Reaction Details |
| Report a problem with these data |
Target | High affinity choline transporter 1 |
---|
Ligand | BDBM78815 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | Dose responses of compounds that activate the Choline Transporter (CHT) - 10 point CRC |
---|
EC50 | 13440±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
|
|
|
BDBM78815 |
---|
n/a |
---|
Name | BDBM78815 |
Synonyms: | 3-cyclohexyl-N-[2-[(3S,6R)-6-[(4-hydroxyphenyl)methyl]-3-(phenylmethyl)-2,3,5,6-tetrahydroimidazo[1,2-a]imidazol-7-yl]ethyl]propanamide | MLS000697929 | N-[2-[(3S,6R)-3-benzyl-6-(4-hydroxybenzyl)-2,3,5,6-tetrahydroimidaz[1,2-a]imidazol-7-yl]ethyl]-3-cyclohexyl-propionamide | N-[2-[(3S,6R)-3-benzyl-6-[(4-hydroxyphenyl)methyl]-2,3,5,6-tetrahydroimidazo[1,2-a]imidazol-7-yl]ethyl]-3-cyclohexylpropanamide | SMR000386396 | cid_16195653 |
Type | Small organic molecule |
Emp. Form. | C30H40N4O2 |
Mol. Mass. | 488.6642 |
SMILES | Oc1ccc(C[C@@H]2CN3[C@@H](Cc4ccccc4)CN=C3N2CCNC(=O)CCC2CCCCC2)cc1 |c:19| |
Structure |
|