(Q5274515)

Dieckol (English)

7 October 2016

C₃₆H₂₂O₁₈

1 reference

Dieckol (English)

7 October 2016

C1=C(C=C(C=C1O)OC2=C(C=C(C3=C2OC4=C(C=C(C=C4O3)OC5=C(C=C(C=C5O)OC6=C(C=C(C7=C6OC8=C(C=C(C=C8O7)O)O)O)O)O)O)O)O)O

1 reference

A new phloroglucinol derivative from the brown alga Eisenia bicyclis: potential for the effective treatment of diabetic complications

Dieckol (English)

7 October 2016

2 references

Molecular docking studies of phlorotannins from Eisenia bicyclis with BACE1 inhibitory activity

Ecklonia kurome

2 references

An Anti-plasmin Inhibitor, Eckol, Isolated from the Brown AlgaEcklonia kuromeOkamura

ECKOLS, NOVEL PHLOROTANNINS WITH A DIBENZO-p-DIOXIN SKELETON POSSESSING INHIBITORY EFFECTS ON α2-MACROGLOBULIN FROM THE BROWN ALGAECKLONIA KUROMEOKAMURA

Ecklonia cava

5 references

Chemical components and its antioxidant properties in vitro: an edible marine brown alga, Ecklonia cava

Dieckol, a SARS-CoV 3CL(pro) inhibitor, isolated from the edible brown algae Ecklonia cava

Dieckol from Ecklonia cava Regulates Invasion of Human Fibrosarcoma Cells and Modulates MMP-2 and MMP-9 Expression via NF-κB Pathway.

Molecular docking studies of a phlorotannin, dieckol isolated from Ecklonia cava with tyrosinase inhibitory activity

Inhibition of HIV-1 reverse transcriptase and protease by phlorotannins from the brown alga Ecklonia cava

Ecklonia stolonifera

5 references

Dieckol, isolated from Ecklonia stolonifera, induces apoptosis in human hepatocellular carcinoma Hep3B cells

A new phlorotannin from the brown alga Ecklonia stolonifera

Hepatoprotective constituents of the edible brown alga Ecklonia stolonifera on tacrine-induced cytotoxicity in Hep G2 cells

Isolation and identification of phlorotannins from Ecklonia stolonifera with antioxidant and anti-inflammatory properties.

The inhibitory effects of eckol and dieckol from Ecklonia stolonifera on the expression of matrix metalloproteinase-1 in human dermal fibroblasts

Identifiers

InChI

InChI=1S/C36H22O18/c37-12-1-13(38)3-15(2-12)49-31-22(44)10-25(47)34-35(31)54-30-21(43)8-17(9-27(30)52-34)48-28-19(41)6-16(7-20(28)42)50-32-23(45)11-24(46)33-36(32)53-29-18(40)4-14(39)5-26(29)51-33/h1-11,37-47H

1 reference

Dieckol (English)

7 October 2016

2 references

imported from Wikimedia project

Dieckol (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

88095-77-6

2 references

English Wikipedia

https://commonchemistry.cas.org/detail?cas_rn=88095-77-6

10 April 2021

1 reference

Dieckol (English)

7 October 2016

2 references

English

title

Dieckol (English)

retrieved

7 October 2016

Reaxys registry number

5714171

1 reference

dieckol (English)

7 October 2016

mapping relation type

2 references

English

title

dieckol (English)

retrieved

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C36H22O18/c37-12-1-13(38)3-15(2-12)49-31-22(44)10-25(47)34-35(31)54-30-21(43)8-17(9-27(30)52-34)48-28-19(41)6-16(7-20(28)42)50-32-23(45)11-24(46)33-36(32)53-29-18(40)4-14(39)5-26(29)51-33/h1-11,37-47H

1 reference

DIECKOL (English)

7 October 2016

2 references

inferred from InChIKey

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

1 reference

2 references

DSSTOX compound identifier

DTXCID00339387

0 references

Human Metabolome Database ID

HMDB0251228

2 references

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00031747

2 references

based on heuristic

inferred from InChIKey

UNII

ZU0ESU4399

1 reference