kaempferol 3-robinobioside (Q50318427)

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chemical compound

Language	Label	Description	Also known as
English	kaempferol 3-robinobioside	chemical compound

Statements

type of chemical entity

0 references

kaempferol 3-robinobioside

1 reference

based on heuristic

inferred from SMILES

5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

based on heuristic

inferred from SMILES

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

1 reference

based on heuristic

inferred from SMILES

863.15847026 dalton

1 reference

based on heuristic

inferred from isomeric SMILES

stereoisomer of

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

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

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

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-({[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one

1 reference

based on heuristic

inferred from InChI

Kaempferol-3-rutinoside

1 reference

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

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

1 reference

based on heuristic

inferred from InChI

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

1 reference

based on heuristic

inferred from InChI

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

1 reference

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

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

1 reference

based on heuristic

inferred from InChI

4',5,7-Trihydroxy-3-(6-O-beta-D-rhamnopyranosyl-beta-D-glucopyranosyloxy)flavone

1 reference

based on heuristic

inferred from InChI

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

1 reference

based on heuristic

inferred from InChI

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

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₇H₃₀O₁₅

0 references

canonical SMILES

O=C1C(OC2OC(COC3OC(C)C(O)C(O)C3O)C(O)C(O)C2O)=C(OC=4C=C(O)C=C(O)C14)C=5C=CC(O)=CC5

0 references

isomeric SMILES

C([H])([H])([H])[C@@]1([H])[C@@]([H])([C@@]([H])([C@]([H])([C@]([H])(OC([H])([H])[C@@]2([H])[C@@]([H])([C@@]([H])([C@@]([H])([C@@]([H])(O2)OC3=C(C4=C([H])C([H])=C(C([H])=C4[H])O[H])OC5=C(C(=C([H])C(=C5[H])O[H])O[H])C3=O)O[H])O[H])O[H])O1)O[H])O[H])O[H]

0 references

Trigonella spicata

1 reference

A comparative study of the flavonoids of Medicago radiata with other Medicago and related Trigonella species

Strychnos variabilis

1 reference

Four acylated flavonol glycosides from leaves of Strychnos variabilis

Chenopodium pallidicaule

1 reference

Studies on the Constituents of Chenopodium pallidicaule (Canihua) Seeds. Isolation and Characterization of Two New Flavonol Glycosides

Lathyrus articulatus

1 reference

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

Lathyrus clymenum

1 reference

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

Physalis peruviana

1 reference

Kaempferol and quercetin di- and triglycosides from Physalis peruviana leaves

Camellia sinensis

2 references

Medicinal flowers. XIV. New acylated oleanane-type triterpene oligoglycosides with antiallergic activity from flower buds of chinese tea plant (Camellia sinensis).

Medicinal flowers. XXII. Structures of chakasaponins V and VI, chakanoside I, and chakaflavonoside A from flower buds of Chinese tea plant (Camellia sinensis).

Capsicum annuum

1 reference

Integrative analysis of metabolome and transcriptome reveals the mechanism of color formation in pepper fruit (Capsicum annuum L.).

Annona muricata

5 references

Novel cytotoxic annonaceous acetogenins from Annona muricata

New cytotoxic monotetrahydrofuran annonaceous acetogenins from Annona muricata

Five novel mono-tetrahydrofuran ring acetogenins from the seeds of Annona muricata

Cohibins C and D, two important metabolites in the biogenesis of acetogenins from Annona muricata and Annona nutans

Annona muricata (Annonaceae): A Review of Its Traditional Uses, Isolated Acetogenins and Biological Activities

Identifiers

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

0 references

RTATXGUCZHCSNG-DKBMUQCHSA-N

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CAS Registry Number

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2 references

26 December 2021

matched by identifier from

RTATXGUCZHCSNG-DKBMUQCHSA-N

UniChem compound ID

1 reference

0 references

Sitelinks

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Wikiquote(0 entries)

Wikisource(0 entries)

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Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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