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3-Benzyl-7,8-dihydroxy-4-methyl-2H-chromen-2-one is a complex organic compound belonging to the flavonoid class, specifically a flavanone. It is characterized by a 2H-chromen-2-one core structure, which features a benzyl group at the 3-position, two hydroxyl groups at the 7 and 8 positions, and a methyl group at the 4-position. 3-Benzyl-7,8-dihydroxy-4-methyl-2H-chromen-2-one exhibits a range of biological activities, including antioxidant and anti-inflammatory properties, and is found in various plants. Its chemical structure endows it with potential therapeutic applications, particularly in the context of natural products research and development.

1658-77-1

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1658-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1658-77-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1658-77:
(6*1)+(5*6)+(4*5)+(3*8)+(2*7)+(1*7)=101
101 % 10 = 1
So 1658-77-1 is a valid CAS Registry Number.

1658-77-1Downstream Products

1658-77-1Relevant academic research and scientific papers

Inhibitor daphnetin derivative and application and pharmaceutical composition thereof

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Paragraph 0147-0155, (2020/11/25)

The invention provides an inhibitor daphnetin derivative and application and a pharmaceutical composition thereof. The daphnetin derivative (1-13) or the pharmaceutically acceptable salt or solvent compound thereof is shown as the following formula. The p

Syntheses and evaluation of daphnetin derivatives as novel G protein-coupled receptor inhibitors and activators

Wang, Yinan,Wang, Jiangming,Fu, Zhe,Sheng, Ruilong,Wu, Wenhui,Fan, Junting,Guo, Ruihua

, (2020/10/13)

A series of daphnetin (7,8-dihydroxycoumarin) derivatives 1–22 were synthesized including sixteen new compounds (1–5, 7–14, 18, 21 and 22) and six known compounds (6, 15–17, 19 and 20). Their pharmacological activities on G protein-coupled receptors (GPCRs) were evaluated by double antibody sandwich ELISA (DAS-ELISA) in vitro. Daphnetin derivatives with various substitution patterns/groups were obtained from inhibitors to activators on GPCRs. Derivatives 2–5, 8, 15, 16 and 18–20 possessed moderate activation potency on GPCRs. Among them, derivatives 3–5, 16 and 19 presented significant activation potency on GPCRs with EC50 values in the range of 1.18–1.91 nM. Derivatives 6, 11, 14 and 18 showed significant inhibitory potency on GPCRs with IC50 values in the range of 1.26–1.38 nM. Moreover, the structure-activity relationships (SARs) of daphnetin derivatives were discussed in detail. The new daphnetic-based GPCRs activators and inhibitors have potentials as future drug candidates for the treatment of metabolic diseases.

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