prostaglandin E2 (Q416554)

Prostaglandin E2 (English)

9-oxo-11S,15S-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8R,12S]

19 October 2016

stereoisomer of

2 references

9-oxo-11S,15R-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8R,12S]

2 references

(8beta,11beta,12alpha,15R)-11,15-Dihydroxy-9-oxoprosta-5,13-dien-1-oic acid

2 references

7-[(1R,2R,3R)-3-hydroxy-2-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-5-oxocyclopentyl]hept-5-enoic acid

2 references

8-isoprostaglandin E2

2 references

15-epi-prostaglandin E2

2 references

7-[(1R,2R,3R)-3-hydroxy-2-[(3S)-3-hydroxyoct-1-enyl]-5-oxocyclopentyl]-5-heptenoic acid

2 references

9-oxo-11S,15R-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8S,12S]

1 reference

1 reference

9-oxo-11S,15R-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8R,12R]

1 reference

(Z)-7-[(1S,2S,3R)-3-hydroxy-2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopentyl]hept-5-enoic acid

1 reference

9-oxo-11R,15S-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8R,12S]

1 reference

9-oxo-11R,15R-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8S,12R]

1 reference

9-oxo-11R,15R-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8R,12S]

1 reference

(Z)-7-[(1S,2R,3S)-3-hydroxy-2-[(E,3R)-3-hydroxyoct-1-enyl]-5-oxocyclopentyl]hept-5-enoic acid

1 reference

5-trans-prostaglandin E2

1 reference

9-oxo-11S,15S-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8S,12R]

1 reference

9-oxo-11S,15S-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8S,12S]

1 reference

chemical formula

C₂₀H₃₂O₅

1 reference

Prostaglandin E2 (English)

19 November 2016

canonical SMILES

CCCCCC(C=CC1C(CC(=O)C1CC=CCCCC(=O)O)O)O

1 reference

Prostaglandin E2 (English)

19 November 2016

isomeric SMILES

CCCCC[C@@H](/C=C/[C@H]1[C@@H](CC(=O)[C@@H]1C/C=C\CCCC(=O)O)O)O

1 reference

Prostaglandin E2 (English)

https://www.whocc.no/atc_ddd_index/?code=G02AD02

19 November 2016

defined daily dose

0.5 milligram

route of administration

oral administration

1 reference

reference URL

1 reference

14 February 2018

1 reference

14 February 2018

1 reference

14 February 2018

World Health Organisation international non-proprietary name

dinoprostone (English)

1 reference

Prostaglandins from the horns of the spotted deer (Cervus nippon)

prostaglandin E2 (English)

19 October 2016

1 reference

Gersemia fruticosa

1 reference

In vitro biosynthesis of prostaglandins in the White Sea soft coral Gersemia fruticosa: Formation of optically active PGD2, PGE2, PGF2α and 15-keto-PGF2α from arachidonic acid

Larix sibirica

2 references

Identification of prostaglandins E (series 1 and 2) isolated from the living tissues ofLarix sibirica andPopulus balzamifera

Detection of prostaglandin F2? in tissues of Populus balsamifera and Larix sibirica

Populus balsamifera

1 reference

Identification of prostaglandins E (series 1 and 2) isolated from the living tissues ofLarix sibirica andPopulus balzamifera

Homo sapiens

2 references

Recon 2.2: from reconstruction to model of human metabolism

A community-driven global reconstruction of human metabolism.

Populus candicans

1 reference

Identification of prostaglandins E (series 1 and 2) isolated from the living tissues ofLarix sibirica andPopulus balzamifera

Populus alba

1 reference

Identification of prostaglandins E (series 1 and 2) isolated from the living tissues ofLarix sibirica andPopulus balzamifera

medical condition treated

1 reference

13 December 2016

1 reference

physically interacts with

13 December 2016

Prostaglandin E receptor 1

1 reference

Prostaglandin E receptor 2

17 August 2016

1 reference

Prostaglandin E receptor 2 (subtype EP2)

17 August 2016

1 reference

Prostaglandin E receptor 3

17 August 2016

1 reference

Prostaglandin E receptor 4

17 August 2016

1 reference

Solute carrier organic anion transporter family member 2A1

17 August 2016

1 reference

Solute carrier organic anion transporter family member 3A1

17 August 2016

1 reference

imported from Wikimedia project

17 August 2016

pregnancy category

US pregnancy category C

1 reference

1 reference

Medical Subject Headings

15 March 2018

0 references

1 reference

https://reactome.org/PathwayBrowser/#/R-HSA-1430728&DTAB=MT

Commons category

Prostaglandin E2

0 references

Identifiers

InChI

InChI=1S/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h4,7,12-13,15-17,19,21,23H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t15-,16+,17+,19+/m0/s1

1 reference

Prostaglandin E2 (English)

19 November 2016

2 references

Prostaglandin E2 (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

363-24-6

2 references

dinoprostone (English)

19 November 2016

https://commonchemistry.cas.org/detail?cas_rn=363-24-6

10 April 2021

1 reference

Dinoprostone (English)

19 November 2016

2 references

Prostaglandin E2 (English)

19 November 2016

Reaxys registry number

2224724

1 reference

prostaglandin E2 (English)

19 October 2016

ChEBI ID

15551

mapping relation type

2 references

DINOPROSTONE (English)

19 November 2016

International Chemical Identifier

InChI

InChI=1S/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h4,7,12-13,15-17,19,21,23H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t15-,16+,17+,19+/m0/s1

1 reference

DINOPROSTONE (English)

19 November 2016

2 references

splash10-00di-0495000000-78584a9b664c5155b473

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

splash10-00dr-0592000000-b37d658cf7b0d590aad4

0 references

splash10-00dr-0590000000-985f93ab468aa6a8a1b8

0 references

splash10-00dr-0890000000-5757ca5e8720a47086dc

0 references

splash10-0079-0960000000-c67461d3bd965cbf289c

0 references

splash10-000i-0920000000-830ad149a4fe8f36e211

0 references

splash10-07br-0910000000-35e5bd204c947e2c4bcc

0 references

splash10-05fs-0900000000-573b0c5a4593210b387a

0 references

splash10-00di-0294000000-9d89acbe9e631d718a4b

0 references

splash10-00or-0096000000-67e3460a07ad1397b529

0 references

splash10-0059-4920000000-6108934d406ea4062761

0 references

DSSTox substance ID

DTXSID4022947

2 references

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

DSSTOX compound identifier

0 references

0 references

0 references

1 reference

dinoprostone (English)

ECHA Substance Infocard ID

19 November 2016

100.006.052

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.006.052

27 December 2018

Dinoprostone (English)

quotation

CAS no.: 363-24-6 (English)

1 reference

Dinoprostone (English)

publication date

17 November 2015

1883

1 reference

1883

PGE2 (English)

19 November 2016

1 reference

D10.251.355.255.550.250.200

5 February 2021

Dinoprostone

0 references

MeSH concept ID

M0023405

0 references

MeSH tree code

0 references

D23.469.050.175.725.250.200

0 references

RxNorm ID

3478

1 reference

dinoprostone (English)

19 November 2016

DrugBank ID

DB00917

1 reference

Human Metabolome Database ID

HMDB0001220

2 references

2 references

dinoprostone (English)

19 November 2016

MedlinePlus drug identifier

0 references

1 reference

dinoprostone (English)

19 November 2016

0 references

1 reference

1 reference

https://docs.openalex.org/download-snapshot/snapshot-data-format

prostaglandin E2 (English)

19 October 2016

0 references

0 references

1 reference

28 October 2013

1 reference

9 July 2020

Microsoft Academic ID

0 references

0 references

1 reference

26 January 2022

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

3WFH (English)

19 October 2016

1 reference

dinoprostone (English)