Catenarin

Catenarin
	Skeletal formula of catenarin
Names
	Preferred IUPAC name 1,4,5,7-tetrahydroxy-2-methylanthracene-9,10-dione
	Other names 4-Hydroxyemodin; Katenarin; Caterarin;
Identifiers
CAS Number	476-46-0;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL29860;
ChemSpider	9744;
PubChem CID	10150;
UNII	EHN5P96V6S;
CompTox Dashboard (EPA)	DTXSID50197212 ;
	InChI InChI=1S/C15H10O6/c1-5-2-8(17)11-12(13(5)19)14(20)7-3-6(16)4-9(18)10(7)15(11)21/h2-4,16-19H,1H3 Key: VWDXGKUTGQJJHJ-UHFFFAOYSA-N;
	SMILES CC1=CC(=C2C(=C1O)C(=O)C3=C(C2=O)C(=CC(=C3)O)O)O;
Properties
Chemical formula	C15H10O6
Molar mass	286.239 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Catenarin is a derivative chemical compound of anthraquinone.^[1]^[2] Its formula is C₁₅H₁₀O₆. 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

↑ Yang WC, Shen MY, Jang YS, Chen ZW, Chang C (May 1, 2012). "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.
↑ Martorell M, Castro N, Victoriano M, Capó X, Tejada S, Vitalini S, et al. (September 20, 2021). "An Update of Anthraquinone Derivatives Emodin, Diacerein, and Catenarin in Diabetes". Evidence-Based Complementary and Alternative Medicine. 2021 3313419. doi:10.1155/2021/3313419. PMC 8476274. PMID 34589130.
↑ Engström K, Brishammar S, Svensson C, Bengtsson M, Andersson R (March 1, 1993). "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.
↑ Lin LC, Chou CJ, Kuo YC (May 2001). "Cytotoxic principles from Ventilago leiocarpa". Journal of Natural Products. 64 (5): 674–676. doi:10.1021/np000569d. ISSN 0163-3864. PMID 11374975.
↑ Arai K, Aoki Y, Yamamoto Y (1989). "Asperinines A and B, Dimeric Tetrahydroanthracene Derivatives from Aspergillus ruber". Chemical & Pharmaceutical Bulletin. 37 (3): 621–625. doi:10.1248/cpb.37.621.
↑ Du L, Zhu T, Liu H, Fang Y, Zhu W, Gu Q (December 1, 2008). "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.
↑ Søchting U, Søgaard MZ, Elix JA, Arup U, Elvebakk A, Sancho LG (2014). "Catenarina (Teloschistaceae, Ascomycota), a new Southern Hemisphere genus with 7-chlorocatenarin". The Lichenologist. 46 (2): 175–187. doi:10.1017/s002428291300087x.
↑ Bu'Lock JD, Smith JR (January 1, 1968). "Modified anthraquinones from Penicillium islandicum". Journal of the Chemical Society C: Organic: 1941–1943. doi:10.1039/J39680001941. ISSN 0022-4952.
↑ van Eijk GW (May 1, 1973). "Anthraquinones in the fungus Talaromyces stipitatus". Experientia. 29 (5): 522–523. doi:10.1007/BF01926640. ISSN 0014-4754. PMID 4730274.

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[1] Yang WC, Shen MY, Jang YS, Chen ZW, Chang C (May 1, 2012). "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.

[2] Martorell M, Castro N, Victoriano M, Capó X, Tejada S, Vitalini S, et al. (September 20, 2021). "An Update of Anthraquinone Derivatives Emodin, Diacerein, and Catenarin in Diabetes". Evidence-Based Complementary and Alternative Medicine. 2021 3313419. doi:10.1155/2021/3313419. PMC 8476274. PMID 34589130.

[3] Engström K, Brishammar S, Svensson C, Bengtsson M, Andersson R (March 1, 1993). "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.

[4] Lin LC, Chou CJ, Kuo YC (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 K, Aoki Y, Yamamoto Y (1989). "Asperinines A and B, Dimeric Tetrahydroanthracene Derivatives from Aspergillus ruber". Chemical & Pharmaceutical Bulletin. 37 (3): 621–625. doi:10.1248/cpb.37.621.

[6] Du L, Zhu T, Liu H, Fang Y, Zhu W, Gu Q (December 1, 2008). "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.

[Søchting_et_al._2014-7] Søchting U, Søgaard MZ, Elix JA, Arup U, Elvebakk A, Sancho LG (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 JD, Smith JR (January 1, 1968). "Modified anthraquinones from Penicillium islandicum". Journal of the Chemical Society C: Organic: 1941–1943. doi:10.1039/J39680001941. ISSN 0022-4952.

[9] van Eijk GW (May 1, 1973). "Anthraquinones in the fungus Talaromyces stipitatus". Experientia. 29 (5): 522–523. doi:10.1007/BF01926640. ISSN 0014-4754. PMID 4730274.

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Occurrence

References