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Target
Ephrin type-B receptor 3
Ligand
BDBM50551201
Substrate
n/a
Meas. Tech.
ChEMBL_2030719 (CHEMBL4684877)
IC50
11000±n/a nM
Citation
 Incerti, M; Russo, S; Corrado, M; Giorgio, C; Ballabeni, V; Chiodelli, P; Rusnati, M; Scalvini, L; Callegari, D; Castelli, R; Vacondio, F; Ferlenghi, F; Tognolini, M; Lodola, A Optimization of EphA2 antagonists based on a lithocholic acid core led to the identification of UniPR505, a new 3?-carbamoyloxy derivative with antiangiogenetic properties. Eur J Med Chem 189:0 (2020) [PubMed]  Article 
Target
Name:
Ephrin type-B receptor 3
Synonyms:
2.7.10.1 | Developmental kinase 5 | EPHB3_MOUSE | Ephb3 | Ephrin type-B receptor 3 | Etk2 | Mdk5 | Sek4 | Tyrosine-protein kinase receptor SEK-4 | mDK-5
Type:
PROTEIN
Mol. Mass.:
109657.93
Organism:
Mouse
Description:
ChEMBL_120143
Residue:
993
Sequence:
MAGARPPPGLLPLLAPLLLPLLLPAGCWALEETLMDTKWVTSELAWTSHPESGWEEVSGYDEAMNPIRTYQVCNVRESSQNNWLRTGFIWRREVQRVYVELKFTVRDCNSIPNIPGSCKETFNLFYYEADSDVASASSPFWMENPYVKVDTIAPDESFSRLDAGRVNTKVRSFGPLSKAGFYLAFQDQGACMSLISVRAFYKKCASTTAGFALFPETLTGAEPTSLVIAPGTCIANAVEVSVPLKLYCNGDGEWMVPVGACTCATGHEPAAKESQCRACPPGSYKAKQGEGPCLPCPPNSRTTSPAASICTCHNNFYRADSDSADSACTTVPSPPRGVISNVNETSLILEWSEPRDLGGRDDLLYNVICKKCRGSSGAGGPATCSRCDDNVEFVPRQLGLTERRVHISHLLAHTRYTFEVQAVNGVSGKSPLPPRYAAVNITTNQAAPSEVPTLHLHSSSGSSLTLSWAPPERPNGVILDYEMKYFEKSKGIASTVTSQKNSVQLDGLQPDARYVVQVRARTVAGYGQYSHPAEFETTSERGSGAQQLQEQLPLIVGSTVAGFVFMVVVVVIALVCLRKQRHGPDAEYTEKLQQYIAPGMKVYIDPFTYEDPNEAVREFAKEIDVSCVKIEEVIGAGEFGEVCRGRLKLPGRREVFVAIKTLKVGYTERQRRDFLSEASIMGQFDHPNIIRLEGVVTKSRPVMILTEFMENCALDSFLRLNDGQFTVIQLVGMLRGIAAGMKYLSEMNYVHRDLAARNILVNSNLVCKVSDFGLSRFLEDDPSDPTYTSSLGGKIPIRWTAPEAIAYRKFTSASDVWSYGIVMWEVMSYGERPYWDMSNQDVINAVEQDYRLPPPMDCPTALHQLMLDCWVRDRNLRPKFSQIVNTLDKLIRNAASLKVTASAPSGMSQPLLDRTVPDYTTFTTVGDWLDAIKMGRYKESFVGAGFASFDLVAQMTAEDLLRIGVTLAGHQKKILCSIQDMRLQMNQTLPVQV
  
Inhibitor
Name:
BDBM50551201
Synonyms:
CHEMBL4761556
Type:
Small organic molecule
Emp. Form.:
C39H57N3O5
Mol. Mass.:
647.887
SMILES:
[H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@@H](CC[C@]4(C)[C@@]3([H])CC[C@]12C)OC(=O)NCC)[C@H](C)CCC(=O)N[C@H](CC(O)=O)Cc1c[nH]c2ccccc12 |r|
Structure:
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