kaempferol-7-rhamnoside

chemical compound

C₂₁H₂₀O₁₀

kaempferol-7-rhamnoside is …
instance of (P31):
type of chemical entityQ113145171

sublass of (P279):
flavoneQ424525

External links are
P233canonical SMILESCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O
P231CAS Registry Number20196-89-8
P592ChEMBL IDCHEMBL1289337
P661ChemSpider ID26367429
P8494DSSTOX compound identifierDTXCID9096525
P3117DSSTox substance IDDTXSID60174034
P234InChIInChI=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
P235InChIKeyHQNOUCSPWAGQND-GKLNBGJFSA-N
P2017isomeric SMILESC[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
P6689MassBank accession IDMSBNK-RIKEN-PR100941
MSBNK-RIKEN-PR100942
MSBNK-RIKEN-PR101008
P11199Probes And Drugs IDPD164904
P662PubChem CID25079965
P4964SPLASHsplash10-000i-0090000000-bf3229a51b726d4cb146
splash10-0zgr-0590000000-157fd3edfb39e660bb57
P11089UniChem compound ID918600
P652UNII79YJI9GIF1

P703found in taxonEquisetum palustreQ21122
Equisetum arvenseQ107592
Actinidia kolomiktaQ132741
Cephalocereus senilisQ312190
Bambara groundnutQ338219
Vigna mungoQ369447
Lotus pedunculatusQ158164
Dioscorea communisQ161378
Robinia pseudoacaciaQ157417
Hibiscus cannabinusQ1137540
Vigna umbellataQ1368391
Vigna angularisQ380279
Vigna unguiculataQ498940
Vigna radiataQ484447
Vigna aconitifoliaQ511249
Eryngium campestreQ839771
Bupleurum chinenseQ1031631
Maclura pomiferaQ1066106
Celastrus flagellarisQ4167985
Rorippa indicaQ5768150
Chenopodium muraleQ1911022
Dryopteris crassirhizomaQ2043064
Cissus verticillataQ2714097
Hylotelephium ewersiiQ1383053
Ixora coccineaQ1856114
Cardamine leucanthaQ6747475
Annulohypoxylon squamulosumQ10412537
Sinocrassula indicaQ10910388
Hypericum japonicumQ10928400
Viola diamantiacaQ10933933
Rhodiola crenulataQ10937567
Indigofera hebepetalaQ11127769
Cleome droserifoliaQ12156640
Lespedeza virgataQ15245347
Aconitum vulpariaQ15362154
Delphinium formosumQ15372362
Lepidium cartilagineumQ15431302
Cleome brachycarpaQ15516775
Cleome amblyocarpaQ15517762
Cleome chrysanthaQ15517942
Hylotelephium caucasicumQ17767955
Tamus communisQ21877561
Lotus uliginosusQ22112213
Lepidium syvaschicumQ81734343
Cissus discolorQ87599449
Cissus sicyoidesQ87615974
Stylidocleome brachycarpaQ104387057
Thulinella chrysanthaQ104415551
Maclura aurantiacaQ104916878
P2067mass432.106
P3364stereoisomer of3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-oneQ105032328
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-oneQ105032329
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-oneQ105032335
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-oneQ105032338

Reverse relations

stereoisomer of (P3364)
Q1050323383,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
Q1050323283,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
Q1050323353,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
Q1050323293,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

main subject (P921)
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Q46592055Antioxidant 2-phenylbenzofurans and a coumestan from Lespedeza virgata
Q105032333Antioxidant flavonoids from Tamus communis ssp. cretica
Q81163948Bioactive 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),
Q104847944Chemical Constituents of the Aerial Part of Bupleurum longicaule
Q104847867Chromone glycosides and flavonoids from hypericum japonicum
Q105032331Constitutive flavonoids and induced isoflavonoids as taxonomic markers in the genus Vigna
Q104918235Dolabellane Diterpenes from Cleome Droserifolia
Q42906615Doubly linked, A-type proanthocyanidin trimer and other constituents of Ixora coccinea leaves and their antioxidant and antibacterial properties.
Q104847701Flavonoids and hydroxycoumarins of Sedum ewersii
Q104975914Flavonoids from seeds of Maclura aurantiaca growing in Georgia
Q79580394Flavonoids from the Aboveground Parts of Lycopus virginicus
Q104968071Flavonoids from the leaves of Actinidia kolomikta
Q104852482Flavonoids of four Cleome and three Capparis species
Q105032330Flavonoids of the leaves ofHibiscus cannabinus
Q104933974Flavonol 3,7-diglycosides ofLepidium syvaschicum
Q47867687Flavonol glycosides from Aconitum vulparia.
Q72273225Flavonol glycosides from Cephalocereus senilis
Q104400100Flavonol glycosides from Rhodiola crenulata
Q104385698Hydroxycoumarins and flavonol 7-monorhamnosides ofSedum caucasicum
Q104386698Interspecific and intraspecific variation of phenolics in the genus Equisetum subgenus Equisetum
Q39627968Ixorapeptide I and ixorapeptide II, bioactive peptides isolated from Ixora coccinea
Q83232624Localized Changes in Flavonoid Biosynthesis in Roots of Lotus pedunculatus after Infection by Rhizobium loti
Q46409275Nectar Flavonol rhamnosides are floral markers of acacia (Robinia pseudacacia) honey
Q104847859Roripanoside, a New Kaempferol Rhamnoside fromRorippa Indica (L.) Hiern
Q105013440Secondary metabolites and cytotoxic activities from the endophytic fungus Annulohypoxylon squamulosum
Q39791698Structures of new flavonoids and benzofuran-type stilbene and degranulation inhibitors of rat basophilic leukemia cells from the Brazilian herbal medicine Cissus sicyoides
Q105032332Studies on the Flavonoid Glycoside of the Leaves of Viola diamantiaca
Q104998886Three New Kaempferol Glycosides fromCardamine leucantha
Q71955196Two flavonol triglycosides from flowers of Indigofera hebepetala
Q83378833Two new lignans from Celastrus flagellaris Rupr
Q45395373Two new triterpenes from the Rhizome of Dryopteris crassirhizoma, and inhibitory activities of its constituents on human immunodeficiency virus-1 protease

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