3-Chloro-4-hydroxybenzoic acid

Details

Top
Internal ID 3b61437d-fc6f-4a8a-b60f-ec8889a91a94
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives
IUPAC Name 3-chloro-4-hydroxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H5ClO3/c8-5-3-4(7(10)11)1-2-6(5)9/h1-3,9H,(H,10,11)
InChI Key QGNLHMKIGMZKJX-UHFFFAOYSA-N
Popularity 37 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H5ClO3
Molecular Weight 172.56 g/mol
Exact Mass 171.9927217 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.74
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
3964-58-7
Benzoic acid, 3-chloro-4-hydroxy-
3-Chloro-4-hydroxybenzoate
4WF3LNJ6Q5
4-hydroxy-3-chlorobenzoic acid
MFCD00002549
NSC-21186
3-chloro-4-hydroxy-benzoic acid
EINECS 223-574-6
NSC 21186
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 3-Chloro-4-hydroxybenzoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.6452 64.52%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.9440 94.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9620 96.20%
OATP1B3 inhibitior + 0.9345 93.45%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9662 96.62%
P-glycoprotein inhibitior - 0.9831 98.31%
P-glycoprotein substrate - 0.9955 99.55%
CYP3A4 substrate - 0.7462 74.62%
CYP2C9 substrate - 0.6241 62.41%
CYP2D6 substrate - 0.8835 88.35%
CYP3A4 inhibition - 0.9361 93.61%
CYP2C9 inhibition - 0.7761 77.61%
CYP2C19 inhibition - 0.8839 88.39%
CYP2D6 inhibition - 0.9494 94.94%
CYP1A2 inhibition - 0.8581 85.81%
CYP2C8 inhibition - 0.6591 65.91%
CYP inhibitory promiscuity - 0.8842 88.42%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.5656 56.56%
Carcinogenicity (trinary) Non-required 0.6105 61.05%
Eye corrosion + 0.7150 71.50%
Eye irritation + 0.9947 99.47%
Skin irritation + 0.9393 93.93%
Skin corrosion - 0.7339 73.39%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8830 88.30%
Micronuclear + 0.5998 59.98%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.9001 90.01%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.6916 69.16%
Acute Oral Toxicity (c) III 0.8539 85.39%
Estrogen receptor binding - 0.7330 73.30%
Androgen receptor binding - 0.6836 68.36%
Thyroid receptor binding - 0.8169 81.69%
Glucocorticoid receptor binding - 0.7527 75.27%
Aromatase binding - 0.8534 85.34%
PPAR gamma - 0.7153 71.53%
Honey bee toxicity - 0.9842 98.42%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7904 79.04%
Fish aquatic toxicity + 0.9840 98.40%

Targets

Top

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
CHEMBL3194 P02766 Transthyretin 96.87% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.15% 91.11%
CHEMBL1811 P34995 Prostanoid EP1 receptor 90.76% 95.71%
CHEMBL4208 P20618 Proteasome component C5 89.61% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.53% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.81% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.57% 94.42%
CHEMBL3401 O75469 Pregnane X receptor 81.08% 94.73%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

Top
PubChem 19860
LOTUS LTS0266080
wikiData Q27458813