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CHEBI ONTOLOGY - ANNOTATIONS

The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/. The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/). For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.

Term:cyclopentafuran
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Accession:CHEBI:47783 term browser browse the term
Synonyms:related_synonym: cyclopentafurans


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prostaglandin I2 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ace angiotensin I converting enzyme multiple interactions ISO ACE inhibits the reaction [Cocaine affects the abundance of Epoprostenol] CTD PMID:14738173 NCBI chr10:90,910,316...90,930,437
Ensembl chr10:90,910,316...90,931,131
JBrowse link
G Agt angiotensinogen multiple interactions
increases abundance
EXP 1-Butanol inhibits the reaction [AGT protein results in increased abundance of Epoprostenol]; arachidonyltrifluoromethane inhibits the reaction [AGT protein results in increased abundance of Epoprostenol]; midostaurin inhibits the reaction [AGT protein results in increased abundance of Epoprostenol]; PTGS2 protein affects the reaction [AGT protein results in increased abundance of Epoprostenol]
AGT protein results in increased abundance of Epoprostenol; AGT results in increased abundance of Epoprostenol
CTD PMID:3888613 PMID:14613874 NCBI chr19:52,529,139...52,549,618
Ensembl chr19:52,529,185...52,540,977
JBrowse link
G Ccl2 C-C motif chemokine ligand 2 increases expression ISO Epoprostenol results in increased expression of CCL2 protein CTD PMID:15302794 NCBI chr10:67,005,424...67,007,222
Ensembl chr10:67,005,424...67,007,226
JBrowse link
G Fbn1 fibrillin 1 multiple interactions ISO FBN1 protein affects the reaction [Phenylephrine results in increased secretion of Epoprostenol metabolite] CTD PMID:17641673 NCBI chr 3:112,554,257...112,750,835
Ensembl chr 3:112,554,925...112,750,889
JBrowse link
G Il10 interleukin 10 multiple interactions EXP IL10 protein inhibits the reaction [Carbon Tetrachloride results in increased abundance of Epoprostenol] CTD PMID:12632514 NCBI chr13:42,472,625...42,477,308
Ensembl chr13:42,472,839...42,477,313
JBrowse link
G Il1a interleukin 1 alpha increases abundance ISO IL1A protein results in increased abundance of Epoprostenol CTD PMID:21513769 NCBI chr 3:116,526,601...116,537,055
Ensembl chr 3:116,526,604...116,536,822
JBrowse link
G Il1b interleukin 1 beta increases secretion EXP IL1B protein results in increased secretion of Epoprostenol CTD PMID:11882577 NCBI chr 3:116,577,005...116,583,386
Ensembl chr 3:116,577,010...116,583,415
JBrowse link
G Kng2 kininogen 2 increases abundance EXP KNG1 results in increased abundance of Epoprostenol CTD PMID:3888613 NCBI chr11:77,913,876...77,936,247 JBrowse link
G Mapk1 mitogen activated protein kinase 1 increases activity ISO Epoprostenol results in increased activity of MAPK1 protein CTD PMID:19201774 NCBI chr11:83,957,813...84,023,629
Ensembl chr11:83,957,813...84,023,616
JBrowse link
G Mapk3 mitogen activated protein kinase 3 increases activity ISO Epoprostenol results in increased activity of MAPK3 protein CTD PMID:19201774 NCBI chr 1:181,366,646...181,372,863
Ensembl chr 1:181,366,637...181,372,863
JBrowse link
G Pdgfa platelet derived growth factor subunit A multiple interactions
increases abundance
ISO 5,5-dimethyl-3-(3-fluorophenyl)-4-(4-methylsulfonyl)phenyl-2(5H)-furanone inhibits the reaction [PDGFA results in increased abundance of Epoprostenol]; celecoxib inhibits the reaction [PDGFA results in increased abundance of Epoprostenol]; Ibuprofen inhibits the reaction [PDGFA results in increased abundance of Epoprostenol]; N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide inhibits the reaction [PDGFA results in increased abundance of Epoprostenol] CTD PMID:19201774 NCBI chr12:15,645,549...15,667,056
Ensembl chr12:15,645,541...15,666,497
JBrowse link
G Ppargc1a PPARG coactivator 1 alpha increases expression ISO Epoprostenol results in increased expression of PPARGC1A mRNA CTD PMID:23056435 NCBI chr14:58,860,752...59,516,525
Ensembl chr14:58,861,144...59,512,656
JBrowse link
G Ptgs2 prostaglandin-endoperoxide synthase 2 multiple interactions EXP PTGS2 protein affects the reaction [AGT protein results in increased abundance of Epoprostenol] CTD PMID:14613874 NCBI chr13:62,164,080...62,169,770
Ensembl chr13:62,163,932...62,172,188
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 19821
    chemical entity 19821
      atom 19819
        nonmetal atom 19707
          oxygen atom 19445
            oxygen molecular entity 19445
              organooxygen compound 19014
                oxacycle 17587
                  cyclopentafuran 13
                    N-s-butyl-N-[(2R,3S)-3-(\{[(3aS,5R,6aR)-hexahydro-2H-cyclopenta[b]furan-5-yloxy]carbonyl\}amino)-2-hydroxy-4-phenylbutyl]-4-(hydroxymethyl)benzenesulfonamide 0
                    prostaglandins I + 13
Path 2
Term Annotations click to browse term
  CHEBI ontology 19821
    subatomic particle 19819
      composite particle 19819
        hadron 19819
          baryon 19819
            nucleon 19819
              atomic nucleus 19819
                atom 19819
                  main group element atom 19716
                    p-block element atom 19716
                      carbon group element atom 19640
                        carbon atom 19630
                          organic molecular entity 19630
                            organic molecule 19569
                              organic cyclic compound 19360
                                organic heterocyclic compound 18591
                                  organic heteropolycyclic compound 18064
                                    organic heterobicyclic compound 16868
                                      cyclopentafuran 13
                                        N-s-butyl-N-[(2R,3S)-3-(\{[(3aS,5R,6aR)-hexahydro-2H-cyclopenta[b]furan-5-yloxy]carbonyl\}amino)-2-hydroxy-4-phenylbutyl]-4-(hydroxymethyl)benzenesulfonamide 0
                                        prostaglandins I + 13
paths to the root