2-(1-Methylethylidene)cyclohexanone

Details

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Internal ID 3b282693-78f3-41da-ad68-11b1ec09839b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 2-propan-2-ylidenecyclohexan-1-one
SMILES (Canonical) CC(=C1CCCCC1=O)C
SMILES (Isomeric) CC(=C1CCCCC1=O)C
InChI InChI=1S/C9H14O/c1-7(2)8-5-3-4-6-9(8)10/h3-6H2,1-2H3
InChI Key MMTBDIDPDFBJIC-UHFFFAOYSA-N
Popularity 4 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 2.40
Atomic LogP (AlogP) 2.47
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Cyclohexanone, 2-(1-methylethylidene)-
2-propan-2-ylidenecyclohexan-1-one
2-(1-METHYLETHYLIDENE)CYCLOHEXANONE
Cyclohexanone, 2-isopropylidene-
2-Isopropylidenecyclohexanone
isopropylidenecyclohexanone
SCHEMBL7177738
DTXSID40160197
AKOS015907383
2-(1-Methylethylidene)cyclohexanone #

2D Structure

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2D Structure of 2-(1-Methylethylidene)cyclohexanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.9467 94.67%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.7118 71.18%
OATP2B1 inhibitior - 0.8450 84.50%
OATP1B1 inhibitior + 0.9743 97.43%
OATP1B3 inhibitior + 0.9392 93.92%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9282 92.82%
P-glycoprotein inhibitior - 0.9763 97.63%
P-glycoprotein substrate - 0.9886 98.86%
CYP3A4 substrate - 0.7371 73.71%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8590 85.90%
CYP3A4 inhibition - 0.9558 95.58%
CYP2C9 inhibition - 0.9297 92.97%
CYP2C19 inhibition - 0.8800 88.00%
CYP2D6 inhibition - 0.9340 93.40%
CYP1A2 inhibition - 0.7813 78.13%
CYP2C8 inhibition - 0.9957 99.57%
CYP inhibitory promiscuity - 0.8258 82.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.6264 62.64%
Eye corrosion - 0.6313 63.13%
Eye irritation + 0.9907 99.07%
Skin irritation + 0.7631 76.31%
Skin corrosion - 0.9745 97.45%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6911 69.11%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.9000 90.00%
skin sensitisation + 0.9231 92.31%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.6590 65.90%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5116 51.16%
Acute Oral Toxicity (c) III 0.5004 50.04%
Estrogen receptor binding - 0.9818 98.18%
Androgen receptor binding - 0.8850 88.50%
Thyroid receptor binding - 0.8598 85.98%
Glucocorticoid receptor binding - 0.8953 89.53%
Aromatase binding - 0.8885 88.85%
PPAR gamma - 0.8762 87.62%
Honey bee toxicity - 0.9547 95.47%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9577 95.77%

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 92.98% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.29% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.05% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.98% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.38% 85.14%

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.
Crocus sativus
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 26252
NPASS NPC243368