3-(Methylamino)cycloheptan-1-one

Details

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Internal ID 81c4c392-9749-40f8-b9f3-2fc8b5d0968d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 3-(methylamino)cycloheptan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H15NO/c1-9-7-4-2-3-5-8(10)6-7/h7,9H,2-6H2,1H3
InChI Key TZEMYNIWYNDOLG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H15NO
Molecular Weight 141.21 g/mol
Exact Mass 141.115364102 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 0.40
Atomic LogP (AlogP) 1.11
H-Bond Acceptor 2
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 3-(Methylamino)cycloheptan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9894 98.94%
Caco-2 + 0.8286 82.86%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Lysosomes 0.5933 59.33%
OATP2B1 inhibitior - 0.8344 83.44%
OATP1B1 inhibitior + 0.9660 96.60%
OATP1B3 inhibitior + 0.9468 94.68%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior - 0.9645 96.45%
P-glycoprotein inhibitior - 0.9801 98.01%
P-glycoprotein substrate - 0.9344 93.44%
CYP3A4 substrate - 0.6465 64.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4793 47.93%
CYP3A4 inhibition - 0.9848 98.48%
CYP2C9 inhibition - 0.9422 94.22%
CYP2C19 inhibition - 0.9387 93.87%
CYP2D6 inhibition - 0.9222 92.22%
CYP1A2 inhibition - 0.8441 84.41%
CYP2C8 inhibition - 0.9592 95.92%
CYP inhibitory promiscuity - 0.9590 95.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.7232 72.32%
Eye corrosion + 0.4559 45.59%
Eye irritation + 0.9457 94.57%
Skin irritation + 0.6070 60.70%
Skin corrosion - 0.4937 49.37%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5839 58.39%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.8770 87.70%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.5277 52.77%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.4944 49.44%
Acute Oral Toxicity (c) III 0.6564 65.64%
Estrogen receptor binding - 0.9102 91.02%
Androgen receptor binding - 0.8990 89.90%
Thyroid receptor binding - 0.9033 90.33%
Glucocorticoid receptor binding - 0.8866 88.66%
Aromatase binding - 0.7655 76.55%
PPAR gamma - 0.7980 79.80%
Honey bee toxicity - 0.9348 93.48%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.8284 82.84%

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
CHEMBL2581 P07339 Cathepsin D 90.52% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.62% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.26% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.37% 91.11%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.12% 93.03%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.89% 96.09%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 82.56% 92.88%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.10% 93.04%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 81.55% 83.14%

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.
Physalis peruviana

Cross-Links

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PubChem 55287488
LOTUS LTS0223930
wikiData Q105268083