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Dapagliflozin (BMS-512148)

Catalog No.
C007B-136815
Mfr. No.
D408687-1ml
Mfr. Name
Aladdin Scientific
Qty/UOM
1
UOM
EA
Price: $87.80
List Price: $97.56

InformationDapagliflozin (BMS-512148) is a potent and selectivehSGLT2inhibitor withEC50of 1.1 nM, exhibiting 1200-fold selectivity over hSGLT1. Phase 4.In vitroDapagliflozin is not sensitive to hSGLT1 with a 1200-fold IC50. Dapagliflozin is 32-fold

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InformationDapagliflozin (BMS-512148) is a potent and selectivehSGLT2inhibitor withEC50of 1.1 nM, exhibiting 1200-fold selectivity over hSGLT1. Phase 4.In vitroDapagliflozin is not sensitive to hSGLT1 with a 1200-fold IC50. Dapagliflozin is 32-fold more potent than phlorizin against hSGLT2 but 4-fold less than phlorizin against hSGLT1. Dapagliflozin is highly selective versus GLUT transporters and displays 8–9% inhibition in protein-free buffer at 20 μM and virtually no inhibition in the presence of 4% bovine serum albumin. Dapagliflozin has good permeability across Caco-2 cell membranes and is a substrate for P-glycoprotein (P-gp) but not a significant P-gp inhibitor. Dapagliflozin is stable in rat, dog, monkey, and human serum at 10 μM. Dapagliflozin shows no inhibitory responses or induction to human P450 enzymes. The in vitro metabolic pathways Dapagliflozin are glucuronidation, hydroxylation, and O-deethylation.In vivoDapagliflozin reduces blood glucose levels by 55% after 0.1 mg/kg oral dose in hyperglycemic streptozotocin (STZ) rats, which is in part to the metabolic stability conferred by the C-glucoside linkage. Dapagliflozin displays a favorable absorption, distribution, metabolism, and excretion (ADME) profile and is orally bioavailable. Dapagliflozin (1 mg/kg) causes significant dose-dependent glucosuria and increase in urine volume in normal rats over 24 hours post-dose. Dapagliflozin induces increase in urine glucose and urine volume excretion at 6 hours post-dose in Zucker diabetic fatty (ZDF) rats. Dapagliflozin lowers fasting and fed glucose levels in ZDF rats even by 2 weeks of treatment, without any marker of renal or liver toxicity. Dapagliflozin significantly reduces the development of hyperglycaemia, with lowered blood glucose. Dapagliflozin could improve the insulin sensitivity, reduce β-cell mass and the development of impaired pancreatic function.Cell Datacell lines:Concentrations:Incubation Time:Powder Purity:≥98%. Specification: 10mM in DMSO Molecular Formula: C21H25ClO6 Molecular Weight: 408.87 Related Documents: https://ald-pub-files.oss-cn-shanghai.aliyuncs.com/aladdinsci/pdp/sds/1/D408687-SCI_4554288f7f552ecf2cab84b903a39ae8.pdf
UPC:
51142560
Condition:
New
Availability:
2 weeks
Weight:
0.85 Ounces
HazmatClass:
No
WeightUOM:
LB
MPN:
D408687-1ml
CAS:
461432-26-8
Product Size:
1ml
Hazard Statement Codes:
H227
Precautionary Statement Codes:
P210:P280:P370+P378:P403+P235:P501

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