3-Isopropylphenol

Details

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Internal ID 7e492ec0-5530-486e-9467-22c102425ac0
Taxonomy Benzenoids > Benzene and substituted derivatives > Cumenes
IUPAC Name 3-propan-2-ylphenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12O/c1-7(2)8-4-3-5-9(10)6-8/h3-7,10H,1-2H3
InChI Key VLJSLTNSFSOYQR-UHFFFAOYSA-N
Popularity 57 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O
Molecular Weight 136.19 g/mol
Exact Mass 136.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.52
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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618-45-1
M-ISOPROPYLPHENOL
m-Cumenol
3-propan-2-ylphenol
Phenol, m-isopropyl-
Phenol, 3-(1-methylethyl)-
meta-isopropylphenol
ERD00478GH
DTXSID0044571
NSC-2209
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Isopropylphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.7691 76.91%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7706 77.06%
OATP2B1 inhibitior - 0.8706 87.06%
OATP1B1 inhibitior + 0.9412 94.12%
OATP1B3 inhibitior + 0.9739 97.39%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9581 95.81%
P-glycoprotein inhibitior - 0.9845 98.45%
P-glycoprotein substrate - 0.8886 88.86%
CYP3A4 substrate - 0.7327 73.27%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate + 0.3457 34.57%
CYP3A4 inhibition - 0.9246 92.46%
CYP2C9 inhibition - 0.9147 91.47%
CYP2C19 inhibition - 0.9280 92.80%
CYP2D6 inhibition - 0.9541 95.41%
CYP1A2 inhibition + 0.6879 68.79%
CYP2C8 inhibition - 0.9793 97.93%
CYP inhibitory promiscuity - 0.8935 89.35%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6088 60.88%
Carcinogenicity (trinary) Non-required 0.7456 74.56%
Eye corrosion + 0.9890 98.90%
Eye irritation + 0.9722 97.22%
Skin irritation + 0.8231 82.31%
Skin corrosion + 0.9665 96.65%
Ames mutagenesis - 0.8037 80.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6686 66.86%
Micronuclear - 0.8841 88.41%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.8787 87.87%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.7317 73.17%
Acute Oral Toxicity (c) III 0.7928 79.28%
Estrogen receptor binding - 0.9243 92.43%
Androgen receptor binding - 0.8262 82.62%
Thyroid receptor binding - 0.7678 76.78%
Glucocorticoid receptor binding - 0.9191 91.91%
Aromatase binding - 0.8554 85.54%
PPAR gamma - 0.8902 89.02%
Honey bee toxicity - 0.9398 93.98%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.7792 77.92%

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
CHEMBL2581 P07339 Cathepsin D 95.86% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.65% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.69% 99.15%
CHEMBL2535 P11166 Glucose transporter 89.15% 98.75%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 89.01% 97.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.90% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.03% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.55% 94.73%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.53% 93.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.32% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.27% 94.45%

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.
Chamaecyparis obtusa var. formosana
Thujopsis dolabrata

Cross-Links

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PubChem 12059
LOTUS LTS0073143
wikiData Q27277323