(Q6345965)

Kaempferitrin (English)

5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

7 October 2016

stereoisomer of

1 reference

5-Hydroxy-2-(4-hydroxyphenyl)-3,7-bis[[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]chromen-4-one

inferred from InChIKey

1 reference

5-hydroxy-2-(4-hydroxyphenyl)-7-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

inferred from InChIKey

2 references

inferred from InChIKey

5-Hydroxy-2-(4-hydroxyphenyl)-3,7-bis[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]chromen-4-one

1 reference

5-hydroxy-2-(4-hydroxyphenyl)-3,7-bis[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]chromen-4-one

1 reference

5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

1 reference

5-hydroxy-2-(4-hydroxyphenyl)-3,7-bis[[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]chromen-4-one

1 reference

5-hydroxy-2-(4-hydroxyphenyl)-3,7-bis[[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]chromen-4-one

1 reference

Kaempferol-3,7-O-bis-alpha-L-rhamnoside

1 reference

5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

1 reference

chemical formula

C₂₇H₃₀O₁₄

1 reference

Kaempferitrin (English)

20 November 2016

canonical SMILES

CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O

1 reference

Kaempferitrin (English)

20 November 2016

isomeric SMILES

C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O[C@H]4[C@@H]([C@@H]([C@H]([C@@H](O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O

1 reference

Antidiabetic effects of Justicia spicigera Schltdl (Acanthaceae).

Kaempferitrin (English)

20 November 2016

2 references

Isolation of Kaempferitrin From Justicia spicigera

Lespedeza virgata

2 references

A novel flavonoid from Lespedeza virgata (Thunb.) DC.: structural elucidation and antioxidative activity.

Antioxidant 2-phenylbenzofurans and a coumestan from Lespedeza virgata

Ixora coccinea

2 references

Ixorapeptide I and ixorapeptide II, bioactive peptides isolated from Ixora coccinea

Doubly linked, A-type proanthocyanidin trimer and other constituents of Ixora coccinea leaves and their antioxidant and antibacterial properties.

broad bean

1 reference

Catalytic inhibition of eukaryotic topoisomerases I and II by flavonol glycosides extracted from Vicia faba and Lotus edulis

Lotus edulis

1 reference

Catalytic inhibition of eukaryotic topoisomerases I and II by flavonol glycosides extracted from Vicia faba and Lotus edulis

Dryopteris crassirhizoma

1 reference

In vivo anthelmintic effect of flavonol rhamnosides from Dryopteris crassirhizoma against Dactylogyrus intermedius in goldfish (Carassius auratus).

Sedum dendroideum

1 reference

Antidiabetic activity of Sedum dendroideum: metabolic enzymes as putative targets for the bioactive flavonoid kaempferitrin

Annulohypoxylon bovei

1 reference

Secondary metabolites from the endophytic fungus Annulohypoxylon boveri var. microspora BCRC 34012

Agrimonia pilosa

1 reference

Phenolic glycosides from Agrimonia pilosa.

Androsace umbellata

1 reference

Two New Kaempferol Glycosides fromAndrosace umbellata

Bauhinia forficata

2 references

Hypoglycemic effect and antioxidant potential of kaempferol-3,7-O-(alpha)-dirhamnoside from Bauhinia forficata leaves

Phytochemical and pharmacognositc investigation of Bauhinia forficata Link (Leguminosae)

Cardamine leucantha

1 reference

Three New Kaempferol Glycosides fromCardamine leucantha

Celastrus orbiculatus

1 reference

On the Flavone-Glycoside of Celastrus Orbiculatus

Chenopodium murale

4 references

A flavonol triglycoside from Chenopodium murale

A comparative study of the flavonoids and some biological activities of two Chenopodium species

Two flavonoid glycosides from Chenopodium murale

Isolation of hypotensive flavonoids fromChenopodium species growing in Egypt

Cinnamomum yabunikkei

1 reference

Chemical constituents from the stems of Cinnamomum insulari-montanum

Cinnamomum osmophloeum

1 reference

Inhibitory effects of flavonol glycosides from Cinnamomum osmophloeum on inflammatory mediators in LPS/IFN-gamma-activated murine macrophages

Cinnamomum burmanni

1 reference

Four kaempferol glycosides from leaves of Cinnamomum sieboldii

Cinnamomum sieboldii

1 reference

Four kaempferol glycosides from leaves of Cinnamomum sieboldii

Cissus sicyoides

1 reference

Structures of new flavonoids and benzofuran-type stilbene and degranulation inhibitors of rat basophilic leukemia cells from the Brazilian herbal medicine Cissus sicyoides

Cissus verticillata

1 reference

Structures of new flavonoids and benzofuran-type stilbene and degranulation inhibitors of rat basophilic leukemia cells from the Brazilian herbal medicine Cissus sicyoides

Colocasia antiquorum

1 reference

Lignans from the tuber-barks of Colocasia antiquorum var. esculenta and their antimelanogenic Activity

Colocasia esculenta

1 reference

Lignans from the tuber-barks of Colocasia antiquorum var. esculenta and their antimelanogenic Activity

Dorycnium hirsutum

1 reference

Antioxidant flavonol glycosides from Dorycnium hirsutum

Farsetia aegyptia

1 reference

A new kaempferol trioside from Farsetia aegyptia

Ficus septica

1 reference

Phenanthroindolizidine Alkaloids and Their Cytotoxicity from the Leaves of Ficus septica

Garcinia dulcis

1 reference

Phenolic compounds from the fruit of Garcinia dulcis.

Humulus lupulus

1 reference

Flavonol glycoside from Humulus lupulus

Ligustrum vulgare

2 references

HPLC analysis of flavonoids and secoiridoids in leaves of Ligustrum vulgare L. (Oleaceae)

Secoiridoid glucosides and unusual recyclized secoiridoid aglycones from Ligustrum vulgare

Pterogyne nitens

1 reference

Flavonols from Pterogyne nitens and their evaluation as myeloperoxidase inhibitors

radish

1 reference

Antioxidant constituents of radish sprout (Kaiware-daikon), Raphanus sativus L.

Hylotelephium telephium

1 reference

Flavonol glycosides from sedum telephium subspecies Maximum leaves

Macrothelypteris torresiana

1 reference

New cytotoxic flavonoids from Thelypteris torresiana

Tilia tomentosa

1 reference

Hepatoprotective principles from the flowers of Tilia argentea (linden): structure requirements of tiliroside and mechanisms of action

Trichosanthes cucumeroides

1 reference

A chemotaxonomic study of flavonoids in the leaves of six Trichosanthes species

Trichosanthes ovigera

1 reference

A chemotaxonomic study of flavonoids in the leaves of six Trichosanthes species

Camellia sinensis

1 reference

Separation of the components in black tea infusion by chromatography on Toyopearl.

Asplenium trichomanes-ramosum

1 reference

New and rare flavonol glycosides from asplenium trichomanes-ramosum as stable chemotaxonomic markers

Asplenium viride

1 reference

New and rare flavonol glycosides from asplenium trichomanes-ramosum as stable chemotaxonomic markers

Prunus spinosa

1 reference

Constituents of Prunus spinosa

Epimedium acuminatum

1 reference

New tetrasaccharide flavonol glycoside from Epimedium acuminatum

Chromolaena subscandens

1 reference

Flavonoids from the Leaves of Chromolaena subscandens

Hibiscus cannabinus

1 reference

Lignanamides and other phenolic constituents from the bark of kenaf (Hibiscus cannabinus).

Cleome amblyocarpa

1 reference

Flavonoids of four Cleome and three Capparis species

Cleome brachycarpa

1 reference

Flavonoids of four Cleome and three Capparis species

Thulinella chrysantha

1 reference

Flavonoids of four Cleome and three Capparis species

Vancouveria hexandra

1 reference

Flavonol glycosides production in cell suspension cultures of Vancouveria hexandra

Hedyotis verticillata

1 reference

Kaempferitrin from the leaves of Hedyotis verticillata and its biological activity

Adesmia incana

1 reference

Hydrophilic components in twoAdesmia species

Geranium thunbergii

1 reference

Studies on the activities of tannins and related compounds from medicinal plants and drugs. IV. Effects of various extracts of Geranii herba and geraniin on liver injury and lipid metabolism in rats fed peroxidized oil

Pilularia minuta

1 reference

Extended flavonoid biosynthetic capability in the aquatic fern genus Pilularia

Pilularia globulifera

1 reference

Extended flavonoid biosynthetic capability in the aquatic fern genus Pilularia

Ostericum sieboldii

1 reference

Separation of Ostericum from Angelica on the Basis of Leaf and Mericarp Flavonoids

Panax trifolius

1 reference

Studies on the constituents of dwarf ginseng

Viola diamantiaca

1 reference

Studies on the Flavonoid Glycoside of the Leaves of Viola diamantiaca

Chengiopanax sciadophylloides

1 reference

Studies on the Constituents of Acanthopanax sciadophylloides FR. et SAV. Leaves

Cissus discolor

1 reference

Structures of new flavonoids and benzofuran-type stilbene and degranulation inhibitors of rat basophilic leukemia cells from the Brazilian herbal medicine Cissus sicyoides

Lotus hirsutus

1 reference

Antioxidant flavonol glycosides from Dorycnium hirsutum

Stylidocleome brachycarpa

1 reference

Flavonoids of four Cleome and three Capparis species

Scleromitrion verticillatum

1 reference

Kaempferitrin from the leaves of Hedyotis verticillata and its biological activity

Cleome droserifolia

2 references

Flavonoids of four Cleome and three Capparis species

Dolabellane Diterpenes from Cleome Droserifolia

Raphanus raphanistrum

1 reference

Antioxidant constituents of radish sprout (Kaiware-daikon), Raphanus sativus L.

Cleome chrysantha

1 reference

Flavonoids of four Cleome and three Capparis species

Aconitum vulparia

1 reference

Flavonol glycosides from Aconitum vulparia.

Tilia mandshurica

1 reference

Hepatoprotective principles from the flowers of Tilia argentea (linden): structure requirements of tiliroside and mechanisms of action

Arabidopsis thaliana

1 reference

The structure of the major anthocyanin in Arabidopsis thaliana

Lotus tenuis

1 reference

Antioxidant flavonol glycosides from Dorycnium hirsutum

Lotus herbaceus

1 reference

Flavonoids of Dorycnium intermedium

Arivela viscosa

1 reference

Flavonoids with hepatoprotective activity from the leaves of Cleome viscosa L.

Identifiers

InChI

InChI=1S/C27H30O14/c1-9-17(30)20(33)22(35)26(37-9)39-13-7-14(29)16-15(8-13)40-24(11-3-5-12(28)6-4-11)25(19(16)32)41-27-23(36)21(34)18(31)10(2)38-27/h3-10,17-18,20-23,26-31,33-36H,1-2H3/t9-,10-,17-,18-,20+,21+,22+,23+,26-,27-/m0/s1

1 reference

Kaempferitrin (English)

PUPKKEQDLNREIM-QNSQPKOQSA-N

20 November 2016

InChIKey

2 references

Kaempferitrin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

482-38-2

2 references

Global Substance Registration System

UNII

VPV01U3R59

PUPKKEQDLNREIM-QNSQPKOQSA-N

lespedin (English)

20 November 2016

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=482-38-2

1 reference

Kaempferitrin (English)

20 November 2016

1 reference

Kaempferitrin (English)

20 November 2016

Reaxys registry number

73958

1 reference

kaempferol 3-O-alpha-L-rhamnopyranosyl-7-O-alpha-L-rhamnopyranoside (English)

7 October 2016

ChEBI ID

68883

mapping relation type

1 reference

KAEMPFERITRIN (English)

20 November 2016

1 reference

MSBNK-Univ_Toyama-TY000224

KAEMPFERITRIN (English)

20 November 2016

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

MSBNK-Univ_Toyama-TY000228

0 references

MSBNK-Univ_Toyama-TY000237

0 references

MSBNK-BS-BS001024

0 references

MSBNK-BS-BS001025

0 references

SPLASH

splash10-001i-0020900000-cff5cebd77d8af55155a

0 references

splash10-001i-0000930000-4528a8c0efd5cd7d384e

0 references

splash10-001i-0000930000-05546880dd0ca8b27efa

0 references

splash10-0a4i-0000900000-b238e2a54490a257d8a1

0 references

splash10-0a4i-0000900000-9e02282b01a62b20b286

0 references

splash10-00di-0000900000-5e715ddda0be047858cb

0 references

splash10-00di-0000900000-3451d5bb54395bbc27e6

0 references

splash10-0a4i-0000020900-c0b427176429de0e1049

0 references

splash10-0002-0092400100-ebbbe04721d3116536ec

0 references

splash10-0019-0090520000-8e9b49560ef1c495512d

0 references

splash10-003r-0080890000-90954644aa8be4f3e3d7

0 references

splash10-000i-0090100000-f7cb5208cc787bcfb1a3

0 references

splash10-000i-1090400000-7b252fa24dc92328e1d9

0 references

splash10-001r-0090440000-fe4ddd1e95a23c5456c3

0 references

DSSTox substance ID

DTXSID90197458

1 reference

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

DSSTOX compound identifier

DTXCID00119949

0 references

Human Metabolome Database ID

0 references

0 references

1 reference

Global Substance Registration System

UNII

VPV01U3R59

lespedin (English)

20 November 2016

0 references

1 reference