(Q27266794)

Alpha-Rhamnoisorobin (English)

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

14 October 2016

stereoisomer of

2 references

inferred from InChIKey

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

2 references

inferred from InChIKey

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

1 reference

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

1 reference

chemical formula

C₂₁H₂₀O₁₀

1 reference

Alpha-Rhamnoisorobin (English)

14 October 2016

canonical SMILES

CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O

1 reference

Alpha-Rhamnoisorobin (English)

14 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)C4=CC=C(C=C4)O)O)O)O)O

1 reference

Interspecific and intraspecific variation of phenolics in the genus Equisetum subgenus Equisetum

Alpha-Rhamnoisorobin (English)

14 October 2016

1 reference

Equisetum palustre

1 reference

Interspecific and intraspecific variation of phenolics in the genus Equisetum subgenus Equisetum

Hylotelephium caucasicum

1 reference

Hydroxycoumarins and flavonol 7-monorhamnosides ofSedum caucasicum

Bupleurum chinense

1 reference

Chemical Constituents of the Aerial Part of <I>Bupleurum longicaule</I>

Chenopodium murale

1 reference

A flavonol triglycoside from Chenopodium murale

Cleome amblyocarpa

1 reference

Flavonoids of four Cleome and three Capparis species

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

2 references

Flavonoids of four Cleome and three Capparis species

Dolabellane Diterpenes from Cleome Droserifolia

Eryngium campestre

1 reference

Flavonoids from the Aboveground Parts of Lycopus virginicus

Hibiscus cannabinus

1 reference

Flavonoids of the leaves ofHibiscus cannabinus

Hypericum japonicum

1 reference

Chromone glycosides and flavonoids from hypericum japonicum

Indigofera hebepetala

1 reference

Two flavonol triglycosides from flowers of Indigofera hebepetala

Lepidium cartilagineum

1 reference

Flavonol 3,7-diglycosides ofLepidium syvaschicum

Rorippa indica

1 reference

Roripanoside, a New Kaempferol Rhamnoside fromRorippa Indica (L.) Hiern

Vigna aconitifolia

1 reference

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

Vigna angularis

1 reference

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

Vigna mungo

1 reference

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

Vigna radiata

1 reference

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

Bambara groundnut

1 reference

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

Vigna umbellata

1 reference

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

Vigna unguiculata

1 reference

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

Viola diamantiaca

1 reference

Studies on the Flavonoid Glycoside of the Leaves of Viola diamantiaca

Actinidia kolomikta

1 reference

Flavonoids from the leaves of Actinidia kolomikta

Annulohypoxylon squamulosum

1 reference

Secondary metabolites and cytotoxic activities from the endophytic fungus Annulohypoxylon squamulosum

Cardamine leucantha

1 reference

Three New Kaempferol Glycosides fromCardamine leucantha

Celastrus flagellaris

1 reference

Two new lignans from Celastrus flagellaris Rupr

Cephalocereus senilis

1 reference

Flavonol glycosides from Cephalocereus senilis

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

Sinocrassula indica

1 reference

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

Dryopteris crassirhizoma

1 reference

Two new triterpenes from the Rhizome of Dryopteris crassirhizoma, and inhibitory activities of its constituents on human immunodeficiency virus-1 protease

Ixora coccinea

2 references

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

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

Lespedeza virgata

1 reference

Antioxidant 2-phenylbenzofurans and a coumestan from Lespedeza virgata

Maclura aurantiaca

1 reference

Flavonoids from seeds of Maclura aurantiaca growing in Georgia

Maclura pomifera

1 reference

Flavonoids from seeds of Maclura aurantiaca growing in Georgia

Rhodiola crenulata

1 reference

Flavonol glycosides from Rhodiola crenulata

Tamus communis

1 reference

Antioxidant flavonoids from Tamus communis ssp. cretica

Dioscorea communis

1 reference

Antioxidant flavonoids from Tamus communis ssp. cretica

Robinia pseudoacacia

1 reference

Nectar Flavonol rhamnosides are floral markers of acacia (Robinia pseudacacia) honey

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

Aconitum vulparia

1 reference

Flavonol glycosides from Aconitum vulparia.

Lepidium syvaschicum

1 reference

Flavonol 3,7-diglycosides ofLepidium syvaschicum

Lotus pedunculatus

1 reference

Localized Changes in Flavonoid Biosynthesis in Roots of Lotus pedunculatus after Infection by Rhizobium loti

Thulinella chrysantha

1 reference

Flavonoids of four Cleome and three Capparis species

Stylidocleome brachycarpa

1 reference

Flavonoids of four Cleome and three Capparis species

Lotus uliginosus

1 reference

Localized Changes in Flavonoid Biosynthesis in Roots of Lotus pedunculatus after Infection by Rhizobium loti

Hylotelephium ewersii

1 reference

Flavonoids and hydroxycoumarins of Sedum ewersii

Identifiers

InChI

InChI=1S/C21H20O10/c1-8-15(24)17(26)19(28)21(29-8)30-11-6-12(23)14-13(7-11)31-20(18(27)16(14)25)9-2-4-10(22)5-3-9/h2-8,15,17,19,21-24,26-28H,1H3/t8-,15-,17+,19+,21-/m0/s1

1 reference

Alpha-Rhamnoisorobin (English)

14 October 2016

1 reference

Global Substance Registration System

Alpha-Rhamnoisorobin (English)

14 October 2016

2 references

UNII

79YJI9GIF1

kaempferol-7-rhamnoside (English)

14 October 2016

https://commonchemistry.cas.org/detail?cas_rn=20196-89-8

9 April 2021

1 reference

Kaempferol-7-O-alpha-L-rhamnoside (English)

14 October 2016

2 references

Alpha-Rhamnoisorobin (English)

matched by identifier from

14 October 2016

1 reference

splash10-0zgr-0590000000-157fd3edfb39e660bb57

ALPHA-RHAMNOISOROBIN (English)

14 October 2016

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

splash10-000i-0090000000-bf3229a51b726d4cb146

0 references

DSSTox substance ID

DTXSID60174034

2 references

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

matched by identifier from

DSSTOX compound identifier

0 references

2 references

Global Substance Registration System

UNII

79YJI9GIF1

kaempferol-7-rhamnoside (English)

matched by identifier from

14 October 2016