Leucosceptoside A (Q105379836)

inferred from SMILES

mass

638.2210705159999 dalton

1 reference

inferred from isomeric SMILES

stereoisomer of

cis-Leucosceptoside A

2 references

[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

2 references

[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

2 references

[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

1 reference

[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

1 reference

chemical formula

C₃₀H₃₈O₁₅

0 references

canonical SMILES

O=C(OC1C(OC(OCCC2=CC=C(O)C(O)=C2)C(O)C1OC3OC(C)C(O)C(O)C3O)CO)C=CC4=CC=C(O)C(OC)=C4

0 references

isomeric SMILES

COc1cc(/C=C/C(=O)O[C@@H]2[C@@H](CO)O[C@@H](OCCc3ccc(O)c(O)c3)[C@H](O)[C@H]2O[C@@H]2O[C@@H](C)[C@H](O)[C@@H](O)[C@H]2O)ccc1O

0 references

found in taxon

Acanthus ebracteatus

2 references

Megastigmane, aliphatic alcohol and benzoxazinoid glycosides from Acanthus ebracteatus

Megastigmane, aliphatic alcohol and benzoxazinoid glycosides from Acanthus ebracteatus

Santisukia kerrii

1 reference

Phenolic glycosides from Barnettia kerrii

Fernandoa adenophylla

2 references

Lignan and phenylpropanoid glycosides from Fernandoa adenophylla

Lignan and phenylpropanoid glycosides from Fernandoa adenophylla

Firmiana simplex

1 reference

Isoprenylated naphthoquinone dimers firmianones A, B, and C from Firmiana platanifolia

Lamium purpureum

2 references

Five new phenylethanoid glycosides from the whole plants of Lamium purpureum L.

Five new phenylethanoid glycosides from the whole plants of Lamium purpureum L.

Leonurus persicus

2 references

Iridoid glycosides of Leonurus persicus

Iridoid glycosides of Leonurus persicus

Marrubium velutinum

3 references

Acylated flavonoid and phenylethanoid glycosides from Marrubium velutinum

Identification of tyrosinase inhibitors from Marrubium velutinum and Marrubium cylleneum

Acylated flavonoid and phenylethanoid glycosides from Marrubium velutinum

Verbena brasiliensis

2 references

New iridoid glucosides from the aerial parts of Verbena brasiliensis

New iridoid glucosides from the aerial parts of Verbena brasiliensis

Marrubium alysson

2 references

Phenylpropanoid glycosides from Marrubium alysson

Phenylpropanoid glycosides from Marrubium alysson

Digitalis purpurea

1 reference

Phenylethanoid glycosides from Digitalis purpurea and Penstemon linarioides with PKCalpha-inhibitory activity

Penstemon linarioides

2 references

Phenylethanoid glycosides from Digitalis purpurea and Penstemon linarioides with PKCalpha-inhibitory activity

Phenylethanoid glycosides from Digitalis purpurea and Penstemon linarioides with PKCalpha-inhibitory activity

Acanthus montanus

1 reference

Acanmontanoside, a new phenylethanoid diglycoside from Acanthus montanus.

Betonica macrantha

1 reference

Iridoid and phenylpropanoid glycosides fromStachys macrantha

Stachys macrantha

1 reference

Iridoid and phenylpropanoid glycosides fromStachys macrantha

Buddleja davidii

1 reference

Phenylethanoid and lignan-iridoid complex glycosides from roots of Buddleja davidii

Lantana trifolia

1 reference

Flavones and phenylpropanoids from a sedative extract of Lantana trifolia L.

Pedicularis artselaeri

1 reference

Iridoid and phenylpropanoid glycosides from Pedicularis artselaeri

Penstemon centranthifolius

1 reference

Antibiofilm phenylethanoid glycosides from Penstemon centranthifolius.

Penstemon crandallii

1 reference

Verbascoside derivatives and iridoid glycosides from Penstemon crandallii

Phlomis armeniaca

1 reference

Studies on constituents with cytotoxic and cytostatic activity of two Turkish medicinal plants Phlomis armeniaca and Scutellaria salviifolia

Plantago lacustris

1 reference

Phenylethanoid glucosides from in vitro propagated plants and callus cultures of Plantago lanceolata

Plantago lanceolata

1 reference

Phenylethanoid glucosides from in vitro propagated plants and callus cultures of Plantago lanceolata

Rehmannia glutinosa

3 references

Phytochemical Studies of Rehmannia glutinosa Rhizones

Hydroxycinnamic acid esters of phenethylalcohol glycosides from Rehmannia glutinosa var. Purpurea

Study on antioxidant effect and chemical constituents of Taohong Siwu decoction

Scutellaria baicalensis

1 reference

Flavonoids and phenylethanoids from hairy root cultures of Scutellaria baicalensis

Sideritis ozturkii

1 reference

Three acylated flavone glycosides from Sideritis ozturkii Aytac & Aksoy

Stachys lavandulifolia

1 reference

Lavandulifolioside B: a new phenylethanoid glycoside from the aerial parts of Stachys lavandulifolia Vahl

Tynanthus panurensis

1 reference

Phenylpropanoid glycosides from Tynanthus panurensis: characterization and LC-MS quantitative analysis

Osmanthus × fortunei

1 reference

Studies on the Constituents of Osmanthus Species. IV. On the Components of the Leaves of Osmanthus fortunei CARR.

Scutellaria prostrata

1 reference

Studies on the nepalese crude drugs. XII. On the phenolic compounds from the root of Scutellaria prostrata JAcq. ex Benth.

Plantago major

1 reference

Phenylethanoid glycosides from Plantago asiatica

Plantago asiatica

1 reference

Phenylethanoid glycosides from Plantago asiatica

Stachytarpheta cayennensis

1 reference

Phenylethanoid glycosides from Stachytarpheta cayennensis (Rich.) Vahl, Verbenaceae, a traditional antimalarial medicinal plant

Sideritis perfoliata

1 reference

Antioxidant and antiinflammatory activities of Sideritis perfoliata subsp. perfoliata (Lamiaceae).

Penstemon secundiflorus

1 reference

Iridoid glycosides from Penstemon species: A C-5, C-9 trans iridoid and C-8 epimeric pairs

Scutellaria orientalis

1 reference

Two phenethyl alcohol glycosides from Scutellaria orientalis subsp. pinnatifida

Globularia davisiana

1 reference

Iridoid glycosides from Globularia davisiana

Globularia orientalis

1 reference

Sugar esters from Globularia orientalis

Globularia dumulosa

1 reference

Iridoids from Globularia dumulosa

Penstemon serrulatus

1 reference

Phenolics from Cell Suspension Cultures of Penstemon serrulatus; Relation to Plant Organs

Scutellaria salviifolia

1 reference

Studies on constituents with cytotoxic and cytostatic activity of two Turkish medicinal plants Phlomis armeniaca and Scutellaria salviifolia

Sideritis lyciae

1 reference

Polyphenolic Compounds of Sideritis lycia and Their Anti-Inflammatory Activity

Clerodendrum trichotomum

1 reference

Angiotensin converting enzyme inhibitory phenylpropanoid glycosides from Clerodendron trichotomum

Phtheirospermum japonicum

1 reference

A New Phenolic Glycoside from Phtheirospermum japonicum

Pedicularis nordmanniana

1 reference

Iridoids and phenylpropanoid glycosides from Pedicularis nordmanniana

Plantago coronopus

1 reference

Phenylethanoid glucosides from in vitro propagated plants and callus cultures of Plantago lanceolata

Plantago depressa

1 reference

A novel strategy for target profiling analysis of bioactive phenylethanoid glycosides in Plantago medicinal plants using ultra-performance liquid chromatography coupled with tandem quadrupole mass spectrometry

Phyla nodiflora var. minor

1 reference

Antiproliferative constituents in plants 9. Aerial parts of Lippia dulcis and Lippia canescens

Volkameria inermis

1 reference

Megastigmane and iridoid glucosides from Clerodendrum inerme

Identifiers

InChI

InChI=1S/C30H38O15/c1-14-23(36)24(37)25(38)30(42-14)45-28-26(39)29(41-10-9-16-3-6-17(32)19(34)11-16)43-21(13-31)27(28)44-22(35)8-5-15-4-7-18(33)20(12-15)40-2/h3-8,11-12,14,21,23-34,36-39H,9-10,13H2,1-2H3/b8-5+/t14-,21+,23-,24+,25+,26+,27+,28+,29+,30-/m0/s1

0 references

InChIKey

ZMYQRHSOVRDQDL-CPPDSBOHSA-N

0 references

1 reference

17 September 2022