Eupatolide (Q27106567)

eupatolide synthase activity

inferred from SMILES

part of

1 reference

reference URL

http://geneontology.org/external2go/rhea2go

25 May 2022

mass

248.141245±0 dalton

1 reference

(3aR,4S,6E,10E,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one

Eupatolide (English)

5 October 2016

2 references

(3aR,4S,6E,11aS)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one

1 reference

Neobritannilactone B

1 reference

(3aR,4S,6Z,10E,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one

2 references

(3aR,4R,6E,10E,11aS)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one

1 reference

(3aR,4S,6Z,10E,11aS)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one

1 reference

(3aS,4S,6E,10E,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one

1 reference

(3aS,4R,6E,10E,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one

1 reference

chemical formula

C₁₅H₂₀O₃

1 reference

Eupatolide (English)

5 October 2016

CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2

1 reference

Eupatolide (English)

5 October 2016

C/C/1=C\[C@@H]2[C@@H]([C@@H](C/C(=C/CC1)/C)O)C(=C)C(=O)O2

1 reference

Eudesmane derivatives other constituents fromApalochlamys spectabilis Cassinia species

Eupatolide (English)

5 October 2016

1 reference

Cassinia subtropica

1 reference

Sesquiterpene lactones and other constituents from Cassinia, actinobole and an axeton species

Eupatorium chinense

2 references

Seven germacranolides, eupaglehnins A, B, C, D, E, and F, and 2alpha-acetoxyepitulipinolide from Eupatorium glehni

Seven Germacranolides, Eupaglehnins A, B, C, D, E, and F, and 2α-Acetoxyepitulipinolide from Eupatorium glehni.

Helianthus argophyllus

3 references

Sesquiterpene lactones and diterpenoids from Helianthus argophyllus

Three sesquiterpene lactones from Helianthus niveus subsp. canescens and H. argophyllus

Chemosystematic Investigation of the Annual Species of Helianthus (Asteraceae)

Rhodanthe floribunda

1 reference

Sesquiterpene lactones and other constituents from Australian Helipterum species

Inula britannica

2 references

New sesquiterpene dimers from Inula britannica inhibit NF-kappaB activation and NO and TNF-alpha production in LPS-stimulated RAW264.7 cells

Secoeudesmanolides from Inula japonica

Inula japonica

1 reference

Secoeudesmanolides from Inula japonica

Inula salsoloides

2 references

Further sesquiterpene lactones from Inula salsoloides

Sesquiterpene lactones from Inula salsoloides

Stevia alpina

1 reference

Sesquiterpene lactones from Stevia alpina var. glutinosa

Gonzalezia hypargyrea

2 references

Sesquiterpene lactones from Viguiera hypargyrea

Sesquiterpene lactones from Viguiera hypargyrea

Aldama tucumanensis

2 references

Terpenoid constituents of Viguiera tucumanensis

Antifeedant activity of metabolites from Viguiera tucumanensis.

Ophryosporus floribundus

1 reference

Seco-labdanes and other constituents fromOphryosporus floribundus

Disynaphia multicrenulata

1 reference

Sesquiterpene lactones and other constituents of Disynaphia multicrenulata from Argentina

Cassinia arcuata

1 reference

Eremophilane derivatives and other constituents from Haeckeria species and further Australian inuleae

Eupatoriastrum nelsonii

1 reference

Germacranolides from Eupatoriastrum nelsonii

Aldama atacamensis

1 reference

Further sesquiterpene lactones from Calea and Viguiera species

Eupatorium cannabinum

1 reference

Eupatoriopicrin 19-O-Linolenoate and Other Constituents from Eupatorium cannabium

Eupatorium formosanum

1 reference

Structure and stereochemistry of eupaformonin, a novel cytotoxic sesquiterpene lactone from eupatorium formosanum hay.

Florestina tripteris

1 reference

Eupatolide and borneol derivatives from Florestina tripteris

Kyrsteniopsis dibollii

1 reference

Unusual norhomoditerpenes and other constituents from Kyrsteniopsis dibollii

Tithonia pedunculata

1 reference

An acyclic diterpene and sesquiterpene lactones from Tithonia pedunculata

Aldama linearis

1 reference

Further sesquiterpene lactones from Calea and Viguiera species

Aldama tukumanensis

2 references

Antifeedant activity of metabolites from Viguiera tucumanensis.

Terpenoid constituents of Viguiera tucumanensis

Pentanema britannicum

2 references

Secoeudesmanolides from Inula japonica

New sesquiterpene dimers from Inula britannica inhibit NF-kappaB activation and NO and TNF-alpha production in LPS-stimulated RAW264.7 cells

Identifiers

InChI

InChI=1S/C15H20O3/c1-9-5-4-6-10(2)8-13-14(12(16)7-9)11(3)15(17)18-13/h5,8,12-14,16H,3-4,6-7H2,1-2H3/b9-5+,10-8+/t12-,13-,14-/m1/s1

1 reference

PDEJECFRCJOMEN-OURLZOILSA-N

Eupatolide (English)

5 October 2016

2 references

Eupatolide (English)

5 October 2016

ChEBI release 2020-09-01

2 references

PDEJECFRCJOMEN-OURLZOILSA-N

Eupatolide (English)

5 October 2016

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=6750-25-0

1 reference

English

(3aR,4R,6E,10E,11aR)-4-Hydroxy-6,10-dimethyl-3-methylene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2(3H)-one (English)

5 October 2016

1 reference

Eupatolide (English)

5 October 2016

mapping relation type

1 reference

Eupatolide (English)

5 October 2016

1 reference

EUPATOLIDE (English)

5 October 2016

1 reference

0 references

683-136-9

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.208.652

27 December 2018

ECHA Substance Infocard ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 6750-25-0 (English)

100.208.652

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.208.652

27 December 2018

[No public or meaningful name is available] (English)

quotation

CAS no.: 6750-25-0 (English)

1 reference

Eupatolide (English)

5 October 2016

1 reference

English

Eupatolide (English)