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| Cas No.: | 842133-18-0 |
| Chemical Name: | (3R,4R,5S,6R)-2-(3-((5-(4-fluorophenyl)thiophen-2-yl)methyl)-4-methylphenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol |
| Synonyms: | JNJ 24831754; INJ24831754; JNJ-24831754; JNJ24831754AAA; JNJ24831754ZAE; TA 7284; TA-7284; TA7284; Canagliflozin; Trade name: Invokana. |
| SMILES: | FC1=CC=C(C2=CC=C(CC3=C(C=CC([C@@H]4O[C@@H]([C@H]([C@@H]([C@H]4O)O)O)CO)=C3)C)S2)C=C1 |
| Formula: | C24H25FO5S |
| M.Wt: | 444.52 |
| Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
| Description: | Canagliflozin is a selective SGLT2 inhibitor with IC50s of 2 nM, 3.7 nM, and 4.4 nM for mSGLT2, rSGLT2, and hSGLT2 in CHOK cells, respectively. |
| In Vivo: | Canagliflozin treatment (1 mg/kg) notably lowers renal threshold for glucose excretion (RTG) in Zucker diabetic fatty (ZDF) rats to 94±10 mg/dL. In the second study, an insulin infusion is given to lower blood glucose (BG) to approximately 25 mg/dL, and then the graded glucose infusion (GGI) is given to slowly raise BG to approximately 300 mg/dL. In ZDF rats treated with Canagliflozin (1 mg/kg), the relationship between BG and urinary glucose excretion (UGE) remains well-described by a threshold relationship with negligible UGE occurring when BG<90 mg/dL and UGE increases in proportion to BG at higher BG levels. In db/db mice, single doses of Canagliflozin dose-dependently reduces non-fasting BG concentrations. The onset of the BG-lowering effect after a single dose is rapid, and BG levels in Canagliflozin-treated mice (at 1 and 10 mg/kg doses) are significantly different from those of vehicle-treated mice at 1 hour after treatment (22% and 36% reduction of BG levels compared with that in vehicle-treated mice, respectively)[1]. |
| In Vitro: | Canagliflozin is a sodium glucose co-transporter (SGLT) 2 inhibitor. In a concentration-dependent fashion, Canagliflozin inhibits Na+-dependent 14C-AMG uptake in CHO-hSGLT2 cells, with an IC50 of 4.4±1.2 nM. Similar IC50 values are obtained in CHO-rSGLT2 and CHO-mSGLT2 cells (IC50=3.7 and 2.0 nM for rat and mouse SGLT2, respectively). Canagliflozin inhibits 14C-AMG uptake in CHO-hSGLT1 and mSGLT1 cells with IC50 of 684±159 nM and >1,000 nM, respectively. At 10 µM, Canagliflozin inhibits the facilitative (non-Na+-linked) GLUT-mediated 3H-2-DG uptake in L6 myoblasts by less than 50%[1]. |
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