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TargetMonocarboxylate transporter 4
LigandBDBM345280
Substrate/Competitorn/a
Meas. Tech.MCT4-Mediated Lactate Transport in MDA-MB-231 Breast Cancer Cells
IC50 9.40±n/a nM
Citation Parnell, KMMcCall, JRomero, D Heterocyclic inhibitors of MCT4 US Patent US10214492 Publication Date 2/26/2019
More Info.:Get all data from this article,  Assay Method
 
Monocarboxylate transporter 4
Name:Monocarboxylate transporter 4
Synonyms:MCT 4 | MCT3 | MCT4 | MOT4_HUMAN | SLC16A3 | Solute carrier family 16 member 3
Type:PROTEIN
Mol. Mass.:49474.36
Organism:Homo sapiens (Human)
Description:ChEMBL_104604
Residue:465
Sequence:
MGGAVVDEGPTGVKAPDGGWGWAVLFGCFVITGFSYAFPKAVSVFFKELIQEFGIGYSDT
AWISSILLAMLYGTGPLCSVCVNRFGCRPVMLVGGLFASLGMVAASFCRSIIQVYLTTGV
ITGLGLALNFQPSLIMLNRYFSKRRPMANGLAAAGSPVFLCALSPLGQLLQDRYGWRGGF
LILGGLLLNCCVCAALMRPLVVTAQPGSGPPRPSRRLLDLSVFRDRGFVLYAVAASVMVL
GLFVPPVFVVSYAKDLGVPDTKAAFLLTILGFIDIFARPAAGFVAGLGKVRPYSVYLFSF
SMFFNGLADLAGSTAGDYGGLVVFCIFFGISYGMVGALQFEVLMAIVGTHKFSSAIGLVL
LMEAVAVLVGPPSGGKLLDATHVYMYVFILAGAEVLTSSLILLLGNFFCIRKKPKEPQPE
VAAAEEEKLHKPPADSGVDLREVEHFLKAEPEKNGEVVHTPETSV
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM345280
n/a
NameBDBM345280
Synonyms:2-[[1-[(2-Fluorophenyl)methyl]-5-(3- isobutoxyphenyl)pyrazol-3-yl]methoxy]-2- methyl-propanoic acid 1HNMR (CDCl3): $#948; 0.97 (s, 3H), 0.99 (s, 3H), 1.55 (s, 6H), 2.00-2.06 (m, 1H), 3.70 (d, 2H), 4.62 (s, 2H), 5.39 (s, 2H), 6.37 (s, 1H), 6.79-6.80 (m, 1H), 6.87-7.09 (M, 5H), 7.22-7.30 (m, 2H) | US10202350, Example 26 | US10214492, Example 26 | US11292767, Example 26 | US11724989, Example 26
TypeSmall organic molecule
Emp. Form.C25H29FN2O4
Mol. Mass.440.5072
SMILESCC(C)COc1cccc(c1)-c1cc(COC(C)(C)C(O)=O)nn1Cc1ccccc1F
Structure
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