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ChemicalBook--->CAS DataBase List--->102841-46-3

102841-46-3

102841-46-3 Structure

102841-46-3 Structure
IdentificationBack Directory
[Name]

Moracin P
[CAS]

102841-46-3
[Synonyms]

Moracin P
(9R)-moracin P
5-(6-hydroxy-7,7-dimethyl-3a,4,5,6-tetrahydrofuro[3,2-g]chromen-2-yl)benzene-1,3-diol
5-[(6R)-6,7-Dihydro-6-hydroxy-7,7-dimethyl-5H-furo[3,2-g][1]benzopyran-2-yl]-1,3-benzenediol
1,3-Benzenediol, 5-[(6R)-6,7-dihydro-6-hydroxy-7,7-dimethyl-5H-furo[3,2-g][1]benzopyran-2-yl]-
[Molecular Formula]

C19H18O5
[MDL Number]

MFCD21333739
[MOL File]

102841-46-3.mol
[Molecular Weight]

326.34
Chemical PropertiesBack Directory
[Boiling point ]

560.6±50.0 °C(Predicted)
[density ]

1.349±0.06 g/cm3(Predicted)
[solubility ]

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
[form ]

Powder
[pka]

9.10±0.10(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

Moracin P is a 2-arylbenzofuran isolated from the Mori Cortex Radicis. Moracin P exhibits potent in vitro inhibitory activity against hypoxia-inducible factor (HIF-1). Moracin P reduces oxygen-glucose deprivation (OGD)-induced reactive oxygen species (ROS) production. Moracin P has neuroprotective and anti-inflammatory effects[1][2][3].
[target]

ROS | HIF | NO
[References]

[1] Hak Ju Lee, et al. Inhibitory effect of 2-arylbenzofurans from the Mori Cortex Radicis (Moraceae) on oxygen glucose deprivation (OGD)-induced cell death of SH-SY5Y cells. Arch Pharm Res. 2011 Aug;34(8):1373-80. DOI:10.1007/s12272-011-0818-4
[2] Yan Xia, et al. HIF-1α inhibitors: synthesis and biological evaluation of novel moracin O and P analogues. Eur J Med Chem. 2011 Jun;46(6):2386-96. DOI:10.1016/j.ejmech.2011.03.022
[3] Besse Hardianti, et al. Anti-inflammatory compounds moracin O and P from Morus alba Linn. (Sohakuhi) target the NF?κB pathway. Mol Med Rep. 2020 Dec;22(6):5385-5391. DOI:10.3892/mmr.2020.11615
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