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Details

Stereochemistry MIXED
Molecular Formula C18H25N3O2
Molecular Weight 315.41
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SAXAGLIPTIN ANHYDROUS

SMILES

N[C@H](C(=O)N1[C@H]2C[C@H]2C[C@H]1C#N)C34CC5CC(CC(O)(C5)C3)C4

InChI

InChIKey=QGJUIPDUBHWZPV-SGTAVMJGSA-N
InChI=1S/C18H25N3O2/c19-8-13-2-12-3-14(12)21(13)16(22)15(20)17-4-10-1-11(5-17)7-18(23,6-10)9-17/h10-15,23H,1-7,9,20H2/t10?,11?,12-,13+,14+,15-,17?,18?/m1/s1

HIDE SMILES / InChI

Description

Saxagliptin is an orally active hypoglycemic (anti-diabetic drug) of the new dipeptidyl peptidase-4 (DPP-4) inhibitor class of drugs. FDA approved on July 31, 2009. Saxagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor antidiabetic for the treatment of type 2 diabetes. DPP-4 inhibitors are a class of compounds that work by affecting the action of natural hormones in the body called incretins. Incretins decrease blood sugar by increasing consumption of sugar by the body, mainly through increasing insulin production in the pancreas, and by reducing production of sugar by the liver. [Bristol-Myers Squibb Press Release] DPP-4 is a membrane associated peptidase which is found in many tissues, lymphocytes and plasma. DPP-4 has two main mechanisms of action, an enzymatic function and another mechanism where DPP-4 binds adenosine deaminase, which conveys intracellular signals via dimerization when activated. Saxagliptin forms a reversible, histidine-assisted covalent bond between its nitrile group and the S630 hydroxyl oxygen on DPP-4. The inhibition of DPP-4 increases levels active of glucagon like peptide 1 (GLP-1), which inhibits glucagon production from pancreatic alpha cells and increases production of insulin from pancreatic beta cells.

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
30.3 nM [IC50]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Onglyza

Cmax

ValueDoseCo-administeredAnalytePopulation
24 ng/mL
5 mg single, oral
SAXAGLIPTIN plasma
Homo sapiens

AUC

ValueDoseCo-administeredAnalytePopulation
78 ng × h/mL
5 mg single, oral
SAXAGLIPTIN plasma
Homo sapiens

T1/2

ValueDoseCo-administeredAnalytePopulation
2.5 h
5 mg single, oral
SAXAGLIPTIN plasma
Homo sapiens

Funbound

ValueDoseCo-administeredAnalytePopulation
100%
5 mg single, oral
SAXAGLIPTIN plasma
Homo sapiens

Doses

AEs

Drug as perpetrator​

Drug as victim

Tox targets

PubMed

Sample Use Guides

In Vivo Use Guide
Diabetes Mellitus Monotherapy Oral 2.5 or 5 mg once daily.1 Higher dosages (e.g., 10 mg once daily) did not provide additional benefit in clinical trials and are not recommended by manufacturer.
Route of Administration: Oral
In Vitro Use Guide
Saxagliptin inhibited rat plasma DPP-IV activity in vitro with an IC(50) value of 2.00 nmol/l