3-Methylcyclotridecan-1-one

Details

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Internal ID 8d720729-2ecc-434e-9cf1-f2701f193166
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 3-methylcyclotridecan-1-one
SMILES (Canonical) CC1CCCCCCCCCCC(=O)C1
SMILES (Isomeric) CC1CCCCCCCCCCC(=O)C1
InChI InChI=1S/C14H26O/c1-13-10-8-6-4-2-3-5-7-9-11-14(15)12-13/h13H,2-12H2,1H3
InChI Key CVMWCRDXSQGRSJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H26O
Molecular Weight 210.36 g/mol
Exact Mass 210.198365449 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.50
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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61415-11-0
Cyclotridecanone,3-methyl-
EINECS 262-772-7
3-Methylcyclotridecanone
Cyclotridecanone, 3-methyl-
SCHEMBL14118250
DTXSID40976972
3 - methylcyclotridecan - 1 - one

2D Structure

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2D Structure of 3-Methylcyclotridecan-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 + 0.9970 99.70%
Caco-2 + 0.9402 94.02%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.5081 50.81%
OATP2B1 inhibitior - 0.8440 84.40%
OATP1B1 inhibitior + 0.9595 95.95%
OATP1B3 inhibitior + 0.9702 97.02%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8123 81.23%
P-glycoprotein inhibitior - 0.9333 93.33%
P-glycoprotein substrate - 0.9619 96.19%
CYP3A4 substrate - 0.6402 64.02%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.9742 97.42%
CYP2C9 inhibition - 0.9243 92.43%
CYP2C19 inhibition - 0.9544 95.44%
CYP2D6 inhibition - 0.9666 96.66%
CYP1A2 inhibition - 0.6002 60.02%
CYP2C8 inhibition - 0.9566 95.66%
CYP inhibitory promiscuity - 0.9685 96.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6782 67.82%
Eye corrosion + 0.9272 92.72%
Eye irritation + 0.9724 97.24%
Skin irritation + 0.8266 82.66%
Skin corrosion + 0.7968 79.68%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6083 60.83%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.8053 80.53%
skin sensitisation + 0.8404 84.04%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.7405 74.05%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.4794 47.94%
Acute Oral Toxicity (c) III 0.8804 88.04%
Estrogen receptor binding - 0.8510 85.10%
Androgen receptor binding - 0.8912 89.12%
Thyroid receptor binding - 0.7333 73.33%
Glucocorticoid receptor binding - 0.8016 80.16%
Aromatase binding - 0.8188 81.88%
PPAR gamma - 0.7915 79.15%
Honey bee toxicity - 0.9587 95.87%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.7272 72.72%

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 94.08% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.64% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.43% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.90% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.63% 96.09%
CHEMBL3012 Q13946 Phosphodiesterase 7A 84.55% 99.29%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.55% 93.04%
CHEMBL1902 P62942 FK506-binding protein 1A 83.51% 97.05%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 82.95% 95.27%
CHEMBL5255 O00206 Toll-like receptor 4 80.62% 92.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.05% 95.89%

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.
Bupleurum chinense

Cross-Links

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PubChem 3017257
NPASS NPC107206