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TargetBroad substrate specificity ATP-binding cassette transporter ABCG2
LigandBDBM50500539
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1546423 (CHEMBL3748978)
IC50 1700±n/a nM
Citation Li, YWoo, JChmielecki, JXia, CQLiao, MChuang, BCYang, JJGuan, MYPlesescu, MPrakash, SR Synthesis of a new inhibitor of breast cancer resistance protein with significantly improved pharmacokinetic profiles. Bioorg Med Chem Lett26:551-555 (2016) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Broad substrate specificity ATP-binding cassette transporter ABCG2
Name:Broad substrate specificity ATP-binding cassette transporter ABCG2
Synonyms:ABCG2 | ABCG2_HUMAN | ABCP | ATP-Binding Cassette Transporter ABCG2 | ATP-binding cassette sub-family G member 2 | ATP-binding cassette transporter (ABCG2) | ATP-binding cassette, sub-family G, member 2 | BCRP | BCRP1 | Breast cancer resistance protein | CDw338 | MXR | Mitoxantrone resistance-associated protein | Placenta-specific ATP-binding cassette transporter | Urate exporter
Type:Multi-pass membrane protein; monomer or homodimer; disulfide-linked
Mol. Mass.:72329.48
Organism:Homo sapiens (Human)
Description:Q9UNQ0
Residue:655
Sequence:
MSSSNVEVFIPVSQGNTNGFPATASNDLKAFTEGAVLSFHNICYRVKLKSGFLPCRKPVE
KEILSNINGIMKPGLNAILGPTGGGKSSLLDVLAARKDPSGLSGDVLINGAPRPANFKCN
SGYVVQDDVVMGTLTVRENLQFSAALRLATTMTNHEKNERINRVIQELGLDKVADSKVGT
QFIRGVSGGERKRTSIGMELITDPSILFLDEPTTGLDSSTANAVLLLLKRMSKQGRTIIF
SIHQPRYSIFKLFDSLTLLASGRLMFHGPAQEALGYFESAGYHCEAYNNPADFFLDIING
DSTAVALNREEDFKATEIIEPSKQDKPLIEKLAEIYVNSSFYKETKAELHQLSGGEKKKK
ITVFKEISYTTSFCHQLRWVSKRSFKNLLGNPQASIAQIIVTVVLGLVIGAIYFGLKNDS
TGIQNRAGVLFFLTTNQCFSSVSAVELFVVEKKLFIHEYISGYYRVSSYFLGKLLSDLLP
MRMLPSIIFTCIVYFMLGLKPKADAFFVMMFTLMMVAYSASSMALAIAAGQSVVSVATLL
MTICFVFMMIFSGLLVNLTTIASWLSWLQYFSIPRYGFTALQHNEFLGQNFCPGLNATGN
NPCNYATCTGEEYLVKQGIDLSPWGLWKNHVALACMIVIFLTIAYLKLLFLKKYS
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  Blast E-value cutoff:
BDBM50500539
n/a
NameBDBM50500539
Synonyms:CHEMBL3746825
TypeSmall organic molecule
Emp. Form.C21H27N3O4
Mol. Mass.385.4568
SMILES[H][C@]12Cc3c([nH]c4cc(OC)c(OC)cc34)[C@H](CC(C)C)N1C(=O)[C@H](C)NC2=O |r|
Structure
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