3-Isopropyl-2-methylphenol

Details

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Internal ID 89108813-d2bd-4ef7-8d33-1f24f1cfa7c0
Taxonomy Benzenoids > Benzene and substituted derivatives > Cumenes
IUPAC Name 2-methyl-3-propan-2-ylphenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O/c1-7(2)9-5-4-6-10(11)8(9)3/h4-7,11H,1-3H3
InChI Key NKXINWNCBKRRIC-UHFFFAOYSA-N
Popularity 38 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.82
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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4371-48-6
2-methyl-3-propan-2-ylphenol
DTXSID90195914
RefChem:94492
DTXCID30118405
2-methyl-3-(propan-2-yl)phenol
isopropylkresol
SCHEMBL36322
SCHEMBL997260
SCHEMBL16951421
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-Isopropyl-2-methylphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.7090 70.90%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.8502 85.02%
OATP2B1 inhibitior - 0.8667 86.67%
OATP1B1 inhibitior + 0.9451 94.51%
OATP1B3 inhibitior + 0.9689 96.89%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9628 96.28%
P-glycoprotein inhibitior - 0.9842 98.42%
P-glycoprotein substrate - 0.9428 94.28%
CYP3A4 substrate - 0.6594 65.94%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate + 0.3457 34.57%
CYP3A4 inhibition - 0.9196 91.96%
CYP2C9 inhibition - 0.9070 90.70%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9368 93.68%
CYP1A2 inhibition + 0.9107 91.07%
CYP2C8 inhibition - 0.9382 93.82%
CYP inhibitory promiscuity - 0.7429 74.29%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6729 67.29%
Carcinogenicity (trinary) Non-required 0.7172 71.72%
Eye corrosion + 0.9828 98.28%
Eye irritation + 0.8733 87.33%
Skin irritation + 0.7899 78.99%
Skin corrosion + 0.9671 96.71%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7380 73.80%
Micronuclear - 0.8541 85.41%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.8963 89.63%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6785 67.85%
Acute Oral Toxicity (c) III 0.8351 83.51%
Estrogen receptor binding - 0.8852 88.52%
Androgen receptor binding - 0.8446 84.46%
Thyroid receptor binding - 0.7719 77.19%
Glucocorticoid receptor binding - 0.9166 91.66%
Aromatase binding - 0.8669 86.69%
PPAR gamma - 0.8816 88.16%
Honey bee toxicity - 0.9662 96.62%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9193 91.93%

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 94.80% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.42% 99.15%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.54% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.93% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.52% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.18% 91.11%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 82.36% 83.10%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 80.56% 97.23%
CHEMBL2535 P11166 Glucose transporter 80.39% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.32% 93.99%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.10% 93.65%

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.
Artemisia carvifolia

Cross-Links

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PubChem 138205
LOTUS LTS0213988
wikiData Q83068980