1-Isopentyl-1-cyclohexene

Details

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Internal ID e7c3cfbd-334a-49e8-b147-b5f8cc8fa80a
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1-(3-methylbutyl)cyclohexene
SMILES (Canonical) CC(C)CCC1=CCCCC1
SMILES (Isomeric) CC(C)CCC1=CCCCC1
InChI InChI=1S/C11H20/c1-10(2)8-9-11-6-4-3-5-7-11/h6,10H,3-5,7-9H2,1-2H3
InChI Key QATQACDSNXQUEE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20
Molecular Weight 152.28 g/mol
Exact Mass 152.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.92
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Cyclohexene, 1-isopentyl-
1-Isopentyl-1-cyclohexene
3983-04-8
1-Isopentyl-1-cyclohexene #
QATQACDSNXQUEE-UHFFFAOYSA-N
cyclohexene, 1-(3-methylbutyl)-

2D Structure

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2D Structure of 1-Isopentyl-1-cyclohexene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.8970 89.70%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.4346 43.46%
OATP2B1 inhibitior - 0.8385 83.85%
OATP1B1 inhibitior + 0.9506 95.06%
OATP1B3 inhibitior + 0.9230 92.30%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9311 93.11%
P-glycoprotein inhibitior - 0.9705 97.05%
P-glycoprotein substrate - 0.8908 89.08%
CYP3A4 substrate - 0.6696 66.96%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9425 94.25%
CYP2C9 inhibition - 0.9245 92.45%
CYP2C19 inhibition - 0.9187 91.87%
CYP2D6 inhibition - 0.9309 93.09%
CYP1A2 inhibition - 0.7223 72.23%
CYP2C8 inhibition - 0.9704 97.04%
CYP inhibitory promiscuity - 0.5973 59.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Warning 0.5076 50.76%
Eye corrosion + 0.7568 75.68%
Eye irritation + 0.9647 96.47%
Skin irritation + 0.7039 70.39%
Skin corrosion - 0.9591 95.91%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4762 47.62%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.9664 96.64%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.8672 86.72%
Acute Oral Toxicity (c) III 0.8381 83.81%
Estrogen receptor binding - 0.9685 96.85%
Androgen receptor binding - 0.8307 83.07%
Thyroid receptor binding - 0.8284 82.84%
Glucocorticoid receptor binding - 0.8960 89.60%
Aromatase binding - 0.8795 87.95%
PPAR gamma - 0.8938 89.38%
Honey bee toxicity - 0.9415 94.15%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9964 99.64%

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 93.89% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.25% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.98% 97.25%
CHEMBL4208 P20618 Proteasome component C5 87.35% 90.00%
CHEMBL230 P35354 Cyclooxygenase-2 85.89% 89.63%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.83% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.83% 93.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.76% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.78% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.50% 95.56%

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.
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

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PubChem 520965
NPASS NPC177372