10-Methyl-10-pyrrolidin-2-yloxecan-2-one

Details

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Internal ID 7163557e-4eb2-4c67-bdcd-515c4a70904c
Taxonomy Organoheterocyclic compounds > Pyrrolidines
IUPAC Name 10-methyl-10-pyrrolidin-2-yloxecan-2-one
SMILES (Canonical) CC1(CCCCCCCC(=O)O1)C2CCCN2
SMILES (Isomeric) CC1(CCCCCCCC(=O)O1)C2CCCN2
InChI InChI=1S/C14H25NO2/c1-14(12-8-7-11-15-12)10-6-4-2-3-5-9-13(16)17-14/h12,15H,2-11H2,1H3
InChI Key HXFUVYFNBRBBPM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H25NO2
Molecular Weight 239.35 g/mol
Exact Mass 239.188529040 g/mol
Topological Polar Surface Area (TPSA) 38.30 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.78
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-Methyl-10-pyrrolidin-2-yloxecan-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 + 0.9967 99.67%
Caco-2 + 0.8040 80.40%
Blood Brain Barrier + 0.9379 93.79%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.5568 55.68%
OATP2B1 inhibitior - 0.8452 84.52%
OATP1B1 inhibitior + 0.9106 91.06%
OATP1B3 inhibitior + 0.9370 93.70%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.8779 87.79%
P-glycoprotein inhibitior - 0.9376 93.76%
P-glycoprotein substrate - 0.8972 89.72%
CYP3A4 substrate + 0.5622 56.22%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.7345 73.45%
CYP3A4 inhibition - 0.9808 98.08%
CYP2C9 inhibition - 0.9218 92.18%
CYP2C19 inhibition - 0.8254 82.54%
CYP2D6 inhibition - 0.8663 86.63%
CYP1A2 inhibition - 0.8938 89.38%
CYP2C8 inhibition - 0.9072 90.72%
CYP inhibitory promiscuity - 0.8954 89.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6248 62.48%
Eye corrosion - 0.9761 97.61%
Eye irritation - 0.7804 78.04%
Skin irritation - 0.7089 70.89%
Skin corrosion - 0.8335 83.35%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4767 47.67%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5106 51.06%
skin sensitisation - 0.8006 80.06%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6435 64.35%
Acute Oral Toxicity (c) III 0.5951 59.51%
Estrogen receptor binding - 0.8064 80.64%
Androgen receptor binding - 0.6410 64.10%
Thyroid receptor binding - 0.6045 60.45%
Glucocorticoid receptor binding - 0.7925 79.25%
Aromatase binding - 0.6921 69.21%
PPAR gamma - 0.8514 85.14%
Honey bee toxicity - 0.9325 93.25%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.7278 72.78%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.73% 97.25%
CHEMBL2581 P07339 Cathepsin D 94.21% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.78% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.44% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 89.78% 94.75%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 89.20% 96.38%
CHEMBL4040 P28482 MAP kinase ERK2 88.54% 83.82%
CHEMBL3012 Q13946 Phosphodiesterase 7A 87.91% 99.29%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.54% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.69% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.76% 90.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.29% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.32% 95.89%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.91% 96.21%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.81% 92.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.25% 100.00%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 81.29% 94.78%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.19% 93.99%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.09% 80.96%
CHEMBL325 Q13547 Histone deacetylase 1 80.92% 95.92%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.81% 93.04%

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.
Carica papaya

Cross-Links

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PubChem 162885099
LOTUS LTS0108879
wikiData Q105034969