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TargetHigh affinity choline transporter 1
LigandBDBM89156
Substrate/Competitorn/a
Meas. Tech.Dose responses of compounds that activate the Choline Transporter (CHT) - 10 point CRC
EC50 8220±n/a nM
Citation PubChem, PC Dose responses of compounds that activate the Choline Transporter (CHT) - 10 point CRC PubChem Bioassay(2012)[AID]
More Info.:Get all data from this article,  Assay Method
 
High affinity choline transporter 1
Name:High affinity choline transporter 1
Synonyms:CHT1 | High-affinity choline transporter | SC5A7_HUMAN | SLC5A7 | high affinity choline transporter 1
Type:PROTEIN
Mol. Mass.:63194.33
Organism:Homo sapiens (Human)
Description:ChEMBL_1464247
Residue:580
Sequence:
MAFHVEGLIAIIVFYLLILLVGIWAAWRTKNSGSAEERSEAIIVGGRDIGLLVGGFTMTA
TWVGGGYINGTAEAVYVPGYGLAWAQAPIGYSLSLILGGLFFAKPMRSKGYVTMLDPFQQ
IYGKRMGGLLFIPALMGEMFWAAAIFSALGATISVIIDVDMHISVIISALIATLYTLVGG
LYSVAYTDVVQLFCIFVGLWISVPFALSHPAVADIGFTAVHAKYQKPWLGTVDSSEVYSW
LDSFLLLMLGGIPWQAYFQRVLSSSSATYAQVLSFLAAFGCLVMAIPAILIGAIGASTDW
NQTAYGLPDPKTTEEADMILPIVLQYLCPVYISFFGLGAVSAAVMSSADSSILSASSMFA
RNIYQLSFRQNASDKEIVWVMRITVFVFGASATAMALLTKTVYGLWYLSSDLVYIVIFPQ
LLCVLFVKGTNTYGAVAGYVSGLFLRITGGEPYLYLQPLIFYPGYYPDDNGIYNQKFPFK
TLAMVTSFLTNICISYLAKYLFESGTLPPKLDVFDAVVARHSEENMDKTILVKNENIKLD
ELALVKPRQSMTLSSTFTNKEAFLDVDSSPEGSGTEDNLQ
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM89156
n/a
NameBDBM89156
Synonyms:(3aS,5S,9aS)-2-(3-chlorobenzyl)-5-(1-pyridin-2-yl-1H-pyrrol-2-yl)hexahydro-7H-pyrrolo[3,4-g]pyrrolizin-1(2H)-one | (3aS,5S,9aS)-2-(3-chlorobenzyl)-5-[1-(2-pyridyl)pyrrol-2-yl]-3a,4,5,7,8,9-hexahydro-3H-pyrrolo[3,4-h]pyrrolizin-1-one | (3aS,5S,9aS)-2-[(3-chlorophenyl)methyl]-5-(1-pyridin-2-ylpyrrol-2-yl)-3a,4,5,7,8,9-hexahydro-3H-pyrrolo[3,4-h]pyrrolizin-1-one | (3aS,5S,9aS)-2-[(3-chlorophenyl)methyl]-5-[1-(2-pyridinyl)-2-pyrrolyl]-3a,4,5,7,8,9-hexahydro-3H-pyrrolo[3,4-h]pyrrolizin-1-one | MLS000732939 | SMR000316090 | cid_16189940
TypeSmall organic molecule
Emp. Form.C25H25ClN4O
Mol. Mass.432.945
SMILESClc1cccc(CN2C[C@@H]3C[C@H](N4CCC[C@@]34C2=O)c2cccn2-c2ccccn2)c1
Structure
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