Isopentylbenzene

Details

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Internal ID c5ff2686-78b8-431a-964a-fbb8e12454ff
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 3-methylbutylbenzene
SMILES (Canonical) CC(C)CCC1=CC=CC=C1
SMILES (Isomeric) CC(C)CCC1=CC=CC=C1
InChI InChI=1S/C11H16/c1-10(2)8-9-11-6-4-3-5-7-11/h3-7,10H,8-9H2,1-2H3
InChI Key XNXIYYFOYIUJIW-UHFFFAOYSA-N
Popularity 38 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16
Molecular Weight 148.24 g/mol
Exact Mass 148.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.28
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Isoamylbenzene
2049-94-7
(3-METHYLBUTYL)BENZENE
3-methylbutylbenzene
Benzene, (3-methylbutyl)-
Benzene, isopentyl-
iso-Pentylbenzene
1-Phenyl-3-methylbutane
2-Methyl-4-phenylbutane
3-Methyl-1-phenylbutane
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isopentylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.9337 93.37%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.5189 51.89%
OATP2B1 inhibitior - 0.8726 87.26%
OATP1B1 inhibitior + 0.9606 96.06%
OATP1B3 inhibitior + 0.9467 94.67%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8456 84.56%
P-glycoprotein inhibitior - 0.9868 98.68%
P-glycoprotein substrate - 0.7151 71.51%
CYP3A4 substrate - 0.7148 71.48%
CYP2C9 substrate - 0.8214 82.14%
CYP2D6 substrate + 0.3542 35.42%
CYP3A4 inhibition - 0.9730 97.30%
CYP2C9 inhibition - 0.9587 95.87%
CYP2C19 inhibition - 0.9425 94.25%
CYP2D6 inhibition - 0.9102 91.02%
CYP1A2 inhibition - 0.7768 77.68%
CYP2C8 inhibition - 0.9745 97.45%
CYP inhibitory promiscuity - 0.8417 84.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.5436 54.36%
Eye corrosion + 0.9527 95.27%
Eye irritation + 0.9287 92.87%
Skin irritation + 0.8588 85.88%
Skin corrosion - 0.9017 90.17%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5879 58.79%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6359 63.59%
skin sensitisation + 0.9595 95.95%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7588 75.88%
Acute Oral Toxicity (c) III 0.6734 67.34%
Estrogen receptor binding - 0.8788 87.88%
Androgen receptor binding - 0.6963 69.63%
Thyroid receptor binding - 0.8529 85.29%
Glucocorticoid receptor binding - 0.9129 91.29%
Aromatase binding - 0.8514 85.14%
PPAR gamma - 0.8721 87.21%
Honey bee toxicity - 0.9368 93.68%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9709 97.09%

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 97.23% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 91.94% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.62% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 91.33% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.16% 94.62%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 89.20% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 86.68% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.62% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.15% 86.33%

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.
Angelica sinensis
Vaccinium corymbosum

Cross-Links

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PubChem 16294
NPASS NPC47570
LOTUS LTS0017019
wikiData Q83044546