59163-53-0

59163-53-0 structure
59163-53-0 structure
  • Name: Aloenin aglycone
  • Chemical Name: 6-(2,4-dihydroxy-6-methylphenyl)-4-methoxypyran-2-one
  • CAS Number: 59163-53-0
  • Molecular Formula: C13H12O5
  • Molecular Weight: 248.23100
  • Catalog: Signaling Pathways Immunology/Inflammation NO Synthase
  • Create Date: 2016-11-05 10:48:12
  • Modify Date: 2024-01-08 18:31:00
  • Aloenin aglycone (compound 13) is an NF-κB inhibitor that can be isolated from aloe exudate. Aloenin aglycone inhibits TNFα-induced NF-κB transcriptional activity (IC50: 18.7 μM). Aloenin aglycone (10 μM) also reduced inducible nitric oxide synthase (iNOS) and intercellular adhesion molecule 1 (ICAM-1) gene expression after treatment of HepG2 cells with 10 ng/mL TNFα[1].

Name 6-(2,4-dihydroxy-6-methylphenyl)-4-methoxypyran-2-one
Synonyms 4-methoxy-6-(2',4'-dihydroxy-6'-methylphenyl)pyran-2-one
Aloenin-Aglycon
6-(2',4'-dihydroxy-6'-methylphenyl)-4-methoxy-2-pyrone
6-(2,4-dihydroxy-6-methyl-phenyl)-4-methoxy-pyran-2-one
2H-Pyran-2-one,6-(2,4-dihydroxy-6-methylphenyl)-4-methoxy
aloenin aglycone
Description Aloenin aglycone (compound 13) is an NF-κB inhibitor that can be isolated from aloe exudate. Aloenin aglycone inhibits TNFα-induced NF-κB transcriptional activity (IC50: 18.7 μM). Aloenin aglycone (10 μM) also reduced inducible nitric oxide synthase (iNOS) and intercellular adhesion molecule 1 (ICAM-1) gene expression after treatment of HepG2 cells with 10 ng/mL TNFα[1].
Related Catalog
Target

intercellular adhesion molecule-1 (ICAM-1)[1]

References

[1]. Sun Y N, et al. Isolation and identification of chromone and pyrone constituents from Aloe and their anti-inflammatory activities[J]. Journal of Functional Foods, 2016, 21: 232-239.

[2]. Sun Y N. et al. Isolation and identification of chromone and pyrone constituents from Aloe and their anti-inflammatory activities[J]. Journal of Functional Foods, 2016, 21: 232-239.

Molecular Formula C13H12O5
Molecular Weight 248.23100
Exact Mass 248.06800
PSA 79.90000
LogP 2.03500

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59163-53-0 structure

59163-53-0

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59163-53-0 structure

59163-53-0

Literature: Bringmann; Schneider 1985 , vol. 1985, # 4 p. 765 - 774

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59163-53-0 structure

59163-53-0

Literature: Bringmann; Schneider 1985 , vol. 1985, # 4 p. 765 - 774

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59163-53-0 structure

59163-53-0

Literature: Bringmann; Schneider 1985 , vol. 1985, # 4 p. 765 - 774

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59163-53-0 structure

59163-53-0

Literature: Bringmann; Schneider 1985 , vol. 1985, # 4 p. 765 - 774

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59163-53-0 structure

59163-53-0

Literature: Bringmann; Schneider 1985 , vol. 1985, # 4 p. 765 - 774

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59163-53-0 structure

59163-53-0

Literature: Bringmann; Schneider 1985 , vol. 1985, # 4 p. 765 - 774

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59163-53-0 structure

59163-53-0

Literature: Conner, John M.; Gray, Alexander I.; Reynolds, Tom; Waterman, Peter G. Phytochemistry (Elsevier), 1987 , vol. 26, # 11 p. 2995 - 2998