4,6-Dimethylhept-5-en-2-ylbenzene

Details

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Internal ID d834020f-f1a9-4b68-9edb-535a9d672849
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 4,6-dimethylhept-5-en-2-ylbenzene
SMILES (Canonical) CC(CC(C)C1=CC=CC=C1)C=C(C)C
SMILES (Isomeric) CC(CC(C)C1=CC=CC=C1)C=C(C)C
InChI InChI=1S/C15H22/c1-12(2)10-13(3)11-14(4)15-8-6-5-7-9-15/h5-10,13-14H,11H2,1-4H3
InChI Key VJZKAUPZUWIWLQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.78
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,6-Dimethylhept-5-en-2-ylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.9506 95.06%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.3709 37.09%
OATP2B1 inhibitior - 0.8682 86.82%
OATP1B1 inhibitior + 0.9122 91.22%
OATP1B3 inhibitior + 0.9249 92.49%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5120 51.20%
P-glycoprotein inhibitior - 0.9644 96.44%
P-glycoprotein substrate - 0.9390 93.90%
CYP3A4 substrate - 0.7306 73.06%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.6701 67.01%
CYP3A4 inhibition - 0.8125 81.25%
CYP2C9 inhibition - 0.8230 82.30%
CYP2C19 inhibition - 0.8644 86.44%
CYP2D6 inhibition - 0.8550 85.50%
CYP1A2 inhibition - 0.7220 72.20%
CYP2C8 inhibition - 0.9597 95.97%
CYP inhibitory promiscuity + 0.5958 59.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5864 58.64%
Carcinogenicity (trinary) Warning 0.5720 57.20%
Eye corrosion + 0.5501 55.01%
Eye irritation - 0.7911 79.11%
Skin irritation + 0.7528 75.28%
Skin corrosion - 0.8975 89.75%
Ames mutagenesis - 0.7237 72.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7128 71.28%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6642 66.42%
skin sensitisation + 0.9728 97.28%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.7024 70.24%
Acute Oral Toxicity (c) III 0.9230 92.30%
Estrogen receptor binding - 0.8721 87.21%
Androgen receptor binding - 0.7607 76.07%
Thyroid receptor binding - 0.7222 72.22%
Glucocorticoid receptor binding - 0.7995 79.95%
Aromatase binding - 0.7253 72.53%
PPAR gamma - 0.8173 81.73%
Honey bee toxicity - 0.8948 89.48%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9921 99.21%

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 97.14% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 95.79% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.31% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.19% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.02% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.94% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.98% 94.73%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 86.18% 94.08%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.22% 93.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.17% 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.
Artemisia monosperma

Cross-Links

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PubChem 86138847
LOTUS LTS0004677
wikiData Q105287622