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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:neoflavonoid
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Accession:CHEBI:71971 term browser browse the term
Definition:Any 1-benzopyran with an aryl substituent at position 4. The term was originally restricted to natural products, but is now also used to describe semi-synthetic and fully synthetic compounds.
Synonyms:related_synonym: 4-aryl-1-benzopyran;   4-aryl-1-benzopyrans;   neoflavonoids
 xref: Wikipedia:Neoflavonoid


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4-phenylcoumarin term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Abl1 ABL proto-oncogene 1, non-receptor tyrosine kinase increases expression ISO 4-phenylcoumarin analog results in increased expression of ABL1 mRNA CTD PMID:27773722 NCBI chr 3:14,979,853...15,083,065
Ensembl chr 3:14,979,853...15,083,065 		JBrowse link
G Ddit3 DNA-damage inducible transcript 3 increases expression ISO 4-phenylcoumarin analog results in increased expression of DDIT3 mRNA CTD PMID:27773722 NCBI chr 7:63,115,645...63,121,203
Ensembl chr 7:63,116,380...63,121,201 		JBrowse link
G Gadd45a growth arrest and DNA-damage-inducible, alpha increases expression ISO 4-phenylcoumarin analog results in increased expression of GADD45A mRNA CTD PMID:27773722 NCBI chr 4:96,154,789...96,157,091
Ensembl chr 4:96,154,789...96,157,115 		JBrowse link
G Gadd45g growth arrest and DNA-damage-inducible, gamma increases expression ISO 4-phenylcoumarin analog results in increased expression of GADD45G mRNA CTD PMID:27773722 NCBI chr17:13,376,842...13,378,587
Ensembl chr17:13,376,839...13,378,610 		JBrowse link
G Mlh3 mutL homolog 3 increases expression ISO 4-phenylcoumarin analog results in increased expression of MLH3 mRNA CTD PMID:27773722 NCBI chr 6:104,881,483...104,917,686
Ensembl chr 6:104,881,483...104,917,728 		JBrowse link
G Ppp1r15a protein phosphatase 1, regulatory subunit 15A increases expression ISO 4-phenylcoumarin analog results in increased expression of PPP1R15A mRNA CTD PMID:27773722 NCBI chr 1:96,000,053...96,003,128
Ensembl chr 1:96,000,058...96,003,171 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 20089
    chemical entity 20088
      atom 20058
        nonmetal atom 19979
          oxygen atom 19674
            oxygen molecular entity 19674
              flavonoids 11202
                neoflavonoid 6
                  (S)-4'-Hydroxy-4-methoxydalbergione 0
                  1,2-Dihydro-5-hydroxy-2-(1-hydroxy-1-methylethyl)-4-(isobutyryl)-6-phenylfurano[2,3-h][1]benzopyran-8-one 0
                  2-[(8-methyl-2-oxo-4-phenyl-1-benzopyran-7-yl)oxy]acetic acid 0
                  4'-Hydroxy-5,7-dimethoxy-4-phenylcoumarin 0
                  4-(4-Methoxyphenyl)-5,7-dihydroxychroman-2-one 0
                  5,3',4'-Trihydroxy-7-methoxy-4-phenylcoumarin 0
                  5-hydroxy-8-(hydroxymethyl)-8-methyl-6-(2-methylpropanoyl)-4-phenyl-2H,8H-pyrano[2,3-f]chromen-2-one 0
                  6-Butyryl-5,7-dihydroxy-8-(3',3'-dimethylallyl)-4-phenylcoumarin 0
                  6-Butyryl-5-hydroxy-4-phenylseselin 0
                  6-hydroxy-7,8-dimethoxy-4-phenyl-1-benzopyran-2-one 0
                  7',3',4'-Trihydroxy-5-methoxy-4-phenylcoumarin 0
                  7'-hydroxy-4'-(4-methoxyphenyl)-4,4,5'-trimethyl-2-spiro[1,3-diazinane-6,2'-3,4-dihydro-2H-1-benzopyran]thione 0
                  7,3'-Dihydroxy-5,4'-dimethoxy-4-phenylcoumarin 0
                  7-hydroxy-4-phenyl-8-(1-piperidinylmethyl)-1-benzopyran-2-one 0
                  8-(diethylaminomethyl)-7-hydroxy-4-phenyl-1-benzopyran-2-one 0
                  8-Hydroxy-5,7,3',4'-tetramethoxy-4-phenylcoumarin 0
                  8-[[butyl(ethyl)amino]methyl]-7-hydroxy-4-phenyl-1-benzopyran-2-one 0
                  Calophyllolide 0
                  Crolibulin 0
                  Cyclomammeisin 0
                  Dalbergin 0
                  Dalbergione, 4-methoxy-4'-hydroxy- 0
                  Glycobismine A 0
                  LSM-26505 0
                  Leucadenone A 0
                  Leucadenone B 0
                  Leucadenone C 0
                  Mammea A/AA 0
                  Mammea A/AB 0
                  Mammea A/AB cyclo F 0
                  Mammea A/AB, (-)- 0
                  Mammea A/BA 0
                  Mammea A/BB 0
                  Mammea A/BB, (-)- 0
                  Mammeigin 0
                  Melannin 0
                  Mesuagin 0
                  Mesuol 0
                  Nordalbergin 0
                  S-3'-hydroxy-4,4'-dimethoxydalbergione 0
                  Stevenin 0
                  Tomentolide A 0
                  cis-and-trans-Inophyllolide 0
                  inophyllolide chromanol 0
                  melannein 0
                  neoflavans + 0
                  neoflavones + 6
                  pterolinus J 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 20089
    subatomic particle 20058
      composite particle 20058
        hadron 20088
          baryon 20088
            nucleon 20088
              atomic nucleus 20088
                atom 20058
                  main group element atom 19960
                    p-block element atom 19990
                      carbon group element atom 19916
                        carbon atom 19909
                          organic molecular entity 19909
                            organic molecule 19856
                              organic cyclic compound 19612
                                organic heterocyclic compound 18824
                                  oxacycle 17688
                                    benzopyran 11213
                                      1-benzopyran 10951
                                        neoflavonoid 6
                                          (S)-4'-Hydroxy-4-methoxydalbergione 0
                                          1,2-Dihydro-5-hydroxy-2-(1-hydroxy-1-methylethyl)-4-(isobutyryl)-6-phenylfurano[2,3-h][1]benzopyran-8-one 0
                                          2-[(8-methyl-2-oxo-4-phenyl-1-benzopyran-7-yl)oxy]acetic acid 0
                                          4'-Hydroxy-5,7-dimethoxy-4-phenylcoumarin 0
                                          4-(4-Methoxyphenyl)-5,7-dihydroxychroman-2-one 0
                                          5,3',4'-Trihydroxy-7-methoxy-4-phenylcoumarin 0
                                          5-hydroxy-8-(hydroxymethyl)-8-methyl-6-(2-methylpropanoyl)-4-phenyl-2H,8H-pyrano[2,3-f]chromen-2-one 0
                                          6-Butyryl-5,7-dihydroxy-8-(3',3'-dimethylallyl)-4-phenylcoumarin 0
                                          6-Butyryl-5-hydroxy-4-phenylseselin 0
                                          6-hydroxy-7,8-dimethoxy-4-phenyl-1-benzopyran-2-one 0
                                          7',3',4'-Trihydroxy-5-methoxy-4-phenylcoumarin 0
                                          7'-hydroxy-4'-(4-methoxyphenyl)-4,4,5'-trimethyl-2-spiro[1,3-diazinane-6,2'-3,4-dihydro-2H-1-benzopyran]thione 0
                                          7,3'-Dihydroxy-5,4'-dimethoxy-4-phenylcoumarin 0
                                          7-hydroxy-4-phenyl-8-(1-piperidinylmethyl)-1-benzopyran-2-one 0
                                          8-(diethylaminomethyl)-7-hydroxy-4-phenyl-1-benzopyran-2-one 0
                                          8-Hydroxy-5,7,3',4'-tetramethoxy-4-phenylcoumarin 0
                                          8-[[butyl(ethyl)amino]methyl]-7-hydroxy-4-phenyl-1-benzopyran-2-one 0
                                          Calophyllolide 0
                                          Crolibulin 0
                                          Cyclomammeisin 0
                                          Dalbergin 0
                                          Dalbergione, 4-methoxy-4'-hydroxy- 0
                                          Glycobismine A 0
                                          LSM-26505 0
                                          Leucadenone A 0
                                          Leucadenone B 0
                                          Leucadenone C 0
                                          Mammea A/AA 0
                                          Mammea A/AB 0
                                          Mammea A/AB cyclo F 0
                                          Mammea A/AB, (-)- 0
                                          Mammea A/BA 0
                                          Mammea A/BB 0
                                          Mammea A/BB, (-)- 0
                                          Mammeigin 0
                                          Melannin 0
                                          Mesuagin 0
                                          Mesuol 0
                                          Nordalbergin 0
                                          S-3'-hydroxy-4,4'-dimethoxydalbergione 0
                                          Stevenin 0
                                          Tomentolide A 0
                                          cis-and-trans-Inophyllolide 0
                                          inophyllolide chromanol 0
                                          melannein 0
                                          neoflavans + 0
                                          neoflavones + 6
                                          pterolinus J 0
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