Benzene, 1-ethyl-2,4,5-trimethyl-

Details

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Internal ID 255cd09a-02d9-402a-804a-fdbec7ed985a
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 1-ethyl-2,4,5-trimethylbenzene
SMILES (Canonical) CCC1=C(C=C(C(=C1)C)C)C
SMILES (Isomeric) CCC1=C(C=C(C(=C1)C)C)C
InChI InChI=1S/C11H16/c1-5-11-7-9(3)8(2)6-10(11)4/h6-7H,5H2,1-4H3
InChI Key IYFUQKGDILUVJG-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16
Molecular Weight 148.24 g/mol
Exact Mass 148.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.17
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Benzene, 1-ethyl-2,4,5-trimethyl-
2,4,5-TRIMETHYLETHYLBENZENE
DTXSID20170496
1,2,4-Trimethyl,5-Ethylbenzene
Benzene, 1,2,4-trimethyl-5-ethyl
Benzene, 5-ethyl-1,2,4-trimethyl
RefChem:117318
DTXCID7092987
IYFUQKGDILUVJG-UHFFFAOYSA-N
1-Ethyl-2,4,5-trimethylbenzene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Benzene, 1-ethyl-2,4,5-trimethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.9196 91.96%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.4964 49.64%
OATP2B1 inhibitior - 0.8626 86.26%
OATP1B1 inhibitior + 0.9564 95.64%
OATP1B3 inhibitior + 0.9404 94.04%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8393 83.93%
P-glycoprotein inhibitior - 0.9732 97.32%
P-glycoprotein substrate - 0.9835 98.35%
CYP3A4 substrate - 0.7793 77.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9605 96.05%
CYP2C9 inhibition - 0.8918 89.18%
CYP2C19 inhibition - 0.8432 84.32%
CYP2D6 inhibition - 0.8983 89.83%
CYP1A2 inhibition - 0.6353 63.53%
CYP2C8 inhibition - 0.9727 97.27%
CYP inhibitory promiscuity + 0.5125 51.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.4490 44.90%
Eye corrosion + 0.8122 81.22%
Eye irritation + 0.9691 96.91%
Skin irritation + 0.8580 85.80%
Skin corrosion - 0.9293 92.93%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5670 56.70%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.9564 95.64%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.5924 59.24%
Acute Oral Toxicity (c) III 0.7661 76.61%
Estrogen receptor binding - 0.9121 91.21%
Androgen receptor binding - 0.7892 78.92%
Thyroid receptor binding - 0.8160 81.60%
Glucocorticoid receptor binding - 0.8324 83.24%
Aromatase binding - 0.7118 71.18%
PPAR gamma - 0.8977 89.77%
Honey bee toxicity - 0.9589 95.89%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9884 98.84%

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
CHEMBL3401 O75469 Pregnane X receptor 89.75% 94.73%
CHEMBL2581 P07339 Cathepsin D 89.73% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.29% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.54% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.05% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.39% 96.00%

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.
Panax ginseng

Cross-Links

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PubChem 28812
NPASS NPC58995