(Q3387412)

7-O-Methyleriodictyol (English)

(2R)-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one

21 September 2016

stereoisomer of

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₆H₁₄O₆

1 reference

7-O-Methyleriodictyol (English)

21 September 2016

canonical SMILES

COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)O)O

1 reference

7-O-Methyleriodictyol (English)

21 September 2016

isomeric SMILES

COC1=CC(=C2C(=O)C[C@H](OC2=C1)C3=CC(=C(C=C3)O)O)O

1 reference

p-Coumaric acid derivatives from Artemisia monosperma

7-O-Methyleriodictyol (English)

21 September 2016

2 references

Bioactive constituents of Artemisia monosperma.

Artemisia campestris

2 references

Flavonoids from Artemisia campestris ssp. glutinosa

Chromones and flavanones from artemisia campestris subsp. maritima

Encelia asperifolia

1 reference

Encelia canescens

1 reference

Encelia frutescens

1 reference

Encelia laciniata

1 reference

Encelia stenophylla

1 reference

Ophryosporus charua

1 reference

Diterpenoids and flavonoids from Ophryosporus charrua

Tessaria dodoneifolia

1 reference

Sesquiterpenes and flavonoids from Tessaria species

Adenothamnus validus

1 reference

Flavonoids of Adenothamnus validus

Artemisia halodendron

1 reference

Flavonoid composition ofArtemisia halodendron

Baccharis salicifolia

1 reference

Neo-clerodane diterpenoids and other constituents from Baccharis species

Baccharis scandens

1 reference

2α,3α-Dihydroxycativic acid, a diterpenoid from Baccharis petiolata

Blumea balsamifera

1 reference

Sesquiterpenoids and plasmin-inhibitory flavonoids from Blumea balsamifera.

Blumea glomerata

1 reference

Isolation of austroinulin possessing cell cycle inhibition activity from Blumea glomerata and revision of its absolute configuration

Gochnatia glutinosa

1 reference

Two homofarnesane derivatives and other constituents from Gochnatia glutinosa

Heliotropium taltalense

1 reference

Chemical analysis of the resinous exudate isolated from Heliotropium taltalense and evaluation of the antioxidant activity of the phenolics components and the resin in homogeneous and heterogeneous systems.

Holocarpha obconica

1 reference

Flavonoid aglycones of Holocarpha obconica☆

Dittrichia viscosa

1 reference

Exudate flavonoids of Inula viscosa

Perymenium hintonii

1 reference

Acyclic diterpenes from perymenium HINTONIIfn1fn1Contribution No. 1653 of Instituto de Quimica, UNAM.

Pulicaria undulata

1 reference

A new thymol derivative from Pulicaria undulata.

Traversia baccharoides

1 reference

A new truxillate and some flavonoid esters from the leaf gum of Traversiabaccharoides Hook. f.

Wyethia glabra

1 reference

Flavonoids from Wyethia glabra

Blumea fistulosa

1 reference

Isolation of austroinulin possessing cell cycle inhibition activity from Blumea glomerata and revision of its absolute configuration

Identifiers

InChI

InChI=1S/C16H14O6/c1-21-9-5-12(19)16-13(20)7-14(22-15(16)6-9)8-2-3-10(17)11(18)4-8/h2-6,14,17-19H,7H2,1H3/t14-/m0/s1

1 reference

7-O-Methyleriodictyol (English)

21 September 2016

1 reference

7-O-Methyleriodictyol (English)

imported from Wikimedia project

21 September 2016

CAS Registry Number

51857-11-5

2 references

English Wikipedia

https://commonchemistry.cas.org/detail?cas_rn=51857-11-5

8 April 2021

1 reference

Sterubin (English)

21 September 2016

2 references

7-O-Methyleriodictyol (English)

21 September 2016

SureChEMBL ID

SCHEMBL17626618

2 references

based on heuristic

inferred from InChIKey

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

1 reference

2 references

DSSTOX compound identifier

DTXCID80122310

0 references

UNII

0IT00NY6AC

1 reference