1,5,6-Trimethyl-6-(3-methylpenta-2,4-dienyl)cyclohexene

Details

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Internal ID bb7c2064-ee03-4c73-8d5d-beb548beeee4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name 1,5,6-trimethyl-6-(3-methylpenta-2,4-dienyl)cyclohexene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24/c1-6-12(2)10-11-15(5)13(3)8-7-9-14(15)4/h6,8,10,14H,1,7,9,11H2,2-5H3
InChI Key SDGBQFYYFDSSQI-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 5.30
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 1,5,6-Trimethyl-6-(3-methylpenta-2,4-dienyl)cyclohexene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9872 98.72%
Caco-2 + 0.9171 91.71%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.6547 65.47%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.9136 91.36%
OATP1B3 inhibitior - 0.2397 23.97%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8752 87.52%
P-glycoprotein inhibitior - 0.9785 97.85%
P-glycoprotein substrate - 0.8339 83.39%
CYP3A4 substrate + 0.5074 50.74%
CYP2C9 substrate - 0.8128 81.28%
CYP2D6 substrate - 0.7875 78.75%
CYP3A4 inhibition - 0.8292 82.92%
CYP2C9 inhibition - 0.8784 87.84%
CYP2C19 inhibition - 0.8578 85.78%
CYP2D6 inhibition - 0.9430 94.30%
CYP1A2 inhibition - 0.8082 80.82%
CYP2C8 inhibition - 0.8291 82.91%
CYP inhibitory promiscuity - 0.6265 62.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Warning 0.5013 50.13%
Eye corrosion - 0.7670 76.70%
Eye irritation - 0.8134 81.34%
Skin irritation + 0.5393 53.93%
Skin corrosion - 0.9890 98.90%
Ames mutagenesis - 0.7528 75.28%
Human Ether-a-go-go-Related Gene inhibition - 0.4624 46.24%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5233 52.33%
skin sensitisation + 0.8874 88.74%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6696 66.96%
Nephrotoxicity - 0.6812 68.12%
Acute Oral Toxicity (c) III 0.8727 87.27%
Estrogen receptor binding - 0.9144 91.44%
Androgen receptor binding - 0.7847 78.47%
Thyroid receptor binding - 0.8307 83.07%
Glucocorticoid receptor binding - 0.8491 84.91%
Aromatase binding - 0.7014 70.14%
PPAR gamma - 0.7480 74.80%
Honey bee toxicity - 0.9303 93.03%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.37% 97.25%
CHEMBL3492 P49721 Proteasome Macropain subunit 91.61% 90.24%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.59% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.59% 96.09%
CHEMBL4072 P07858 Cathepsin B 88.34% 93.67%
CHEMBL4208 P20618 Proteasome component C5 86.89% 90.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.55% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.97% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.72% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.60% 95.89%
CHEMBL2581 P07339 Cathepsin D 81.03% 98.95%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.80% 86.00%
CHEMBL1937 Q92769 Histone deacetylase 2 80.49% 94.75%

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.
Ptychanthus striatus

Cross-Links

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PubChem 74975867
LOTUS LTS0267539
wikiData Q105250623