CAS 4880-92-6
:Apovincamine
Description:
Apovincamine is an alkaloid derived from the Vinca minor plant, commonly known as lesser periwinkle. It is characterized by its chemical structure, which includes a tetracyclic framework typical of many indole alkaloids. The substance is known for its potential pharmacological properties, particularly as a nootropic agent, which may enhance cognitive function and improve blood circulation in the brain. Apovincamine exhibits vasodilatory effects, making it useful in treating conditions related to cerebral insufficiency. It is often utilized in various formulations aimed at improving cognitive performance and memory. The compound is typically administered in the form of its salts, which can enhance its solubility and bioavailability. While it has been studied for its therapeutic effects, further research is necessary to fully understand its mechanisms of action and potential side effects. As with any pharmacological agent, it is essential to consider dosage and individual patient factors when evaluating its use in clinical settings.
Formula:C21H24N2O2
InChI:InChI=1S/C21H24N2O2/c1-3-21-10-6-11-22-12-9-15-14-7-4-5-8-16(14)23(18(15)19(21)22)17(13-21)20(24)25-2/h4-5,7-8,13,19H,3,6,9-12H2,1-2H3/t19-,21+/m1/s1
InChI key:InChIKey=OZDNDGXASTWERN-CTNGQTDRSA-N
SMILES:C(C)[C@]12[C@]3(C=4N(C=5C(C4CCN3CCC1)=CC=CC5)C(C(OC)=O)=C2)[H]
Synonyms:- (+)-cis-Apovincamine
- 1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine, eburnamenine-14-carboxylic acid deriv.
- Apovincamina
- Apovincamina [Spanish]
- Apovincamine [INN]
- Apovincaminum
- Apovincaminum [Latin]
- Eburnamenine-14-carboxylic acid, methyl ester, (3-alpha,16-alpha)-
- Eburnamenine-14-carboxylic acid, methyl ester, (3α,16α)-
- Methyl (13aS,13bS)-13a-ethyl-2,3,4,6,13a,14b-hexahydro-1H-indilol(3.2.1-de)pyrido(3,2,1-ij)(1,5)naphthylridin-12-carboxylat
- Methyl (3α,16α)-eburnamenine-14-carboxylate
- Methyl(3alpha,16alpha)-eburnamenine-14-carboxylate
- Unii-504R182Zx7
- Apovincamine
- See more synonyms
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Found 8 products.
Vinpocetine Related Compound B (Methyl(13aS,13bS)-13a-ethyl-2,3,5,6,13a,13b-hexahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]-naphthyridine-12-carboxylate)
CAS:Vegetable alkaloids, natural or reproduced by synthesis, their salts and other derivatives, nesoiFormula:C21H24N2O2Color and Shape:PowderMolecular weight:336.18378Apovincamine
CAS:<p>Apovincamine is a vinca alkaloid and a chemical precursor of Vinpocetine, which is a derivative of Vincamine with vasodilating activity.</p>Formula:C21H24N2O2Purity:98%Color and Shape:SolidMolecular weight:336.44Vinpocetine EP Impurity B (Vincamine EP Impurity D)
CAS:Controlled ProductFormula:C21H24N2O2Color and Shape:NeatMolecular weight:336.43cis-Apovincamine-d3
CAS:Controlled Product<p>Applications cis-Apovincamine-d3 is labelled cis-Apovincamine (A729245) which is a vinca alkaloid and a chemical precursor of Vinpocetine (V332500), a derivative of Vincamine with vasodilating activity. Vasodilator (cerebral).<br>References Han, et al.: J. Biol. Chem., 274, 22337 (1999), O’Donnell, et al.: Pharmacol. Biochem. Behav., 63, 185 (1999),<br></p>Formula:C21D3H21N2O2Color and Shape:NeatMolecular weight:339.446cis-Apovincamine
CAS:Controlled Product<p>Impurity Vinpocetine USP Related Compound B<br>Applications cis-Apovincamine (Vinpocetine USP Related Compound B), is a vinca alkaloid and a chemical precursor of Vinpocetine (V332500), a derivative of Vincamine with vasodilating activity. Vasodilator (cerebral).<br>References Han, et al.: J. Biol. Chem., 274, 22337 (1999), O’Donnell, et al.: Pharmacol. Biochem. Behav., 63, 185 (1999),<br></p>Formula:C21H24N2O2Color and Shape:NeatMolecular weight:336.43
