6-Phenylundecane

Details

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Internal ID 838f0a2f-d039-4f9f-8052-80e165be38e1
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name undecan-6-ylbenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H28/c1-3-5-8-12-16(13-9-6-4-2)17-14-10-7-11-15-17/h7,10-11,14-16H,3-6,8-9,12-13H2,1-2H3
InChI Key WCABIRIFXVXGQH-UHFFFAOYSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C17H28
Molecular Weight 232.40 g/mol
Exact Mass 232.219100893 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 7.40
Atomic LogP (AlogP) 5.93
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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4537-14-8
DTXSID5075446
CHEBI:77514
RefChem:1074135
DTXCID1040407
Benzene, (1-pentylhexyl)-
undecan-6-ylbenzene
Undecane, 6-phenyl-
(1-Pentylhexyl)benzene
alpha-pentylhexylbenzene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 6-Phenylundecane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.9871 98.71%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.5187 51.87%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9391 93.91%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6022 60.22%
P-glycoprotein inhibitior - 0.8758 87.58%
P-glycoprotein substrate - 0.8236 82.36%
CYP3A4 substrate - 0.7050 70.50%
CYP2C9 substrate - 0.8214 82.14%
CYP2D6 substrate + 0.3542 35.42%
CYP3A4 inhibition - 0.9532 95.32%
CYP2C9 inhibition - 0.9126 91.26%
CYP2C19 inhibition - 0.8998 89.98%
CYP2D6 inhibition - 0.8645 86.45%
CYP1A2 inhibition - 0.5996 59.96%
CYP2C8 inhibition - 0.9621 96.21%
CYP inhibitory promiscuity - 0.6643 66.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5389 53.89%
Eye corrosion + 0.9561 95.61%
Eye irritation - 0.6049 60.49%
Skin irritation + 0.6425 64.25%
Skin corrosion - 0.9659 96.59%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6464 64.64%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7276 72.76%
skin sensitisation + 0.9274 92.74%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7740 77.40%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6006 60.06%
Acute Oral Toxicity (c) III 0.7630 76.30%
Estrogen receptor binding - 0.8398 83.98%
Androgen receptor binding - 0.6726 67.26%
Thyroid receptor binding + 0.5760 57.60%
Glucocorticoid receptor binding - 0.8489 84.89%
Aromatase binding - 0.8925 89.25%
PPAR gamma - 0.6446 64.46%
Honey bee toxicity - 0.9846 98.46%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7950 79.50%
Fish aquatic toxicity + 0.9969 99.69%

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%
CHEMBL240 Q12809 HERG 97.36% 89.76%
CHEMBL221 P23219 Cyclooxygenase-1 93.51% 90.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.33% 92.08%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 91.16% 94.08%
CHEMBL1907 P15144 Aminopeptidase N 89.99% 93.31%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.95% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.53% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 88.31% 89.63%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.47% 93.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.25% 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%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.78% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 84.12% 94.73%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 83.09% 95.00%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.85% 93.81%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.55% 91.11%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.39% 91.81%

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.
Panax quinquefolius

Cross-Links

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PubChem 20660
NPASS NPC101122