Page last updated: 2024-09-21

3,5-di-tert-butyl-4-hydroxybenzoic acid

Cross-References

ID SourceID
PubMed CID15007
CHEMBL ID119696
SCHEMBL ID227202
MeSH IDM0172550

Synonyms (60)

Synonym
unii-9f0i7yag34
9f0i7yag34 ,
4-10-00-00765 (beilstein handbook reference)
benzoic acid, 3,5-di-tert-butyl-4-hydroxy-
benzoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-
3,5-di-tert-butyl-4-hydroxybenzoic acid
einecs 215-823-2
3,5-bis-tert-butyl-4-hydroxybenzoic acid
3,5-di-t-butyl-4-hydroxybenzoic acid
brn 2216948
OPREA1_044717 ,
inchi=1/c15h22o3/c1-14(2,3)10-7-9(13(17)18)8-11(12(10)16)15(4,5)6/h7-8,16h,1-6h3,(h,17,18
3,5-di-tert-butyl-4-hydroxybenzoic acid, 98%
AC-11916
HMS1648L07
3,5-ditert-butyl-4-hydroxybenzoic acid
CHEMBL119696
AKOS001082280
1421-49-4
D2381
A807856
FT-0633532
AE-562/43460589
SCHEMBL227202
AB01334268-02
3,5-bis(1,1-dimethylethyl)-4-hydroxybenzoic acid
f 2 (antioxidant)
2,6-di-tert-butyl-4-carboxyphenol
4-carboxy-2,6-di-tert-butylphenol
DTXSID3061683
TS-00782
3,5-bis-(1,1-dimetyletyl)-4-hydroxybenzenecarboxylic acid
4-hydroxy-3,5-di(tert.-butyl)benzoic acid
3,5-di-tert-butyl-4-hydroxy benzoic acid
3,5-di-tert-butyl4-hydroxybenzoic acid
3,5-di-tert-butyl4-hydroxy-benzoic acid
3,5-di-tert.-butyl-4-hydroxybenzoic acid
3,5-di-tert-butyl-4-hydroxy-benzoic acid
3,5-di-t-butyl-4-hydroxy-benzoic acid
4-hydroxy-3,5-di-tert-butyl benzoic acid
3,5-di-tert-butyl-4-hydroxybezoic acid
3,5-di-t-butyl4-hydroxybenzoic acid
3,5-bis(1,1-dimethylethyl)-4-hydroxy benzoic acid
3,5-di(t-butyl)-4-hydroxybenzoic acid
3,5-bis(1,1-dimethyethyl)-4-hydroxybenzoic acid
W-108178
3,5-di-tert-butyl-4-hydroxybenzoicacid
3,5-di(tert-butyl)-4-hydroxybenzoic acid
STR04340
3,5-di-t-butyl-4-hydroxy benzoic acid
mfcd00008827
sr-01000597216
SR-01000597216-1
SY048732
EN300-16635
D71197
Q27272465
NCGC00342102-01
CS-0154929
Z56347242

Bioassays (10)

Assay IDTitleYearJournalArticle
AID540299A screen for compounds that inhibit the MenB enzyme of Mycobacterium tuberculosis2010Bioorganic & medicinal chemistry letters, Nov-01, Volume: 20, Issue:21
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.
AID588519A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities2011Antiviral research, Sep, Volume: 91, Issue:3
High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2014Journal of biomolecular screening, Jul, Volume: 19, Issue:6
A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).
AID736211Antidyslipidemic activity against triton WR1339-induced hyperlipidemia in rat assessed as reduction in plasma triglyceride level at 56 umol/kg, ip after 24 hrs (Rvb = 580%)2013Journal of medicinal chemistry, Apr-25, Volume: 56, Issue:8
New multifunctional Di-tert-butylphenoloctahydro(pyrido/benz)oxazine derivatives with antioxidant, antihyperlipidemic, and antidiabetic action.
AID438491Antioxidant activity in rat brain homogenate assessed as malondialdehyde release2009Journal of medicinal chemistry, Nov-26, Volume: 52, Issue:22
Novel compounds designed as antistress agents.
AID1365821Antioxidant activity in rat hepatic microsomes assessed as inhibition of FeSO4-induced lipid peroxidation measured after 45 mins by spectrophotometry2017Bioorganic & medicinal chemistry letters, 11-01, Volume: 27, Issue:21
Dual antioxidant structures with potent anti-inflammatory, hypolipidemic and cytoprotective properties.
AID736212Antidyslipidemic activity against triton WR1339-induced hyperlipidemia in rat assessed as reduction in plasma total cholesterol level at 56 umol/kg, ip after 24 hrs (Rvb = 260%)2013Journal of medicinal chemistry, Apr-25, Volume: 56, Issue:8
New multifunctional Di-tert-butylphenoloctahydro(pyrido/benz)oxazine derivatives with antioxidant, antihyperlipidemic, and antidiabetic action.
AID169468Comparative activity versus Dihydrodimethylbenzofurans in the CPE (Carrageenan paw edema) assay; (-) indicates the compound is inactive1998Journal of medicinal chemistry, Aug-27, Volume: 41, Issue:18
New cyclooxygenase-2/5-lipoxygenase inhibitors. 3. 7-tert-butyl-2, 3-dihydro-3,3-dimethylbenzofuran derivatives as gastrointestinal safe antiinflammatory and analgesic agents: variations at the 5 position.
AID647625Antioxidant activity assessed as trolox equivalent of ABTS radical scavenging activity relative to control2012European journal of medicinal chemistry, Apr, Volume: 50New losartan-hydrocaffeic acid hybrids as antihypertensive-antioxidant dual drugs: Ester, amide and amine linkers.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (15)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (6.67)18.7374
1990's4 (26.67)18.2507
2000's1 (6.67)29.6817
2010's6 (40.00)24.3611
2020's3 (20.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other15 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research Highlights

Dosage (1)

ArticleYear
Further metabolism of 3,5-di-tert-butyl-4-hydroxybenzoic acid, a major metabolite of butylated hydroxytoluene, in rats.
Chemical & pharmaceutical bulletin, Volume: 39, Issue: 2
1991
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]