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  • Product Name: Ononetin
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  • Purity: 98.0%
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487-49-0

487-49-0 structure
487-49-0 structure
  • Name: Ononetin
  • Chemical Name: 1-(2,4-dihydroxyphenyl)-2-(4-methoxyphenyl)ethanone
  • CAS Number: 487-49-0
  • Molecular Formula: C15H14O4
  • Molecular Weight: 258.26900
  • Catalog: Signaling Pathways Membrane Transporter/Ion Channel TRP Channel
  • Create Date: 2017-11-04 18:24:37
  • Modify Date: 2024-01-14 18:14:23
  • Ononetin, a natural deoxybenzoin, is a potent and selective TRPM3 channel blocker with an IC50 of 0.3 μM[1].

Name 1-(2,4-dihydroxyphenyl)-2-(4-methoxyphenyl)ethanone
Synonyms Phenobarbital sodium salt
2,4-dihydroxy-4'-methoxy deoxybenzoin
Description Ononetin, a natural deoxybenzoin, is a potent and selective TRPM3 channel blocker with an IC50 of 0.3 μM[1].
Related Catalog
Target

TRPM3:0.3 μM (IC50)

In Vitro Ononetin (1-10 μM) completely and reversibly abrogates Ca2+ entry and ionic currents through recombinantly expressed TRPM3α2 and block the pregnenolone sulphate-inducible Ca2+ entry in primary cultures of mouse or rat dorsal root ganglia (DRG) neurones, indicating biological activity towards endogenously expressed TRPM3[1]. Oxidative intermediates of Ononetin may be involved in activating TRPA1, but not in the block of TRPM3 by Ononetin[1].
In Vivo Ononetin (10 mg/kg, i.p.) treatment completely reverses established Freund's Complete Adjuvant (FCA)-induced heat hypersensitivity, demonstrating that the loss of hypersensitivity in Trpm3-/- mice is unlikely to be caused by developmental or compensatory mechanisms and suggests that TRPM3 may be a tractable target for inflammatory pain[2].
References

[1]. I Straub, et al. Citrus fruit and fabacea secondary metabolites potently and selectively block TRPM3. Br J Pharmacol. 2013 Apr;168(8):1835-50.

[2]. Omar Alkhatib, et al. Promiscuous G-Protein-Coupled Receptor Inhibition of Transient Receptor Potential Melastatin 3 Ion Channels by Gβγ Subunits. J Neurosci. 2019 Oct 2;39(40):7840-7852.

Density 1.275g/cm3
Boiling Point 464.7ºC at 760mmHg
Melting Point 158.0-162.0°C
Molecular Formula C15H14O4
Molecular Weight 258.26900
Flash Point 176.9ºC
Exact Mass 258.08900
PSA 66.76000
LogP 2.53180
Vapour Pressure 2.95E-09mmHg at 25°C
Index of Refraction 1.62
HS Code 2914509090

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Literature: Waehaelae, Kristiina; Hase, Tapio A. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1991 , # 12 p. 3005 - 3008

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Literature: HANBUL COSMETIC CO., LTD. Patent: WO2005/54169 A1, 2005 ; Location in patent: Page/Page column 8; 9 ;

~94%

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Literature: Pazenok, Sergii; Lui, Norbert Patent: US2010/121082 A1, 2010 ; Location in patent: Page/Page column 2 ;

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Literature: Walz Justus Liebigs Annalen der Chemie, 1931 , vol. 489, p. 118,127, 140

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Literature: Virtanen; Hietala Acta Chemica Scandinavica (1947-1973), 1958 , vol. 12, p. 579 Full Text Show Details Bradbury; White Journal of the Chemical Society, 1951 , p. 3447 Full Text Show Details Bose; Siddiqui Journal of Scientific and Industrial Research, 1951 , vol. 10 B, p. 291,292

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Literature: Whalley Journal of the Chemical Society, 1957 , p. 1833,1834

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487-49-0 structure

487-49-0

Literature: Whalley Journal of the Chemical Society, 1957 , p. 1833,1834

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487-49-0 structure

487-49-0

Literature: Baker; Eastwood Journal of the Chemical Society, 1929 , p. 2907

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487-49-0 structure

487-49-0

Literature: Whalley Journal of the Chemical Society, 1957 , p. 1833,1834
HS Code 2914509090
Summary HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%