{"id":11831,"date":"2022-12-05T06:02:39","date_gmt":"2022-12-04T22:02:39","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=11831"},"modified":"2022-12-05T06:02:39","modified_gmt":"2022-12-04T22:02:39","slug":"vannam-raghus-team-published-research-in-cell-chemical-biology-in-28-cas-1936429-06-9","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=11831","title":{"rendered":"Vannam, Raghu&#8217;s team published research in Cell Chemical Biology  in 28 | CAS: 1936429-06-9"},"content":{"rendered":"<p>Vannam, Raghu published the artcile<b><i>Targeted degradation of the enhancer lysine acetyltransferases CBP and p300<\/i><\/b>,  <a href=\"https:\/\/www.ambeed.com\/products\/1936429-06-9.html\">Application of tert-Butyl 3-bromo-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate<\/a>,  the publication is  Cell Chemical Biology (2021), 28(4), 503-514.e12, database is CAplus and MEDLINE.<\/p>\n<p>The enhancer factors CREB-binding protein (CBP) and p300 (also known as KAT3A and KAT3B) maintain gene expression programs through lysine acetylation of chromatin and transcriptional regulators and by scaffolding functions mediated by several protein-protein interaction domains. Small mol. inhibitors that target some of these domains have been developed; however, they cannot completely ablate p300\/CBP function in cells. Here we describe a chem. degrader of p300\/CBP, dCBP-1. Leveraging structures of ligand-bound p300\/CBP domains, we use in silico modeling of ternary complex formation with the E3 ubiquitin ligase cereblon to enable degrader design. dCBP-1 is exceptionally potent at killing multiple myeloma cells and can abolish the enhancer that drives MYC oncogene expression. As an efficient degrader of this unique class of acetyltransferases, dCBP-1 is a useful tool alongside domain inhibitors for dissecting the mechanism by which these factors coordinate enhancer activity in normal and diseased cells.<\/p>\n<p>Cell Chemical Biology published new progress about 1936429-06-9. 1936429-06-9 belongs to pyrazoles-derivatives, auxiliary class Pyrazoles, name is tert-Butyl 3-bromo-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate, and the molecular formula is C14H10O4, <a href=\"https:\/\/www.ambeed.com\/products\/1936429-06-9.html\">Application of tert-Butyl 3-bromo-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate<\/a>.<\/p>\n<p>Referemce:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">https:\/\/en.wikipedia.org\/wiki\/Pyrazole<\/a>,<br \/><a href=\"Pyrazole - Wikipedia\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Cell Chemical Biology published new progress about 1936429-06-9. 1936429-06-9 belongs to pyrazoles-derivatives, auxiliary class Pyrazoles, name is tert-Butyl 3-bromo-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate, and the molecular formula is C14H10O4, <a href=\"https:\/\/www.ambeed.com\/products\/1936429-06-9.html\">Application of tert-Butyl 3-bromo-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate<\/a>.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[828,131],"tags":[811],"class_list":["post-11831","post","type-post","status-publish","format-standard","hentry","category-1936429-06-9","category-pyrazoles-derivatives","tag-m-w300-350"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - 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