(6-Methylheptyl)benzene

Details

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Internal ID 4a96bc75-6377-40fe-87e7-9c30ba96c92c
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 6-methylheptylbenzene
SMILES (Canonical) CC(C)CCCCCC1=CC=CC=C1
SMILES (Isomeric) CC(C)CCCCCC1=CC=CC=C1
InChI InChI=1S/C14H22/c1-13(2)9-5-3-6-10-14-11-7-4-8-12-14/h4,7-8,11-13H,3,5-6,9-10H2,1-2H3
InChI Key TUFDHHZZUWXWRD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H22
Molecular Weight 190.32 g/mol
Exact Mass 190.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 4.45
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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Q63399678

2D Structure

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2D Structure of (6-Methylheptyl)benzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.9864 98.64%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.5061 50.61%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.9519 95.19%
OATP1B3 inhibitior + 0.9422 94.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8643 86.43%
P-glycoprotein inhibitior - 0.9533 95.33%
P-glycoprotein substrate - 0.6217 62.17%
CYP3A4 substrate - 0.6015 60.15%
CYP2C9 substrate - 0.8214 82.14%
CYP2D6 substrate + 0.3542 35.42%
CYP3A4 inhibition - 0.9678 96.78%
CYP2C9 inhibition - 0.9303 93.03%
CYP2C19 inhibition - 0.9270 92.70%
CYP2D6 inhibition - 0.9089 90.89%
CYP1A2 inhibition - 0.7267 72.67%
CYP2C8 inhibition - 0.9192 91.92%
CYP inhibitory promiscuity - 0.8276 82.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.5558 55.58%
Eye corrosion + 0.9323 93.23%
Eye irritation + 0.9327 93.27%
Skin irritation + 0.6815 68.15%
Skin corrosion - 0.9486 94.86%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6460 64.60%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5068 50.68%
skin sensitisation + 0.9338 93.38%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.7969 79.69%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.7074 70.74%
Acute Oral Toxicity (c) III 0.7477 74.77%
Estrogen receptor binding - 0.8926 89.26%
Androgen receptor binding - 0.7192 71.92%
Thyroid receptor binding - 0.5684 56.84%
Glucocorticoid receptor binding - 0.8758 87.58%
Aromatase binding - 0.7183 71.83%
PPAR gamma - 0.8077 80.77%
Honey bee toxicity - 0.9624 96.24%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.9963 99.63%

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 98.17% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 93.09% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.85% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.22% 94.62%
CHEMBL3401 O75469 Pregnane X receptor 88.14% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 86.16% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.49% 95.56%
CHEMBL2885 P07451 Carbonic anhydrase III 84.29% 87.45%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 83.74% 100.00%
CHEMBL3902 P09211 Glutathione S-transferase Pi 83.58% 93.81%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.34% 86.33%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.36% 96.25%
CHEMBL3761 Q9HCG7 Beta-glucosidase 81.87% 99.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.04% 92.08%

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.
Vaccinium corymbosum

Cross-Links

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PubChem 19019642
LOTUS LTS0168397
wikiData Q63399678