(Q27137238)

CHEMBL1929193 (English)

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

7 October 2016

stereoisomer of

2 references

Kaempferol 3-galactoside-7-rhamnoside

2 references

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

2 references

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

2 references

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

2 references

kaempferol 3-O-beta-D-galactopyranosyl-7-O-alpha-L-rhamnopyranoside

2 references

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

1 reference

Kaempferol 3-glucoside-7-rhamnoside

1 reference

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

1 reference

kaempferol 3-O-beta-D-glucopyranosyl-7-O-beta-L-rhamnopyranoside

1 reference

chemical formula

C₂₇H₃₀O₁₅

1 reference

CHEMBL1929193 (English)

7 October 2016

canonical SMILES

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

1 reference

CHEMBL1929193 (English)

7 October 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)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O

1 reference

Flavonoids and a proanthocyanidin from rhizomes of Selliguea feei

CHEMBL1929193 (English)

7 October 2016

1 reference

Arabidopsis thaliana

3 references

The structure of the major anthocyanin in Arabidopsis thaliana

Metabolomics-oriented isolation and structure elucidation of 37 compounds including two anthocyanins from Arabidopsis thaliana

Major flavonoids from Arabidopsis thaliana leaves

Chenopodium murale

3 references

Two flavonoid glycosides from Chenopodium murale

Two flavonoid glycosides from Chenopodium murale

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

Cissus sicyoides

2 references

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

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

Cleome brachycarpa

1 reference

Flavonoids of four Cleome and three Capparis species

Cleome chrysantha

1 reference

Flavonoids of four Cleome and three Capparis species

Cleome droserifolia

1 reference

Flavonoids of four Cleome and three Capparis species

Eryngium campestre

1 reference

Flavonolacyl glycosides of the aerial parts of Eryngium campestre

Erythroxylum vacciniifolium

1 reference

Flavonoid variation in Erythroxylum

Lathyrus sativus

1 reference

The flavonoids of the genus Lathyrus and a comparison of flavonoid patterns within the tribe vicieae

Ostericum sieboldii

1 reference

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

Asplenium scolopendrium var. scolopendrium

1 reference

Kaempferol Glycosides in Asplenium scolopendvium Newm

Trichosanthes cucumeroides

2 references

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

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

Bambara groundnut

1 reference

Constitutive flavonoids and induced isoflavonoids as taxonomic markers in the genus Vigna

Lotus edulis

2 references

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

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

broad bean

2 references

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

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

Aconitum lycoctonum

1 reference

Flavonol glycosides from Aconitum vulparia.

Androsace umbellata

1 reference

Two New Kaempferol Glycosides fromAndrosace umbellata

Camellia reticulata

1 reference

Five New Flavonol Glycosides from the Fresh Flowers ofCamellia reticulata

Sinocrassula indica

3 references

Bioactive constituents from Chinese natural medicines. XXXII. aminopeptidase N and aldose reductase inhibitors from Sinocrassula indica: structures of sinocrassosides B(4), B(5), C(1), and D(1)-D(3).

Bioactive Constituents from Chinese Natural Medicines. XXXI. Hepatoprotective Principles from Sinocrassula indica: Structures of Sinocrassosides A8, A9, A10, A11, and A12

Bioactive constituents from chinese natural medicines. XXIV. Hypoglycemic effects of Sinocrassula indica in sugar-loaded rats and genetically diabetic KK-A(y) mice and structures of new acylated flavonol glycosides, sinocrassosides A(1), A(2), B(1),

Delphinium formosum

1 reference

Acylated pelargonidin 3,7-glycosides from red flowers of Delphinium hybridum

Dorycnium hirsutum

1 reference

Antioxidant flavonol glycosides from Dorycnium hirsutum

Lespedeza virgata

1 reference

Antioxidant 2-phenylbenzofurans and a coumestan from Lespedeza virgata

Ligustrum vulgare

1 reference

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

Luculia pinceana

1 reference

Flavonoids in Luculia pinceana

Nephelium lappaceum

1 reference

Monoterpene lactones from the seeds of Nephelium lappaceum.

Reseda luteola

1 reference

Flavonoids ofPsoralea drupaceae andReseda luteola

Breynia androgyna

1 reference

Active Chemical Constituents fromSauropus androgynus

Sauropus androgynus

1 reference

Active Chemical Constituents fromSauropus androgynus

Sorbus aria

1 reference

Activity-guided isolation and identification of free radical-scavenging components from various leaf extracts of Sorbus aria (L.) Crantz

Lotus hirsutus

1 reference

Antioxidant flavonol glycosides from Dorycnium hirsutum

Aria edulis

1 reference

Activity-guided isolation and identification of free radical-scavenging components from various leaf extracts of Sorbus aria (L.) Crantz

Lotus tenuis

1 reference

Antioxidant flavonol glycosides from Dorycnium hirsutum

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

Stylidocleome brachycarpa

1 reference

Flavonoids of four Cleome and three Capparis species

Thulinella chrysantha

1 reference

Flavonoids of four Cleome and three Capparis species

Identifiers

InChI

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

1 reference

CHEMBL1929193 (English)

JYXSWDCPHRTYGU-RVCYDTIBSA-N

7 October 2016

InChIKey

2 references

CHEMBL1929193 (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

2392-95-2

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

1 reference

Kaempferol-3-O-beta-glucopyranosyl-7-O-alpha-rhamnopyranoside (English)

7 October 2016

1 reference

CHEMBL1929193 (English)

7 October 2016

Reaxys registry number

74580

1 reference

kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside (English)

7 October 2016

ChEBI ID

68882

mapping relation type

1 reference

kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside (English)

7 October 2016

1 reference

splash10-0002-0010900000-39bf1345b5539749ec9f

CHEMBL1929193 (English)

7 October 2016

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

splash10-001i-0020900000-6c83c9ce518723675abe

0 references

splash10-001i-0030900000-29057181fb009cba28cc

0 references

splash10-00di-0000900000-f4c2e9040560413a0415

0 references

splash10-00di-0000900000-8b1cd7a95af611ebc7a1

0 references

splash10-000i-0090000000-05026344170e7e50f70f

0 references

splash10-001i-0070950000-52f7fc32dd1be6479bf7

0 references

splash10-014i-0090000000-c3b0cbea94af7ffdc699

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download