2,4'-bisphenol F is a synthetic organic compound with the formula (HOC6H3(CH3))2C(CH3)2. It is a white solid that is used in the production of epoxy resins and other polymers. 2,4'-bisphenol F is synthesized by the reaction of phenol with acetone in the presence of a catalyst. It has been studied for its potential health effects, including its endocrine-disrupting activity. 2,4'-bisphenol F has been found to be an estrogen mimic and may affect reproductive health. It is also a potential allergen and irritant. 2,4'-bisphenol F is studied because of its widespread use in consumer products and its potential health risks. Research is ongoing to understand the effects of 2,4'-bisphenol F on human health.'
2,4'-bisphenol F: contact allergen; structure given in first source
ID Source | ID |
---|---|
PubMed CID | 75576 |
CHEMBL ID | 3187039 |
SCHEMBL ID | 68653 |
MeSH ID | M0138261 |
Synonym |
---|
unii-lix5ymk20b |
lix5ymk20b , |
phenol, 2,4'-methylenedi- |
2,4'-methylenebis(phenol) |
nsc36395 |
(2-hydroxyphenyl)(4-hydroxyphenyl)methane |
2,4'-dihydroxydiphenylmethane |
2,4'-methylenediphenol |
o-(p-hydroxybenzyl)phenol |
nsc-36395 |
phenol, 2-[(4-hydroxyphenyl)methyl]- |
2467-03-0 |
2,4'-bisphenol f |
nsc 36395 |
o-((4-hydroxyphenyl)methyl)phenol |
ccris 8451 |
einecs 219-579-8 |
phenol, 2-((4-hydroxyphenyl)methyl)- |
2-[(4-hydroxyphenyl)methyl]phenol |
2-(4-hydroxybenzyl)phenol |
FT-0691237 |
lvlnpxcisnphle-uhfffaoysa- |
inchi=1/c13h12o2/c14-12-7-5-10(6-8-12)9-11-3-1-2-4-13(11)15/h1-8,14-15h,9h2 |
D1940 |
NCGC00249140-01 |
dtxcid0024890 |
tox21_303514 |
cas-2467-03-0 |
dtxsid2044890 , |
NCGC00257335-01 |
NCGC00259502-01 |
tox21_201953 |
2,4'-methylenebisphenol |
2,4'-bis(hydroxyphenyl)methane |
o,p'-bis(hydroxyphenyl)methane |
SCHEMBL68653 |
oxybenzylphenol |
o-[(4-hydroxyphenyl)methyl]phenol |
W-109789 |
CHEMBL3187039 , |
2,4'-dihydroxydiphenylmethane, aldrichcpr |
mfcd00060113 |
4-[(2-hydroxyphenyl)methyl]phenol |
AKOS027320950 |
AS-62687 |
2,4 inverted exclamation marka-dihydroxydiphenylmethane |
CS-0207438 |
2,4-dihydroxydiphenylmethane |
Q27283009 |
A877837 |
bdbm50607374 |
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Luciferase | Photinus pyralis (common eastern firefly) | Potency | 22.7391 | 0.0072 | 15.7588 | 89.3584 | AID1224835 |
GLI family zinc finger 3 | Homo sapiens (human) | Potency | 29.1240 | 0.0007 | 14.5928 | 83.7951 | AID1259369; AID1259392 |
AR protein | Homo sapiens (human) | Potency | 26.8928 | 0.0002 | 21.2231 | 8,912.5098 | AID1259243; AID1259247; AID743035; AID743036; AID743042; AID743054; AID743063 |
estrogen receptor 2 (ER beta) | Homo sapiens (human) | Potency | 12.1923 | 0.0006 | 57.9133 | 22,387.1992 | AID1259377; AID1259378; AID1259394 |
nuclear receptor subfamily 1, group I, member 3 | Homo sapiens (human) | Potency | 57.8678 | 0.0010 | 22.6508 | 76.6163 | AID1224838; AID1224839; AID1224893 |
progesterone receptor | Homo sapiens (human) | Potency | 46.1818 | 0.0004 | 17.9460 | 75.1148 | AID1346795 |
pregnane X nuclear receptor | Homo sapiens (human) | Potency | 58.1800 | 0.0054 | 28.0263 | 1,258.9301 | AID1346982 |
estrogen nuclear receptor alpha | Homo sapiens (human) | Potency | 26.9589 | 0.0002 | 29.3054 | 16,493.5996 | AID743069; AID743075; AID743077; AID743078; AID743079 |
peroxisome proliferator activated receptor gamma | Homo sapiens (human) | Potency | 10.9635 | 0.0010 | 19.4141 | 70.9645 | AID743191 |
aryl hydrocarbon receptor | Homo sapiens (human) | Potency | 61.8773 | 0.0007 | 23.0674 | 1,258.9301 | AID743085 |
Histone H2A.x | Cricetulus griseus (Chinese hamster) | Potency | 90.9125 | 0.0391 | 47.5451 | 146.8240 | AID1224845 |
thyroid hormone receptor beta isoform 2 | Rattus norvegicus (Norway rat) | Potency | 65.2334 | 0.0003 | 23.4451 | 159.6830 | AID743065; AID743067 |
nuclear factor erythroid 2-related factor 2 isoform 1 | Homo sapiens (human) | Potency | 29.2304 | 0.0006 | 27.2152 | 1,122.0200 | AID743202; AID743219 |
Cellular tumor antigen p53 | Homo sapiens (human) | Potency | 69.4275 | 0.0023 | 19.5956 | 74.0614 | AID651631 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Kelch-like ECH-associated protein 1 | Homo sapiens (human) | Kd | 1,000.0000 | 1.0000 | 1.7667 | 2.4000 | AID1918095 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1918095 | Binding affinity to Keap1 kelch domain (unknown origin) by surface plasmon resonance assay | 2022 | Journal of medicinal chemistry, 11-10, Volume: 65, Issue:21 | Development of Noncovalent Small-Molecule Keap1-Nrf2 Inhibitors by Fragment-Based Drug Discovery. |
AID1869400 | Antifungal activity against Penicillium chrysogenum IBWF assessed as reduction in fungal growth at 25 to 50 ug/ml incubated for 16 to 24 hrs by serial dilution assay | |||
AID1869402 | Antifungal activity against Phytophthora infestans CBS 430.90 assessed as reduction in fungal growth at 25 to 50 ug/ml incubated for 16 to 24 hrs by serial dilution assay | |||
AID1869403 | Antifungal activity against Candida albicans ATCC 90028 assessed as reduction in fungal growth at 25 to 50 ug/ml incubated for 16 to 24 hrs by serial dilution assay | |||
AID1869399 | Antifungal activity against Rhizomucor miehei assessed as reduction in fungal growth at 25 to 50 ug/ml incubated for 16 to 24 hrs by serial dilution assay | |||
AID1869395 | Cytotoxicity against human HeLa S3 cells assessed as cell viability incubated for 48 hrs by microscopic analysis | |||
AID1869397 | Antibacterial activity against Staphylococcus aureus ATCC 11632 assessed as reduction in bacterial growth at 25 to 50 ug/ml incubated for 16 to 24 hrs by serial dilution assay | |||
AID1869401 | Antifungal activity against Paecilomyces variotii ETH 114646 assessed as reduction in fungal growth at 25 to 50 ug/ml incubated for 16 to 24 hrs by serial dilution assay | |||
AID1869396 | Antibacterial activity against Aneurinibacillus migulanus ATCC 9999 assessed as reduction in bacterial growth at 25 to 50 ug/ml incubated for 16 to 24 hrs by serial dilution assay | |||
AID1869398 | Antibacterial activity against Pseudomonas aeruginosa ATCC 15442 assessed as reduction in bacterial growth at 25 to 50 ug/ml incubated for 16 to 24 hrs by serial dilution assay | |||
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 2 (33.33) | 18.7374 |
1990's | 1 (16.67) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 2 (33.33) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.64) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 1 (16.67%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 5 (83.33%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |