Ask about this productRelated genes to: CBR4 Blocking Peptide
- Gene:
- CBR4 NIH gene
- Name:
- carbonyl reductase 4
- Previous symbol:
- -
- Synonyms:
- FLJ14431, SDR45C1
- Chromosome:
- 4q32.3
- Locus Type:
- gene with protein product
- Date approved:
- 2006-03-21
- Date modifiied:
- 2015-09-11
Related products to: CBR4 Blocking Peptide
Related articles to: CBR4 Blocking Peptide
- Utilizing a readily available and highly efficient organic photocatalyst (QXPT-NPy, 0.5 mol %) and inexpensive CBr (0.5 mol %) as a bromine radical precursor, the [3 + 2] cycloadditions of vinylcyclopropanes with alkenes/alkynes were successfully achieved under irradiation of 420 nm blue LEDs. A broad scope of alkenes and alkynes participated efficiently in the reaction, and structurally diverse cyclopentane and cyclopentene derivatives were afforded in up to 97% yield and 95:5 dr. - Source: PubMed
Publication date: 2026/02/03
Sun YiYang YantingHuang XiaobingYuan LinBian QiangRen JunWang Zhongwen - To investigate the causal relationship between mitochondrial genes and the pathogenesis of carotid plaque (CP), a multiomics-integrated Mendelian randomization (MR) analysis was performed in this study. - Source: PubMed
Publication date: 2025/11/01
Yu ZhuyuanMeng XiangyuanZong ZiyuSong QiHuo YingchaoChen Hao - A new photocatalytic cascade involving Kharasch-type cyclization, 1,5-(S″)-substitution, and elimination has been developed for the reactions of secondary alcohol-tethered 1,6-diynes with polyhalomethanes such as BrCCl and CBr. This method affords a series of functionalized β--dihalovinyl 1-indanones in good yields with high stereoselectivity. Moreover, when ene-diynes were employed as radical acceptors, the reaction proceeded readily to deliver polyhalogenated indenes in a completely stereoselective manner. - Source: PubMed
Publication date: 2026/01/16
Zhang YanXu Zi-YangFu RongChen KeHao Wen-JuanJiang Bo - An electrochemical bromination of diazo compounds with CBr as a bromine source via convergent paired electrolysis has been developed, which affords α-bromo phosphonates as products in up to 96% yields. This work represents the first example of direct anodic oxidation of diazos to couple with an -generated nucleophile from the cationic reduction of CBr by using CHCl as a hydrogen source. This reaction features mild conditions, good substrate compatibility, and scale-up applicability, which represents a new electrochemical reaction mode of diazo compounds and also provides easy access to α-bromo phosphonates. - Source: PubMed
Publication date: 2026/01/13
Wang QianWu WentianMei HaiboEscorihuela JorgePajkert RomanaRöschenthaler Gerd-VolkerHan Jianlin - A metal-free synthesis of indolo[2,1-]isoquinolines is achieved via a one-pot C-H oxidation/intramolecular carbene insertion cascade. The strategy employs CBr as a mild oxidant and diazoacetates to form key α-diazo intermediates, which undergo visible-light-induced denitrogenative cyclization to forge the target framework. This protocol features operational simplicity, excellent functional group tolerance, and scalability, enabling the discovery of derivatives with aggregation-induced emission properties. - Source: PubMed
Publication date: 2025/12/12
Ma QiyuanZhu YuhaoWang JinchengZhang ShuweiYuan YuJia Xiaodong