435306-99-3
Chemical Structure
Erinacine Q
- CAS No.: 435306-99-3
- Formula:C27H42O8
- Molecular Weight:494.63
IUPAC Name: (3aR,5aR,6S,9R,10aR)-8-(hydroxymethyl)-1-isopropyl-3a,5a-dimethyl-6-(((2S,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)-2,3,3a,4,5,5a,6,9,10,10a-decahydrocyclohepta[e]inden-9-yl acetate
InChIKey: BNEKFVWNEHVFNT-JGSLRZJPSA-N
SMILES: C[C@]12C([C@@]3([C@](C)([C@@H](O[C@H]4[C@H](O)[C@@H](O)[C@H](O)CO4)C=C(CO)[C@H](OC(C)=O)C3)CC1)[H])=C(C(C)C)CC2
Biological Activity: Erinacine Q is a cyathane diterpenoid compound. Erinacine Q is produced by the mycelium of H. erinaceum. Erinacine Q serves as the direct substrate for the biosynthesis of Erinacine P (HY-N11019). Erinacine Q is used in the study of peripheral nerve injury[1][2][3][4].
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Erinacine Q | Erinacine Q is a cyathane diterpenoid compound. Erinacine Q is produced by the mycelium of H. erinaceum. Erinacine Q serves as the direct substrate for the biosynthesis of Erinacine P (HY-N11019). Erinacine Q is used in the study of peripheral nerve injury. | |||||||||||||||||||||
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References
- [1]. Li IC, et al. Neurohealth properties of Hericium erinaceus mycelia enriched with erinacines. Behavioural Neurology. 2018;2018(1):5802634.
- [2]. Lin CF, et al. A xanthurenate and an isoindolinone from the mycelia of Hericium erinaceum. Phytochemistry Letters. 2018 Aug 1;26:218-21.
- [3]. Wong KH, et al. Neuroregenerative potential of lion's mane mushroom, Hericium erinaceus (Bull.: Fr.) Pers. (higher Basidiomycetes), in the treatment of peripheral nerve injury (review). International journal of medicinal mushrooms. 2012;14(5):427-46.
- [4]. Trzeciak-Ryczek A, et al. Neurotrophic and Neuroprotective Effects of Hericium erinaceus. [Content Brief]
