Dihydromorin

Dihydromorin
Names
	IUPAC name (2R,3R)-2′,3,4′,5,7-Pentahydroxyflavan-4-one
	Systematic IUPAC name (2R,3R)-2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one
Identifiers
CAS Number	18422-83-8 ;
3D model (JSmol)	Interactive image;
ChemSpider	4572618 ;
PubChem CID	5458714;
UNII	BHC9FB8RFH ;
CompTox Dashboard (EPA)	DTXSID60939807 ;
	InChI InChI=1S/C15H12O7/c16-6-1-2-8(9(18)3-6)15-14(21)13(20)12-10(19)4-7(17)5-11(12)22-15/h1-5,14-19,21H/t14-,15+/m0/s1 Key: QIWOFDHUQPJCJF-LSDHHAIUSA-N ; InChI=1/C15H12O7/c16-6-1-2-8(9(18)3-6)15-14(21)13(20)12-10(19)4-7(17)5-11(12)22-15/h1-5,14-19,21H/t14-,15+/m0/s1 Key: QIWOFDHUQPJCJF-LSDHHAIUBR;
	SMILES C1=CC(=C(C=C1O)O)[C@@H]2[C@H](C(=O)C3=C(C=C(C=C3O2)O)O)O;
Properties
Chemical formula	C15H12O7
Molar mass	304.25 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

Dihydromorin is a flavanonol, a type of flavonoid. It can be found in plants of the family Moraceae including Morus nigra (Black mulberry),^[1] in Morus alba,^[2] Maclura pomifera (Maclura aurantiaca or Osage-Orange),^[2] in the jackfruit (Artocarpus heterophyllus)^[3] and in Artocarpus dadah.^[4]

Dihydromorin is an inhibitor of tyrosinase.^[3]

References

^ Black mulberry on naturalstandard.com
^ ^a ^b Dihydromorin on liberherbarum.com
^ ^a ^b Zheng, Zong-Ping; Chen, Sibao; Wang, Shiyun; Wang, Xia-Chang; Cheng, Ka-Wing; Wu, Jia-Jun; Yang, Dajiang; Wang, Mingfu (2009). "Chemical Components and Tyrosinase Inhibitors from the Twigs of Artocarpus heterophyllus". Journal of Agricultural and Food Chemistry. 57 (15): 6649–55. doi:10.1021/jf9014685. PMID 19588925.
^ Su, BN; Cuendet, M; Hawthorne, ME; Kardono, LB; Riswan, S; Fong, HH; Mehta, RG; Pezzuto, JM; Kinghorn, AD (2002). "Constituents of the bark and twigs of Artocarpus dadah with cyclooxygenase inhibitory activity". Journal of Natural Products. 65 (2): 163–9. doi:10.1021/np010451c. PMID 11858749.

v t e Flavanonols and their glycosides
3-Hydroxyflavanones:	Ampelopsin (Dihydromyricetin) Aromadedrin (Dihydrokaempferol) Dihydrogossypetin Dihydromorin Fustin (Dihydrofisetin) Garbanzol Pinobanksin Taxifolin (Dihydroquercetin)
O-methylated flavanonols	Dihydrokaempferide
dihydroflavonol 3-O-glycosides	Lecontin (+)-fustin glucoside
Glycosides	Astilbin Chrysandroside A Chrysandroside B Engeletin Eucryphin Smitilbin (Isoastilbin B) Xeractinol
Acetylated glycosides	Phellamurin

Names

IUPAC name (2R,3R)-2′,3,4′,5,7-Pentahydroxyflavan-4-one
Systematic IUPAC name (2R,3R)-2-(2,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one
Identifiers
CAS Number	18422-83-8^Y
3D model (JSmol)	Interactive image
ChemSpider	4572618^N
PubChem CID	5458714
UNII	BHC9FB8RFH^Y
CompTox Dashboard (EPA)	DTXSID60939807
InChI InChI=1S/C15H12O7/c16-6-1-2-8(9(18)3-6)15-14(21)13(20)12-10(19)4-7(17)5-11(12)22-15/h1-5,14-19,21H/t14-,15+/m0/s1^N Key: QIWOFDHUQPJCJF-LSDHHAIUSA-N^N InChI=1/C15H12O7/c16-6-1-2-8(9(18)3-6)15-14(21)13(20)12-10(19)4-7(17)5-11(12)22-15/h1-5,14-19,21H/t14-,15+/m0/s1 Key: QIWOFDHUQPJCJF-LSDHHAIUBR
SMILES C1=CC(=C(C=C1O)O)[C@@H]2[C@H](C(=O)C3=C(C=C(C=C3O2)O)O)O
Properties
Chemical formula	C₁₅H₁₂O₇
Molar mass	304.25 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is ^YN ?) Infobox references