4-Prop-1-enyl-1,1-bis(prop-1-en-2-yl)cyclohexane

Details

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Internal ID b89e83b4-7a11-472a-abe7-c2f20ffad315
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 4-prop-1-enyl-1,1-bis(prop-1-en-2-yl)cyclohexane
SMILES (Canonical) CC=CC1CCC(CC1)(C(=C)C)C(=C)C
SMILES (Isomeric) CC=CC1CCC(CC1)(C(=C)C)C(=C)C
InChI InChI=1S/C15H24/c1-6-7-14-8-10-15(11-9-14,12(2)3)13(4)5/h6-7,14H,2,4,8-11H2,1,3,5H3
InChI Key WSYPQZYSZXUDTO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 4.89
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Prop-1-enyl-1,1-bis(prop-1-en-2-yl)cyclohexane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 + 0.8020 80.20%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.7401 74.01%
OATP2B1 inhibitior - 0.8455 84.55%
OATP1B1 inhibitior + 0.9420 94.20%
OATP1B3 inhibitior + 0.8859 88.59%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8686 86.86%
P-glycoprotein inhibitior - 0.9340 93.40%
P-glycoprotein substrate - 0.9363 93.63%
CYP3A4 substrate - 0.5551 55.51%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate - 0.7751 77.51%
CYP3A4 inhibition - 0.8717 87.17%
CYP2C9 inhibition - 0.8432 84.32%
CYP2C19 inhibition - 0.8225 82.25%
CYP2D6 inhibition - 0.9430 94.30%
CYP1A2 inhibition - 0.8435 84.35%
CYP2C8 inhibition - 0.9321 93.21%
CYP inhibitory promiscuity - 0.7671 76.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Warning 0.5033 50.33%
Eye corrosion + 0.5539 55.39%
Eye irritation + 0.5995 59.95%
Skin irritation + 0.6974 69.74%
Skin corrosion - 0.9905 99.05%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5053 50.53%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8878 88.78%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.8093 80.93%
Nephrotoxicity + 0.5507 55.07%
Acute Oral Toxicity (c) III 0.7532 75.32%
Estrogen receptor binding - 0.8179 81.79%
Androgen receptor binding - 0.7525 75.25%
Thyroid receptor binding - 0.6622 66.22%
Glucocorticoid receptor binding - 0.6572 65.72%
Aromatase binding - 0.6040 60.40%
PPAR gamma - 0.6894 68.94%
Honey bee toxicity - 0.7965 79.65%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9950 99.50%

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
CHEMBL1951 P21397 Monoamine oxidase A 91.12% 91.49%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.30% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.38% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.69% 91.11%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.52% 93.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.36% 100.00%
CHEMBL2061 P19793 Retinoid X receptor alpha 80.34% 91.67%

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 capillaris

Cross-Links

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PubChem 163194643
LOTUS LTS0089265
wikiData Q105312222