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C32H28FN5O4S, also known as Ramelteon, is a synthetic compound that functions as a melatonin receptor agonist. It is characterized by its chemical structure comprising 32 carbon atoms, 28 hydrogen atoms, 1 fluorine atom, 5 nitrogen atoms, 4 oxygen atoms, and 1 sulfur atom. Ramelteon is instrumental in regulating the sleep-wake cycle by binding to melatonin receptors in the brain. With a molecular weight of 585.66 g/mol, C32H28FN5O4S is available in oral tablet form and is recommended for short-term use to promote healthy sleep patterns.

1264908-75-9

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1264908-75-9 Usage

Uses

Used in Pharmaceutical Industry:
C32H28FN5O4S is used as a sleep aid for individuals experiencing difficulty falling asleep due to its melatonin receptor agonist properties. It helps regulate the sleep-wake cycle, making it an essential pharmacological agent for treating insomnia and promoting restful sleep.
Used in Sleep Management:
Ramelteon is utilized as a therapeutic agent for managing sleep disorders, particularly insomnia. It is taken once daily before bedtime to facilitate the onset of sleep, making it a valuable tool for individuals with sleep initiation issues.
Used in Insomnia Treatment:
In the medical field, C32H28FN5O4S is used as a treatment for insomnia, specifically for patients who have trouble falling asleep. Its mechanism of action involves binding to melatonin receptors in the brain, which aids in the regulation of the sleep-wake cycle, thus improving sleep quality and duration.

Check Digit Verification of cas no

The CAS Registry Mumber 1264908-75-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,4,9,0 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1264908-75:
(9*1)+(8*2)+(7*6)+(6*4)+(5*9)+(4*0)+(3*8)+(2*7)+(1*5)=179
179 % 10 = 9
So 1264908-75-9 is a valid CAS Registry Number.

1264908-75-9Downstream Products

1264908-75-9Relevant academic research and scientific papers

Inhibitors of HCV NS5A: From iminothiazolidinones to symmetrical stilbenes

Romine, Jeffrey L.,St. Laurent, Denis R.,Leet, John E.,Martin, Scott W.,Serrano-Wu, Michael H.,Yang, Fukang,Gao, Min,O'Boyle, Donald R,Lemm, Julie A.,Sun, Jin-Hua,Nower, Peter T.,Huang, Xiaohua,Deshpande, Milind S.,Meanwell, Nicholas A.,Snyder, Lawrence B.

, p. 224 - 229 (2011/04/26)

The iminothiazolidinone BMS-858 (2) was identified as a specific inhibitor of HCV replication in a genotype 1b replicon assay via a high-throughput screening campaign. A more potent analogue, BMS-824 (18), was used in resistance mapping studies, which rev

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