461432-25-7: Dapagliflozin Tetraacetate

It is a biotransformation product of Dapagliflozin which is a sodium-glucose cotransporter 2 blocker dapagliflozin lowered the composite endpoint of cardiovascular death in a large population of patients having type 2 diabetes mellitus.

Additional information on CAS 461432-25-7

Catalogue No.

VE006659

CAS No.

461432-25-7

Molecular Formula

C29H33ClO10

Molecular Weight

577.02

Parent drug

Dapagliflozin

IUPAC Name

(2R, 3R, 4R, 5S, 6S)-2-(acetoxymethyl)-6-(4-chloro-3-(4-ethoxybenzyl)phenyl)tetrahydro-2H-pyran-3, 4, 5-triyl triacetate

Synonyms

N/A

References

Lemaire, Sébastien, and Didier Schils. “Development of Efficient Routes to Access C-Glycosides as SGLT-2 Inhibitors for the Treatment of Type 2 Diabetes.” Topics in Heterocyclic Chemistry, 2015, pp. 29–50, https://doi.org/10.1007/7081_2015_166.?Kato, Eri T., et al. “Effect of Dapagliflozin on Heart Failure and Mortality in Type 2 Diabetes Mellitus.” Circulation, vol. 139, no. 22, May 2019, pp. 2528–36, https://doi.org/10.1161/circulationaha.119.040130.?

Status

In-stock

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461432-25-7: Dapagliflozin Tetraacetate

461432-25-7: Dapagliflozin Tetraacetate
Catalogue No.

VE006659

CAS No.

461432-25-7

Molecular Formula

C29H33ClO10

Molecular Weight

577.02

Parent drug

Dapagliflozin

IUPAC Name

(2R, 3R, 4R, 5S, 6S)-2-(acetoxymethyl)-6-(4-chloro-3-(4-ethoxybenzyl)phenyl)tetrahydro-2H-pyran-3, 4, 5-triyl triacetate

Synonyms

N/A

References

Lemaire, Sébastien, and Didier Schils. “Development of Efficient Routes to Access C-Glycosides as SGLT-2 Inhibitors for the Treatment of Type 2 Diabetes.” Topics in Heterocyclic Chemistry, 2015, pp. 29–50, https://doi.org/10.1007/7081_2015_166.?Kato, Eri T., et al. “Effect of Dapagliflozin on Heart Failure and Mortality in Type 2 Diabetes Mellitus.” Circulation, vol. 139, no. 22, May 2019, pp. 2528–36, https://doi.org/10.1161/circulationaha.119.040130.?

Status

In-stock

ListName

Dapagliflozin Tetraacetate

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