(4R)-4-ethenyl-4-methyl-3-propan-2-ylidenecyclohexene

Details

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Internal ID cfd8aeab-cff4-47ab-9f1f-c57c2bd9f7e7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name (4R)-4-ethenyl-4-methyl-3-propan-2-ylidenecyclohexene
SMILES (Canonical) CC(=C1C=CCCC1(C)C=C)C
SMILES (Isomeric) CC(=C1C=CCC[C@]1(C)C=C)C
InChI InChI=1S/C12H18/c1-5-12(4)9-7-6-8-11(12)10(2)3/h5-6,8H,1,7,9H2,2-4H3/t12-/m0/s1
InChI Key DDDUDPZNWNWAHI-LBPRGKRZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18
Molecular Weight 162.27 g/mol
Exact Mass 162.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.87
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R)-4-ethenyl-4-methyl-3-propan-2-ylidenecyclohexene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.9557 95.57%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.6482 64.82%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.9359 93.59%
OATP1B3 inhibitior - 0.3738 37.38%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8878 88.78%
P-glycoprotein inhibitior - 0.9766 97.66%
P-glycoprotein substrate - 0.9424 94.24%
CYP3A4 substrate - 0.5701 57.01%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.8810 88.10%
CYP2C9 inhibition - 0.8806 88.06%
CYP2C19 inhibition - 0.8393 83.93%
CYP2D6 inhibition - 0.9387 93.87%
CYP1A2 inhibition - 0.8399 83.99%
CYP2C8 inhibition - 0.9385 93.85%
CYP inhibitory promiscuity - 0.6848 68.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Warning 0.5079 50.79%
Eye corrosion - 0.7794 77.94%
Eye irritation + 0.9512 95.12%
Skin irritation + 0.7273 72.73%
Skin corrosion - 0.9687 96.87%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5298 52.98%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6825 68.25%
skin sensitisation + 0.9170 91.70%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.6891 68.91%
Nephrotoxicity + 0.5405 54.05%
Acute Oral Toxicity (c) III 0.9040 90.40%
Estrogen receptor binding - 0.9615 96.15%
Androgen receptor binding - 0.8104 81.04%
Thyroid receptor binding - 0.8724 87.24%
Glucocorticoid receptor binding - 0.8599 85.99%
Aromatase binding - 0.9162 91.62%
PPAR gamma - 0.8935 89.35%
Honey bee toxicity - 0.8988 89.88%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9949 99.49%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.96% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.29% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.99% 96.09%
CHEMBL4208 P20618 Proteasome component C5 88.61% 90.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.85% 85.30%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.88% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.39% 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.
Ruta graveolens

Cross-Links

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PubChem 162918166
LOTUS LTS0049295
wikiData Q104976257