1-Ethyl-4-isobutylbenzene

Details

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Internal ID 4eae0656-5c62-4819-84b0-f28225234516
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name 1-ethyl-4-(2-methylpropyl)benzene
SMILES (Canonical) CCC1=CC=C(C=C1)CC(C)C
SMILES (Isomeric) CCC1=CC=C(C=C1)CC(C)C
InChI InChI=1S/C12H18/c1-4-11-5-7-12(8-6-11)9-10(2)3/h5-8,10H,4,9H2,1-3H3
InChI Key FMHWAAZOTFVMKR-UHFFFAOYSA-N
Popularity 13 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18
Molecular Weight 162.27 g/mol
Exact Mass 162.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.45
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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1-ethyl-4-(2-methylpropyl)benzene
100319-40-2
p-Isobutylethylbenzene
1-Ethyl-4-isobutylbenzene #
DTXSID00341920
FMHWAAZOTFVMKR-UHFFFAOYSA-N
MFCD08275587
AKOS006287445
Benzene, 1-ethyl-4-(2-methylpropyl)-
BS-45944
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Ethyl-4-isobutylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9793 97.93%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.9143 91.43%
Subcellular localzation Lysosomes 0.4646 46.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9518 95.18%
OATP1B3 inhibitior + 0.9507 95.07%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9053 90.53%
P-glycoprotein inhibitior - 0.9765 97.65%
P-glycoprotein substrate - 0.9392 93.92%
CYP3A4 substrate - 0.7736 77.36%
CYP2C9 substrate - 0.8214 82.14%
CYP2D6 substrate + 0.3542 35.42%
CYP3A4 inhibition - 0.9358 93.58%
CYP2C9 inhibition - 0.8972 89.72%
CYP2C19 inhibition - 0.9477 94.77%
CYP2D6 inhibition - 0.8757 87.57%
CYP1A2 inhibition - 0.6965 69.65%
CYP2C8 inhibition - 0.9715 97.15%
CYP inhibitory promiscuity - 0.7085 70.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5581 55.81%
Carcinogenicity (trinary) Warning 0.5786 57.86%
Eye corrosion + 0.9394 93.94%
Eye irritation + 0.9406 94.06%
Skin irritation + 0.7863 78.63%
Skin corrosion - 0.9502 95.02%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4653 46.53%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6965 69.65%
skin sensitisation + 0.9625 96.25%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7845 78.45%
Acute Oral Toxicity (c) III 0.8720 87.20%
Estrogen receptor binding - 0.9548 95.48%
Androgen receptor binding - 0.7282 72.82%
Thyroid receptor binding - 0.6906 69.06%
Glucocorticoid receptor binding - 0.9223 92.23%
Aromatase binding - 0.8582 85.82%
PPAR gamma - 0.8273 82.73%
Honey bee toxicity - 0.9441 94.41%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9759 97.59%

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 97.78% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 92.46% 90.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 91.49% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.58% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.69% 94.45%
CHEMBL1944 P08473 Neprilysin 84.57% 92.63%
CHEMBL4072 P07858 Cathepsin B 82.79% 93.67%

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.
Curcuma longa

Cross-Links

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PubChem 576929
NPASS NPC179376