2-Hydroxy-5-butoxyphenylacetic acid

Details

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Internal ID 049b605a-247c-40fd-935f-37aa359f9a01
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylacetic acids > 2(hydroxyphenyl)acetic acids
IUPAC Name 2-(5-butoxy-2-hydroxyphenyl)acetic acid
SMILES (Canonical) CCCCOC1=CC(=C(C=C1)O)CC(=O)O
SMILES (Isomeric) CCCCOC1=CC(=C(C=C1)O)CC(=O)O
InChI InChI=1S/C12H16O4/c1-2-3-6-16-10-4-5-11(13)9(7-10)8-12(14)15/h4-5,7,13H,2-3,6,8H2,1H3,(H,14,15)
InChI Key TUTWQVWAOIMZDH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O4
Molecular Weight 224.25 g/mol
Exact Mass 224.10485899 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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5-Butoxy-2-hydroxybenzeneacetic acid

2D Structure

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2D Structure of 2-Hydroxy-5-butoxyphenylacetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.7345 73.45%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.9397 93.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9219 92.19%
OATP1B3 inhibitior + 0.9483 94.83%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9157 91.57%
P-glycoprotein inhibitior - 0.9838 98.38%
P-glycoprotein substrate - 0.9464 94.64%
CYP3A4 substrate - 0.6117 61.17%
CYP2C9 substrate + 0.5427 54.27%
CYP2D6 substrate - 0.8105 81.05%
CYP3A4 inhibition - 0.9143 91.43%
CYP2C9 inhibition - 0.8445 84.45%
CYP2C19 inhibition - 0.6868 68.68%
CYP2D6 inhibition - 0.9090 90.90%
CYP1A2 inhibition + 0.6245 62.45%
CYP2C8 inhibition + 0.5631 56.31%
CYP inhibitory promiscuity - 0.8950 89.50%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7710 77.10%
Carcinogenicity (trinary) Non-required 0.6839 68.39%
Eye corrosion - 0.9842 98.42%
Eye irritation + 0.9012 90.12%
Skin irritation - 0.6096 60.96%
Skin corrosion - 0.9381 93.81%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5808 58.08%
Micronuclear - 0.8426 84.26%
Hepatotoxicity + 0.5051 50.51%
skin sensitisation - 0.6579 65.79%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5647 56.47%
Acute Oral Toxicity (c) III 0.8566 85.66%
Estrogen receptor binding + 0.7168 71.68%
Androgen receptor binding + 0.7056 70.56%
Thyroid receptor binding - 0.6486 64.86%
Glucocorticoid receptor binding + 0.5935 59.35%
Aromatase binding + 0.5357 53.57%
PPAR gamma + 0.8888 88.88%
Honey bee toxicity - 0.9901 99.01%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9699 96.99%

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 98.22% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.86% 99.17%
CHEMBL2581 P07339 Cathepsin D 96.58% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.40% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.02% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.35% 99.15%
CHEMBL4208 P20618 Proteasome component C5 89.15% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 87.10% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.64% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.72% 95.56%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.96% 92.08%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.20% 96.00%
CHEMBL1951 P21397 Monoamine oxidase A 80.50% 91.49%

Cross-Links

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PubChem 15108711
NPASS NPC85040
LOTUS LTS0148860
wikiData Q105265043