109741-24-4 Usage
Description
Apovincaminic Acid Ethyl Ester N-Oxide is a metabolite of Vinpocetine (V332502), a vasodilator cerebral. It is a chemical compound derived from the parent compound Vinpocetine, which is known for its ability to improve blood flow in the brain and enhance cognitive function.
Uses
Used in Pharmaceutical Industry:
Apovincaminic Acid Ethyl Ester N-Oxide is used as a vasodilator for improving blood flow in the brain. It is employed in the development of medications aimed at enhancing cognitive function and treating conditions related to reduced cerebral blood flow.
Used in Cognitive Enhancement:
Apovincaminic Acid Ethyl Ester N-Oxide is used as a cognitive enhancer for improving memory, focus, and overall brain function. Its ability to increase blood flow in the brain may contribute to better cognitive performance and support brain health.
Used in Neuroprotection:
Apovincaminic Acid Ethyl Ester N-Oxide is used as a neuroprotective agent for safeguarding the brain against damage caused by various factors, such as oxidative stress, inflammation, and neurodegenerative diseases. Its vasodilatory properties may help maintain optimal brain function and protect against age-related cognitive decline.
Check Digit Verification of cas no
The CAS Registry Mumber 109741-24-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,7,4 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109741-24:
(8*1)+(7*0)+(6*9)+(5*7)+(4*4)+(3*1)+(2*2)+(1*4)=124
124 % 10 = 4
So 109741-24-4 is a valid CAS Registry Number.
109741-24-4Relevant articles and documents
Synthesis of vinca alkaloids and related compounds XXXVIII. Formation of dimers under Polonovski reaction conditions
Moldvai, Istvan,Szantay, Csaba,Toth, Gabor,Vedres, Andras,Kalman, Alajos,Szantay, Csaba
, p. 335 - 342 (2007/10/02)
The dimeric products (1a-c) have ben prepared by treatment of N-oxides derived from some indole alkaloids.Their structures have been elucidated by detailed NMR investigations and the structure of 1c determined by X-ray analysis.The importance of the E2-type trans-axial elimination of the N-acyloxy intermediate in the dimer formation has also been established.The iminium salts 4a-b and the derived pseudocyanide 6 have been prepared.
