(3-Methylpentyl)benzene

Details

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Internal ID 092216c3-1d79-4b5b-aaf9-0dedce4a6a59
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 3-methylpentylbenzene
SMILES (Canonical) CCC(C)CCC1=CC=CC=C1
SMILES (Isomeric) CCC(C)CCC1=CC=CC=C1
InChI InChI=1S/C12H18/c1-3-11(2)9-10-12-7-5-4-6-8-12/h4-8,11H,3,9-10H2,1-2H3
InChI Key PVXCNEZDIJHZQB-UHFFFAOYSA-N
Popularity 7 references 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 4.60
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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Benzene, (3-methylpentyl)-
54410-69-4
26372-59-8
3-methylpentylbenzene
(3-methyl-pentyl)benzene
(3-methylpentyl)-benzene
(3-Methylpentyl)benzene #
DTXSID90871428
PVXCNEZDIJHZQB-UHFFFAOYSA-N
AKOS006331696

2D Structure

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2D Structure of (3-Methylpentyl)benzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.9822 98.22%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.5569 55.69%
OATP2B1 inhibitior - 0.8654 86.54%
OATP1B1 inhibitior + 0.9321 93.21%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8422 84.22%
P-glycoprotein inhibitior - 0.9914 99.14%
P-glycoprotein substrate - 0.7037 70.37%
CYP3A4 substrate - 0.7228 72.28%
CYP2C9 substrate - 0.8214 82.14%
CYP2D6 substrate + 0.3542 35.42%
CYP3A4 inhibition - 0.9536 95.36%
CYP2C9 inhibition - 0.9110 91.10%
CYP2C19 inhibition - 0.8878 88.78%
CYP2D6 inhibition - 0.8493 84.93%
CYP1A2 inhibition - 0.5303 53.03%
CYP2C8 inhibition - 0.9397 93.97%
CYP inhibitory promiscuity - 0.6287 62.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.5031 50.31%
Eye corrosion + 0.9242 92.42%
Eye irritation + 0.7078 70.78%
Skin irritation + 0.7583 75.83%
Skin corrosion - 0.9665 96.65%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4360 43.60%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5235 52.35%
skin sensitisation + 0.9470 94.70%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity - 0.7652 76.52%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.7382 73.82%
Acute Oral Toxicity (c) III 0.7481 74.81%
Estrogen receptor binding - 0.7757 77.57%
Androgen receptor binding - 0.6309 63.09%
Thyroid receptor binding - 0.8091 80.91%
Glucocorticoid receptor binding - 0.9062 90.62%
Aromatase binding - 0.8257 82.57%
PPAR gamma - 0.8057 80.57%
Honey bee toxicity - 0.9397 93.97%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9929 99.29%

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 97.53% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.48% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 90.50% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.85% 94.62%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 89.48% 100.00%
CHEMBL1907 P15144 Aminopeptidase N 89.07% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 87.03% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.15% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.64% 95.56%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.34% 93.81%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.27% 95.50%

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.
Conioselinum anthriscoides
Ligusticum officinale

Cross-Links

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PubChem 521502
NPASS NPC190803