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2643-85-8

2643-85-8 structure
2643-85-8 structure
  • Name: Oxypeucedanin hydrate
  • Chemical Name: Oxypeucedanin hydrate
  • CAS Number: 2643-85-8
  • Molecular Formula: C16H16O6
  • Molecular Weight: 304.295
  • Catalog: Research Areas Cancer
  • Create Date: 2018-02-25 08:00:00
  • Modify Date: 2024-01-01 18:27:03
  • Oxypeucedanin hydrate ((+)-Oxypeucedanin hydrate) is a natural product isolated from D. anethifolia. Prangol exhibits mild toxicity on fibroblasts and parental lymphoma cells[1].

Name Oxypeucedanin hydrate
Synonyms 4-[(2R)-2,3-Dihydroxy-3-methylbutoxy]-7H-furo[3,2-g]chromen-7-one
7H-Furo[3,2-g][1]benzopyran-7-one, 4-[(2R)-2,3-dihydroxy-3-methylbutoxy]-
oxypeucedaninhydrate
Description Oxypeucedanin hydrate ((+)-Oxypeucedanin hydrate) is a natural product isolated from D. anethifolia. Prangol exhibits mild toxicity on fibroblasts and parental lymphoma cells[1].
Related Catalog
References

[1]. Mottaghipisheh J, et al. Antiproliferative and cytotoxic activities of furocoumarins of Ducrosia anethifolia. Pharm Biol. 2018 Dec;56(1):658-664.

Density 1.4±0.1 g/cm3
Boiling Point 544.3±50.0 °C at 760 mmHg
Molecular Formula C16H16O6
Molecular Weight 304.295
Flash Point 283.0±30.1 °C
Exact Mass 304.094696
PSA 93.04000
LogP 1.31
Vapour Pressure 0.0±1.5 mmHg at 25°C
Index of Refraction 1.630
Storage condition 2-8℃

~92%

2643-85-8 structure

2643-85-8

Literature: Row; Brown; Stachulski; Lennard Organic and Biomolecular Chemistry, 2006 , vol. 4, # 8 p. 1604 - 1610

~%

2643-85-8 structure

2643-85-8

Literature: Row; Brown; Stachulski; Lennard Organic and Biomolecular Chemistry, 2006 , vol. 4, # 8 p. 1604 - 1610

~%

2643-85-8 structure

2643-85-8

Literature: Row; Brown; Stachulski; Lennard Organic and Biomolecular Chemistry, 2006 , vol. 4, # 8 p. 1604 - 1610

~%

2643-85-8 structure

2643-85-8

Literature: Row; Brown; Stachulski; Lennard Organic and Biomolecular Chemistry, 2006 , vol. 4, # 8 p. 1604 - 1610

~%

2643-85-8 structure

2643-85-8

Literature: Row; Brown; Stachulski; Lennard Organic and Biomolecular Chemistry, 2006 , vol. 4, # 8 p. 1604 - 1610
Precursor  5

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