Results 71 to 80 of about 20,504 (258)

Clinical and Neurodevelopmental Characteristics of Paralogous Gain‐of‐Function Variants at GRIA2 p.Gly792 and GRIA3 p.Gly803

Clinical Genetics, Volume 108, Issue 5, Page 553-565, November 2025.
Key features of paralogous GRIA2 and GRIA3 gain‐of‐function variants. ABSTRACT GRIA‐related disorders arise from disease‐causing variants in GRIA1, GRIA2, GRIA3, or GRIA4 that encode α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazole propionic acid (AMPA)‐type glutamate receptors (AMPARs).
Emilie Sjøstrøm, Dorota Studniarczyk, Xinyao Dou, Rebekka S. Dahl, Vincent Cruz, Heng Wang, Sandra Mercier, Wallid Deb, Thomas Besnard, Jennifer Friedman, Miriam Essid, Sana Karoui, Lamia Ben Jemaa, Thouraya Benyounes, Gaetan Lesca, Davide Tonduti, Maria Iascone, Simona Orcesi, Melanie Fradin, Christèle Dubourg, Silvia Napuri, Stuart G. Cull‐Candy, Ian D. Coombs, Mark Farrant, Allan Bayat   +24 more
wiley   +1 more source

Recent developments in chemical reactivity of N,N-dimethylenamino ketones as synthons for various heterocycles [PDF]

, 2017
The current review presents recent progress in the utility of N,N-dimethyl enaminones as building blocks for a diverse range of acyclic, carbocyclic, five- and six-membered heterocyclic a broad range of heterocyclic and fused heterocyclic derivatives ...
Abbas, Abdallah, Abdallah, Abdallah, Abdel-Khalik, Abdel-Khalik, Abdel-Khalik, Abdel-Megid, Abdel-Motaleb, Abdel-Motaleb, Abdelhamid, Abdelhamid, AbdelKhalik, Abu-Shanab, Abu-Shanab, Adams, Agamy, Agamy, Al-Awadi, Al-Awadi, Al-Awadi, Al-Enezi, Al-Etaibi, Al-Mousawi, Al-Mousawi, Al-Mousawi, Al-Mousawi, Al-Mousawi, Al-Mousawi, Al-Mousawi, Al-Omran, Al-Omran, Al-Omran, Al-Omran, Al-Omran, Al-Omran, Al-Omran, Al-Omran, Al-Saleh, Al-Saleh, Al-Saleh, Al-Saleh, Al-Saleh, Al-Saleh, Al-Saleh, Al-Saleh, Al-Shiekh, Al-Shiekh, Al-Shiekh, Al-Zaydi, Al-Zaydi, Al-Zaydi, Al-Zaydi, Al-Zaydi, Al-Zaydi, Al-Zaydi, Alinezhad, Alinezhad, Almazroa, Anwer, Behbehani, Cao, Dawood, Domínguez, El-Desoky, El-Dusouqui, El-Taweel, Eldebss, Elghamry, Farghaly, Figueiredo, Gaber, Gaber, Gaber, Gaber, Gaber, Gaber, Gad-Elkareem, Gad-Elkareem, Ghozlan, Ghozlan, Ghozlan, Gomha, Gomha, Gomha, Gomha, Gomha, Greenhill, Hassanien, Hassanien, Hassanien, Hernández, Ho, Ho, Ho, Hughes, Ibrahim, Igarashi, Ingham, Jiang, Kandeel, Kantevari, Kascheres, Katritzky, Katritzky, Kenawi, Kepe, Kepe, Kim, Kirschbaum, Liu, Lue, Macba, Macba, Makhseed, Manley, Martins, Michael, Mokhtar, Mousawi, Moustafa, Mukhanova, Murphy, Negri, Nishimura, Nishiyama, Pichon, Pigge, Pleier, Raghunadh, Rasmussen, Reidlinger, Sabnis, Saleh, Salomone, Schenone, Shaaban, Shankaraiah, Sherif, Toche, Tois, Trautwein, Verma, Wan, Wan, Wan, Wan, Wan, Wang, Witherington, Xiang, Zhao, Zhou, Šimůnek   +153 more
core   +1 more source

(1RS,3SR)-1-(4-Methylbenzyl)-7-phenyl-5-oxa-6-azaspiro[2.4]hept-6-en-4-one

Molbank
The previously unknown cyclopropane spiro-fused with isoxazol-5-one ((1RS,3SR)-1-(4-methylbenzyl)-7-phenyl-5-oxa-6-azaspiro[2.4]hept-6-en-4-one) was synthesized from benzylideneisoxazol-5-one in 34% yield via double methylene transfer from diazomethane ...
Gleb D. Titov, Nikolai V. Rostovskii
doaj   +1 more source

Synthesis and Antimicrobial Activity of N′-Heteroarylidene-1-adamantylcarbohydrazides and (±)-2-(1-Adamantyl)-4-acetyl-5-[5-(4-substituted phenyl-3-isoxazolyl)]-1,3,4-oxadiazolines

Molecules, 2012
The reaction of adamantane-1-carbohydrazide (1) with heterocyclic aldehydes, namely 5-(4-chlorophenyl)isoxazole-3-carboxaldehyde (2a), 5-(4-methylphenyl)isoxazole-3-carboxaldehyde (2b), 5-(4-methoxyphenyl)isoxazole-3-carboxaldehyde (2c), 1H-imidazole-2 ...
Abdul-Malek S. Al-Tamimi, Ali A. El-Emam, Mohamed A. Al-Omar, Khalid A. Alrashood   +3 more
doaj   +1 more source

The Nuclear Receptor Nurr1 Modulates the Expression and Activity of PPARγ in Human Pro‐Inflammatory Macrophages

Scandinavian Journal of Immunology, Volume 102, Issue 5, November 2025.
Nurr1 activation in human primary macrophages induced the increment of PPARγ expression through protein stabilisation and reduction of the proportion of PPARγ phosphorylated at Ser84, a repressive mark for PPARγ transcriptional activity. The Nurr1 agonist C‐DIM12 enhanced the rosiglitazone‐induced expression of PPARγ‐responsive genes. ABSTRACT Nurr1 is
Eduardo Santana‐Cisneros, Miguel A. Solís‐Barbosa, Norma C. Segovia‐Gamboa, Marco A. Meraz‐Ríos, Erika González‐Domínguez, Rosaura Hernández‐Rivas, Daniel Marrero‐Rodríguez, Carmen Sanchez‐Torres   +7 more
wiley   +1 more source

Toxic Tau Oligomers Modulated by Novel Curcumin Derivatives [PDF]

, 2019
The pathological aggregation and accumulation of tau, a microtubule-associated protein, is a common feature amongst more than 18 different neurodegenerative diseases that are collectively known as tauopathies.
Bucchieri, Fabio, Ellsworth, Anna, Kayed, Rakez, Lo Cascio, Filippa, Pace, Andrea, Palumbo Piccionello, Antonio, Puangmalai, Nicha   +6 more
core   +1 more source

A Dive Into Forty Years of Research on Organic Superbases: From Design to Applications

Journal of Computational Chemistry, Volume 46, Issue 28, October 30, 2025.
This review covers the design and application of various neutral organic superbases with carbon, nitrogen, boron, silicon and germanium centers as basic sites. Their utility as organocatalysts has been reported with particular attention given to applications of commercially accessible organic superbases in some pivotal reactions.
Rabindranath Lo, Bishwajit Ganguly
wiley   +1 more source

Gold-catalyzed bicyclic annulations of 4-methoxy-1,2-dienyl-5-ynes with isoxazoles to form indolizine derivatives via an Au-π-allene intermediate

Chemical Science, 2019
Gold-catalyzed bicyclic annulations of 4-methoxy-1,2-dienyl-5-ynes with isoxazoles afford indolizine derivatives; the reaction mechanism involves alkyne attack on a gold π-allene to yield a vinyl gold carbene.
Antony Sekar Kulandai Raj, Kuo-Chen Tan, Liang-Yu Chen, M. Cheng, Rai‐Shung Liu   +4 more
semanticscholar   +1 more source

Rational Design, Synthesis and Biological Evaluation of Pyrimidine-4,6-diamine derivatives as Type-II inhibitors of FLT3 Selective Against c-KIT. [PDF]

, 2018
FMS-like Tyrosine Kinase 3 (FLT3) is a clinically validated target for acute myeloid leukemia (AML). Inhibitors targeting FLT3 have been evaluated in clinical studies and have exhibited potential to treat FLT3-driven AML.
Bharate, Jaideep B, Ding, Lucky, Frett, Brendan, Lakkaniga, Naga Rajiv, Li, Hong-Yu, McConnell, Nicholas, Naresh, Gunaganti, Shah, Neil P, Zhang, Lingtian   +8 more
core   +2 more sources

Regioselective synthesis of heterocyclic N-sulfonyl amidines from heteroaromatic thioamides and sulfonyl azides

Beilstein Journal of Organic Chemistry, 2020
N-Sulfonyl amidines bearing 1,2,3-triazole, isoxazole, thiazole and pyridine substituents were successfully prepared for the first time by reactions of primary, secondary and tertiary heterocyclic thioamides with alkyl- and arylsulfonyl azides.
Vladimir Ilkin, Vera Berseneva, Tetyana Beryozkina, Tatiana Glukhareva, Lidia Dianova, Wim Dehaen, Eugenia Seliverstova, Vasiliy Bakulev   +7 more
doaj   +1 more source