Butylbenzene

Details

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Internal ID e56224c6-6e81-4a64-be5a-e7ac951ca18b
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name butylbenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14/c1-2-3-7-10-8-5-4-6-9-10/h4-6,8-9H,2-3,7H2,1H3
InChI Key OCKPCBLVNKHBMX-UHFFFAOYSA-N
Popularity 1,534 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 4.40
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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N-BUTYLBENZENE
104-51-8
1-Phenylbutane
Benzene, butyl-
1-Butylbenzene
butyl-benzene
CHEMBL195441
S8XZ2901RZ
DTXSID6022472
CHEBI:44194
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Butylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.9789 97.89%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4925 49.25%
OATP2B1 inhibitior - 0.8725 87.25%
OATP1B1 inhibitior + 0.8491 84.91%
OATP1B3 inhibitior + 0.9514 95.14%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8662 86.62%
P-glycoprotein inhibitior - 0.9904 99.04%
P-glycoprotein substrate - 0.7433 74.33%
CYP3A4 substrate - 0.7275 72.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9642 96.42%
CYP2C9 inhibition - 0.9322 93.22%
CYP2C19 inhibition - 0.8715 87.15%
CYP2D6 inhibition - 0.9085 90.85%
CYP1A2 inhibition - 0.5406 54.06%
CYP2C8 inhibition - 0.5585 55.85%
CYP inhibitory promiscuity - 0.6562 65.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.5015 50.15%
Eye corrosion + 0.9797 97.97%
Eye irritation + 0.9901 99.01%
Skin irritation + 0.9019 90.19%
Skin corrosion - 0.9208 92.08%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6910 69.10%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5682 56.82%
skin sensitisation + 0.9457 94.57%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.8145 81.45%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.6081 60.81%
Acute Oral Toxicity (c) III 0.5347 53.47%
Estrogen receptor binding - 0.8308 83.08%
Androgen receptor binding - 0.7243 72.43%
Thyroid receptor binding - 0.8518 85.18%
Glucocorticoid receptor binding - 0.8998 89.98%
Aromatase binding - 0.8356 83.56%
PPAR gamma - 0.8777 87.77%
Honey bee toxicity - 0.9888 98.88%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.8600 86.00%
Fish aquatic toxicity + 0.9705 97.05%

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 98.04% 98.95%
CHEMBL240 Q12809 HERG 94.89% 89.76%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.26% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.28% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 90.04% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.63% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 86.64% 93.31%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.19% 94.62%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.69% 96.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.28% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 82.81% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.56% 99.17%

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.
Ducrosia ismaelis

Cross-Links

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PubChem 7705
LOTUS LTS0209972
wikiData Q105104753