Reaction Details | |||
---|---|---|---|
Report a problem with these data | |||
Target | Isoform Truncated 1 of E3 ubiquitin-protein ligase CBL-B [36-427] | ||
Ligand | BDBM585805 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Cbl-b Displacement Assay (Cbl-b Inhibition Assay low) | ||
IC50 | <1±n/a nM | ||
Citation | Sands, AT; Bence, NF; Zapf, CW; Cohen, F; Wang, C; Cummins, T; Tanaka, H; Shunatona, H; Cardozo, M; Weiss, D; Gosling, J Cyano cyclobutyl compounds for CBL-B inhibition and uses thereof US Patent US11530229 Publication Date 12/20/2022 | ||
More Info.: | Get all data from this article, Assay Method | ||
Isoform Truncated 1 of E3 ubiquitin-protein ligase CBL-B [36-427] | |||
Name: | Isoform Truncated 1 of E3 ubiquitin-protein ligase CBL-B [36-427] | ||
Synonyms: | CBLB | CBLB_HUMAN | E3 ubiquitin-protein ligase CBL-B [36-427] | RNF56 | ||
Type: | Enzyme Catalytic Domain | ||
Mol. Mass.: | 45487.32 | ||
Organism: | Homo sapiens (Human) | ||
Description: | aa 36-427 (sequence in paper SEQ ID No: 1) | ||
Residue: | 392 | ||
Sequence: |
| ||
BDBM585805 | |||
n/a | |||
Name | BDBM585805 | ||
Synonyms: | US11530229, Compound 20 | ||
Type | Small organic molecule | ||
Emp. Form. | C30H29F5N6O | ||
Mol. Mass. | 584.5829 | ||
SMILES | Cn1cnnc1C[C@@]1(C[C@@H](C1)C#N)c1cccc(c1)N1Cc2c(cc(CN[C@H]3CCC(F)(F)C3)cc2C(F)(F)F)C1=O |r,wU:9.12,wD:7.14,27.29,(7.67,-1.35,;6.2,-1.83,;5.73,-3.29,;4.19,-3.29,;3.71,-1.83,;4.96,-.92,;4.96,.62,;6.29,1.39,;7.38,.3,;8.47,1.39,;7.38,2.48,;10.01,1.39,;11.55,1.39,;4.96,2.16,;4.96,3.7,;3.62,4.47,;2.29,3.7,;2.29,2.16,;3.62,1.39,;.96,1.39,;.8,-.15,;-.71,-.47,;-1.48,.87,;-3.02,.87,;-3.79,-.47,;-5.33,-.47,;-6.1,-1.8,;-7.64,-1.8,;-8.55,-.55,;-10.01,-1.03,;-10.01,-2.57,;-11.55,-2.57,;-10.01,-4.11,;-8.55,-3.04,;-3.02,-1.8,;-1.48,-1.8,;-.71,-3.13,;-1.48,-4.47,;.83,-3.13,;.06,-4.47,;-.45,2.01,;-.77,3.52,)| | ||
Structure |