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4H-1-Benzopyran-4-one, 7-[2-(diethylamino)ethoxy]-3-(4-methoxyphenyl)- is a complex organic compound belonging to the class of benzopyran derivatives. It features a benzopyran-4-one core structure, with a diethylaminoethoxy group at the 7-position and a 4-methoxyphenyl group at the 3-position. 4H-1-Benzopyran-4-one, 7-[2-(diethylamino)ethoxy]-3-(4-methoxyphenyl)- is known for its potential pharmacological properties, particularly as a serotonin receptor agonist. It is used in the synthesis of various drugs and has been studied for its effects on the central nervous system. The specific arrangement of functional groups in this molecule contributes to its unique chemical and biological activities, making it a subject of interest in medicinal chemistry and drug development.

6650-31-3

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6650-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6650-31-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,5 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6650-31:
(6*6)+(5*6)+(4*5)+(3*0)+(2*3)+(1*1)=93
93 % 10 = 3
So 6650-31-3 is a valid CAS Registry Number.

6650-31-3Downstream Products

6650-31-3Relevant academic research and scientific papers

Synthetic analogs of daidzein, having more potent osteoblast stimulating effect

Yadav, Dinesh K.,Gautam, Abnish K.,Kureel, Jyoti,Srivastava, Kamini,Sahai, Mahendra,Singh, Divya,Chattopadhyay, Naibedya,Maurya, Rakesh

supporting information; experimental part, p. 677 - 681 (2011/03/18)

A series of didzein derivatives were synthesized and assessed for stimulation of osteoblast differentiation using primary cultures of rat calvarial osteoblasts. Data suggested that three synthetic analogs, 1c, 3a and 3c were several folds more potent than daidzein in stimulating differentiation and mineralization of osteoblasts. Further, these three compounds did not show any estrogen agonistic activity, however had mild estrogen antagonistic effect. Out of the three compounds, 3c was found to maximally increase the mineralization of bone marrow osteoprogenitor cells. Compound 3c also robustly increased the mRNA levels of osteogenic genes including bone morphogenetic protein-2 and osteocalcin in osteoblasts. Unlike daidzein, 3c did not inhibit osteoclastogenesis. Collectively, we demonstrate osteogenic activity of daidzein analogs at significantly lower concentrations than daidzein.

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