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Vincamine

Catalog No.
C3338
An alkaloid with cerebral vasodilatory effects and improved glucose homeostasis.
Grouped product items
SizePriceStock Qty
500mg
$50.00
In stock
1g
$63.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Background

Vincamine (CAS No.: 1617-90-9) is a naturally occurring monoterpenoid indole alkaloid isolated from the leaves of Vinca minor and related species, widely studied in biomedical research for its vasoactive and neurovascular regulatory properties. It functions primarily as a peripheral vasodilator with selective effects on cerebral microcirculation, enhancing regional cerebral blood flow and oxygen delivery, which underpins its investigation in models of cerebrovascular and metabolic disorders. Mechanistically, vincamine has been reported to modulate vascular tone and exhibit activity as a GPR40 agonist, contributing to β-cell protection, improved glucose-stimulated insulin secretion, and enhanced glucose homeostasis in metabolic disease models. In vitro studies indicate pharmacological activity in the low micromolar range in cerebrovascular tissues, supporting its utility in probing smooth muscle responsiveness and microvascular function. Vincamine is commonly employed in cellular and animal studies to investigate neuroprotection, cerebral ischemia, and metabolic regulation, as well as in drug discovery programs targeting vascular dysfunction and type 2 diabetes, with experimental concentrations or dosing regimens varying according to specific study designs and endpoints.

Chemical Properties

Physical AppearanceA solid
Storage-20°C
M.Wt354.44
Cas No.1617-90-9
FormulaC21H26N2O3
SynonymsAngiopac; Devincan; Equipur; Minorin; NSC 91998; Novicet; Oxybral; Perval; Sostenil; Tripervan
Solubility≥9.11 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O
Chemical Name(41S,12S,13aS)-methyl 13a-ethyl-12-hydroxy-2,3,41,5,6,12,13,13a-octahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylate
Canonical SMILESCC[C@]1(CCC2)C[C@@](C(OC)=O)(O)N3C4=CC=CC=C4C5=C3[C@@]1([H])N2CC5
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

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