Ethylbenzene

Details

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Internal ID fc2f99ca-267f-4500-953d-8826847f531c
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name ethylbenzene
SMILES (Canonical) CCC1=CC=CC=C1
SMILES (Isomeric) CCC1=CC=CC=C1
InChI InChI=1S/C8H10/c1-2-8-6-4-3-5-7-8/h3-7H,2H2,1H3
InChI Key YNQLUTRBYVCPMQ-UHFFFAOYSA-N
Popularity 13,111 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10
Molecular Weight 106.16 g/mol
Exact Mass 106.078250319 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.25
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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100-41-4
Phenylethane
Ethylbenzol
Ethyl benzene
Benzene, ethyl-
Aethylbenzol
Ethylenzene
Ethylbenzeen
Etilbenzene
Etylobenzen
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethylbenzene

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 + 0.9711 97.11%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Lysosomes 0.4751 47.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9421 94.21%
OATP1B3 inhibitior + 0.9600 96.00%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8856 88.56%
P-glycoprotein inhibitior - 0.9926 99.26%
P-glycoprotein substrate - 0.9715 97.15%
CYP3A4 substrate - 0.8112 81.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9568 95.68%
CYP2C9 inhibition - 0.8849 88.49%
CYP2C19 inhibition - 0.9040 90.40%
CYP2D6 inhibition - 0.9423 94.23%
CYP1A2 inhibition - 0.5540 55.40%
CYP2C8 inhibition - 0.8692 86.92%
CYP inhibitory promiscuity - 0.6250 62.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6081 60.81%
Carcinogenicity (trinary) Warning 0.5524 55.24%
Eye corrosion + 0.9950 99.50%
Eye irritation + 0.9951 99.51%
Skin irritation + 0.9401 94.01%
Skin corrosion - 0.8453 84.53%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7130 71.30%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6557 65.57%
skin sensitisation + 0.9828 98.28%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7119 71.19%
Acute Oral Toxicity (c) III 0.8651 86.51%
Estrogen receptor binding - 0.9398 93.98%
Androgen receptor binding - 0.8459 84.59%
Thyroid receptor binding - 0.8747 87.47%
Glucocorticoid receptor binding - 0.8995 89.95%
Aromatase binding - 0.8610 86.10%
PPAR gamma - 0.9228 92.28%
Honey bee toxicity - 0.9739 97.39%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.9058 90.58%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL4096 P04637 Cellular tumor antigen p53 6.3 nM
6.3 nM
Potency
Potency
via CMAUP
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 95.57% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 95.51% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.17% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.48% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 82.24% 94.73%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 81.17% 92.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.37% 95.56%

Cross-Links

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PubChem 7500
NPASS NPC65873
ChEMBL CHEMBL371561
LOTUS LTS0122434
wikiData Q409184