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24:
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The low solubility of
Tangeretin is one of the main reasons for the low bioavailability of Tangeretin (and other flavonoids in general), and has been reported as a major challenge when using the compound in laboratory procedures. However, methods for tangeretin extraction are currently being tested
590:
Mizuno, H.; Yoshikawa, H.; Usuki, T. Extraction of
Nobiletin and Tangeretin From Peels of Shekwasha and Ponkan Using and Centrifugation. Natural Product Communications 2019, 14, 1-6.
532:
Tangeretin is commercially available as a dietary supplement. Tangeretin has also demonstrated beneficial applications in other pharmaceutical, nutraceutical, and cosmetic processes.
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1228:
1233:
841:
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to maximize efficiency and percent yields as its uses in treatment of cancer and other diseases are becoming better understood.
1223:
492:
peels. Tangeretin strengthens the cell wall and acts as a plant's defensive mechanism against disease-causing pathogens.
244:
265:
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728:
465:
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Panche, A. N.; Diwan, A. D.; Chandra, S. R. Flavonoids: an overview. Journal of
Nutritional Science. 2016, 5, 47.
181:
310:
InChI=1S/C20H20O7/c1-22-12-8-6-11(7-9-12)14-10-13(21)15-16(23-2)18(24-3)20(26-5)19(25-4)17(15)27-14/h6-10H,1-5H3
1093:
320:
InChI=1/C20H20O7/c1-22-12-8-6-11(7-9-12)14-10-13(21)15-16(23-2)18(24-3)20(26-5)19(25-4)17(15)27-14/h6-10H,1-5H3
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856:
1110:
1106:
1005:
417:
565.3 ± 50.0 °C (1,049.5 ± 90.0 °F; 838.4 ± 50.0 K)
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871:
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1088:
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Tangeretin can be found as various synonyms throughout literature and research, including
32:
286:
173:
87:
436:
131:
1217:
1176:
1158:
936:
495:
It has also been used as a marker compound to detect contamination in citrus juices.
412:
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1181:
774:
498:
The following is a list of methods used to extract tangeretin from citrus peels:
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isolation using ionic liquids and a cycle of centrifugation and decantation
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Except where otherwise noted, data are given for materials in their
514:
a combination of vacuum flash silica gel chromatography and flash C
208:
980:
122:
110:
100:
199:
612:
564:
SciFinder.com (accessed Nov. 6, 2012). Tangeretin (481-53-8).
270:
407:
155 to 156 °C (311 to 313 °F; 428 to 429 K)
453:
598:
596:
344:
O=C2C1=C(OC)C(OC)=C(OC)C(OC)=C1OC(C3=CC=C(OC)C=C3)=C2
1190:
1169:
1153:
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505:preparative-high performance liquid chromatography
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8:
578:Uckoo, RM; et al. Sep. Purif. Technol. 2011.
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60:5,6,7,8-Tetramethoxy-2-(4-methoxyphenyl)-4
15:
511:high speed counter current chromatography
252:
574:
572:
570:
552:
341:
306:
281:
163:
541:5,6,7,8,4’-pentamethoxyflavone (VIII)
313:Key: ULSUXBXHSYSGDT-UHFFFAOYSA-N
130:
7:
508:super critical fluid chromatography
323:Key: ULSUXBXHSYSGDT-UHFFFAOYAG
223:
207:
14:
443:
31:
22:
842:4',7-Dihydroxy-6-methoxyflavone
439:(at 25 °C , 100 kPa).
49:4′,5,6,7,8-Pentamethoxyflavone
1:
1229:Flavonoids found in Rutaceae
1250:
387:372.37 g/mol
1234:4-Methoxyphenyl compounds
433:
352:
332:
297:
70:
54:
44:
39:
30:
21:
1094:Luteolin-7-O-glucuronide
1058:Hypolaetin 8-glucuronide
734:6,7,4'-Trihydroxyflavone
729:7,8,3'-Trihydroxyflavone
482:polymethoxylated flavone
17:Tangeretin (Tangeritin)
1053:Hypolaetin 8-glucoside
1224:O-methylated flavones
835:O-methylated flavones
688:4',7-Dihydroxyflavone
518:column chromatography
502:column chromatography
56:Systematic IUPAC name
784:Pentahydroxyflavones
743:Tetrahydroxyflavones
693:7,8-Dihydroxyflavone
642:and their conjugates
521:flash chromatography
1154:Sulfated glycosides
424:Solubility in water
64:-1-benzopyran-4-one
18:
1146:Artoindonesianin P
702:Trihydroxyflavones
655:Monohydroxyflavone
466:Infobox references
397:1.244 ± 0.06 g/cm
16:
1211:
1210:
1102:
1101:
960:
959:
811:6-Hydroxyluteolin
676:Dihydroxyflavones
484:that is found in
474:Chemical compound
472:
471:
266:CompTox Dashboard
112:Interactive image
1241:
1089:Veronicastroside
971:
667:6-Hydroxyflavone
662:3-Hydroxyflavone
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360:Chemical formula
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770:Norartocarpetin
760:Isoscutellarein
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1141:Artocarpetin A
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437:standard state
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283:DTXSID30197417
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1177:Amentoflavone
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1159:Theograndin I
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1050:
1048:
1046:of hypolaetin
1044:
1038:
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1023:
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938:
937:Techtochrysin
935:
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837:
833:
827:
824:
822:
819:
817:
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812:
809:
807:
806:Nortangeretin
804:
802:
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413:Boiling point
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403:Melting point
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164:ECHA InfoCard
161:
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57:
53:
47:
43:
38:
34:
29:
25:
20:
1182:Ochnaflavone
1025:of baicalein
931:
877:Cirsimaritin
857:Artocarpetin
775:Scutellarein
540:
536:
534:
531:
527:
497:
494:
477:
476:
71:Identifiers
61:
1126:Scutellarin
1107:Giraldiin A
1079:Isoorientin
1067:of luteolin
1006:Schaftoside
974:of apigenin
867:Cirsilineol
862:Chrysoeriol
353:Properties
170:100.006.883
1218:Categories
1135:Acetylated
1074:Cynaroside
991:Isovitexin
966:Glycosides
932:Tangeretin
927:Sinensetin
922:Salvigenin
912:Oroxylin A
897:Hispidulin
821:Hypolaetin
816:Norwightin
791:Herbacetin
755:Kaempferol
724:Norwogonin
547:References
537:Tangeritin
488:and other
478:Tangeretin
429:0.037 g/L
383:Molar mass
254:I4TLA1DLX6
143:ChemSpider
132:CHEBI:9400
99:3D model (
78:CAS Number
46:IUPAC name
1203:Hidrosmin
1121:Oroxindin
1011:Vicenin-2
1001:Saponarin
996:Rhoifolin
986:Apigetrin
907:Nobiletin
892:Genkwanin
887:Eupatilin
882:Diosmetin
872:Cirsiliol
801:Quercetin
714:Baicalein
648:Aglycones
486:tangerine
191:207-570-1
183:EC Number
1170:Polymers
1116:Nepitrin
1084:Orientin
1032:Baicalin
847:Acacetin
826:Tricetin
765:Luteolin
719:Galangin
709:Apigenin
640:Flavones
480:is an O-
88:481-53-8
1198:Diosmin
1016:Vitexin
952:Zapotin
947:Wogonin
902:Nepetin
852:Alnetin
750:Fisetin
683:Chrysin
459:what is
457: (
393:Density
377:
221:PubChem
1037:Tetuin
942:Tricin
917:Pratol
490:citrus
454:verify
451:
337:SMILES
209:C10190
40:Names
1191:Drugs
981:Apiin
796:Morin
302:InChI
234:68077
152:61389
123:ChEBI
101:JSmol
1161:and
1109:and
539:and
245:UNII
200:KEGG
271:EPA
224:CID
1220::
1163:II
595:^
583:^
569:^
555:^
543:.
371:20
367:20
1111:B
632:e
625:t
618:v
516:8
449:N
375:7
373:O
369:H
365:C
273:)
269:(
103:)
62:H
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