Diarylheptanoid

The diarylheptanoids (also known as diphenylheptanoids) are a relatively small class of plant secondary metabolites. Diarylheptanoids consist of two aromatic rings (aryl groups) joined by a seven carbons chain (heptane) and having various substituents.[1] They can be classified into linear (curcuminoids) and cyclic diarylheptanoids. The best known member is curcumin, which is isolated from turmeric (Curcuma longa) and is known as food coloring E100. Some other Curcuma species, such as Curcuma comosa also produce diarylheptanoids.

Curcumin, a linear diarylheptanoid.

They have been reported from plants in 10 different families, e.g. Betulaceae and Zingiberaceae.

A diarylheptanoid is an intermediate in the biosynthesis of phenylphenalenones in Anigozanthos preissii[2] or Wachendorfia thyrsiflora (Haemodoraceae).[3]

Cyclic diarylheptanoids
Myricanone, a cyclic diarylheptanoid.

Cyclic diarylheptanoids formed from myricanone can be isolated from the bark of Myrica rubra (Myricaceae).[4] Two cyclic diarylheptanoids, named ostryopsitrienol and ostryopsitriol, can be isolated from the stems of endemic Chinese medicinal plant Ostryopsis nobilis (Betulaceae).[5] Acerogenin M can be found in Acer nikoense (Sapindaceae).[6] Jugcathayenoside and (+)-galeon can be found in the root bark of Juglans cathayensis (Juglandaceae).[7]

Health effects

The antioxidant activity of diarylheptanoids isolated from rhizomes of Etlingera elatior (Zingiberaceae) is greater than that of α-tocopherol.[8]

gollark: You should probably not be hardcoding sizes.
gollark: Not just "it's like WINDOWS, but for ComputerCraft, and actually not really like Windows as much as just a start menu, desktop and one GUI program".
gollark: They're typically significantly more interesting and creative.
gollark: Copy-pasting this from two months ago:Wild theory on new people constantly wanting to make an OS: they think something like "Oh wow, CC is so unlike Windows! And I have never seen any desktop OS but Windows! I must make it more like Windows so it is more familiar. Clearly nobody else has done this, or it would already be the default, because this is obviously better." Not explicitly/exactly that obviously, but think this might be close to what's going on.
gollark: It uses the CraftOS shell, yes, because I don't like GUIs and this was easier.

References
  1. Brahmachari, Goutam (2013-02-20). Chemistry and Pharmacology of Naturally Occurring Bioactive Compounds. CRC Press. pp. 285–. ISBN 9781439891674. Retrieved 5 July 2013.
  2. Hölscher, Dirk; Schneider, Bernd (1995). "A diarylheptanoid intermediate in the biosynthesis of phenylphenalenones in Anigozanthos preissii". Journal of the Chemical Society, Chemical Communications (5): 525–526. doi:10.1039/C39950000525.
  3. Brand, S; Hölscher, D; Schierhorn, A; Svatos, A; Schröder, J; Schneider, B (2006). "A type III polyketide synthase from Wachendorfia thyrsiflora and its role in diarylheptanoid and phenylphenalenone biosynthesis". Planta. 224 (2): 413–428. doi:10.1007/s00425-006-0228-x. PMID 16496097.
  4. Akazawa, H; Fujita, Y; Banno, N; Watanabe, K; Kimura, Y; Manosroi, A; Manosroi, J; Akihisa, T (2010). "Three new cyclic diarylheptanoids and other phenolic compounds from the bark of Myrica rubra and their melanogenesis inhibitory and radical scavenging activities". Journal of Oleo Science. 59 (4): 213–221. doi:10.5650/jos.59.213. PMID 20299768.
  5. Zhang, Yan-Xia; Xia, Bing; Zhou, Yan; Ding, Li-Sheng; Peng, Shu-Lin (2013). "Two new cyclic diarylheptanoids from the stems of Ostryopsis nobilis". Chinese Chemical Letters. 24 (6): 512–514. doi:10.1016/j.cclet.2013.03.035.
  6. Akihisa, T; Taguchi, Y; Yasukawa, K; Tokuda, H; Akazawa, H; Suzuki, T; Kimura, Y (2006). "Acerogenin M, a cyclic diarylheptanoid, and other phenolic compounds from Acer nikoense and their anti-inflammatory and anti-tumor-promoting effects". Chemical & Pharmaceutical Bulletin. 54 (5): 735–739. doi:10.1248/cpb.54.735. PMID 16651781.
  7. Li, Juan; Sun, Jia-Xiang; Yu, Heng-Yi; Chen, Zu-Yu; Zhao, Xiao-Ya; Ruan, Han-Li (2013). "Diarylheptanoids from the root bark of Juglans cathayensis". Chinese Chemical Letters. 24 (6): 521–523. doi:10.1016/j.cclet.2013.03.050.
  8. Mohamad, Habsah; Lajis, Nordin H.; Abas, Faridah; Ali, Abdul Manaf; Sukari, Mohamad Aspollah; Kikuzaki, Hiroe; Nakatani, Nobuji (2005). "Antioxidative constituents of Etlingera elatior". Journal of Natural Products. 68 (2): 285–288. doi:10.1021/np040098l. PMID 15730265.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.