5.33436
Monocarboxylate Transport Inhibitor, AR-C155858
别名:
Monocarboxylate Transport Inhibitor, AR-C155858, (S)-6-((3,5-dimethyl-1H-pyrazol-4-yl)methyl)-5-(4-hydroxyisoxazolidine-2-carbonyl)-1-isobutyl-3-methylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dione , Monocarboxylate transporter 1 inhibitor, AR-C155858, SR13801
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关于此项目
经验公式（希尔记法）:
C21H27N5O5S
化学文摘社编号:
分子量:
461.53
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.77
Assay:
≥95% (HPLC)
Form:
solid
Storage condition:
OK to freeze, protect from light
assay
≥95% (HPLC)
Quality Segment
form
solid
potency
1.2 nM Ki
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze, protect from light
color
brown
solubility
DMSO: 50 mg/mL
storage temp.
−20°C
SMILES string
[s]1c2[n]([c]([n]([c](c2c(c1Cc4c([nH]nc4C)C)C(=O)N3OC[C@H](C3)O)=O)C)=O)CC(C)C
InChI
1S/C21H27N5O5S/c1-10(2)7-25-20-17(18(28)24(5)21(25)30)16(19(29)26-8-13(27)9-31-26)15(32-20)6-14-11(3)22-23-12(14)4/h10,13,27H,6-9H2,1-5H3,(H,22,23)/t13-/m0/s1
InChI key
ISIVOJWVBJIOFM-ZDUSSCGKSA-N
General description
A cell-permeable thieno[2,3-d]pyrimidinedione compound that acts as a highly potent inhibitor of monocarboxylate transporter 1 (MCT1; Ki = 2.3 nM for lactate uptake in rat erythrocytes). Also shown to inhibit MCT2 when associated with basigin (IC50 = 10 nM). Does not affect the activity of MCT4 even at higher concentration. Also shown to block MCT1 expressed in Xenopus oocytes Binds to MCT1 from the intracellular side involving transmembrane helices 7-10. Its inhibitory effect is significantly reduced with either F360Y or S364G mutations (~100 nM) and the inhibitory effect is lost with both sites are mutated (~5 µM). Displays high metabolic stability and low inhibition of CYP. Shown to block lactate transport and increase intracellular lactate levels in Raji Burkitt and MCF-7 cells and reduces their proliferation.
Monocarboxylate Transport Inhibitor, AR-C155858, CAS 496791-37-8, is a cell-permeable, potent inhibitor of monocarboxylate transporter 1 (MCT1; Ki = 2.3 nM for lactate uptake in rat erythrocytes).
Biochem/physiol Actions
Cell permeable: yes
Primary Target
MCT1
MCT1
Preparation Note
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Other Notes
Nancolas, B., et al. 2015. Biochem. J.467, 192.
Ovens, M. J. et al. 2010. Biochem. J.425, 523.
Guile, S. D., et al. 2007. J. Med. Chem.50, 254.
Ovens, M. J. et al. 2010. Biochem. J.425, 523.
Guile, S. D., et al. 2007. J. Med. Chem.50, 254.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Toxicity: Standard Handling (A)
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable