4-substituted and 2-substituted-vinyl quinazoline derivatives. These 4-substituted and 2-substituted-vinyl quinazoline derivatives with various substituents at the C-4 position of quinazoline skeleton and at the vinyl moiety have been synthesized and evaluated for their antiproliferatve activities. Results indicated that most of these newly synthesized compounds exhibited potent activities against the

APA, Harvard, Vancouver, ISO, and other styles

More sources

Books on the topic "Quinazolinone derivatives"

1

Gamal Al-kaf, Ali, ed. Quinazolinone and Quinazoline Derivatives. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.85315.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Quinazolinone derivatives"

1

Dangi, R. R., N. S. Chundawat, and K. L. Ameta. "Synthesis and Biological Evaluation of Some Quinazoline Heterocyclic Derivatives." In Green Chemistry: Synthesis of Bioactive Heterocycles. Springer India, 2014. http://dx.doi.org/10.1007/978-81-322-1850-0_13.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Gamal Al-kaf, Ali. "Introductory Chapter: The Newest Research in Quinazolinone and Quinazoline Derivatives." In Quinazolinone and Quinazoline Derivatives. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.88913.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Chiriţă, Cornel, Carmen Limban, Diana Camelia Nuţă, et al. "Synthesis and Pharmacological Research Regarding New Compounds with Quinazolin-4-One Structure." In Quinazolinone and Quinazoline Derivatives. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.89164.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

E. Hashem, Heba. "Synthesis of Quinazoline and Quinazolinone Derivatives." In Quinazolinone and Quinazoline Derivatives. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.89180.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Mishra, Satyendra. "Quinazolinone and Quinazoline Derivatives: Synthesis and Biological Application." In Quinazolinone and Quinazoline Derivatives. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.89203.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Bhanudas Zangade, Sainath. "Quinazoline Based Synthesis of some Heterocyclic Schiff Bases." In Quinazolinone and Quinazoline Derivatives. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.89871.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Y. Abbas, Samir. "4(3H)-Quinazolinone Derivatives: Syntheses, Physical Properties, Chemical Reaction, and Biological Properties." In Quinazolinone and Quinazoline Derivatives. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.90104.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

A. Radwan, Awwad, and Fars K. Alanazi. "Biological Activity of Quinazolinones." In Quinazolinone and Quinazoline Derivatives. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.90621.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Bhat, Mahesh, S. L. Belagali, S. V. Mamatha, B. K. Sagar, and E. Vijaya Sekhar. "Importance of quinazoline and quinazolinone derivatives in medicinal chemistry." In Studies in Natural Products Chemistry. Elsevier, 2021. http://dx.doi.org/10.1016/b978-0-323-91095-8.00005-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Wahan, Simranpreet K., Sangeeta Sharma, and Pooja A. Chawla. "2 Synthesis of quinazolinone and quinazoline derivatives using green chemistry approach." In Synthesis of Bioactive Scaffolds. De Gruyter, 2022. http://dx.doi.org/10.1515/9783110797428-002.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Quinazolinone derivatives"

1

Al-Majedy, Yasmien, Ahmed Al-Amiery, and Redha Al-Bayati. "Novel quinazolinone derivatives: Synthesis and Antimicrobial Activity." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00413.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Rammohan, Aluru, and Grigory V. Zyryanov. "Synthesis and characterization of 1,2,3-triazole integrated quinazolinone derivatives." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0018182.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Maleki, Ali, Jamal Rahimi, and Razieh Firouzi Haji. "Green synthesis of quinazolinone derivatives by using a recyclable heteropoly acid catalyst." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04722.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Maleki, Ali, and Nakisa Ghamari. "A three-component one-pot procedure for the synthesis benzimidazolo-quinazolinone derivatives in the presence of chitosan-supported metal nanocomposite as a green and reusable catalyst." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a034.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Naimi-Jamal, Mohammad Reza, and Maryam karimi. "A simple, convenient three component one-pot procedure for the synthesis of benzimidazolo-quinazolinone derivatives in the presence Silica-based sulfonic acid (MCM-41-SO3H): a efficient and practical catalyst." In The 19th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a001.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Guerreiro Souzedo, Gabriela, LJUBICA TASIC, and Caio Henrique Nasi De Barros. "Synthesis of Quinazoline Derivatives for Adenosine Kinase Inhibition." In XXV Congresso de Iniciação Cientifica da Unicamp. Galoa, 2017. http://dx.doi.org/10.19146/pibic-2017-78452.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Militaru, Andra, Adriana Smarandache, Abdallah Mahamoud, et al. "Stability Characterization of Quinazoline Derivative BG1188 by Optical Methods." In ADVANCES IN LASEROLOGY - SELECTED PAPERS OF LASER FLORENCE 2010: The 50th Birthday of Laser Medicine World. AIP, 2011. http://dx.doi.org/10.1063/1.3626907.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Hussein, AL-Shaimaa Anas, and Fawzi Hameed Jumaa. "Preparation and evaluation of quinazoline derivatives as antimicrobial agents and liquid crystals." In 4TH INTERNATIONAL CONFERENCE ON INNOVATION IN IOT, ROBOTICS AND AUTOMATION (IIRA 4.0). AIP Publishing, 2025. https://doi.org/10.1063/5.0254204.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Yen, Shih Chieh, Shao-Zheng Peng, Hung-Jyun Huang, et al. "Abstract 2809: Novel 2,5,8-trihydro-6,7-disubstituted-4-(3'-alkylsulfonamidoanilino) quinazoline derivatives as RAF inhibitor." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-2809.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Ayvazyan, A. S., A. I. Markosyan, F. H. Arsenyan, and Kh S. Hakobyan. "SYNTHESIS AND BIOLOGICAL ACTIVITY OF SPIRO[BENZO[H]QUINAZOLINE-5,1’-CYCLOHEPTANE]- 4(6H)-ONE DERIVATIVES." In MedChem-Russia 2021. 5-я Российская конференция по медицинской химии с международным участием «МедХим-Россия 2021». Издательство Волгоградского государственного медицинского университета, 2021. http://dx.doi.org/10.19163/medchemrussia2021-2021-240.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!