Hericenone

Last updated
Hericenone C-H Hericenone C-H.png
Hericenone C-H

Hericenones is a class of substituted benzaldehydes that are isolated from fungi in the genus Hericium (the lion's mane mushrooms) that promote nerve growth factor synthesis in vitro . [1] [2]

Hericenones

Hericenones
NameIUPAC nameReference
Hericenone A5-[(2E)-3,7-dimethyl-5-oxoocta-2,6-dienyl]-4-hydroxy-6-methoxy-3H-2-benzofuran-1-one [3] [4]
Hericenone B6-[(2Z)-3,7-dimethyl-5-oxoocta-2,6-dienyl]-7-hydroxy-5-methoxy-2-(2-phenylethyl)-3H-isoindol-1-one [5] [4]
Hericenone C[4-[(2E)-3,7-dimethyl-5-oxoocta-2,6-dienyl]-2-formyl-3-hydroxy-5-methoxyphenyl]methyl hexadecanoate [6] [7]
Hericenone D[4-[(2E)-3,7-dimethyl-5-oxoocta-2,6-dienyl]-2-formyl-3-hydroxy-5-methoxyphenyl]methyl octadecanoate [8] [7]
Hericenone E[4-[(2E)-3,7-dimethyl-5-oxoocta-2,6-dienyl]-2-formyl-3-hydroxy-5-methoxyphenyl]methyl (9E,12E)-octadeca-9,12-dienoate [7]
Hericenone F[8-formyl-5-methoxy-2-methyl-2-(4-methyl-2-oxopent-3-enyl)-3,4-dihydrochromen-7-yl]methyl hexadecanoate [9] [10]
Hericenone G[8-formyl-5-methoxy-2-methyl-2-(4-methyl-2-oxopent-3-enyl)-3,4-dihydrochromen-7-yl]methyl octadecanoate [11] [10]
Hericenone H[8-formyl-5-methoxy-2-methyl-2-(4-methyl-2-oxopent-3-enyl)-3,4-dihydrochromen-7-yl]methyl (9E,12E)-octadeca-9,12-dienoate [12] [10]
Hericenone I
Hericenone J6-[(2E)-3,7-dimethylocta-2,6-dienyl]-7-hydroxy-5-methoxy-3H-2-benzofuran-1-one [13]
Hericenone K2-(4-hydroxy-4-methyl-2-oxopentyl)-5-methoxy-2-methyl-4,7-dihydro-3H-furo[3,4-h]chromen-9-one [14]

References

  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. ↑ 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. ↑ "Hericenone A". PubChem. Retrieved 2021-04-11.
  4. 1 2 "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. ↑ "Hericenone B". PubChem. Retrieved 2021-04-11.
  6. ↑ "Hericenone C". PubChem. Retrieved 2021-04-11.
  7. 1 2 3 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. ↑ "Hericenone D". PubChem. Retrieved 2021-04-11.
  9. ↑ "Hericenone F". PubChem. Retrieved 2021-04-11.
  10. 1 2 3 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. ↑ "Hericenone G". PubChem. Retrieved 2021-04-11.
  12. ↑ "Hericenone H". PubChem. Retrieved 2021-04-11.
  13. ↑ "Hericenone J". PubChem. Retrieved 2021-04-12.
  14. ↑ "Hericenone K". PubChem. Retrieved 2021-04-12.


This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.