2-Methylcycloheptanone

Details

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Internal ID 6080968e-3e02-4826-9038-e56ca3534731
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 2-methylcycloheptan-1-one
SMILES (Canonical) CC1CCCCCC1=O
SMILES (Isomeric) CC1CCCCCC1=O
InChI InChI=1S/C8H14O/c1-7-5-3-2-4-6-8(7)9/h7H,2-6H2,1H3
InChI Key FDMAFOTXGNYBFG-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O
Molecular Weight 126.20 g/mol
Exact Mass 126.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.16
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2-methylcycloheptan-1-one
932-56-9
2-methyl-cycloheptanone
Cycloheptanone, 2-methyl-
2-methyl-cycloheptan-1-one
SCHEMBL107928
DTXSID60337586
DTXSID80870804
AKOS011021491
AT33106
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Methylcycloheptanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.7587 75.87%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6235 62.35%
OATP2B1 inhibitior - 0.8261 82.61%
OATP1B1 inhibitior + 0.9484 94.84%
OATP1B3 inhibitior + 0.9567 95.67%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9500 95.00%
P-glycoprotein inhibitior - 0.9909 99.09%
P-glycoprotein substrate - 0.9711 97.11%
CYP3A4 substrate - 0.6640 66.40%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.9841 98.41%
CYP2C9 inhibition - 0.9247 92.47%
CYP2C19 inhibition - 0.9492 94.92%
CYP2D6 inhibition - 0.9547 95.47%
CYP1A2 inhibition - 0.7045 70.45%
CYP2C8 inhibition - 0.9859 98.59%
CYP inhibitory promiscuity - 0.9762 97.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6980 69.80%
Eye corrosion + 0.8478 84.78%
Eye irritation + 0.9862 98.62%
Skin irritation + 0.8543 85.43%
Skin corrosion - 0.5696 56.96%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7784 77.84%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6803 68.03%
skin sensitisation + 0.7498 74.98%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.6783 67.83%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.6841 68.41%
Acute Oral Toxicity (c) III 0.8145 81.45%
Estrogen receptor binding - 0.9599 95.99%
Androgen receptor binding - 0.8466 84.66%
Thyroid receptor binding - 0.9300 93.00%
Glucocorticoid receptor binding - 0.8947 89.47%
Aromatase binding - 0.8409 84.09%
PPAR gamma - 0.8458 84.58%
Honey bee toxicity - 0.9672 96.72%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.8399 83.99%

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 93.28% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.33% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.08% 95.56%
CHEMBL3012 Q13946 Phosphodiesterase 7A 86.31% 99.29%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.10% 97.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.55% 93.04%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.04% 96.09%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 81.14% 95.27%
CHEMBL5255 O00206 Toll-like receptor 4 80.76% 92.50%

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.
Nepeta racemosa

Cross-Links

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PubChem 543503
LOTUS LTS0167327
wikiData Q82105463