(Q105262980)

4-hydroxy-3,5,5-trimethyl-4-[(1E,3R)-3-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}but-1-en-1-yl]cyclohex-2-en-1-one

inferred from SMILES

1 reference

inferred from SMILES

mass

386.19406792 dalton

1 reference

(3Z)-4-[(1S)-1-Hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl]-3-buten-2-yl beta-D-glucopyranoside

inferred from SMILES

stereoisomer of

2 references

2 references

(4S)-4-hydroxy-3,5,5-trimethyl-4-[(E,3R)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one

2 references

(4S)-4-hydroxy-3,5,5-trimethyl-4-[(E,3R)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one

2 references

(4S)-4-hydroxy-3,5,5-trimethyl-4-[(1E,3R)-3-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}but-1-en-1-yl]cyclohex-2-en-1-one

1 reference

(4R)-4-hydroxy-3,5,5-trimethyl-4-[(E,3R)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one

1 reference

1 reference

(4R)-4-hydroxy-3,5,5-trimethyl-4-[(E,3S)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one

1 reference

(4S)-4-hydroxy-3,5,5-trimethyl-4-[(E,3R)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one

1 reference

chemical formula

C₁₉H₃₀O₈

0 references

canonical SMILES

O=C1C=C(C)C(O)(C=CC(OC2OC(CO)C(O)C(O)C2O)C)C(C)(C)C1

0 references

isomeric SMILES

CC1=CC(=O)CC(C)(C)[C@@]1(O)/C=C/[C@H](C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

0 references

found in taxon

Capparis spinosa

2 references

(6S)-Hydroxy-3-oxo-alpha-ionol glucosides from Capparis spinosa fruits.

(6S)-Hydroxy-3-oxo-alpha-ionol glucosides from Capparis spinosa fruits.

Cibotium barometz

3 references

Inhibitors of osteoclast formation from rhizomes of Cibotium barometz

Inhibitors of osteoclast formation from rhizomes of Cibotium barometz

Inhibitors of osteoclast formation from rhizomes of Cibotium barometz

Sauropus androgynus

3 references

Lignan and megastigmane glycosides from Sauropus androgynus

Lignan and megastigmane glycosides from Sauropus androgynus

Lignan and megastigmane glycosides from Sauropus androgynus

Ixora undulata

1 reference

Structure elucidation of secondary metabolites isolated from the leaves of Ixora undulate and their inhibitory activity toward advanced glycation end-products formation

Ajuga salicifolia

1 reference

Ionone, Iridoid and Phenylethanoid Glycosides from Ajuga salicifolia

Anoectochilus formosanus

2 references

Glycosidic constituents from in vitro Anoectochilus formosanus

Glycosidic constituents from in vitro Anoectochilus formosanus

Camellia amplexicaulis

1 reference

New neolignan component from Camellia amplexicaulis and effects on osteoblast differentiation.

Corchorus olitorius

2 references

Medicinal foodstuffs. V. Moroheiya. (1): Absolute stereostructures of corchoionosides A, B, and C, histamine release inhibitors from the leaves of Vietnamese Corchorus olitorius L. (Tiliaceae)

Medicinal foodstuffs. V. Moroheiya. (1): Absolute stereostructures of corchoionosides A, B, and C, histamine release inhibitors from the leaves of Vietnamese Corchorus olitorius L. (Tiliaceae)

Euphorbia hirta

1 reference

Hirtionosides A-C, gallates of megastigmane glucosides, 3-hydroxyoctanoic acid glucosides and a phenylpropanoid glucoside from the whole plants of Euphorbia hirta

Brassica rapa

1 reference

Inhibitory effects of chalcone glycosides isolated from Brassica rapa L. 'hidabeni' and their synthetic derivatives on LPS-induced NO production in microglia.

Kandelia candel

1 reference

Chemical constituents from Kandelia candel with their inhibitory effects on pro-inflammatory cytokines production in LPS-stimulated bone marrow-derived dendritic cells (BMDCs).

Piper umbellatum

1 reference

Flavonas, lignanas e terpeno de Piper umbellata (Piperaceae)

Baccharis dracunculifolia

1 reference

Studies on the constituents from the aerial part of Baccharis dracunculifolia DC.

Santisukia kerrii

1 reference

Phenolic glycosides from Barnettia kerrii

Breynia fruticosa

1 reference

Glycosides from Breynia fruticosa and Breynia rostrata

Breynia rostrata

1 reference

Glycosides from Breynia fruticosa and Breynia rostrata

Cananga odorata

1 reference

The unusual canangafruticosides A-E: five monoterpene glucosides, two monoterpenes and a monoterpene glucoside diester of the aryldihydronaphthalene lignan dicarboxylic acid from leaves of Cananga odorata var. fruticosa

Cardamine komarovii

1 reference

Three New Megastigmane Glucopyranosides from the Cardamine komarovii

Juniperus communis

1 reference

A monoterpene glucoside and three megastigmane glycosides from Juniperus communis var. depressa

Juniperus communis depressa

1 reference

A monoterpene glucoside and three megastigmane glycosides from Juniperus communis var. depressa

Collinsonia japonica

1 reference

Hyaluronidase inhibitors from Keiskea japonica

Markhamia stipulata

1 reference

Phenolic glycosides from Markhamia stipulata

Peperomia obtusifolia

1 reference

Isoswertisin flavones and other constituents from Peperomia obtusifolia

Kali collinum

1 reference

Chemical and biologically active constituents of Salsola collina

Salsola collina

1 reference

Chemical and biologically active constituents of Salsola collina

Salvia nemorosa

1 reference

Megastigmane glycosides from Salvia nemorosa

Salvia × sylvestris

1 reference

Megastigmane glycosides from Salvia nemorosa

Sonchus erzincanicus

1 reference

A new sulfated alpha-ionone glycoside from Sonchus erzincanicus Matthews

Zanthoxylum schinifolium

1 reference

Cytotoxic Constituents from the Leaves of Zanthoxylum schinifolium

Persicaria salicifolia

1 reference

Absolute configuration of (6S,9S)-roseoside from Polygonum hydropiper

Persicaria decipiens

1 reference

Absolute configuration of (6S,9S)-roseoside from Polygonum hydropiper

Tetradium glabrifolium

1 reference

Euodionosides A-G: megastigmane glucosides from leaves of Euodia meliaefolia

Juniperus communis var. depressa

1 reference

A monoterpene glucoside and three megastigmane glycosides from Juniperus communis var. depressa

Persicaria lapathifolia

1 reference

Absolute configuration of (6S,9S)-roseoside from Polygonum hydropiper

Breynia androgyna

1 reference

Lignan and megastigmane glycosides from Sauropus androgynus

Araucaria cunninghamii

1 reference

Antimicrobial activity of Araucaria cunninghamii Sweet and the chemical constituents of its twigs and leaves

Identifiers

InChI

InChI=1S/C19H30O8/c1-10-7-12(21)8-18(3,4)19(10,25)6-5-11(2)26-17-16(24)15(23)14(22)13(9-20)27-17/h5-7,11,13-17,20,22-25H,8-9H2,1-4H3/b6-5+/t11-,13+,14+,15-,16+,17+,19+/m0/s1

0 references

InChIKey

SWYRVCGNMNAFEK-PUVRWCMWSA-N

0 references

CAS Registry Number

185414-25-9

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

2 references

17 September 2022