Hericenone

Hericenone

Hericenone

Class of chemical compounds

Hericenones is a class of benzaldehydes that are isolates of the fruiting body of Hericium erinaceum (lion's mane mushroom) that promote nerve growth factor synthesis in vitro.[1] [2]

Hericenone C-H

Hericenones

More information Name, IUPAC name ...

References

  1. [1]
    Kawagishi, Hirokazu; Ando, Motoharu; Shinba, Kayoko; Sakamoto, Hideki; Yoshida, Satoshi; Ojima, Fumihiro; Ishiguro, Yukio; Ukai, Nobuo; Furukawa, Shoei (1992). "Chromans, hericenones F, G and H from the mushroom Hericium erinaceum". Phytochemistry. 32: 175–178. doi:10.1016/0031-9422(92)80127-Z.
  2. [2]
    Ma, B-J; Shen, J-W; Yu, H-Y; Ruan, Yuan; Wu, T-T; Zhao, X (Jun 2010). "Hericenones and erinacines: stimulators of nerve growth factor (NGF) biosynthesis in Hericium erinaceus". Mycology. 1 (2): 92–98. doi:10.1080/21501201003735556.
  3. [3]
    "Hericenone A". PubChem. Retrieved 2021-04-11.
  4. [4]
    "Hericenone A and B as cytotoxic principles from the mushroom hericium erinaceum". Tetrahedron Letters. 31 (3): 373–376. 1990-01-01. doi:10.1016/S0040-4039(00)94558-1. ISSN 0040-4039. Retrieved 2021-04-11.
  5. [5]
    "Hericenone B". PubChem. Retrieved 2021-04-11.
  6. [6]
    "Hericenone C". PubChem. Retrieved 2021-04-11.
  7. [7]
    Kawagishi, Hirokazu; Ando, Motoharu; Sakamoto, Hideki; Yoshida, Satoshi; Ojima, Fumihiro; Ishiguro, Yukio; Ukai, Nobuo; Furukawa, Shoei (1991-01-01). "Hericenones C, D and E, stimulators of nerve growth factor (NGF)-synthesis, from the mushroom Hericium erinaceum". Tetrahedron Letters. 32 (35): 4561–4564. doi:10.1016/0040-4039(91)80039-9. ISSN 0040-4039. Retrieved 2021-04-11.
  8. [8]
    "Hericenone D". PubChem. Retrieved 2021-04-11.
  9. [9]
    "Hericenone F". PubChem. Retrieved 2021-04-11.
  10. [10]
    Kawagishi, Hirokazu; Ando, Motoharu; Shinba, Kayoko; Sakamoto, Hideki; Yoshida, Satoshi; Ojima, Fumihiro; Ishiguro, Yukio; Ukai, Nobuo; Furukawa, Shoei (1992-12-23). "Chromans, hericenones F, G and H from the mushroom Hericium erinaceum". Phytochemistry. 32 (1): 175–178. doi:10.1016/0031-9422(92)80127-Z. ISSN 0031-9422. Retrieved 2021-04-11.
  11. [11]
    "Hericenone G". PubChem. Retrieved 2021-04-11.
  12. [12]
    "Hericenone H". PubChem. Retrieved 2021-04-11.
  13. [13]
    "Hericenone J". PubChem. Retrieved 2021-04-12.
  14. [14]
    "Hericenone K". PubChem. Retrieved 2021-04-12.


Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.
Share this article:

This article uses material from the Wikipedia article Hericenone, and is written by contributors. Text is available under a CC BY-SA 4.0 International License; additional terms may apply. Images, videos and audio are available under their respective licenses.