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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H31O15
Molecular Weight 595.526
Optical Activity UNSPECIFIED
Defined Stereocenters 10 / 10
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of KERACYANIN CATION

SMILES

C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=C([O+]=C4C=C(O)C=C(O)C4=C3)C5=CC=C(O)C(O)=C5)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O

InChI

InChIKey=USNPULRDBDVJAO-FXCAAIILSA-O
InChI=1S/C27H30O15/c1-9-19(32)21(34)23(36)26(39-9)38-8-18-20(33)22(35)24(37)27(42-18)41-17-7-12-14(30)5-11(28)6-16(12)40-25(17)10-2-3-13(29)15(31)4-10/h2-7,9,18-24,26-27,32-37H,8H2,1H3,(H3-,28,29,30,31)/p+1/t9-,18+,19-,20+,21+,22-,23+,24+,26+,27+/m0/s1

HIDE SMILES / InChI
Keracyanin (antirrhinin) is the pigment originally isolated from the fruit of the cherry. The compound exerts potent antioxidant properties. It is able to inhibit host- and bacteria-derived proteinases. Dietary supplementation with purified keracyanin suppresses body weight gain in high-fat diet fed mice.

Originator

Sources: Willstiitter and Zollinger (1916). Liebig's Ann. 412, 164.
Curator's Comment: refrence retrieved from https://www.ncbi.nlm.nih.gov/pubmed/16744416

Approval Year

PubMed

PubMed

TitleDatePubMed
Black raspberry components inhibit proliferation, induce apoptosis, and modulate gene expression in rat esophageal epithelial cells.
2009
Interaction between gliadins and anthocyan derivatives.
2011 Dec 1
Inhibition of host- and bacteria-derived proteinases by natural anthocyanins.
2011 Oct
Separation and identification of anthocyanin extracted from mulberry fruit and the pigment binding properties toward human serum albumin.
2014 Jul 16
Patents

Sample Use Guides

The results from a 12-week experiment show that consumption of purified mulberry anthocyanin cyanidin-3-O-rutinoside (keracyanin) of 40 or 200mg/kg can significantly inhibit body weight gain, reduce the resistance to insulin, lower the size of adipocytes, attenuate lipid accumulation and decrease the leptin secretion.
Route of Administration: Oral
The effects of cyanidin-3-O-rutinoside (keracyanin), on the growth of RE-149 and RE-149 DHD cells were determined at concentrations ranging from 10–50 µg/ ml
Name Type Language
KERACYANIN CATION
Common Name English
CYANIDIN-3-RUTINOSIDE
Common Name English
CYANIDIN 3-.BETA.-D-O-RUTINOSIDE
Systematic Name English
1-BENZOPYRYLIUM, 3-((6-O-(6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL)-.BETA.-D-GLUCOPYRANOSYL)OXY)-2-(3,4-DIHYDROXYPHENYL)-5,7-DIHYDROXY-
Systematic Name English
CYANIDIN 3-O-RUTINOSIDE
Systematic Name English
KERACYANIN ION
Common Name English
FLAVYLIUM, 3-((6-O-(6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL)-.BETA.-D-GLUCOPYRANOSYL)OXY)-3',4',5,7-TETRAHYDROXY-
Systematic Name English
Code System Code Type Description
CAS
259813-55-3
Created by admin on Sat Dec 16 11:04:45 GMT 2023 , Edited by admin on Sat Dec 16 11:04:45 GMT 2023
SUPERSEDED
EPA CompTox
DTXSID401313656
Created by admin on Sat Dec 16 11:04:45 GMT 2023 , Edited by admin on Sat Dec 16 11:04:45 GMT 2023
PRIMARY
CHEBI
58546
Created by admin on Sat Dec 16 11:04:45 GMT 2023 , Edited by admin on Sat Dec 16 11:04:45 GMT 2023
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CHEBI
28064
Created by admin on Sat Dec 16 11:04:45 GMT 2023 , Edited by admin on Sat Dec 16 11:04:45 GMT 2023
PRIMARY
CAS
28338-59-2
Created by admin on Sat Dec 16 11:04:45 GMT 2023 , Edited by admin on Sat Dec 16 11:04:45 GMT 2023
PRIMARY
PUBCHEM
441674
Created by admin on Sat Dec 16 11:04:45 GMT 2023 , Edited by admin on Sat Dec 16 11:04:45 GMT 2023
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FDA UNII
OR49FC491X
Created by admin on Sat Dec 16 11:04:45 GMT 2023 , Edited by admin on Sat Dec 16 11:04:45 GMT 2023
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WIKIPEDIA
Cyanidin 3-rutinoside
Created by admin on Sat Dec 16 11:04:45 GMT 2023 , Edited by admin on Sat Dec 16 11:04:45 GMT 2023
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