o-Cymene

Details

Top
Internal ID 46d856ca-c1f5-4b2e-b4a1-3f4fc443340c
Taxonomy Benzenoids > Benzene and substituted derivatives > Cumenes
IUPAC Name 1-methyl-2-propan-2-ylbenzene
SMILES (Canonical) CC1=CC=CC=C1C(C)C
SMILES (Isomeric) CC1=CC=CC=C1C(C)C
InChI InChI=1S/C10H14/c1-8(2)10-7-5-4-6-9(10)3/h4-8H,1-3H3
InChI Key WWRCMNKATXZARA-UHFFFAOYSA-N
Popularity 419 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H14
Molecular Weight 134.22 g/mol
Exact Mass 134.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.12
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
2-Isopropyltoluene
527-84-4
o-Cymol
1-Isopropyl-2-methylbenzene
o-Isopropyltoluene
CYMENE, ORTHO
1-Methyl-2-isopropylbenzene
1-methyl-2-propan-2-ylbenzene
1-Methyl-2-(1-methylethyl)benzene
1-Methyl-2-isopropylbenzol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of o-Cymene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9201 92.01%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.5928 59.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9698 96.98%
OATP1B3 inhibitior + 0.9584 95.84%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9333 93.33%
P-glycoprotein inhibitior - 0.9878 98.78%
P-glycoprotein substrate - 0.9628 96.28%
CYP3A4 substrate - 0.7029 70.29%
CYP2C9 substrate - 0.7735 77.35%
CYP2D6 substrate - 0.7071 70.71%
CYP3A4 inhibition - 0.9477 94.77%
CYP2C9 inhibition - 0.8965 89.65%
CYP2C19 inhibition - 0.8981 89.81%
CYP2D6 inhibition - 0.9367 93.67%
CYP1A2 inhibition - 0.5950 59.50%
CYP2C8 inhibition - 0.9729 97.29%
CYP inhibitory promiscuity - 0.6360 63.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Warning 0.5098 50.98%
Eye corrosion + 0.9634 96.34%
Eye irritation + 0.9822 98.22%
Skin irritation + 0.8748 87.48%
Skin corrosion - 0.9801 98.01%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6439 64.39%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.8625 86.25%
skin sensitisation + 0.9348 93.48%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.8175 81.75%
Nephrotoxicity - 0.5830 58.30%
Acute Oral Toxicity (c) III 0.7893 78.93%
Estrogen receptor binding - 0.9633 96.33%
Androgen receptor binding - 0.9277 92.77%
Thyroid receptor binding - 0.8852 88.52%
Glucocorticoid receptor binding - 0.9259 92.59%
Aromatase binding - 0.8570 85.70%
PPAR gamma - 0.9197 91.97%
Honey bee toxicity - 0.9356 93.56%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.8300 83.00%
Fish aquatic toxicity + 0.9734 97.34%

Targets

Top

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 92.71% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.45% 95.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.43% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 87.14% 94.73%

Cross-Links

Top
PubChem 10703
NPASS NPC102091
LOTUS LTS0096514
wikiData Q27161449