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  • Product Name: Obtusifolin
  • Price: ¥600.0/5mg
  • Purity: 98.0%
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  • Contact: Xueping-Zheng


477-85-0

477-85-0 structure
477-85-0 structure
  • Name: Obtusifolin
  • Chemical Name: 2,8-dihydroxy-1-methoxy-3-methylanthracene-9,10-dione
  • CAS Number: 477-85-0
  • Molecular Formula: C16H12O5
  • Molecular Weight: 284.263
  • Catalog: Organic raw materials Terpenoid
  • Create Date: 2018-03-26 08:00:00
  • Modify Date: 2024-01-07 18:58:47
  • Obtusifolin, isolated from the seeds of Cassia obtusifolia, regulates the gene expression and production of MUC5AC mucin in airway epithelial cells via inhibiting NF-kB pathway[1]. Obtusifolin suppresses phthalate esters-induced breast cancer bone metastasis by targeting parathyroid hormone-related protein[2].

Name 2,8-dihydroxy-1-methoxy-3-methylanthracene-9,10-dione
Synonyms Anthraquinone,2,8-dihydroxy-1-methoxy-3-methyl
2,8-dihydroxy-1-methoxy-3-methyl-anthraquinone
Anthraquinone, 2,8-dihydroxy-1-methoxy-3-methyl-
9,10-Anthracenedione, 2,8-dihydroxy-1-methoxy-3-methyl-
2,8-Dihydroxy-1-methoxy-3-methyl-anthrachinon
obtusifoline
Obtusifolin (anthraquinone)
1,7-Dihydroxy-8-methoxy-6-methyl-9,10-anthraquinone
2,8-Dihydroxy-1-methoxy-3-methyl-9,10-anthraquinone
Obtusifolin
2,8-dihydroxy-1-methoxy-3-methylanhraquinone
2,8-Dihydroxy-1-methoxy-3-methyl-9,10-anthracenedione
Description Obtusifolin, isolated from the seeds of Cassia obtusifolia, regulates the gene expression and production of MUC5AC mucin in airway epithelial cells via inhibiting NF-kB pathway[1]. Obtusifolin suppresses phthalate esters-induced breast cancer bone metastasis by targeting parathyroid hormone-related protein[2].
Related Catalog
Target

NF-κB

In Vitro Obtusifolin (1, 10, 100 μM) inhibits MUC5AC gene expression induced by EGF, PMA, or TNF-α in NCI-H292 cells[1].
References

[1]. Choi BS, et al. Obtusifolin isolated from the seeds of Cassia obtusifolia regulates the gene expression and production of MUC5AC mucin in airway epithelial cells via affecting NF-κB pathway. Phytother Res. 2019 Apr;33(4):919-928.

[2]. Hsu YL, et al. Obtusifolin suppresses phthalate esters-induced breast cancer bone metastasis by targeting parathyroid hormone-related protein. J Agric Food Chem. 2014 Dec 10;62(49):11933-40.

Density 1.448±0.06 g/cm3
Boiling Point 528.0±50.0 °C at 760 mmHg
Melting Point 242-243ºC
Molecular Formula C16H12O5
Molecular Weight 284.263
Flash Point 202.2±23.6 °C
Exact Mass 284.068481
PSA 83.83000
LogP 4.18
Vapour Pressure 0.0±1.4 mmHg at 25°C
Index of Refraction 1.678
Storage condition -20℃
Water Solubility Insuluble (2.6E-3 g/L) (25 ºC)

~0%

477-85-0 structure

477-85-0

Literature: Cameron, Donald W.; Feutrill, Geoffrey I.; Gamble, Glenn B.; Stavrakis, John Tetrahedron Letters, 1986 , vol. 27, # 41 p. 4999 - 5002

~%

477-85-0 structure

477-85-0

Literature: Cameron, Donald W.; Feutrill, Geoffrey I.; Gamble, Glenn B.; Stavrakis, John Tetrahedron Letters, 1986 , vol. 27, # 41 p. 4999 - 5002

~98%

477-85-0 structure

477-85-0

Literature: Camerom, Donald W.; Feutrill, Geoffrey I.; Keep, Philip L. C. Tetrahedron Letters, 1989 , vol. 30, # 38 p. 5173 - 5176

~60%

477-85-0 structure

477-85-0

Literature: Cameron, Donald W.; Feutrill, Geoffrey I.; Gamble, Glenn B.; Stavrakis, John Tetrahedron Letters, 1986 , vol. 27, # 41 p. 4999 - 5002

~%

477-85-0 structure

477-85-0

Literature: Cameron, Donald W.; Feutrill, Geoffrey I.; Gamble, Glenn B.; Stavrakis, John Tetrahedron Letters, 1986 , vol. 27, # 41 p. 4999 - 5002

~%

477-85-0 structure

477-85-0

Literature: Camerom, Donald W.; Feutrill, Geoffrey I.; Keep, Philip L. C. Tetrahedron Letters, 1989 , vol. 30, # 38 p. 5173 - 5176

~%

477-85-0 structure

477-85-0

Literature: Camerom, Donald W.; Feutrill, Geoffrey I.; Keep, Philip L. C. Tetrahedron Letters, 1989 , vol. 30, # 38 p. 5173 - 5176

~%

477-85-0 structure

477-85-0

Literature: Camerom, Donald W.; Feutrill, Geoffrey I.; Keep, Philip L. C. Tetrahedron Letters, 1989 , vol. 30, # 38 p. 5173 - 5176

~%

477-85-0 structure

477-85-0

Literature: Krohn, Carsten; Khanbabaee, Karamali Liebigs Annalen der Chemie, 1993 , # 8 p. 905 - 910