(Q6586709)

Wedelolactone (English)

3 October 2016

chemical formula

C₁₆H₁₀O₇

1 reference

Wedelolactone (English)

3 October 2016

canonical SMILES

COC1=CC(=C2C(=C1)OC(=O)C3=C2OC4=CC(=C(C=C43)O)O)O

1 reference

Potential Value of Plants as Sources of New Antifertility Agents II *

Wedelolactone (English)

3 October 2016

8 references

Antihepatotoxic agent in micropropagated plantlets of Eclipta alba

Neutralization of lethal and myotoxic activities of South American rattlesnake venom by extracts and constituents of the plant Eclipta prostrata (Asteraceae)

Inhibition of the myotoxic and hemorrhagic activities of crotalid venoms by Eclipta prostrata (Asteraceae) extracts and constituents

In vitro plant regeneration of Eclipta alba and increased production of coumestans

Coumestans as the Main Active Principles of the Liver DrugsEclipta albaandWedelia calendulacea1

Plants against snakebites

STUDIES ON CHEMICAL CONSTITUENTS OF ECLIPTA PROSTRATA

Hypericum erectum

2 references

Studies on antihemorrhagic substances in herbs classified as hemostatics in Chinese medicine. IV. On antihemorrhagic principles in Hypericum erectum Thunb

Studies on antihemorrhagic substances in herbs classified as hemostatics in Chinese medicine. IV. On antihemorrhagic principles in Hypericum erectum Thunb

Aconitum kongboense

1 reference

Chemical constituents of the aerial parts of Aconitum kongboense

Eclipta prostrata

9 references

Potential Value of Plants as Sources of New Antifertility Agents II *

STUDIES ON CHEMICAL CONSTITUENTS OF ECLIPTA PROSTRATA

Inhibition of the myotoxic and hemorrhagic activities of crotalid venoms by Eclipta prostrata (Asteraceae) extracts and constituents

Neutralization of lethal and myotoxic activities of South American rattlesnake venom by extracts and constituents of the plant Eclipta prostrata (Asteraceae)

Plants against snakebites

Coumestans as the Main Active Principles of the Liver DrugsEclipta albaandWedelia calendulacea1

In vitro plant regeneration of Eclipta alba and increased production of coumestans

Antihepatotoxic agent in micropropagated plantlets of Eclipta alba

Wedelolactone inhibits LPS-induced pro-inflammation via NF-kappaB pathway in RAW 264.7 cells

Sphagneticola calendulacea

5 references

Potential Value of Plants as Sources of New Antifertility Agents II *

Coumestans as the Main Active Principles of the Liver DrugsEclipta albaandWedelia calendulacea1

The benzofuran norwedelic acid from Wedelia calendulaceae

Wedelolactone inhibits LPS-induced pro-inflammation via NF-kappaB pathway in RAW 264.7 cells

126. Chemical examination of Wedelia calendulacea. Part I. Structure of wedelolactone

physically interacts with

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

5551

InChI=1S/C16H10O7/c1-21-6-2-10(19)14-12(3-6)23-16(20)13-7-4-8(17)9(18)5-11(7)22-15(13)14/h2-5,17-19H,1H3

17 August 2016

Identifiers

InChI

1 reference

Wedelolactone (English)

3 October 2016

2 references

Wedelolactone (English)

3 October 2016

ChEBI release 2020-09-01

2 references

wedelolactone (English)

3 October 2016

https://commonchemistry.cas.org/detail?cas_rn=524-12-9

9 April 2021

1 reference

wedelolactone (English)

3 October 2016

2 references

Wedelolactone (English)

3 October 2016

Reaxys registry number

332398

1 reference

wedelolactone (English)

3 October 2016

ChEBI ID

10037

mapping relation type

2 references

wedelolactone (English)

3 October 2016

International Chemical Identifier

InChI

InChI=1S/C16H10O7/c1-21-6-2-10(19)14-12(3-6)23-16(20)13-7-4-8(17)9(18)5-11(7)22-15(13)14/h2-5,17-19H,1H3

1 reference

WEDELOLACTONE (English)

3 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

DTXCID20122899

0 references

EC number

637-054-5

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.164.794

27 December 2018

ECHA Substance Infocard ID

3,13,14-trihydroxy-5-methoxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-1(10),2,4,6,11(16),12,14-heptaen-9-one (English)

quotation

CAS no.: 524-12-9 (English)

100.164.794

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.164.794

27 December 2018

Guide to Pharmacology Ligand ID

3,13,14-trihydroxy-5-methoxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-1(10),2,4,6,11(16),12,14-heptaen-9-one (English)

quotation

CAS no.: 524-12-9 (English)

5551

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

5551

wedelolactone (English)

Human Metabolome Database ID

3 October 2016

HMDB0259891

2 references

based on heuristic

inferred from InChIKey

3 references

wedelolactone (English)

3 October 2016

based on heuristic

inferred from InChIKey

UNII

0K6L725GNS

2 references

Global Substance Registration System

UNII

0K6L725GNS

WEDELOLACTONE (English)

3 October 2016

0 references

1 reference