Lanierone

Details

Top
Internal ID 406dfb50-ef49-4cc0-9e5d-4f3a109e5aa5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 2-hydroxy-4,4,6-trimethylcyclohexa-2,5-dien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12O2/c1-6-4-9(2,3)5-7(10)8(6)11/h4-5,10H,1-3H3
InChI Key GKOBUKITZSFCJC-UHFFFAOYSA-N
Popularity 18 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H12O2
Molecular Weight 152.19 g/mol
Exact Mass 152.083729621 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.98
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
2-hydroxy-4,4,6-trimethylcyclohexa-2,5-dien-1-one
SCHEMBL1301789
GKOBUKITZSFCJC-UHFFFAOYSA-N
DTXSID201031959
28750-52-9
2-Hydroxy-4,4,6-trimethyl-2,5-cyclohexadienone
2-Hydroxy-4,4,6-trimethylcyclohexa-2,5-dienone
2-hydroxy-4,4,6-trimethyl-2,5-cyclohexadien-1-one
4,4,6-Trimethyl-2-hydroxycyclohexa-2,5-diene-1-one
Q19597672
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Lanierone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.7872 78.72%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8188 81.88%
OATP2B1 inhibitior - 0.8675 86.75%
OATP1B1 inhibitior + 0.9269 92.69%
OATP1B3 inhibitior + 0.9665 96.65%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9256 92.56%
P-glycoprotein inhibitior - 0.9686 96.86%
P-glycoprotein substrate - 0.9793 97.93%
CYP3A4 substrate - 0.6042 60.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8725 87.25%
CYP3A4 inhibition - 0.8268 82.68%
CYP2C9 inhibition - 0.8948 89.48%
CYP2C19 inhibition - 0.8320 83.20%
CYP2D6 inhibition - 0.9187 91.87%
CYP1A2 inhibition - 0.8601 86.01%
CYP2C8 inhibition - 0.9834 98.34%
CYP inhibitory promiscuity - 0.7798 77.98%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7244 72.44%
Carcinogenicity (trinary) Non-required 0.6207 62.07%
Eye corrosion - 0.6821 68.21%
Eye irritation + 0.9821 98.21%
Skin irritation + 0.7150 71.50%
Skin corrosion - 0.7909 79.09%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7736 77.36%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.6584 65.84%
skin sensitisation + 0.8951 89.51%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6825 68.25%
Acute Oral Toxicity (c) III 0.8261 82.61%
Estrogen receptor binding - 0.8812 88.12%
Androgen receptor binding - 0.8440 84.40%
Thyroid receptor binding - 0.8240 82.40%
Glucocorticoid receptor binding - 0.9222 92.22%
Aromatase binding - 0.8995 89.95%
PPAR gamma - 0.8157 81.57%
Honey bee toxicity - 0.9603 96.03%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8182 81.82%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.66% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 86.88% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.59% 99.23%
CHEMBL2581 P07339 Cathepsin D 86.34% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.31% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 82.01% 94.73%

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.
There are no matching plants.

Cross-Links

Top
PubChem 642486
LOTUS LTS0209605
wikiData Q19597672