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
Accession: CHEBI:71971
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
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
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
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
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
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
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
Term paths to the root one shortest all shortest one longest all longest one shortest and longest all
Path 1
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
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