| Identification | Back Directory | [Name]
Erinacine C
Erinacin C | [CAS]
156101-09-6 | [Synonyms]
Erinacine C
Erinacin C
β-D-Xylopyranose, 1,2-O-[(3aR,5aR,6R,7R,10aR)-2,3,3a,4,5,5a,6,7,10,10a-decahydro-8-(hydroxymethyl)-3a,5a-dimethyl-1-(1-methylethyl)cyclohept[e]indene-6,7-diyl]- | [Molecular Formula]
C25H38O6 | [MOL File]
156101-09-6.mol | [Molecular Weight]
434.57 |
| Chemical Properties | Back Directory | [Boiling point ]
599.3±50.0 °C(Predicted) | [density ]
1.25±0.1 g/cm3(Predicted) | [solubility ]
DMSO: Soluble: =10 mg/ml
Ethanol: Soluble: =10 mg/ml | [form ]
Solid | [pka]
13.19±0.70(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Uses]
Erinacin C can be used to enhance neurite outgrowth | [References]
[1] HIROKAZU KAWAGISHI ∗ . Erinacines A, B and C, strong stimulators of nerve growth factor (NGF)-synthesis, from the mycelia of Hericium erinaceum[J]. Tetrahedron Letters, 1994, 35 10: Pages 1569-1572. DOI: 10.1016/s0040-4039(00)76760-8
[2] PRIYANKA PREMNATH. Screening for inhibitors of mutacin synthesis in Streptococcus mutans using fluorescent reporter strains.[J]. BMC Microbiology, 2018: 24. DOI: 10.1186/s12866-018-1170-3
[3] JING WEI. Unprecedented Neoverrucosane and Cyathane Diterpenoids with Anti-Neuroinflammatory Activity from Cultures of the Culinary-Medicinal Mushroom Hericium erinaceus.[J]. Molecules, 2023, 28 17. DOI: 10.3390/molecules28176380
[4] LEE K F, HSIEH Y Y, TUNG S Y, et al. The Cerebral Protective Effect of Novel Erinacines from Hericium erinaceus Mycelium on In Vivo Mild Traumatic Brain Injury Animal Model and Primary Mixed Glial Cells via Nrf2-Dependent Pathways[J]. Antioxidants, 2024, 41 1. DOI: 10.3390/antiox13030371 |
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