CAS 57327-92-1
:1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylic acid, 13a-ethyl-2,3,5,6,12,13,13a,13b-octahydro-, ethyl ester, (12R,13aS,13bS)-
Description:
1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylic acid, 13a-ethyl-2,3,5,6,12,13,13a,13b-octahydro-, ethyl ester, with CAS number 57327-92-1, is a complex organic compound characterized by its multi-ring structure that incorporates indole and pyridine moieties. This compound features a carboxylic acid functional group, which contributes to its acidic properties, and an ethyl ester group that enhances its solubility in organic solvents. The stereochemistry indicated by the (12R,13aS,13bS) configuration suggests specific spatial arrangements of its substituents, which can influence its biological activity and reactivity. The presence of multiple fused rings typically suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to their ability to interact with biological targets. Additionally, the octahydro structure indicates that the compound is saturated, which may affect its stability and reactivity compared to unsaturated analogs. Overall, this compound's unique structural features make it of interest for further research in various chemical and biological contexts.
Formula:C22H28N2O2
InChI:InChI=1S/C22H28N2O2/c1-3-22-11-7-12-23-13-10-16-15-8-5-6-9-17(15)24(19(16)20(22)23)18(14-22)21(25)26-4-2/h5-6,8-9,18,20H,3-4,7,10-14H2,1-2H3/t18-,20-,22+/m1/s1
InChI key:InChIKey=UJAQRLRRCXIJFW-UZKOGDIHSA-N
SMILES:C(C)[C@]12[C@]3(C=4N(C=5C(C4CCN3CCC1)=CC=CC5)[C@@H](C(OCC)=O)C2)[H]
Synonyms:- Eburnamenine-14-carboxylic acid, 14,15-dihydro-, ethyl ester, (3α,14α,16α)-
- (-)-(14α)-Dihydrovinpocetine
- 1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine, eburnamenine-14-carboxylic acid deriv.
- Ethyl 14,15-dihydroapovincaminate
- 1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylic acid, 13a-ethyl-2,3,5,6,12,13,13a,13b-octahydro-, ethyl ester, (12R,13aS,13bS)-
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Found 6 products.
Vinpocetine Related Compound D (ethyl(12R,13aS,13bS)-13a-ethyl-2,3,5,6,12,13,13a,13b-octahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylate)
CAS:Other alkaloids,natural or reproduced by synthesis, and their salts, ethers,esters&other derivatives, nesoiFormula:C22H28N2O2Color and Shape:PowderMolecular weight:352.21508(-)-(14α)-Dihydrovinpocetine-d5
CAS:Controlled ProductFormula:C22D5H23N2O2Color and Shape:NeatMolecular weight:357.501(-)-Dihydroapovincaminic Acid Ethyl Ester
CAS:Controlled Product<p>Impurity Vinpocetine USP Related Compound D<br>Applications (-)-Dihydroapovincaminic Acid Ethyl Ester, can be used as a chiral modifier in enantioselective heterogeneous catalytic hydrogenations. It is also structurally related to Vinpocetine (V332500), a Vasodilator (cerebral). Vinpocetine USP Related Compound D<br>References Tungler, A., et al.: Tetrahedron: Asymmetry, 6, 2395 (1995);<br></p>Formula:C22H28N2O2Color and Shape:NeatMolecular weight:352.47



