(Q3484909)

Sinensetin (English)

5 October 2016

C₂₀H₂₀O₇

1 reference

Sinensetin (English)

5 October 2016

COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC

1 reference

High-performance liquid chromatographic determination of naturally occurring flavonoids in Citrus with a photodiode-array detector

Sinensetin (English)

5 October 2016

3 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Biosynthesis of limonoids: Conversion of deacetylnomilinate to nomilin in Citrus limon

Citrus flavicarpa

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus intermedia

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus hassaku

2 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

On the flavonoid constituents from the peels of Citrus hassaku Hort. ex. Tanaka.

Citrus otachibana

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus obovoidea

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus sulcata

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus myrtifolia

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus tankan

3 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Biosynthesis of limonoids: Conversion of deacetylnomilinate to nomilin in Citrus limon

The Chemical Constituents of the Peel of Citrus Tankan Hayata

Citrus ×iyo

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus ujukitsu

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus aurea

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus shunkokan

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus hanaju

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus nippokoreana

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus unshiu

4 references

High-performance liquid chromatographic determination of naturally occurring flavonoids in Citrus with a photodiode-array detector

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Polymethoxylated flavonoids from the peel of Unshiu mandarin fruit

Isolation and identification of polymethoxyflavones from the hybrid Citrus, hallabong

Citrus keraji

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus oto

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus tachibana

2 references

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus erythrosa

2 references

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Cherry Orange

4 references

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Identification and physiological evaluation of the components from citrus fruits as potential drugs for anti-corpulence and anticancer

Citrus depressa

2 references

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus leiocarpa

2 references

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Citrus madurensis

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Chromolaena odorata

2 references

Phenolic compounds of Chromolaena odorata protect cultured skin cells from oxidative damage: implication for cutaneous wound healing

Exudate flavonoids in a tropical weed, Chromolaena odorata (L.) R. M. King et H. Robinson

Ageratum conyzoides

2 references

Methoxyflavones from Ageratum conyzoides

Polyoxygenated flavones from Ageratum conyzoides

Conoclinium coelestinum

1 reference

Two new flavones from Eupatorium coelestinum

Citrus pseudoparadisi

1 reference

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Murraya paniculata

1 reference

PHYTOCHEMICAL STUDY OF MURRAYA EXOTICA L. (RUTACEAE) I- METHOXYLATED FLAVONOIDS OF THE LEAVES

Orthosiphon grandiflorus

4 references

Orthosiphol D and E, minor diterpenes from Orthosiphon stamineus

Flavonoids from Orthosiphon spicatus

Constituents of the Vietnamese medicinal plant Orthosiphon stamineus.

Indonesian medicinal plants. XXIII. Chemical structures of two new migrated pimarane-type diterpenes, neoorthosiphols A and B, and suppressive effects on rat thoracic aorta of chemical constituents isolated from the leaves of Orthosiphon aristatus (

Pulicaria sicula

1 reference

Variations in lipophilic and vacuolar flavonoids among European Pulicaria species

Phanera championii

1 reference

New flavones from Bauhinia championii BENTH.

Croton caudatus

1 reference

Flavonoids from the stems of Croton caudatus Geisel. var. tomentosus Hook.

Citrus × paradisi

3 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Simultaneous separation of flavanone glycosides and polymethoxylated flavones in citrus juices using liquid chromatography

Use of an online extraction liquid chromatography quadrupole time-of-flight tandem mass spectrometry method for the characterization of polyphenols in Citrus paradisi cv. Changshanhuyu peel

pomelo

3 references

High-performance liquid chromatographic determination of naturally occurring flavonoids in Citrus with a photodiode-array detector

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Biosynthesis of limonoids: Conversion of deacetylnomilinate to nomilin in Citrus limon

Kumquat

4 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Identification and physiological evaluation of the components from citrus fruits as potential drugs for anti-corpulence and anticancer

Citrus medica

2 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

On the flavonoid constituents from the peels of Citrus hassaku Hort. ex. Tanaka.

Orthosiphon aristatus

4 references

Flavonoids from Orthosiphon spicatus

Indonesian medicinal plants. XXIII. Chemical structures of two new migrated pimarane-type diterpenes, neoorthosiphols A and B, and suppressive effects on rat thoracic aorta of chemical constituents isolated from the leaves of Orthosiphon aristatus (

Constituents of the Vietnamese medicinal plant Orthosiphon stamineus.

Orthosiphol D and E, minor diterpenes from Orthosiphon stamineus

mandarin orange

15 references

The methoxyflavones in Citrus reticulata Blanco cv. ponkan and their antiproliferative activity against cancer cells

Studies on the constituents of useful plants. V. Multisubstituted flavones in the fruit peel of Citrus reticulata and their examination by gas-liquid chromatography.

High-performance liquid chromatographic determination of naturally occurring flavonoids in Citrus with a photodiode-array detector

The Chemical Constituents of the Peel of Citrus Tankan Hayata

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Polymethoxylated flavonoids from the peel of Unshiu mandarin fruit

Isolation and identification of polymethoxyflavones from the hybrid Citrus, hallabong

Biosynthesis of limonoids: Conversion of deacetylnomilinate to nomilin in Citrus limon

Citrus Polymethoxylated Flavones Can Confer Resistance againstPhytophthora citrophthora,Penicillium digitatum, andGeotrichumSpecies

Studies on the differentiation inducers of myeloid leukemic cells from Citrus species.

Two New Polymethoxylated Flavones, a Class of Compounds with Potential Anticancer Activity, Isolated from Cold Pressed Dancy Tangerine Peel Oil Solids

Isolation and Identification of New Polymethoxyflavonoids from Dancy Tangerine Leaves

Identification and physiological evaluation of the components from citrus fruits as potential drugs for anti-corpulence and anticancer

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Citrus × deliciosa

15 references

High-performance liquid chromatographic determination of naturally occurring flavonoids in Citrus with a photodiode-array detector

The Chemical Constituents of the Peel of Citrus Tankan Hayata

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Identification and physiological evaluation of the components from citrus fruits as potential drugs for anti-corpulence and anticancer

Polymethoxylated flavonoids from the peel of Unshiu mandarin fruit

Isolation and identification of polymethoxyflavones from the hybrid Citrus, hallabong

Biosynthesis of limonoids: Conversion of deacetylnomilinate to nomilin in Citrus limon

Citrus Polymethoxylated Flavones Can Confer Resistance againstPhytophthora citrophthora,Penicillium digitatum, andGeotrichumSpecies

Studies on the differentiation inducers of myeloid leukemic cells from Citrus species.

Isolation and Identification of New Polymethoxyflavonoids from Dancy Tangerine Leaves

The methoxyflavones in Citrus reticulata Blanco cv. ponkan and their antiproliferative activity against cancer cells

Studies on the constituents of useful plants. V. Multisubstituted flavones in the fruit peel of Citrus reticulata and their examination by gas-liquid chromatography.

Two New Polymethoxylated Flavones, a Class of Compounds with Potential Anticancer Activity, Isolated from Cold Pressed Dancy Tangerine Peel Oil Solids

Citrus japonica

4 references

Chemotaxonomy of the genus Citrus based on polymethoxyflavones.

Chemotaxonomic studies on the genus Citrus. I. Distribution of flavones in the subgroup microcarpa.

Isolation and identification of two new flavanones and a chalcone from Citrus kinokuni

Identification and physiological evaluation of the components from citrus fruits as potential drugs for anti-corpulence and anticancer

1 reference

Sinensetin

0 references

Identifiers

InChI

InChI=1S/C20H20O7/c1-22-13-7-6-11(8-15(13)23-2)14-9-12(21)18-16(27-14)10-17(24-3)19(25-4)20(18)26-5/h6-10H,1-5H3

1 reference

Sinensetin (English)

5 October 2016

2 references

Sinensetin (English)

5 October 2016

ChEBI release 2020-09-01

2 references

sinensetin (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=2306-27-6

8 April 2021

1 reference

Sinensetin (English)

5 October 2016

2 references

English

Sinensetin (English)

5 October 2016

Reaxys registry number

345748

1 reference

sinensetin (English)

5 October 2016

mapping relation type

2 references

English

sinensetin (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C20H20O7/c1-22-13-7-6-11(8-15(13)23-2)14-9-12(21)18-16(27-14)10-17(24-3)19(25-4)20(18)26-5/h6-10H,1-5H3

1 reference

SINENSETIN (English)

5 October 2016

2 references

inferred from InChIKey

splash10-0btc-0009000000-d229e25752edb9bfdd4a

1 reference

0 references

splash10-0btc-0009000000-772779fbcb51b0cfefdc

0 references

NMRShiftDB structure ID

20237348

1 reference

DSSTox substance ID

DTXSID60177626

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

DTXCID20100117

0 references

EC number

803-609-7

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.230.396

27 December 2018

ECHA Substance Infocard ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 2306-27-6 (English)

100.230.396

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.230.396

27 December 2018

Human Metabolome Database ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 2306-27-6 (English)

HMDB0036633

2 references

based on heuristic

inferred from InChIKey

3 references

sinensetin (English)

5 October 2016

inferred from InChIKey

UNII

240LNZ51AT

2 references

Global Substance Registration System

UNII

240LNZ51AT

English

SINENSETIN (English)

5 October 2016

0 references

1 reference