262368-44-5 Usage
Description
(R)-[1-(4-aminophenyl)ethyl]carbamic acid tert-butyl ester, commonly known as rufinamide, is a chemical compound with the molecular formula C10H19N3O2. It is a derivative of carbamic acid and is characterized by its anti-epileptic properties. Rufinamide is used to treat seizures, particularly those associated with Lennox-Gastaut syndrome, by inhibiting sodium channels in the brain and stabilizing electrical activity.
Uses
Used in Pharmaceutical Industry:
Rufinamide is used as an anti-epileptic drug for the treatment of seizures, specifically those related to Lennox-Gastaut syndrome. It functions by targeting and inhibiting sodium channels in the brain, which helps to stabilize electrical activity and reduce the frequency of seizures. This application is due to its ability to modulate the electrical activity in the brain, providing a therapeutic effect for patients suffering from this neurological condition.
Additionally, rufinamide is often prescribed in combination with other medications to maximize its effectiveness in managing epilepsy. This combination therapy approach is used to enhance the overall treatment strategy and improve the quality of life for patients with epilepsy.
Check Digit Verification of cas no
The CAS Registry Mumber 262368-44-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,2,3,6 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 262368-44:
(8*2)+(7*6)+(6*2)+(5*3)+(4*6)+(3*8)+(2*4)+(1*4)=145
145 % 10 = 5
So 262368-44-5 is a valid CAS Registry Number.
262368-44-5Relevant articles and documents
SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH
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Page/Page column 47, (2009/04/24)
The present invention relates to a compound of the formula I wherein R1 to R6, A, B, n and m are as defined herein. Such novel sulfonyl amide derivatives are useful in the treatment of abnormal cell growth, such as cancer, in mammals. This invention also relates to a method of using such compounds in the treatment of abnormal cell growth in mammals, especially humans, and to pharmaceutical compositions containing such compounds.
Chain-branched 1,3-dibenzylthioureas as vanilloid receptor 1 antagonists
Ryu, Chong Hyun,Jang, Mi Jung,Jung, Jeong Wha,Park, Ju-Hyun,Choi, Hye Young,Suh, Young-Ger,Oh, Uhtaek,Park, Hyeung-Geun,Lee, Jeewoo,Koh, Hyun-Joo,Mo, Joo-Hyun,Joo, Yung Hyup,Park, Young-Ho,Kim, Hee-Doo
, p. 1751 - 1755 (2007/10/03)
A series of chain-branched 1,3-dibenzylthiourea derivatives were synthesized, and tested their antagonist activity against vanilloid receptor 1. Chain-branching led to a significant change in the mode of action and the potency. (R)-Methyl or ethyl-branched 1,3-dibenzylthiourea derivatives showed the most potent antagonist activity up to the IC50 value of 0.05 μM which is 10-fold more potent than capsazepine.