2,2,3-Trimethyl-3-(4-methylphenyl)cyclopentan-1-ol

Details

Top
Internal ID 76171ee1-499c-4156-aa3c-4dff1ac47936
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2,2,3-trimethyl-3-(4-methylphenyl)cyclopentan-1-ol
SMILES (Canonical) CC1=CC=C(C=C1)C2(CCC(C2(C)C)O)C
SMILES (Isomeric) CC1=CC=C(C=C1)C2(CCC(C2(C)C)O)C
InChI InChI=1S/C15H22O/c1-11-5-7-12(8-6-11)15(4)10-9-13(16)14(15,2)3/h5-8,13,16H,9-10H2,1-4H3
InChI Key AFRLMSOCDMQZOR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.43
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2,2,3-Trimethyl-3-(4-methylphenyl)cyclopentan-1-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9598 95.98%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6511 65.11%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.9511 95.11%
OATP1B3 inhibitior + 0.9330 93.30%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5907 59.07%
P-glycoprotein inhibitior - 0.9731 97.31%
P-glycoprotein substrate - 0.9338 93.38%
CYP3A4 substrate - 0.5559 55.59%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate + 0.3919 39.19%
CYP3A4 inhibition - 0.8980 89.80%
CYP2C9 inhibition - 0.7523 75.23%
CYP2C19 inhibition - 0.8578 85.78%
CYP2D6 inhibition - 0.9337 93.37%
CYP1A2 inhibition - 0.6358 63.58%
CYP2C8 inhibition - 0.9070 90.70%
CYP inhibitory promiscuity - 0.8412 84.12%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.5905 59.05%
Eye corrosion - 0.9238 92.38%
Eye irritation - 0.6571 65.71%
Skin irritation + 0.7531 75.31%
Skin corrosion - 0.7181 71.81%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4439 44.39%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6729 67.29%
skin sensitisation + 0.6595 65.95%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6395 63.95%
Acute Oral Toxicity (c) III 0.7627 76.27%
Estrogen receptor binding - 0.5352 53.52%
Androgen receptor binding - 0.5069 50.69%
Thyroid receptor binding + 0.5440 54.40%
Glucocorticoid receptor binding - 0.7520 75.20%
Aromatase binding - 0.7679 76.79%
PPAR gamma - 0.5248 52.48%
Honey bee toxicity - 0.9720 97.20%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7600 76.00%
Fish aquatic toxicity + 0.8815 88.15%

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 90.65% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.97% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 87.28% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.01% 97.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.36% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 84.87% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.62% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.52% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.95% 95.89%
CHEMBL2581 P07339 Cathepsin D 82.63% 98.95%

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.
Platycladus orientalis

Cross-Links

Top
PubChem 12304243
LOTUS LTS0267961
wikiData Q104911439