1-Isopropyl-2,7-dimethylnaphthalene

Details

Top
Internal ID 00963034-be6a-4011-babd-9f2773e9acfa
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 2,7-dimethyl-1-propan-2-ylnaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H18/c1-10(2)15-12(4)6-8-13-7-5-11(3)9-14(13)15/h5-10H,1-4H3
InChI Key AGPKAOWJJSQKOM-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H18
Molecular Weight 198.30 g/mol
Exact Mass 198.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1-Isopropyl-2,7-dimethylnaphthalene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.9276 92.76%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6103 61.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9372 93.72%
OATP1B3 inhibitior + 0.9571 95.71%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5621 56.21%
P-glycoprotein inhibitior - 0.9515 95.15%
P-glycoprotein substrate - 0.9312 93.12%
CYP3A4 substrate - 0.7078 70.78%
CYP2C9 substrate - 0.7802 78.02%
CYP2D6 substrate + 0.3462 34.62%
CYP3A4 inhibition - 0.8931 89.31%
CYP2C9 inhibition - 0.7689 76.89%
CYP2C19 inhibition - 0.6578 65.78%
CYP2D6 inhibition - 0.8758 87.58%
CYP1A2 inhibition + 0.6486 64.86%
CYP2C8 inhibition - 0.9284 92.84%
CYP inhibitory promiscuity + 0.6588 65.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Warning 0.3944 39.44%
Eye corrosion - 0.8848 88.48%
Eye irritation + 0.8570 85.70%
Skin irritation + 0.6819 68.19%
Skin corrosion - 0.9850 98.50%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3826 38.26%
Micronuclear - 0.8076 80.76%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.8602 86.02%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.5676 56.76%
Acute Oral Toxicity (c) III 0.5055 50.55%
Estrogen receptor binding - 0.5924 59.24%
Androgen receptor binding + 0.5369 53.69%
Thyroid receptor binding - 0.6506 65.06%
Glucocorticoid receptor binding - 0.7390 73.90%
Aromatase binding + 0.5270 52.70%
PPAR gamma - 0.6546 65.46%
Honey bee toxicity - 0.9600 96.00%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.7600 76.00%
Fish aquatic toxicity + 0.9950 99.50%

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
CHEMBL4581 P52732 Kinesin-like protein 1 92.03% 93.18%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 90.33% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.11% 95.56%
CHEMBL260 Q16539 MAP kinase p38 alpha 87.80% 97.78%
CHEMBL2581 P07339 Cathepsin D 87.71% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.40% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 86.22% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 83.69% 93.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.58% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.15% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.42% 93.56%

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 86239706
LOTUS LTS0139278
wikiData Q104911932