94
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MedChemExpress
hy 18637 tcid medchemexpress Hy 18637 Tcid Medchemexpress, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/ldn+57444/LDN-57444/10__1016_slash_j__cpblue__2026__100071-556-16-18 Average 94 stars, based on 1 article reviews
hy 18637 tcid medchemexpress - by Bioz Stars,
2026-08
94/100 stars
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LDN-57444 (Cat No.:I004517) is a potent inhibitor of the deubiquitinating enzyme UCHL1 (ubiquitin carboxyl-terminal hydrolase L1). It acts as a reversible and competitive inhibitor, binding to the active site of UCHL1. By inhibiting UCHL1, LDN-57444
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93
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Selleck Chemicals
ldn 57444 ldn Ldn 57444 Ldn, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/ldn+57444/LDN-57444/pm28726275-68-0-9 Average 93 stars, based on 1 article reviews
ldn 57444 ldn - by Bioz Stars,
2026-08
93/100 stars
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86
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Biosynth Carbosynth
ldn treated animals Ldn Treated Animals, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/ldn+57444/LDN-57444/10__1161_slash_atvbaha__111__240101-45-13-21 Average 86 stars, based on 1 article reviews
ldn treated animals - by Bioz Stars,
2026-08
86/100 stars
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LDN 57444 is a cell permeable ubiquitin C terminal hydrolase UCH L1 inhibitor Ki 0 4 µM Decreases proteasome activity and increases levels of ubiquitinated proteins Induces apoptosis and causes dramatic alterations in synaptic protein
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LDN-57444 is a reversible, competitive proteasome inhibitor for Uch-L1 with IC50 of 0.88 μM, 28-fold selectivity over isoform Uch-L3.A potent, reversible, active site-directed UCH-L1 inhibitor
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LDN-57444 is a cell permeable ubiquitin C-terminal hydrolase (UCH-L1) inhibitor (Ki=0.4 µM). Decreases proteasome activity and increases levels of ubiquitinated proteins. Induces apoptosis and causes dramatic alterations in synaptic protein distribution and spine morphology in
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LDN-57444 is a reversible, competitive proteasome inhibitor for UCH-L1 with IC50 of 0.88 μM, 28-fold greater selectivity over isoform UCH-L3.
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The ubiquitin C terminal hydrolase L1 UCH L1 is a member of a family of de ubiquitinating enzymes that can generate free ubiquitin from ubiquitin precursors via its ubiquitin ligase activity By associating with free
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