1,2-Diethylbenzene

Details

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Internal ID 17369110-b17c-4836-947a-eef8e7a5fc4f
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 1,2-diethylbenzene
SMILES (Canonical) CCC1=CC=CC=C1CC
SMILES (Isomeric) CCC1=CC=CC=C1CC
InChI InChI=1S/C10H14/c1-3-9-7-5-6-8-10(9)4-2/h5-8H,3-4H2,1-2H3
InChI Key KVNYFPKFSJIPBJ-UHFFFAOYSA-N
Popularity 487 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14
Molecular Weight 134.22 g/mol
Exact Mass 134.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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135-01-3
o-Diethylbenzene
Benzene, diethyl-
Benzene, 1,2-diethyl-
Benzene, o-diethyl-
1,2-diethyl-benzene
25HOX6T1LU
Diethylbenzol
DSSTox_CID_7866
DSSTox_RID_78595
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,2-Diethylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.9847 98.47%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.5920 59.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9683 96.83%
OATP1B3 inhibitior + 0.9435 94.35%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8820 88.20%
P-glycoprotein inhibitior - 0.9928 99.28%
P-glycoprotein substrate - 0.9874 98.74%
CYP3A4 substrate - 0.8198 81.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9283 92.83%
CYP2C9 inhibition - 0.8281 82.81%
CYP2C19 inhibition - 0.7478 74.78%
CYP2D6 inhibition - 0.8856 88.56%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9787 97.87%
CYP inhibitory promiscuity + 0.5916 59.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5300 53.00%
Carcinogenicity (trinary) Warning 0.4422 44.22%
Eye corrosion + 0.9079 90.79%
Eye irritation + 0.9830 98.30%
Skin irritation + 0.8292 82.92%
Skin corrosion - 0.9783 97.83%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4640 46.40%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.9645 96.45%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.9198 91.98%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5589 55.89%
Acute Oral Toxicity (c) III 0.8596 85.96%
Estrogen receptor binding - 0.9476 94.76%
Androgen receptor binding - 0.7080 70.80%
Thyroid receptor binding - 0.8728 87.28%
Glucocorticoid receptor binding - 0.9008 90.08%
Aromatase binding - 0.8984 89.84%
PPAR gamma - 0.8976 89.76%
Honey bee toxicity - 0.9663 96.63%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9908 99.08%

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 92.83% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.67% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.27% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 87.14% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.40% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.77% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 80.23% 90.17%

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.
Gossypium hirsutum

Cross-Links

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PubChem 8657
LOTUS LTS0149334
wikiData Q2429316