Page last updated: 2024-11-05

4-hydrazinobenzoic acid

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

4-Hydrazinobenzoic acid (4-HBA) is an organic compound with the formula H2NNHC6H4COOH. It is a white solid that is soluble in water and ethanol. 4-HBA is used as a precursor to the synthesis of various pharmaceuticals, including hydralazine, a vasodilator used to treat high blood pressure. 4-HBA is also a building block for the preparation of polymers and other organic materials. The compound is known to exhibit anti-inflammatory and antioxidant properties, and its biological activities have been studied in various contexts. It is also an important intermediate in the synthesis of pharmaceuticals and other fine chemicals. Research on 4-HBA focuses on its applications in organic synthesis, its biological properties, and its potential as a precursor for new materials.'

4-hydrazinobenzoic acid: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID12089
CHEMBL ID3189010
SCHEMBL ID7034
MeSH IDM0150764

Synonyms (59)

Synonym
HMS1787J10
AC-1781
BB 0220537
benzoic acid, p-hydrazino-
p-hydrazinobenzoic acid
p-carboxyphenylhydrazine
(4-carboxyphenyl)hydrazine
619-67-0
nsc-3813
benzoic acid, 4-hydrazino-
4-hydrazinobenzoic acid
nsc3813
brn 0387378
nsc 3813
einecs 210-609-5
ai3-21063
ccris 7911
4-hydrazinobenzoic acid, 97%
OPREA1_377686
inchi=1/c7h8n2o2/c8-9-6-3-1-5(2-4-6)7(10)11/h1-4,9h,8h2,(h,10,11
STK391437
4-hydrazinylbenzoic acid
H0800
AKOS000119274
A5051
A15703
NCGC00248560-01
NCGC00248560-02
4-hydrazinobenzoicacidhydrochloride
4-hydrazino benzoic acid
BBL008190
tox21_200198
NCGC00257752-01
cas-619-67-0
dtxcid10708
dtxsid3020708 ,
4-carboxyphenylhydrazine
unii-b1r368je7o
4-15-00-01372 (beilstein handbook reference)
b1r368je7o ,
benzoic acid, 4-hydrazinyl-
FT-0618608
(p-carboxyphenyl)hydrazine
deferasirox impurity f [ep impurity]
p-hydrazino benzoic acid
SCHEMBL7034
PS-5959
SY018304
mfcd00007581
Q-200475
F0865-0011
CHEMBL3189010
CS-W018098
BCP27403
EN300-17558
Q27274260
SB75849
HY-W017382
Z56957167
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (17)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
LuciferasePhotinus pyralis (common eastern firefly)Potency32.14570.007215.758889.3584AID1224835
RAR-related orphan receptor gammaMus musculus (house mouse)Potency0.09830.006038.004119,952.5996AID1159521; AID1159523
GLI family zinc finger 3Homo sapiens (human)Potency37.00580.000714.592883.7951AID1259368; AID1259369; AID1259392
AR proteinHomo sapiens (human)Potency32.17380.000221.22318,912.5098AID1259243; AID1259247; AID743040; AID743042; AID743054
caspase 7, apoptosis-related cysteine proteaseHomo sapiens (human)Potency62.00190.013326.981070.7614AID1346978
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency1.81540.001022.650876.6163AID1224838; AID1224839; AID1224893
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency0.42110.003041.611522,387.1992AID1159552; AID1159553; AID1159555
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency25.54450.001530.607315,848.9004AID1224841; AID1224842; AID1224848; AID1224849; AID1259401; AID1259403
pregnane X nuclear receptorHomo sapiens (human)Potency0.04390.005428.02631,258.9301AID1346982
estrogen nuclear receptor alphaHomo sapiens (human)Potency5.16830.000229.305416,493.5996AID1259244; AID1259248; AID743079; AID743080; AID743091
caspase-3Homo sapiens (human)Potency62.00190.013326.981070.7614AID1346978
aryl hydrocarbon receptorHomo sapiens (human)Potency55.25930.000723.06741,258.9301AID743122
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency0.05530.001723.839378.1014AID743083
nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 (p105), isoform CRA_aHomo sapiens (human)Potency0.062519.739145.978464.9432AID1159509
histone deacetylase 9 isoform 3Homo sapiens (human)Potency5.78450.037617.082361.1927AID1259364; AID1259388
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency9.82660.001557.789015,848.9004AID1259244
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency9.82660.001551.739315,848.9004AID1259244
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Ceullar Components (1)

Processvia Protein(s)Taxonomy
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (3)

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.
AID1453183Binding affinity to CK2alpha (unknown origin) assessed as change in melting temperature by thermal shift assay2017Bioorganic & medicinal chemistry, 07-01, Volume: 25, Issue:13
A fragment-based approach leading to the discovery of a novel binding site and the selective CK2 inhibitor CAM4066.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (10)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (10.00)18.7374
1990's1 (10.00)18.2507
2000's3 (30.00)29.6817
2010's4 (40.00)24.3611
2020's1 (10.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 34.13

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index34.13 (24.57)
Research Supply Index2.40 (2.92)
Research Growth Index4.92 (4.65)
Search Engine Demand Index39.93 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (34.13)

All Compounds (24.57)

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%
Other10 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]