Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Phenylurea Derivatives"'
Publikováno v:
Advanced Agrochem, Vol 3, Iss 2, Pp 143-150 (2024)
Plant growth regulators (PGRs) are chemical substances that imitate the functions of phytohormones to enhance the crop yield and the harvest process. Phenylurea-derived plant growth regulators are known for their excellent efficacy in promoting fruit
Externí odkaz:
https://doaj.org/article/7bfab022ea2f4d328835ebc718dd9484
Autor:
Shweta Verma, Sandeep Singh
Publikováno v:
Central Nervous System Agents in Medicinal Chemistry. 21:157-164
Background: A series of phenylurea derivatives were designed and synthesized, The target compounds were subjected to pharmacological studies. Various other parameters such as physicochemical properties, computational studies, and % similarity were al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60d5e142ad081ee168f5671d669a0622
https://doi.org/10.2174/1871524921666210908145356
https://doi.org/10.2174/1871524921666210908145356
Publikováno v:
Bulletin of the Chemical Society of Ethiopia, Vol 27, Iss 2, Pp 295-300 (2013)
Phenylurea groups were introduced into the frame of traditional cyanoacrylate and a series of N-(3-benzylamino-2-cyano-3-methylthioacrylyl)-N'-(substituted phenyl)ureas were synthesized. All compounds are new and their structures were confirmed by 1H
Externí odkaz:
https://doaj.org/article/8d24390c3b5d49c787e12470781e2d6d
Akademický článek
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Autor:
Olivier P. Thomas, Nipun Mahajan, Paul V. Murphy, Enda O' Connell, Kevin Calabro, Rekha Chadda, Hiren Solanki
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2017, 58 (12), pp.1237-1239. ⟨10.1016/j.tetlet.2017.02.037⟩
Tetrahedron Letters, 2017, 58 (12), pp.1237-1239. ⟨10.1016/j.tetlet.2017.02.037⟩
Tetrahedron Letters, Elsevier, 2017, 58 (12), pp.1237-1239. ⟨10.1016/j.tetlet.2017.02.037⟩
Tetrahedron Letters, 2017, 58 (12), pp.1237-1239. ⟨10.1016/j.tetlet.2017.02.037⟩
International audience; A library of 864 extracts prepared from Irish marine organisms was screened in the search for novel antioxidants. Chemical investigation of the most promising extract obtained from the common lichen Lichina pygmaea led to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f807f2d8ead9a5411c569bba06688df3
https://doi.org/10.1016/j.tetlet.2017.02.037
https://doi.org/10.1016/j.tetlet.2017.02.037
Autor:
Kallu Rajender Reddy, Nagireddy Veera Reddy, Peddi Sudhir Reddy, Mannepalli Lakshmi Kantam, Pailla Santhosh Kumar
Publikováno v:
New Journal of Chemistry. 39:805-809
A direct transformation of N-aryl formamides to the corresponding phenylurea derivatives via the formation of isocyanate intermediates is achieved in good yields using hypervalent iodine reagents as external oxidants.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24b9b4e256ed487ddf9125db40c792f0
https://doi.org/10.1039/c4nj01668h
https://doi.org/10.1039/c4nj01668h
Autor:
Ravindra Kulkarni, Aneesa Fatima, Asief Mohammed, Bhagavanraju Mantripagada, V.M. Chandrasheskar, Anusaya Birajdar
Publikováno v:
Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry. 13:112-120
A series of N-(4-phenyl-1, 3-thiazol-2-yl)-N'- phenylureas (5a-z) was synthesized from 2-amino-4-substituted phenylthiazoles and phenylisocyanates. The newly synthesized compounds were characterized by IR, (1)H NMR and Mass spectral data. All the twe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d4b40d812562e0725124a3844d9c3c3
https://doi.org/10.2174/1871523013666140820154843
https://doi.org/10.2174/1871523013666140820154843
Autor:
Feng Jin, Bizhu Chu, Chen Yan, Yuyang Jiang, Dan Gao, Chunyan Tan, Feng Liu, Cunlong Zhang, Yu Zong Chen
Publikováno v:
Bioorganic & Medicinal Chemistry. 21:824-831
Based on the roles of Raf1 and JNK1 in hepatocarcinoma development, scaffold-based drug design was employed to produce a series of compounds, which subsequently were synthesized and explored as potential dual inhibitors Raf1 and JNK1 kinases for anti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba70046945135f601bcf4b0c8c290c95
https://doi.org/10.1016/j.bmc.2012.04.006
https://doi.org/10.1016/j.bmc.2012.04.006
Autor:
Takayuki Imaoka, Shin-ichi Tsukamoto, Tatsuaki Morokata, Ippei Sato, Makoto Takeuchi, Toshiya Takahashi, Yosuke Iura, Hideki Inoue, Mitsuaki Ohta, Hirokazu Kubota, Aiko Nitta, Koichiro Morihira
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 22:6876-6881
Optimization starting with our lead compound 1 (IC(50)=4.9 nM) led to the identification of pyrrolidinyl phenylurea derivatives. Further modification toward improvement of the bioavailability provided (R)-1-(1-((6-fluoronaphthalen-2-yl)methyl)pyrroli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::684ca3932de13368c29c0080b36dffca
https://doi.org/10.1016/j.bmcl.2012.09.035
https://doi.org/10.1016/j.bmcl.2012.09.035
Autor:
Jialong Sun, Yuanming Zhou
Publikováno v:
Molecules
Molecules, Vol 20, Iss 3, Pp 5050-5061 (2015)
Volume 20
Issue 3
Pages 5050-5061
Molecules, Vol 20, Iss 3, Pp 5050-5061 (2015)
Volume 20
Issue 3
Pages 5050-5061
A series of novel phenylurea derivatives were designed and synthesized according to the method of active groups linkage and the principle of aromatic groups bioisosterism in this study. The structures of the novel phenylurea derivatives were confirme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::506309b8aa442fdb558b68fe7fd84b8c
https://pubmed.ncbi.nlm.nih.gov/25808149
https://pubmed.ncbi.nlm.nih.gov/25808149