6-Phenyldodecane

Details

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Internal ID c1f5f64c-3294-4dc4-8b34-6d8a086161bf
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name dodecan-6-ylbenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H30/c1-3-5-7-10-14-17(13-9-6-4-2)18-15-11-8-12-16-18/h8,11-12,15-17H,3-7,9-10,13-14H2,1-2H3
InChI Key ZYHJQFMTTFCBKH-UHFFFAOYSA-N
Popularity 38 references in papers

Physical and Chemical Properties

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Molecular Formula C18H30
Molecular Weight 246.40 g/mol
Exact Mass 246.234750957 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 7.90
Atomic LogP (AlogP) 6.32
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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Benzene, (1-pentylheptyl)-
dodecan-6-ylbenzene
Dodecane, 6-phenyl-
alpha-pentylheptylbenzene
EINECS 220-325-3
CHEBI:77516
DTXSID70875106
RefChem:105231
Benzene, (1pentylheptyl)
DTXCID101013229
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-Phenyldodecane

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 + 0.9794 97.94%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.5187 51.87%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9482 94.82%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.4771 47.71%
P-glycoprotein inhibitior - 0.8478 84.78%
P-glycoprotein substrate - 0.8079 80.79%
CYP3A4 substrate - 0.6845 68.45%
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 - 0.9528 95.28%
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 - 0.5759 57.59%
Skin irritation + 0.6425 64.25%
Skin corrosion - 0.9659 96.59%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7361 73.61%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7276 72.76%
skin sensitisation + 0.9274 92.74%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.7740 77.40%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.5985 59.85%
Acute Oral Toxicity (c) III 0.7630 76.30%
Estrogen receptor binding - 0.7323 73.23%
Androgen receptor binding - 0.6726 67.26%
Thyroid receptor binding + 0.5768 57.68%
Glucocorticoid receptor binding - 0.8197 81.97%
Aromatase binding - 0.8711 87.11%
PPAR gamma - 0.7192 71.92%
Honey bee toxicity - 0.9849 98.49%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.8450 84.50%
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
CHEMBL240 Q12809 HERG 97.60% 89.76%
CHEMBL2581 P07339 Cathepsin D 97.55% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.54% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 94.60% 90.17%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 92.74% 94.08%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.03% 94.62%
CHEMBL230 P35354 Cyclooxygenase-2 90.98% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.05% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 89.99% 93.31%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.47% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.91% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.25% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.05% 96.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.90% 91.81%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.83% 95.56%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 84.42% 85.94%
CHEMBL3401 O75469 Pregnane X receptor 84.25% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.03% 91.11%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 83.09% 95.00%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.50% 93.81%

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 17629
NPASS NPC245819