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Chemical Structure| 1617-90-9 Chemical Structure| 1617-90-9

Structure of Vincamine
CAS No.: 1617-90-9

Chemical Structure| 1617-90-9

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Vincamine is a nootropic monoterpenoid indole alkaloid found in the leaves of Vinca minor (lesser periwinkle), which is used as a memory enhancing prescription medicine for the treatment of primary degenerative and vascular dementia.

Synonyms: Angiopac; Devincan; periwinkle extract

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Product Details of Vincamine

CAS No. :1617-90-9
Formula : C21H26N2O3
M.W : 354.44
SMILES Code : O=C([C@]1(O)N2C3=C(C4=C2C=CC=C4)CCN5[C@@]3([H])[C@](CCC5)(CC)C1)OC
Synonyms :
Angiopac; Devincan; periwinkle extract
MDL No. :MFCD00078054
InChI Key :RXPRRQLKFXBCSJ-GIVPXCGWSA-N
Pubchem ID :15376

Safety of Vincamine

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Isoform Comparison

Biological Activity

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6 mice LPS- or TNF-α-induced lung inflammation model Intraperitoneal injection 10 mg/kg Single dose, lasting 6 hours Vinpocetine significantly inhibited LPS- or TNF-α-induced lung inflammatory responses, including up-regulation of TNF-α, IL-1β, and MIP-2 mRNA expression, and reduced neutrophil infiltration. Proc Natl Acad Sci U S A. 2010 May 25;107(21):9795-800
Drosophila melanogaster DJ-1β mutant fly model Medium supplementation 10 μM During development and 5 days after eclosion Vincamine significantly reduced H2O2 levels and protein carbonylation levels in DJ-1β mutant flies, demonstrating an antioxidant effect. ACS Chem Neurosci. 2023 Jun 21;14(12):2294-2301
Mice STZ-induced type 1 diabetic mice and db/db type 2 diabetic mice Intraperitoneal injection 30 mg/kg/day Once daily for 4 weeks To evaluate the therapeutic potential of Vincamine in ameliorating diabetic peripheral neuropathy (DPN). Vincamine significantly ameliorated neurological dysfunctions, improved blood flow velocities and perfusion areas of foot pads and sciatic nerve tissues, protected against sciatic nerve myelin sheath injury, and ameliorated foot skin intraepidermal nerve fiber (IENF) density impairment in DPN mice. Acta Pharmacol Sin. 2023 Dec;44(12):2388-2403
Rats Bleomycin-induced pulmonary fibrosis model Oral 40 mg/kg Once daily for 9 days Vincamine showed a protective effect against EMT in BLM-induced pulmonary fibrosis through its antioxidant and anti-apoptotic activities. It activated the antioxidant status by elevating SOD and GPX activities. Furthermore, it exerted its anti-apoptotic activity via inhibiting p53/Bax/cleaved caspase 3 pathway. Moreover, vincamine attenuated EMT by suppressing TGF-β1/p38 MAPK/ERK1/2/TWIST/Snai1/Slug/fibronectin/N-cadherin pathway. Molecules. 2023 Jun 9;28(12):4665
Wistar rats Colon ligation puncture (CLP)-induced sepsis model Oral 40 mg/kg Once daily for 4 days To investigate the hepato-protective activity of vincamine during CLP-induced sepsis, results showed that vincamine significantly improved liver function, reduced oxidative stress, inflammation, and apoptosis Sci Rep. 2024 Aug 23;14(1):19572
Wistar rats ANIT-induced intrahepatic cholestasis Oral 40 mg/kg Once daily for 10 days Vincamine alleviated ANIT-induced intrahepatic cholestasis by modulating NF-kB/PDGF/klf6/PPARγ and PI3K/Akt pathways, improving liver function tests, inhibiting inflammation and oxidative stress, and reducing hepatocyte apoptosis. Naunyn Schmiedebergs Arch Pharmacol. 2024 Oct;397(10):7981-7994
Swiss albino mice Ehrlich solid carcinoma model Oral 40 mg/kg/day (VCN), 20 mg/kg/day (VCN-AgNPs) Once daily for 20 days VCN-AgNPs significantly inhibited tumor growth, reduced tumor volume and weight, and improved survival rate Cells. 2024 Oct 24;13(21):1762
Mice Models of opioid reward and relapse Intracerebroventricular administration 60 nmol Pretreatment 20 minutes prior Significantly prevented acute morphine-conditioned place preference (CPP) and stress-induced reinstatement of extinguished morphine-CPP J Med Chem. 2020 May 28;63(10):5119-5138
Male Wistar albino rats Renal ischemia/reperfusion injury (IRI) model Orally single dose of 120 mg/kg or multiple doses of 30 mg/kg Single dose once or multiple doses once daily for 6 days Vincamine alone or in combination with pantoprazole significantly reduced serum creatinine, urea nitrogen, and MDA levels, decreased the release of inflammatory factors TNF-α, IL-1β, and IL-6, and inhibited the MAPK and NF-κB signaling pathways, alleviating renal ischemia/reperfusion injury. Molecules. 2022 Feb 18;27(4):1383

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.82mL

0.56mL

0.28mL

14.11mL

2.82mL

1.41mL

28.21mL

5.64mL

2.82mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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