ChemicalBook--->CAS DataBase List--->27570-38-3

27570-38-3

27570-38-3 Structure

27570-38-3 Structure
IdentificationBack Directory
[Name]

(22R)-5α,17α-Dihydroxy-6α,7α:22,26-diepoxyergosta-2,24-diene-1,26-dione
[CAS]

27570-38-3
[Synonyms]

Withanone
NSC 179884
WITHANONE(SH)
WITHANONE(SH)(NEW)
Withanone 27570-38-3
WITHANONE(P)(NEW)(27570-38-3)
(22R)-5α,17α-Dihydroxy-6α,7α:22,26-diepoxyergosta-2,24-diene-1,26-dione
(22R)-6α,7α-Epoxy-5,17,22-trihydroxy-1-oxo-5α-ergosta-2,24-dien-26-oic acid δ-lactone
(5a,6a,7a,22R)-6,7-Epoxy-5,17,22-trihydroxy-1-oxoergosta-2,24-dien-26-oic acid d-lactone
Ergosta-2,24-dien-26-oicacid, 6,7-epoxy-5,17,22-trihydroxy-1-oxo-, d-lactone, (5a,6a,7a,22R)-
Ergosta-2,24-dien-26-oic acid, 6,7-epoxy-5,17,22-trihydroxy-1-oxo-, δ-lactone, (5α,6α,7α,22R)-
[Molecular Formula]

C28H38O6
[MDL Number]

MFCD09264639
[MOL File]

27570-38-3.mol
[Molecular Weight]

470.6
Chemical PropertiesBack Directory
[Boiling point ]

653.7±55.0 °C(Predicted)
[density ]

1.264
[Fp ]

216℃
[storage temp. ]

-20°C
[solubility ]

Chloroform: soluble,Ethyl Acetate: slightly soluble,Methanol: slightly soluble
[form ]

neat
[pka]

12.98±0.70(Predicted)
[color ]

White to off-white
[InChIKey]

FAZIYUIDUNHZRG-PCTWTJKKSA-N
[SMILES]

O=C1[C@@]2(C)[C@]([C@@H](O3)[C@@H]3[C@]4([H])[C@]2([H])CC[C@@]5(C)[C@@]4([H])CC[C@@]5([C@H](C)[C@]6([H])OC(C(C)=C(C)C6)=O)O)(O)CC=C1
Safety DataBack Directory
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

Withanone is used in biological studies as it has therapeutic uses resulting in the reductase inhibition for cancer chemoprevention.
[in vivo]

Withanone (5-20 mg/kg; oral administration; daily; for 21 days; male Wistar rats) treatment shows significant improvement in the cognitive skill by inhibiting amyloid β-42 and attenuates the elevated levels of pro-inflammatory cytokines like TNF α, IL-1β, IL-6, MCP-1, Nitric oxide, lipid peroxidation and both β- and γ- secretase enzymatic activity. Administration of Withanone also significantly reverses the decline in acetyl choline and Glutathione (GSH) activity[1].

Animal Model:Male Wistar rats (20-24 weeks; 320-360 g) received ICV injection of STZ[1]
Dosage:5 mg/kg, 10 mg/kg and 20 mg/kg
Administration:Oral administration; daily; for 21 days
Result:Showed significant improvement in the cognitive skill by inhibiting amyloid β-42 and attenuated the elevated levels of pro-inflammatory cytokines like TNF alpha, IL-1β, IL-6, MCP-1, Nitric oxide, lipid peroxidation and both β- and γ- secretase enzymatic activity. Also significantly reversed the decline in acetyl choline and Glutathione (GSH) activity.
[IC 50]

NMDA Receptor
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