Methyl 5,5-dimethylcyclohepta-1,3,6-triene-1-carboxylate

Details

Top
Internal ID 78548bea-8e53-4e42-bcf6-dd38aaf38af5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name methyl 5,5-dimethylcyclohepta-1,3,6-triene-1-carboxylate
SMILES (Canonical) CC1(C=CC=C(C=C1)C(=O)OC)C
SMILES (Isomeric) CC1(C=CC=C(C=C1)C(=O)OC)C
InChI InChI=1S/C11H14O2/c1-11(2)7-4-5-9(6-8-11)10(12)13-3/h4-8H,1-3H3
InChI Key QZYLIXQVHZRYQQ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C11H14O2
Molecular Weight 178.23 g/mol
Exact Mass 178.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.24
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Methyl 5,5-dimethylcyclohepta-1,3,6-triene-1-carboxylate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 + 0.9500 95.00%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7005 70.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9256 92.56%
OATP1B3 inhibitior + 0.9461 94.61%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8567 85.67%
P-glycoprotein inhibitior - 0.9709 97.09%
P-glycoprotein substrate - 0.9368 93.68%
CYP3A4 substrate - 0.5162 51.62%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8940 89.40%
CYP3A4 inhibition - 0.9158 91.58%
CYP2C9 inhibition - 0.8378 83.78%
CYP2C19 inhibition - 0.8541 85.41%
CYP2D6 inhibition - 0.9429 94.29%
CYP1A2 inhibition - 0.9084 90.84%
CYP2C8 inhibition - 0.8999 89.99%
CYP inhibitory promiscuity - 0.8254 82.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5629 56.29%
Carcinogenicity (trinary) Non-required 0.5593 55.93%
Eye corrosion + 0.6665 66.65%
Eye irritation + 0.9963 99.63%
Skin irritation + 0.5604 56.04%
Skin corrosion - 0.9703 97.03%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6416 64.16%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5284 52.84%
skin sensitisation + 0.8280 82.80%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.8039 80.39%
Nephrotoxicity + 0.6391 63.91%
Acute Oral Toxicity (c) III 0.8001 80.01%
Estrogen receptor binding - 0.5913 59.13%
Androgen receptor binding - 0.9333 93.33%
Thyroid receptor binding - 0.8548 85.48%
Glucocorticoid receptor binding - 0.9351 93.51%
Aromatase binding - 0.8301 83.01%
PPAR gamma - 0.8733 87.33%
Honey bee toxicity - 0.9350 93.50%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.8657 86.57%

Targets

Top

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.31% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.21% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.43% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.78% 85.14%
CHEMBL4208 P20618 Proteasome component C5 83.85% 90.00%
CHEMBL4040 P28482 MAP kinase ERK2 83.35% 83.82%

Plants that contains it

Top
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.
Thuja plicata

Cross-Links

Top
PubChem 13931941
LOTUS LTS0172308
wikiData Q105232456