1-Methyl-2-propylbenzene

Details

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Internal ID 4d619dcd-4dd4-4616-9b2f-35b76a581024
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name 1-methyl-2-propylbenzene
SMILES (Canonical) CCCC1=CC=CC=C1C
SMILES (Isomeric) CCCC1=CC=CC=C1C
InChI InChI=1S/C10H14/c1-3-6-10-8-5-4-7-9(10)2/h4-5,7-8H,3,6H2,1-2H3
InChI Key YQZBFMJOASEONC-UHFFFAOYSA-N
Popularity 79 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 4.10
Atomic LogP (AlogP) 2.95
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2-Propyltoluene
1074-17-5
2-n-Propyltoluene
o-Propyltoluene
1-Methyl-2-n-propylbenzene
Toluene, o-propyl-
Benzene, 1-methyl-2-propyl-
EINECS 214-037-7
NSC 73977
NSC-73977
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-Methyl-2-propylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.9749 97.49%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4747 47.47%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9511 95.11%
OATP1B3 inhibitior + 0.9367 93.67%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8805 88.05%
P-glycoprotein inhibitior - 0.9932 99.32%
P-glycoprotein substrate - 0.9154 91.54%
CYP3A4 substrate - 0.7263 72.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9825 98.25%
CYP2C9 inhibition - 0.9053 90.53%
CYP2C19 inhibition - 0.8105 81.05%
CYP2D6 inhibition - 0.8617 86.17%
CYP1A2 inhibition - 0.5725 57.25%
CYP2C8 inhibition - 0.7774 77.74%
CYP inhibitory promiscuity - 0.5674 56.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.5010 50.10%
Eye corrosion + 0.8362 83.62%
Eye irritation + 0.9742 97.42%
Skin irritation + 0.7655 76.55%
Skin corrosion - 0.9457 94.57%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5379 53.79%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.9539 95.39%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.6603 66.03%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.5562 55.62%
Acute Oral Toxicity (c) III 0.6728 67.28%
Estrogen receptor binding - 0.9749 97.49%
Androgen receptor binding - 0.8453 84.53%
Thyroid receptor binding - 0.9095 90.95%
Glucocorticoid receptor binding - 0.9274 92.74%
Aromatase binding - 0.9250 92.50%
PPAR gamma - 0.9242 92.42%
Honey bee toxicity - 0.9795 97.95%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9919 99.19%

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 93.78% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.36% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.99% 86.33%
CHEMBL5805 Q9NR97 Toll-like receptor 8 85.87% 96.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.86% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.45% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 81.70% 93.31%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.20% 93.65%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.62% 89.62%
CHEMBL3769292 Q9H773 dCTP pyrophosphatase 1 80.48% 94.40%

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.
Crocus sativus
Gossypium hirsutum

Cross-Links

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PubChem 14091
NPASS NPC213472
LOTUS LTS0194207
wikiData Q63396360