decursin (Q27106347)

[(3R)-2,2-dimethyl-8-oxo-3,4-dihydropyrano[3,2-g]chromen-3-yl] 3-methylbut-2-enoate

Decursin (English)

5 October 2016

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₉H₂₀O₅

1 reference

Decursin (English)

20 November 2016

CC(=CC(=O)OC1CC2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C)C

1 reference

Decursin (English)

20 November 2016

CC(=CC(=O)O[C@H]1CC2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C)C

1 reference

Irritant and cytotoxic coumarins from Angelica glauca Edgew roots

Decursin (English)

20 November 2016

1 reference

Apiaceae

1 reference

Decursin inhibits induction of inflammatory mediators by blocking nuclear factor-kappaB activation in macrophages

Angelica decursiva

2 references

Coumarins from the Roots of Angelica morii HAYATA

Studies on Coumarins from the Root of Angelica decursiva FR. et SAV. I. : The Structure of Decursin and Decursidin

Angelica gigas

10 references

Anti-tumor activities of decursinol angelate and decursin fromAngelica gigas

Decursinol angelate: a cytotoxic and protein kinase C activating agent from the root of Angelica gigas

Gigasol and other coumarins from Angelica gigas

Coumarins isolated from Angelica gigas inhibit acetylcholinesterase: structure-activity relationships

In vivo anti-cancer activity of Korean Angelica gigas and its major pyranocoumarin decursin

Anti-Helicobacter pylori activity of herbal medicines

Coumarins from the Root of Angelica gigas NAKAI

Decursin and decursinol from Angelica gigas inhibit the lung metastasis of murine colon carcinoma.

Decursin inhibits growth of human bladder and colon cancer cells via apoptosis, G1-phase cell cycle arrest and extracellular signal-regulated kinase activation

The simultaneous determination of coumarins in Angelica gigas root by high performance liquid chromatography-diode array detector coupled with electrospray ionization/mass spectrometry

Phlojodicarpus villosus

1 reference

Coumarins ofPhlojodicarpus villosus

Scutellaria lateriflora

2 references

Scuteflorins A and B, dihydropyranocoumarins from Scutellaria lateriflora

Scuteflorins A and B, Dihydropyranocoumarins from Scutellaria lateriflora L.

Angelica

1 reference

Decursin: a cytotoxic agent and protein kinase C activator from the root of Angelica gigas

Prangos ferulacea

1 reference

Coumarins fromCachrys ferulaceaCollected in Sardinia

subject has role

enzyme activator

1 reference

Medical Subject Headings

MeSH descriptor ID

C101278

InChI=1S/C19H20O5/c1-11(2)7-18(21)23-16-9-13-8-12-5-6-17(20)22-14(12)10-15(13)24-19(16,3)4/h5-8,10,16H,9H2,1-4H3/t16-/m0/s1

15 March 2018

Identifiers

InChI

1 reference

Decursin (English)

20 November 2016

2 references

Decursin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

5928-25-6

2 references

Global Substance Registration System

UNII

E95RTO3YQR

decursin (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=5928-25-6

10 April 2021

1 reference

(S)-8,8-Dimethyl-2-oxo-7,8-dihydro-2H,6H-pyrano(3,2-g)chromen-7-yl 3-methyl-2-butenoate (English)

20 November 2016

2 references

Decursin (English)

20 November 2016

InChIKey

ChEBI ID

4353

mapping relation type

2 references

DECURSIN (English)

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C19H20O5/c1-11(2)7-18(21)23-16-9-13-8-12-5-6-17(20)22-14(12)10-15(13)24-19(16,3)4/h5-8,10,16H,9H2,1-4H3/t16-/m0/s1

1 reference

DECURSIN (English)

20 November 2016

1 reference

1 reference

InChIKey

DSSTOX compound identifier

0 references

0 references

1 reference

Medical Subject Headings

14 March 2018

1 reference

Global Substance Registration System

Decursin (English)

5 October 2016

2 references

UNII

E95RTO3YQR

decursin (English)

20 November 2016

InChIKey

0 references

1 reference

Decursin (English)