2-(2-Butynyl)cyclohexanone

Details

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Internal ID f505d5d6-ab81-434d-aed6-4ec167d1a43c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 2-but-2-ynylcyclohexan-1-one
SMILES (Canonical) CC#CCC1CCCCC1=O
SMILES (Isomeric) CC#CCC1CCCCC1=O
InChI InChI=1S/C10H14O/c1-2-3-6-9-7-4-5-8-10(9)11/h9H,4-8H2,1H3
InChI Key JNULPQQVLJEQMV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.16
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Npc32790
2-(2-Butynyl)cyclohexanone
Cyclohexanone, 2-(2-butynyl)-
AC1Q6EOX
2-(2-Butynyl)cyclohexanone #
SCHEMBL7620379
JNULPQQVLJEQMV-UHFFFAOYSA-N
AKOS011594969
DB-312496

2D Structure

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2D Structure of 2-(2-Butynyl)cyclohexanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.5241 52.41%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7787 77.87%
OATP2B1 inhibitior - 0.8401 84.01%
OATP1B1 inhibitior + 0.9508 95.08%
OATP1B3 inhibitior + 0.9616 96.16%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9305 93.05%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.9434 94.34%
CYP3A4 substrate - 0.6015 60.15%
CYP2C9 substrate - 0.6131 61.31%
CYP2D6 substrate - 0.7833 78.33%
CYP3A4 inhibition - 0.8983 89.83%
CYP2C9 inhibition - 0.8197 81.97%
CYP2C19 inhibition - 0.8545 85.45%
CYP2D6 inhibition - 0.9477 94.77%
CYP1A2 inhibition - 0.6275 62.75%
CYP2C8 inhibition - 0.9659 96.59%
CYP inhibitory promiscuity - 0.8510 85.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.7235 72.35%
Eye corrosion + 0.8181 81.81%
Eye irritation + 0.8178 81.78%
Skin irritation + 0.7739 77.39%
Skin corrosion - 0.6364 63.64%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6584 65.84%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6053 60.53%
skin sensitisation + 0.7862 78.62%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6825 68.25%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.5838 58.38%
Acute Oral Toxicity (c) III 0.8851 88.51%
Estrogen receptor binding - 0.8876 88.76%
Androgen receptor binding - 0.8804 88.04%
Thyroid receptor binding - 0.8236 82.36%
Glucocorticoid receptor binding - 0.8243 82.43%
Aromatase binding - 0.8700 87.00%
PPAR gamma - 0.8843 88.43%
Honey bee toxicity - 0.9488 94.88%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.8097 80.97%

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 94.20% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.74% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.63% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.74% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.75% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.19% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.63% 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.
Citrus × aurantium
Citrus × aurantium nothof. deliciosa

Cross-Links

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PubChem 584585
NPASS NPC32790