MW: 350.46
CAS: 42971-09-5
TNP NUMBER: TNP00160
MDL NUMBER: MFCD02114513
Smiles: c1ccc2c(c1)c1c3[C@H]4(N(CC1)CCC[C]4(C=C(n23)C(=O)OCC)CC)
THERAPEUTIC CATEGORY: Vasodilator
SOURCE: Derivative of vincamine - major indole alkaloid of Vinca minor L., Apocynaceae
ACCEPTORS: 2
DONORS: 0
ROTATION BONDS: 3
N+O: 4
Chiral Centers: 2
LogP: 6.37
LogS: -5.67
LIPINSKI: 3
Synonyms: 3A,16A-APOVINCAMINIC ACID ETHYL ESTER;(3A,16A)-EBURNAMENINE-14-CARBOXYLIC ACID ETHYL ESTER;CAVINTON;ETHYL APOVINCAMIN-22-OATE;EBURNAMENINE;EBURNAMENINE-14-CARBOXYLIC ACID ETHYL ESTER;RGH-4405;VINPOCETIN
CAS:42971-09-5
MF:C22H26N2O2
MW:350.45
EINECS:256-028-0
Product Categories:Active Pharmaceutical Ingredients;All Inhibitors;Inhibitors;Intermediates & Fine Chemicals;Pharmaceuticals;Cyclic Nucleotide related Vinpocetine
Chemical Properties: mp 147-153 C dec. storage temp. Store at RT solubility DMSO: 5 mg/mL form solid color white NIST Chemistry ReferenceVinpocetine(42971-09-5) Xn Risk Statements 22 Safety Statements 36 WGK Germany 3 RTECS JW4792000 Ethyl (3alpha,16alpha)-eburnamenine-14-carboxylate Vinpocetine
Usage And Synthesis:
Chemical Properties: White Crystalline Solid UsageA calcium/calmodulin-dependent phosphodiesterase 1 (PDE1) inhibitor Biological ActivityPhosphodiesterase inhibitor, selective for PDE1 (IC 50 = 21 u M). Also blocks voltage-gated Na + channels. Vinpocetine
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