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TargetInduced myeloid leukemia cell differentiation protein Mcl-1 [173-329]/Phorbol-Phorbol-12-myristate-13-acetate-induced protein 1 [26-43]
LigandBDBM562383
Substrate/Competitorn/a
Meas. Tech.Protein-Protein Interaction Assay
IC50 0.640±n/a nM
Citation Furst, LSerrano-Wu, MHLemke, CMcKinney, DFitzgerald, MNasveschuk, CLazarski, KFerrara, SJWei, GMcCarren, PRThede, KMengel, AChrist, CKuhnke, JJohannes, SABuchgraber, PKlar, URauh, UKaulfuss, SFernandez-Montalvan, AEWerbeck, NMönning, UNowak-Reppel, K Macrocyclic indole derivatives US Patent US11401278 Publication Date 8/2/2022
More Info.:Get all data from this article,  Assay Method
 
Induced myeloid leukemia cell differentiation protein Mcl-1 [173-329]/Phorbol-Phorbol-12-myristate-13-acetate-induced protein 1 [26-43]
Name:Induced myeloid leukemia cell differentiation protein Mcl-1 [173-329]/Phorbol-Phorbol-12-myristate-13-acetate-induced protein 1 [26-43]
Synonyms:MCL-1/Noxa BH3
Type:Protein
Mol. Mass.:n/a
Description:n/a
Components:This complex has 2 components.
Component 1
Name:Induced myeloid leukemia cell differentiation protein Mcl-1 [173-329]
Synonyms:BCL2L3 | MCL1 | MCL1_HUMAN
Type:Membrane; Single-pass membrane protein
Mol. Mass.:17924.29
Organism:Homo sapiens (Human)
Description:Q07820[173-329]
Residue:157
Sequence:
ELYRQSLEIISRYLREQATGAKDTKPMGRSGATSRKALETLRRVGDGVQRNHETAFQGML
RKLDIKNEDDVKSLSRVMIHVFSDGVTNWGRIVTLISFGAFVAKHLKTINQESCIEPLAE
SITDVLVRTKRDWLVKQRGWDGFVEFFHVEDLEGGIR
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Component 2
Name:Phorbol-Phorbol-12-myristate-13-acetate-induced protein 1 [26-43]
Synonyms:APR_HUMAN | NOXA | PMAIP1 | Phorbol-12-myristate-13-acetate-induced protein 1 (NOXA)(BH3)
Type:n/a
Mol. Mass.:2208.61
Organism:Homo sapiens (Human)
Description:Q13794[26-43]
Residue:18
Sequence:
ATQLRRFGDKLNFRQKLL
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BDBM562383
n/a
NameBDBM562383
Synonyms:(+)-4-chloro-14-cyclopropyl-3-ethyl-7-{3-[(6-fluoronaphthalen-1-yl)oxy]propyl}-2-methyl-13,13-dioxo-10,11,12,13,14,15-hexahydro-2H-13lambda6-pyrazolo[3',4':4,5][1,2,8]thiadiazacycloundecino[6,7,8-hi]indole-8-carboxylic acid N-ethylethanamine Salt (Enantiomer 1) | US11401278, Example 54
TypeSmall organic molecule
Emp. Form.C35H36ClFN4O5S
Mol. Mass.679.201
SMILESCCc1c-2c(CN(C3CC3)S(=O)(=O)CCCn3c(C(O)=O)c(CCCOc4cccc5cc(F)ccc45)c4ccc(Cl)c-2c34)nn1C
Structure
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