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Compound Detail

CHEMBL101263

4-NITROBENZOIC ACID
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O=C(O)c1ccc([N+](=O)[O-])cc1

Basic Information

ChEMBL ID CHEMBL101263
Name 4-NITROBENZOIC ACID
Phase Preclinical
Structure Type MOL
InChI Key OTLNPYWUJOZPPA-UHFFFAOYSA-N
1
Targets
3
Activities
1
Assay Types
0
PK Parameters
15
Publications
0
Known Names

Molecular Properties

167.1
MW (Da)
1.29
ALogP
3
HBA
1
HBD
80.4
PSA (Ų)
0.53
QED
0
Ro5 Violations
2
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C7H5NO4
MW 167.12
Aromatic Rings 1
Heavy Atoms 12
NP-Likeness -0.99

Activity Summary

IC50 3 meas. best 6.62

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Mus musculus
CHEMBL375
IC50 6.62 6.62 240.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Mus musculus IC50 = 240.0 nM 6.62 Antihemorrhagic activity in ddY mouse assessed as inhibition of Protobothrops fl... 22047800

Literature References

PubMed DOI Target Context # Activities
- 10.6019/CHEMBL3885881 Rattus norvegicus 37
13215 10.1021/jm00211a010 No relevant target 4
1527790 10.1021/jm00096a014 ADMET 2
1527790 10.1021/jm00096a014 Rattus norvegicus 2
8667357 10.1021/jm950589q ADMET 1
1527790 10.1021/jm00096a014 No relevant target 1
8411009 10.1021/jm00072a012 Unchecked 1
3950915 10.1021/jm00153a009 Thiopurine S-methyltransferase 1
19056282 10.1016/j.bmc.2008.11.040 ADMET 1
22047800 10.1016/j.bmc.2011.10.013 Mus musculus 1
22047800 10.1016/j.bmc.2011.10.013 No relevant target 1
- 10.1007/s00044-009-9162-3 Rattus norvegicus 1
24262887 10.1016/j.bmc.2013.10.037 Indoleamine 2,3-dioxygenase 1 1
13215 10.1021/jm00211a010 Neuron 1
32031798 10.1021/acs.jmedchem.9b01746 ATP-dependent Clp protease proteolytic subunit 1

Data from ChEMBL 36 via Core Engine