Nonane, 5-phenyl-

Details

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Internal ID 233af9ba-f63d-4376-be3d-359d175b228c
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name nonan-5-ylbenzene
SMILES (Canonical) CCCCC(CCCC)C1=CC=CC=C1
SMILES (Isomeric) CCCCC(CCCC)C1=CC=CC=C1
InChI InChI=1S/C15H24/c1-3-5-10-14(11-6-4-2)15-12-8-7-9-13-15/h7-9,12-14H,3-6,10-11H2,1-2H3
InChI Key ZUKGIZDDXAWABM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.15
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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Benzene, (1-butylpentyl)-
5-Phenylnonane
20216-88-0
(1-Butylpentyl)benzene
(1-butyl-pentyl)-benzene
(1-Butylpentyl)benzene #
DTXSID00334130
ZUKGIZDDXAWABM-UHFFFAOYSA-N

2D Structure

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2D Structure of Nonane, 5-phenyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.9872 98.72%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.4389 43.89%
OATP2B1 inhibitior - 0.8525 85.25%
OATP1B1 inhibitior + 0.9396 93.96%
OATP1B3 inhibitior + 0.9506 95.06%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8835 88.35%
P-glycoprotein inhibitior - 0.9400 94.00%
P-glycoprotein substrate - 0.8436 84.36%
CYP3A4 substrate - 0.7240 72.40%
CYP2C9 substrate - 0.8214 82.14%
CYP2D6 substrate + 0.3542 35.42%
CYP3A4 inhibition - 0.9353 93.53%
CYP2C9 inhibition - 0.9122 91.22%
CYP2C19 inhibition - 0.8850 88.50%
CYP2D6 inhibition - 0.8775 87.75%
CYP1A2 inhibition - 0.5771 57.71%
CYP2C8 inhibition - 0.9728 97.28%
CYP inhibitory promiscuity - 0.6527 65.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5461 54.61%
Eye corrosion + 0.9628 96.28%
Eye irritation + 0.8064 80.64%
Skin irritation + 0.6483 64.83%
Skin corrosion - 0.9686 96.86%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7426 74.26%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation + 0.9205 92.05%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.7756 77.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.5863 58.63%
Acute Oral Toxicity (c) III 0.7072 70.72%
Estrogen receptor binding - 0.8031 80.31%
Androgen receptor binding - 0.7079 70.79%
Thyroid receptor binding - 0.5271 52.71%
Glucocorticoid receptor binding - 0.9212 92.12%
Aromatase binding - 0.8710 87.10%
PPAR gamma - 0.6979 69.79%
Honey bee toxicity - 0.9847 98.47%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.8100 81.00%
Fish aquatic toxicity + 0.9961 99.61%

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 97.69% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 95.04% 90.17%
CHEMBL1907 P15144 Aminopeptidase N 93.37% 93.31%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 89.89% 94.08%
CHEMBL240 Q12809 HERG 88.95% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.91% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.39% 94.62%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.34% 93.56%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.12% 92.08%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 86.46% 95.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.40% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.06% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.05% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.73% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.24% 99.17%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.01% 93.81%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.24% 91.81%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 519748
LOTUS LTS0091637
wikiData Q82099825