Chemistry:Catenarin

From HandWiki

Catenarin is a derivative chemical compound of anthraquinone.[1][2] Its formula is C
15H
10O
6. It is a natural product.

Occurrence

Catenarin has been identified in plants and fungi from various genera, including Pyrenophora,[3] Ventilago,[4] Aspergillus,[5][6] Catenarina,[7] and Talaromyces.[8][9]

References

  1. ↑ Yang, Wen-Chin; Shen, Ming-Yi; Jang, Yu-Song; Chen, Zeng-Weng; Chang, Cicero (2012-05-01). "Catenarin, an anthraquinone compound, inhibits CXCR4 and CCR5 pathways to protect against type 1 diabetes in NOD mice (72.1)". The Journal of Immunology 188 (1_Supplement): 72.1. doi:10.4049/jimmunol.188.Supp.72.1. ISSN 0022-1767. https://journals.aai.org/jimmunol/article/188/1_Supplement/72.1/50993/Catenarin-an-anthraquinone-compound-inhibits-CXCR4. 
  2. ↑ Martorell, Miquel; Castro, Natalia; Victoriano, Montserrat; Capó, Xavier; Tejada, Silvia; Vitalini, Sara; Pezzani, Raffaele; Sureda, Antoni (2021-09-20). "An Update of Anthraquinone Derivatives Emodin, Diacerein, and Catenarin in Diabetes" (in en). Evidence-Based Complementary and Alternative Medicine 2021. doi:10.1155/2021/3313419. PMID 34589130. 
  3. ↑ Engström, Karin; Brishammar, Sture; Svensson, Christer; Bengtsson, Maria; Andersson, Rolf (1993-03-01). "Anthraquinones from some Drechslera species and Bipolaris sorokiniana". Mycological Research 97 (3): 381–384. doi:10.1016/S0953-7562(09)81142-8. ISSN 0953-7562. https://linkinghub.elsevier.com/retrieve/pii/S0953756209811428. 
  4. ↑ Lin, L. C.; Chou, C. J.; Kuo, Y. C. (May 2001). "Cytotoxic principles from Ventilago leiocarpa". Journal of Natural Products 64 (5): 674–676. doi:10.1021/np000569d. ISSN 0163-3864. PMID 11374975. 
  5. ↑ Arai, Kunizo; Aoki, Yasuji; Yamamoto, Yuzuru (1989). "Asperinines A and B, Dimeric Tetrahydroanthracene Derivatives from Aspergillus ruber". Chemical & Pharmaceutical Bulletin 37 (3): 621–625. doi:10.1248/cpb.37.621. https://www.jstage.jst.go.jp/article/cpb1958/37/3/37_3_621/_article. 
  6. ↑ Du, Lin; Zhu, Tianjiao; Liu, Hongbing; Fang, Yuchun; Zhu, Weiming; Gu, Qianqun (2008-12-01). "Cytotoxic Polyketides from a Marine-derived Fungus Aspergillus glaucus". Journal of Natural Products 71 (11): 1837–1842. doi:10.1021/np800303t. ISSN 0163-3864. PMID 18986198. https://pubs.acs.org/doi/10.1021/np800303t. 
  7. ↑ Søchting, Ulrik; Søgaard, Majbrit Zeuthen; Elix, John A.; Arup, Ulf; Elvebakk, Arve; Sancho, Leopoldo G. (2014). "Catenarina (Teloschistaceae, Ascomycota), a new Southern Hemisphere genus with 7-chlorocatenarin". The Lichenologist 46 (2): 175–187. doi:10.1017/s002428291300087x. 
  8. ↑ Bu'Lock, J. D.; Smith, J. R. (1968-01-01). "Modified anthraquinones from Penicillium islandicum" (in en). Journal of the Chemical Society C: Organic: 1941–1943. doi:10.1039/J39680001941. ISSN 0022-4952. https://pubs.rsc.org/en/content/articlelanding/1968/j3/j39680001941. 
  9. ↑ van Eijk, G. W. (1973-05-01). "Anthraquinones in the fungus Talaromyces stipitatus" (in en). Experientia 29 (5): 522–523. doi:10.1007/BF01926640. ISSN 0014-4754. PMID 4730274. https://link.springer.com/article/10.1007/BF01926640. 




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