Apigeninidin

Apigeninidin (chloride)
Names
	Other names 3-desoxy- pelargonidin; 5,7-dihydroxy-2-(4-hydroxyphenyl)benzopyrilium chloride
Identifiers
CAS Number	1151-98-0 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL590784 ;
ChemSpider	140151 ;
PubChem CID	441647;
UNII	CWI2JJB0W1 ;
CompTox Dashboard (EPA)	DTXSID40921629 ;
	InChI InChI=1S/C15H10O4.ClH/c16-10-3-1-9(2-4-10)14-6-5-12-13(18)7-11(17)8-15(12)19-14;/h1-8H,(H2-,16,17,18);1H Key: GYQDOAKHUGURPD-UHFFFAOYSA-N ;
	SMILES [Cl-].Oc1ccc(cc1)c3[o+]c2cc(O)cc(O)c2cc3;
Properties
Chemical formula	C15H11O4+
Molar mass	255.24 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Apigeninidin (Also, apigenidin,^[1] or Gesneridin) is a chemical compound belonging to the 3-deoxyanthocyanidins and that can be found in the Patagonian plant Ephedra frustillata^[2] and in the soybean.^[3] Apigeninidin is one of the principal pigments found in sorghum.^[4] Extremely high level of apigeninidin (49 mg/g) has been documented in sorghum leaf sheath.^[5] Like all anthocyanidins it exists in a variety of tautomers depending on pH and hydration, several of these bare the distinctive pyrylium core.^[6]

References

^ Asahina, Yasuhiko; Inubuse, Mototaro (1928). "Über die Reduktion der Flavon- und Flavanon-Derivate (III. Mitteilung über die Flavanon-glucoside)". Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 61 (8): 1646–1650. doi:10.1002/cber.19280610810. ISSN 0365-9488.
^ Gurni, Alberto A.; Wagner, Marcelo L. (1982). "Apigeninidin as a leucoderivative in Ephedra frustillata". Phytochemistry. 21 (9): 2428–2429. Bibcode:1982PChem..21.2428G. doi:10.1016/0031-9422(82)85229-1. ISSN 0031-9422.
^ Boveris, AD; Galatro, A; Sambrotta, L; Ricco, R; Gurni, AA; Puntarulo, S (December 2001). "Antioxidant capacity of a 3-deoxyanthocyanidin from soybean". Phytochemistry. 58 (7): 1097–105. Bibcode:2001PChem..58.1097B. doi:10.1016/s0031-9422(01)00378-8. PMID 11730874.
^ Awika, Joseph M.; Rooney, Lloyd W.; Waniska, Ralph D. (2004). "Properties of 3-Deoxyanthocyanins from Sorghum". Journal of Agricultural and Food Chemistry. 52 (14): 4388–4394. doi:10.1021/jf049653f. ISSN 0021-8561. PMID 15237941.
^ Geera, Bhimalingeswarappa; Ojwang, Leonnard O.; Awika, Joseph M. (2012). "New Highly Stable Dimeric 3-Deoxyanthocyanidin Pigments from Sorghum bicolor Leaf Sheath". Journal of Food Science. 77 (5): C566–C572. doi:10.1111/j.1750-3841.2012.02668.x. ISSN 0022-1147. PMID 22489620.
^ Costantino, Luca; Rastelli, Giulio; Rossi, Maria C.; Albasini, Albano (1995). "Quantitative measurement of proton dissociation and tautomeric constants of apigeninidin". Journal of the Chemical Society, Perkin Transactions 2 (2): 227. doi:10.1039/P29950000227.

[AsahinaInubuse1928-1] Asahina, Yasuhiko; Inubuse, Mototaro (1928). "Über die Reduktion der Flavon- und Flavanon-Derivate (III. Mitteilung über die Flavanon-glucoside)". Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 61 (8): 1646–1650. doi:10.1002/cber.19280610810. ISSN 0365-9488.

[GurniWagner1982-2] Gurni, Alberto A.; Wagner, Marcelo L. (1982). "Apigeninidin as a leucoderivative in Ephedra frustillata". Phytochemistry. 21 (9): 2428–2429. Bibcode:1982PChem..21.2428G. doi:10.1016/0031-9422(82)85229-1. ISSN 0031-9422.

[3] Boveris, AD; Galatro, A; Sambrotta, L; Ricco, R; Gurni, AA; Puntarulo, S (December 2001). "Antioxidant capacity of a 3-deoxyanthocyanidin from soybean". Phytochemistry. 58 (7): 1097–105. Bibcode:2001PChem..58.1097B. doi:10.1016/s0031-9422(01)00378-8. PMID 11730874.

[AwikaRooney2004-4] Awika, Joseph M.; Rooney, Lloyd W.; Waniska, Ralph D. (2004). "Properties of 3-Deoxyanthocyanins from Sorghum". Journal of Agricultural and Food Chemistry. 52 (14): 4388–4394. doi:10.1021/jf049653f. ISSN 0021-8561. PMID 15237941.

[GeeraOjwang2012-5] Geera, Bhimalingeswarappa; Ojwang, Leonnard O.; Awika, Joseph M. (2012). "New Highly Stable Dimeric 3-Deoxyanthocyanidin Pigments from Sorghum bicolor Leaf Sheath". Journal of Food Science. 77 (5): C566–C572. doi:10.1111/j.1750-3841.2012.02668.x. ISSN 0022-1147. PMID 22489620.

[6] Costantino, Luca; Rastelli, Giulio; Rossi, Maria C.; Albasini, Albano (1995). "Quantitative measurement of proton dissociation and tautomeric constants of apigeninidin". Journal of the Chemical Society, Perkin Transactions 2 (2): 227. doi:10.1039/P29950000227.

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Names

Other names 3-desoxy- pelargonidin 5,7-dihydroxy-2-(4-hydroxyphenyl)benzopyrilium chloride
Identifiers
CAS Number	1151-98-0^Y
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL590784^Y
ChemSpider	140151^Y
PubChem CID	441647
UNII	CWI2JJB0W1^Y
CompTox Dashboard (EPA)	DTXSID40921629
InChI InChI=1S/C15H10O4.ClH/c16-10-3-1-9(2-4-10)14-6-5-12-13(18)7-11(17)8-15(12)19-14;/h1-8H,(H2-,16,17,18);1H^Y Key: GYQDOAKHUGURPD-UHFFFAOYSA-N^Y
SMILES [Cl-].Oc1ccc(cc1)c3[o+]c2cc(O)cc(O)c2cc3
Properties
Chemical formula	C₁₅H₁₁O₄+
Molar mass	255.24 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is ^YN ?) Infobox references