(1R)-1,4-dimethyl-7-propan-2-yl-2,3-dihydro-1H-azulen-6-one

Details

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Internal ID cebcf96e-e725-434e-9687-09292fd3c81a
Taxonomy Hydrocarbon derivatives > Tropones
IUPAC Name (1R)-1,4-dimethyl-7-propan-2-yl-2,3-dihydro-1H-azulen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O/c1-9(2)13-8-14-10(3)5-6-12(14)11(4)7-15(13)16/h7-10H,5-6H2,1-4H3/t10-/m1/s1
InChI Key UGZCHVLYDNLQTR-SNVBAGLBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O
Molecular Weight 216.32 g/mol
Exact Mass 216.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.53
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R)-1,4-dimethyl-7-propan-2-yl-2,3-dihydro-1H-azulen-6-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9002 90.02%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4851 48.51%
OATP2B1 inhibitior - 0.8624 86.24%
OATP1B1 inhibitior + 0.9588 95.88%
OATP1B3 inhibitior + 0.9594 95.94%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8364 83.64%
P-glycoprotein inhibitior - 0.9407 94.07%
P-glycoprotein substrate - 0.8117 81.17%
CYP3A4 substrate + 0.5135 51.35%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7544 75.44%
CYP3A4 inhibition - 0.9692 96.92%
CYP2C9 inhibition - 0.7534 75.34%
CYP2C19 inhibition - 0.8039 80.39%
CYP2D6 inhibition - 0.9074 90.74%
CYP1A2 inhibition + 0.8505 85.05%
CYP2C8 inhibition - 0.9265 92.65%
CYP inhibitory promiscuity - 0.8891 88.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5294 52.94%
Eye corrosion - 0.8327 83.27%
Eye irritation - 0.5921 59.21%
Skin irritation + 0.5833 58.33%
Skin corrosion - 0.7213 72.13%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3605 36.05%
Micronuclear - 0.9341 93.41%
Hepatotoxicity - 0.5052 50.52%
skin sensitisation + 0.7725 77.25%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.7806 78.06%
Acute Oral Toxicity (c) III 0.6816 68.16%
Estrogen receptor binding - 0.8723 87.23%
Androgen receptor binding - 0.6408 64.08%
Thyroid receptor binding - 0.5315 53.15%
Glucocorticoid receptor binding - 0.8200 82.00%
Aromatase binding - 0.8908 89.08%
PPAR gamma - 0.9143 91.43%
Honey bee toxicity - 0.8766 87.66%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9640 96.40%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.47% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.00% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 93.52% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.67% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.86% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.69% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.08% 93.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.04% 85.14%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 85.06% 90.71%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.49% 99.18%
CHEMBL3238 P23786 Carnitine palmitoyltransferase 2 84.40% 94.05%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.09% 86.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.50% 97.25%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 83.02% 90.24%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.59% 100.00%
CHEMBL4581 P52732 Kinesin-like protein 1 82.24% 93.18%
CHEMBL4444 P04070 Vitamin K-dependent protein C 82.18% 93.89%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.01% 96.77%
CHEMBL1871 P10275 Androgen Receptor 80.97% 96.43%

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.
Orobanche rapum-genistae

Cross-Links

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PubChem 124356410
LOTUS LTS0212759
wikiData Q105272661