ChemicalBook--->CAS DataBase List--->56973-41-2

56973-41-2

56973-41-2 Structure

56973-41-2 Structure
IdentificationBack Directory
[Name]

WITHANOLIDE B(P)(NEW)
[CAS]

56973-41-2
[Synonyms]

Withanolide B
WITHANOLIDE B(SH)
Lycium substance B
WITHANOLIDE B(P)(NEW)
WITHANOLIDE B(SH)(NEW)
Withanolide B 56973-41-2
(5a,6a,7a,22R)-6,7-Epoxy-5,22-dihydroxy-1-oxoergosta-2,24-dien-26-oic acid d-lactone
(5α,6α,7α,22R)-6,7-Epoxy-5,22-dihydroxy-1-oxo-ergosta-2,24-dien-26-oic acid δ-lactone
Ergosta-2,24-dien-26-oic acid, 6,7-epoxy-5,22-dihydroxy-1-oxo-, δ-lactone, (5α,6α,7α,22R)-
[Molecular Formula]

C28H38O5
[MDL Number]

MFCD19053156
[MOL File]

56973-41-2.mol
[Molecular Weight]

454.6
Chemical PropertiesBack Directory
[density ]

1.206
[storage temp. ]

Store at -20°C
[solubility ]

Acetonitrile: 0.1 mg/ml; Methanol: 0.5 mg/ml
[form ]

neat
[color ]

White to off-white
[InChIKey]

ZTEVDTFJUUJBLP-MBMSZCMESA-N
Safety DataBack Directory
[Hazard statements ]

H413
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Withanolide B is an active component of W. somnifera Dunal. Withanolide B promotes osteogenic differentiation of hBMSCs via ERK1/2 and Wnt/β-catenin signaling pathways. Withanolide B exhibits neuroprotective, anti-arthritic, anti-aging and anti-cancer effects[1][2][3].
[Definition]

ChEBI: Withanolide B is a withanolide.
[in vivo]

Withanolide B (10 mg/kg; topical administration) promotes bone healing in a rat tibial defect model[1].

Animal Model:Male Sprague-Dawley rats (8 weeks, 200 g) with tibial defect[1]
Dosage:10 mg/kg
Administration:Injected in situ at the bone defect site at different time points (0, 3, 5, 7, and 9 days)
Result:Increased the trabecular number, trabecular thickness and the thickness of the cortical bone.
[storage]

Store at -20°C
[References]

[1] Kuang Z, et, al. Withanolide B promotes osteogenic differentiation of human bone marrow mesenchymal stem cells via ERK1/2 and Wnt/β-catenin signaling pathways. Int Immunopharmacol. 2020 Nov;88:106960. DOI:10.1016/j.intimp.2020.106960
[2] Dubey S, et, al. Improving the inhibition of β-amyloid aggregation by withanolide and withanoside derivatives. Int J Biol Macromol. 2021 Mar 15;173:56-65. DOI:10.1016/j.ijbiomac.2021.01.094
[3] Sivanandha G, et, al. Enhanced biosynthesis of withanolides by elicitation and precursor feeding in cell suspension culture of Withania somnifera (L.) Dunal in shake-flask culture and bioreactor. PLoS One. 2014 Aug 4;9(8):e104005. DOI:10.1371/journal.pone.0104005
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