4-Hydrazinobenzoic acid

Details

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Internal ID 2d368881-a652-4d0f-be9f-1d20dafb1981
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acids
IUPAC Name 4-hydrazinylbenzoic acid
SMILES (Canonical) C1=CC(=CC=C1C(=O)O)NN
SMILES (Isomeric) C1=CC(=CC=C1C(=O)O)NN
InChI InChI=1S/C7H8N2O2/c8-9-6-3-1-5(2-4-6)7(10)11/h1-4,9H,8H2,(H,10,11)
InChI Key PCNFLKVWBDNNOW-UHFFFAOYSA-N
Popularity 72 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8N2O2
Molecular Weight 152.15 g/mol
Exact Mass 152.058577502 g/mol
Topological Polar Surface Area (TPSA) 75.40 Ų
XlogP -0.90
Atomic LogP (AlogP) 0.67
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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619-67-0
4-hydrazinylbenzoic acid
p-Hydrazinobenzoic acid
Benzoic acid, 4-hydrazino-
p-Carboxyphenylhydrazine
4-Carboxyphenylhydrazine
(4-Carboxyphenyl)hydrazine
BENZOIC ACID, p-HYDRAZINO-
MFCD00007581
Benzoic acid, 4-hydrazinyl-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Hydrazinobenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9741 97.41%
Caco-2 + 0.7656 76.56%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.7109 71.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9786 97.86%
OATP1B3 inhibitior + 0.9524 95.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9675 96.75%
P-glycoprotein inhibitior - 0.9855 98.55%
P-glycoprotein substrate - 0.9787 97.87%
CYP3A4 substrate - 0.8246 82.46%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8835 88.35%
CYP3A4 inhibition + 0.5791 57.91%
CYP2C9 inhibition - 0.6741 67.41%
CYP2C19 inhibition - 0.9134 91.34%
CYP2D6 inhibition - 0.9533 95.33%
CYP1A2 inhibition - 0.6520 65.20%
CYP2C8 inhibition - 0.8753 87.53%
CYP inhibitory promiscuity - 0.9767 97.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6574 65.74%
Carcinogenicity (trinary) Non-required 0.4668 46.68%
Eye corrosion - 0.9783 97.83%
Eye irritation + 0.9952 99.52%
Skin irritation + 0.6034 60.34%
Skin corrosion - 0.8951 89.51%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9355 93.55%
Micronuclear + 0.8200 82.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.9073 90.73%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.6088 60.88%
Acute Oral Toxicity (c) III 0.4693 46.93%
Estrogen receptor binding - 0.7887 78.87%
Androgen receptor binding - 0.5935 59.35%
Thyroid receptor binding - 0.6864 68.64%
Glucocorticoid receptor binding - 0.8211 82.11%
Aromatase binding - 0.6463 64.63%
PPAR gamma - 0.6117 61.17%
Honey bee toxicity - 0.9865 98.65%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 0.7056 70.56%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL1293294 P51151 Ras-related protein Rab-9A 94.06% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 93.91% 81.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.81% 95.56%
CHEMBL4208 P20618 Proteasome component C5 84.16% 90.00%
CHEMBL221 P23219 Cyclooxygenase-1 83.45% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.21% 86.33%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.17% 100.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.61% 94.42%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 80.28% 95.48%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 12089
LOTUS LTS0009039
wikiData Q27274260