1-Butyl-3,5-dimethylbenzene

Details

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Internal ID dcc297ed-96d3-40a6-be1f-22439f475ede
Taxonomy Benzenoids > Benzene and substituted derivatives > Xylenes > m-Xylenes
IUPAC Name 1-butyl-3,5-dimethylbenzene
SMILES (Canonical) CCCCC1=CC(=CC(=C1)C)C
SMILES (Isomeric) CCCCC1=CC(=CC(=C1)C)C
InChI InChI=1S/C12H18/c1-4-5-6-12-8-10(2)7-11(3)9-12/h7-9H,4-6H2,1-3H3
InChI Key GINMJHHVPMUMGK-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H18
Molecular Weight 162.27 g/mol
Exact Mass 162.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.65
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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1601-74-7
starbld0006167
1,3-Dimethyl-5-butylbenzene
1,3-Dimethyl-5-butyl-benzen
benzene-1,3-dimethyl-5-butyl
1,3-Dimethyl-5-n-Butylbenzene
Benzene, 1-butyl-3,5-dimethyl
GINMJHHVPMUMGK-UHFFFAOYSA-N
DTXSID401037096

2D Structure

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2D Structure of 1-Butyl-3,5-dimethylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.9895 98.95%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.5755 57.55%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.8813 88.13%
OATP1B3 inhibitior + 0.9357 93.57%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8178 81.78%
P-glycoprotein inhibitior - 0.9851 98.51%
P-glycoprotein substrate - 0.8700 87.00%
CYP3A4 substrate - 0.6977 69.77%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3634 36.34%
CYP3A4 inhibition - 0.9683 96.83%
CYP2C9 inhibition - 0.9337 93.37%
CYP2C19 inhibition - 0.9186 91.86%
CYP2D6 inhibition - 0.8919 89.19%
CYP1A2 inhibition - 0.6659 66.59%
CYP2C8 inhibition - 0.8569 85.69%
CYP inhibitory promiscuity - 0.6749 67.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.4657 46.57%
Eye corrosion + 0.8828 88.28%
Eye irritation + 0.8390 83.90%
Skin irritation + 0.8137 81.37%
Skin corrosion - 0.8898 88.98%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4479 44.79%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.9398 93.98%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7390 73.90%
Acute Oral Toxicity (c) III 0.7182 71.82%
Estrogen receptor binding - 0.8988 89.88%
Androgen receptor binding - 0.5465 54.65%
Thyroid receptor binding - 0.6784 67.84%
Glucocorticoid receptor binding - 0.8530 85.30%
Aromatase binding - 0.8815 88.15%
PPAR gamma - 0.8223 82.23%
Honey bee toxicity - 0.9861 98.61%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9777 97.77%

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 96.67% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.42% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 87.80% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.29% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.80% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.16% 99.17%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.04% 94.80%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.66% 97.21%
CHEMBL1907 P15144 Aminopeptidase N 82.63% 93.31%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.57% 95.17%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.15% 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.
Crataegus pinnatifida

Cross-Links

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PubChem 528693
NPASS NPC122901