1,7-Dimethylbicyclo[2.2.1]heptan-2-one

Details

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Internal ID 009bcaec-5077-4523-815e-94944db7f69f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 1,7-dimethylbicyclo[2.2.1]heptan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H14O/c1-6-7-3-4-9(6,2)8(10)5-7/h6-7H,3-5H2,1-2H3
InChI Key BDRPBIDNZZQJOI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O
Molecular Weight 138.21 g/mol
Exact Mass 138.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.01
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,7-Dimethylbicyclo[2.2.1]heptan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.7116 71.16%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5093 50.93%
OATP2B1 inhibitior - 0.8478 84.78%
OATP1B1 inhibitior + 0.9365 93.65%
OATP1B3 inhibitior + 0.9722 97.22%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9359 93.59%
P-glycoprotein inhibitior - 0.9834 98.34%
P-glycoprotein substrate - 0.9328 93.28%
CYP3A4 substrate - 0.5556 55.56%
CYP2C9 substrate - 0.7800 78.00%
CYP2D6 substrate - 0.8045 80.45%
CYP3A4 inhibition - 0.9522 95.22%
CYP2C9 inhibition - 0.9454 94.54%
CYP2C19 inhibition - 0.9636 96.36%
CYP2D6 inhibition - 0.9687 96.87%
CYP1A2 inhibition - 0.8817 88.17%
CYP2C8 inhibition - 0.9704 97.04%
CYP inhibitory promiscuity - 0.9831 98.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6104 61.04%
Eye corrosion - 0.7844 78.44%
Eye irritation + 0.9521 95.21%
Skin irritation + 0.8302 83.02%
Skin corrosion - 0.9336 93.36%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7621 76.21%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6737 67.37%
skin sensitisation + 0.8624 86.24%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.6667 66.67%
Acute Oral Toxicity (c) III 0.7123 71.23%
Estrogen receptor binding - 0.9079 90.79%
Androgen receptor binding - 0.6603 66.03%
Thyroid receptor binding - 0.9166 91.66%
Glucocorticoid receptor binding - 0.8877 88.77%
Aromatase binding - 0.8130 81.30%
PPAR gamma - 0.8805 88.05%
Honey bee toxicity - 0.9363 93.63%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.9112 91.12%

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
CHEMBL1937 Q92769 Histone deacetylase 2 87.44% 94.75%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.19% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.94% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.73% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.48% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.82% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.30% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.05% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.47% 99.23%

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.
Mentha suaveolens
Pterocarpus indicus
Santalum album

Cross-Links

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PubChem 5321106
NPASS NPC35472