2'-Methoxykurarinone

Modify Date: 2024-01-10 09:08:37

2'-Methoxykurarinone Structure
2'-Methoxykurarinone structure
Common Name 2'-Methoxykurarinone
CAS Number 270249-38-2 Molecular Weight 452.539
Density 1.171±0.06 g/cm3 (20 ºC 760 Torr) Boiling Point 643.6±55.0 °C at 760 mmHg
Molecular Formula C27H32O6 Melting Point 112-115 ºC
MSDS N/A Flash Point 213.2±25.0 °C

 Use of 2'-Methoxykurarinone


(2S)-2'-Methoxykurarinone, a compound isolated from the roots of Sophora flavescens, has anti-inflammatory, antipyretic, antidiabetic, and antineoplastic effects. (2S)-2'-Methoxykurarinone (MK) inhibits osteoclastogenesis and bone resorption through down-regulation of RANKL signaling. (2S)-2'-Methoxykurarinone (MK) displays cytotoxic activity against human myeloid leukemia HL-60 cells[1][2].

 Names

Name 2'-O-Methylkurarinone
Synonym More Synonyms

 2'-Methoxykurarinone Biological Activity

Description (2S)-2'-Methoxykurarinone, a compound isolated from the roots of Sophora flavescens, has anti-inflammatory, antipyretic, antidiabetic, and antineoplastic effects. (2S)-2'-Methoxykurarinone (MK) inhibits osteoclastogenesis and bone resorption through down-regulation of RANKL signaling. (2S)-2'-Methoxykurarinone (MK) displays cytotoxic activity against human myeloid leukemia HL-60 cells[1][2].
Related Catalog
References

[1]. Kim JY, et al. (2S)-2'-Methoxykurarinone inhibits osteoclastogenesis and bone resorption through down-regulation of RANKL signaling. Biol Pharm Bull. 2014;37(2):255-61.

[2]. Kang TH, et al. Cytotoxic lavandulyl flavanones from Sophora flavescens. J Nat Prod. 2000 May;63(5):680-1.

 Chemical & Physical Properties

Density 1.171±0.06 g/cm3 (20 ºC 760 Torr)
Boiling Point 643.6±55.0 °C at 760 mmHg
Melting Point 112-115 ºC
Molecular Formula C27H32O6
Molecular Weight 452.539
Flash Point 213.2±25.0 °C
Exact Mass 452.219879
PSA 85.22000
LogP 7.05
Vapour Pressure 0.0±2.0 mmHg at 25°C
Index of Refraction 1.575
Water Solubility Insuluble (2.6E-4 g/L) (25 ºC)

 Safety Information

Hazard Codes Xi

 Synonyms

4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-8-[(2R)-5-methyl-2-(1-methylethenyl)-4-hexen-1-yl]-, (2S)-
(2S)-7-Hydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-[(2R)-2-isopropenyl-5-methyl-4-hexen-1-yl]-5-methoxy-2,3-dihydro-4H-chromen-4-one
Kurarinone, 2'-O-methyl-
2'-Methoxykurarinone
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