Results 1 to 10 of about 3,255 (160)

Concise Syntheses of Trifluoromethylated Cyclic and Acyclic Analogues of cADPR

open access: yesMolecules, 2010
A novel trifluoromethylated analogue of cADPR, 8-CF3-cIDPDE (5) was designed and synthesized via construction of N1,N9-disubstituted hypoxanthine, trifluoromethylation and intramolecular condensation.
Min Dong, Zhenjun Yang, Kehui Zhang
exaly   +4 more sources

Direct Gating of the TRPM2 Channel by cADPR via Specific Interactions with the ADPR Binding Pocket [PDF]

open access: yesCell Reports, 2019
Summary: cADPR is a well-recognized signaling molecule by modulating the RyRs, but considerable debate exists regarding whether cADPR can bind to and gate the TRPM2 channel, which mediates oxidative stress signaling in diverse physiological and ...
Lin-Hua Jiang   +2 more
exaly   +4 more sources

Synthesis and Calcium Mobilization Activity of cADPR Analogues Which Integrate Nucleobase, Northern and Southern Ribose Modifications [PDF]

open access: yesMolecules, 2012
Novel cADPR mimics, which integrate nucleobase, northern and southern ribose modifications were synthesized. The key steps of the synthesis were a Cu(I)-catalyzed Hüisgen [3+2] cycloaddition and a microwave-assisted intramolecular pyrophosphorylation ...
Jianbo Yue   +2 more
exaly   +4 more sources

Remifentanil-induced postoperative hyperalgesia is attenuated by inhibition of NMDAR-cADPR-RyRs signaling pathway in the spinal cord of rats [PDF]

open access: yesJichu yixue yu linchuang, 2023
Objective To investigate the role of NMDAR-cADPR-RyRs signaling pathway in remifentanil-induced hyperalgesia(RIH). Methods The rat model of postoperative hyperalgesia induced by remifentanil was established. SD rats were randomly divided into 6 groups as:
QIAN Yue, WANG Fang, ZHANG Jing, XIA Tianjiao, GU Xiaoping
doaj   +2 more sources

Raw defines a TIR-fold cADPR hydrolase cooperating with dSarm in development and axon degeneration [PDF]

open access: yesCell Communication and Signaling
Conserved TIR domain proteins play essential roles in immune signaling, development, and neurodegeneration. SARM1/dSarm, the only known enzymatically active TIR protein in animals, has been established as a key regulator of axon degeneration through its ...
Feng Chen   +15 more
doaj   +2 more sources

Targeting the SARM1–cADPR–Ca2+ pathway attenuates mitochondrial fragmentation and osteoarthritis progression [PDF]

open access: yesArthritis Research & Therapy
Introduction Osteoarthritis (OA) is a prevalent degenerative joint disease accompanied by increased number of senescent chondrocytes. Mitochondrial dysfunction is a well-established hallmark of chondrocyte senescence in OA pathogenesis.
Yu Gu   +7 more
doaj   +2 more sources

A phage-encoded sponge protein suppresses bacterial TIR-Caspase immune signaling [PDF]

open access: yesNature Communications
Triggering immune response through generation of signal molecules is a common immune strategy across all domains of life. In the bacterial type IV Thoeris anti-phage system, a Toll/interleukin-1 receptor (TIR)-domain protein produces adenosine 5 ...
Yu Chen   +13 more
doaj   +2 more sources

Molecular characterisation of the Bacillus subtilis SpbK antiphage defence system [PDF]

open access: yesNature Communications
Bacteria have a variety of mechanisms for limiting predation by phages. SpbK is a Toll/interleukin-1 receptor (TIR) domain-containing antiphage defence protein from Bacillus subtilis that provides protection against the temperate phage SPβ via abortive ...
Biswa P. Mishra   +15 more
doaj   +2 more sources

Does Cyclic ADP-Ribose (cADPR) Activate the Non-selective Cation Channel TRPM2?

open access: yesFrontiers in Immunology, 2020
TRPM2 is a non-selective, Ca2+-permeable cation channel widely expressed in immune cells. It is firmly established that the channel can be activated by intracellular adenosine 5′-diphosphoribose (ADPR).
Andreas Guse, Ralf Fliegert
exaly   +3 more sources

Synthesis and Biological Evaluation of a New Structural Simplified Analogue of cADPR, a Calcium-Mobilizing Secondary Messenger Firstly Isolated from Sea Urchin Eggs

open access: yesMarine Drugs, 2018
Herein, we reported on the synthesis of cpIPP, which is a new structurally-reduced analogue of cyclic ADP-ribose (cADPR), a potent Ca2+-releasing secondary messenger that was firstly isolated from sea urchin eggs extracts.
Agnese Secondo   +2 more
exaly   +3 more sources

Home - About - Disclaimer - Privacy