2-Hydroxybenzenepropanoic acid

Details

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Internal ID 9fee0647-5c6e-488d-b371-19a6d99cff56
Taxonomy Phenylpropanoids and polyketides > Phenylpropanoic acids
IUPAC Name 3-(2-hydroxyphenyl)propanoic acid
SMILES (Canonical) C1=CC=C(C(=C1)CCC(=O)O)O
SMILES (Isomeric) C1=CC=C(C(=C1)CCC(=O)O)O
InChI InChI=1S/C9H10O3/c10-8-4-2-1-3-7(8)5-6-9(11)12/h1-4,10H,5-6H2,(H,11,12)
InChI Key CJBDUOMQLFKVQC-UHFFFAOYSA-N
Popularity 139 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O3
Molecular Weight 166.17 g/mol
Exact Mass 166.062994177 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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495-78-3
3-(2-Hydroxyphenyl)propionic acid
Melilotic acid
Benzenepropanoic acid, 2-hydroxy-
2-hydroxybenzenepropanoic acid
melilotate
o-Hydroxyphenylpropionic acid
3-(o-Hydroxyphenyl) propionic acid
hydrocoumaric acid
2-Hydroxyphenylpropanoate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Hydroxybenzenepropanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9863 98.63%
Caco-2 + 0.8471 84.71%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.9442 94.42%
OATP2B1 inhibitior - 0.8639 86.39%
OATP1B1 inhibitior + 0.9555 95.55%
OATP1B3 inhibitior + 0.9570 95.70%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9642 96.42%
P-glycoprotein inhibitior - 0.9947 99.47%
P-glycoprotein substrate - 0.9794 97.94%
CYP3A4 substrate - 0.7295 72.95%
CYP2C9 substrate + 0.8019 80.19%
CYP2D6 substrate - 0.8141 81.41%
CYP3A4 inhibition - 0.9444 94.44%
CYP2C9 inhibition - 0.8707 87.07%
CYP2C19 inhibition - 0.8105 81.05%
CYP2D6 inhibition - 0.9532 95.32%
CYP1A2 inhibition - 0.9346 93.46%
CYP2C8 inhibition - 0.8673 86.73%
CYP inhibitory promiscuity - 0.9270 92.70%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7927 79.27%
Carcinogenicity (trinary) Non-required 0.6692 66.92%
Eye corrosion - 0.9306 93.06%
Eye irritation + 0.9947 99.47%
Skin irritation + 0.7593 75.93%
Skin corrosion - 0.7372 73.72%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7498 74.98%
Micronuclear - 0.6623 66.23%
Hepatotoxicity + 0.6428 64.28%
skin sensitisation + 0.7385 73.85%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7497 74.97%
Acute Oral Toxicity (c) III 0.7405 74.05%
Estrogen receptor binding - 0.9232 92.32%
Androgen receptor binding - 0.7328 73.28%
Thyroid receptor binding - 0.8721 87.21%
Glucocorticoid receptor binding - 0.5260 52.60%
Aromatase binding - 0.7480 74.80%
PPAR gamma - 0.5241 52.41%
Honey bee toxicity - 0.9769 97.69%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity + 0.7657 76.57%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.10% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.45% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.71% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.70% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.38% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 83.80% 90.20%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.32% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.06% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.70% 99.17%

Plants that contains it

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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.
Dipteryx odorata
Euphorbia helioscopia
Melia azedarach
Melilotus albus
Melilotus officinalis
Melilotus officinalis

Cross-Links

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PubChem 873
NPASS NPC82050
LOTUS LTS0176151
wikiData Q11751633