Propylbenzene

Details

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Internal ID c0522da4-e3f0-4a10-8061-fffdde77f4d9
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name propylbenzene
SMILES (Canonical) CCCC1=CC=CC=C1
SMILES (Isomeric) CCCC1=CC=CC=C1
InChI InChI=1S/C9H12/c1-2-6-9-7-4-3-5-8-9/h3-5,7-8H,2,6H2,1H3
InChI Key ODLMAHJVESYWTB-UHFFFAOYSA-N
Popularity 3,380 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12
Molecular Weight 120.19 g/mol
Exact Mass 120.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.64
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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N-PROPYLBENZENE
103-65-1
1-Phenylpropane
Phenylpropane
Isocumene
Benzene, propyl-
1-Propylbenzene
DTXSID3042219
0WR86ZHG2Z
NSC-16941
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Propylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.9713 97.13%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Lysosomes 0.3956 39.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9168 91.68%
OATP1B3 inhibitior + 0.9551 95.51%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8940 89.40%
P-glycoprotein inhibitior - 0.9933 99.33%
P-glycoprotein substrate - 0.8713 87.13%
CYP3A4 substrate - 0.7857 78.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9643 96.43%
CYP2C9 inhibition - 0.9288 92.88%
CYP2C19 inhibition - 0.8846 88.46%
CYP2D6 inhibition - 0.9183 91.83%
CYP1A2 inhibition - 0.6016 60.16%
CYP2C8 inhibition - 0.6899 68.99%
CYP inhibitory promiscuity - 0.6365 63.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Warning 0.5328 53.28%
Eye corrosion + 0.9840 98.40%
Eye irritation + 0.9887 98.87%
Skin irritation + 0.8694 86.94%
Skin corrosion - 0.9684 96.84%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7041 70.41%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6610 66.10%
skin sensitisation + 0.9523 95.23%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity - 0.7701 77.01%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.5898 58.98%
Acute Oral Toxicity (c) III 0.5186 51.86%
Estrogen receptor binding - 0.9207 92.07%
Androgen receptor binding - 0.8098 80.98%
Thyroid receptor binding - 0.8783 87.83%
Glucocorticoid receptor binding - 0.9086 90.86%
Aromatase binding - 0.9006 90.06%
PPAR gamma - 0.9034 90.34%
Honey bee toxicity - 0.9727 97.27%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.9323 93.23%

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 96.49% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 94.11% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.38% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.03% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.62% 86.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.44% 92.08%
CHEMBL1907 P15144 Aminopeptidase N 82.41% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 82.40% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.08% 95.56%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.36% 96.25%

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.
Brassica juncea
Gossypium hirsutum
Helianthus tuberosus
Pseudocydonia sinensis
Vitis rotundifolia

Cross-Links

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PubChem 7668
NPASS NPC212114
LOTUS LTS0205209
wikiData Q288806