Target
Bone morphogenetic protein receptor type-1B [168-495]
Ligand
BDBM522108
Substrate
n/a
Meas. Tech.
In Vitro Enzyme Inhibition Using a Biochemical Peptide Phosphorylation Assay- Caliper Assay
IC50
>10000±n/a nM
Citation
 Arista, LChamoin, SD''Alessandro, PLLindvall, MLizos, DStiefl, NJTeixeira-Fouchard, SUllrich, TWeiler, S Pyridinone derivatives and their use as selective ALK-2 inhibitors US Patent  US11160797 Publication Date 11/2/2021 
Target
Name:
Bone morphogenetic protein receptor type-1B [168-495]
Synonyms:
BMPR1B | BMR1B_HUMAN | Bone morphogenetic protein receptor type-1B (BMPR1B) aa 168-495
Type:
Enzyme Catalytic Domain
Mol. Mass.:
37241.56
Organism:
Homo sapiens (Human)
Description:
O00238[168-495]
Residue:
328
Sequence:
TYIPPGESLRDLIEQSQSSGSGSGLPLLVQRTIAKQIQMVKQIGKGRYGEVWMGKWRGEKVAVKVFFTTEEASWFRETEIYQTVLMRHENILGFIAADIKGTGSWTQLYLITDYHENGSLYDYLKSTTLDAKSMLKLAYSSVSGLCHLHTEIFSTQGKPAIAHRDLKSKNILVKKNGTCCIADLGLAVKFISDTNEVDIPPNTRVGTKRYMPPEVLDESLNRNHFQSYIMADMYSFGLILWEVARRCVSGGIVEEYQLPYHDLVPSDPSYEDMREIVCIKKLRPSFPNRWSSDECLRQMGKLMTECWAHNPASRLTALRVKKTLAKMS
  
Inhibitor
Name:
BDBM522108
Synonyms:
US11160797, Example 16
Type:
Small organic molecule
Emp. Form.:
C22H18F3N3O2
Mol. Mass.:
413.3924
SMILES:
CN1C(=O)Cc2cc(ccc12)-c1cncc(c1)-c1ccc(=O)n(CCC(F)(F)F)c1
Structure:
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