Spiro(4.5)decan-2-one

Details

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Internal ID 5fc0913d-7def-4200-b71f-226bcf68d043
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name spiro[4.5]decan-3-one
SMILES (Canonical) C1CCC2(CC1)CCC(=O)C2
SMILES (Isomeric) C1CCC2(CC1)CCC(=O)C2
InChI InChI=1S/C10H16O/c11-9-4-7-10(8-9)5-2-1-3-6-10/h1-8H2
InChI Key DJHRXBYWKVQDJY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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3643-16-1
starbld0020979
spiro[4.5]decan-2-on
SCHEMBL708873
DJHRXBYWKVQDJY-UHFFFAOYSA-N
DTXSID201314872
EN300-1725930

2D Structure

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2D Structure of Spiro(4.5)decan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.7281 72.81%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5754 57.54%
OATP2B1 inhibitior - 0.8471 84.71%
OATP1B1 inhibitior + 0.9600 96.00%
OATP1B3 inhibitior + 0.9720 97.20%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8487 84.87%
P-glycoprotein inhibitior - 0.9793 97.93%
P-glycoprotein substrate - 0.9911 99.11%
CYP3A4 substrate - 0.6333 63.33%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.7633 76.33%
CYP3A4 inhibition - 0.9204 92.04%
CYP2C9 inhibition - 0.8047 80.47%
CYP2C19 inhibition - 0.9319 93.19%
CYP2D6 inhibition - 0.9657 96.57%
CYP1A2 inhibition - 0.9239 92.39%
CYP2C8 inhibition - 0.9911 99.11%
CYP inhibitory promiscuity - 0.9689 96.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6095 60.95%
Eye corrosion + 0.7715 77.15%
Eye irritation + 0.9871 98.71%
Skin irritation + 0.7002 70.02%
Skin corrosion - 0.9222 92.22%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6185 61.85%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5219 52.19%
skin sensitisation + 0.6253 62.53%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.5455 54.55%
Acute Oral Toxicity (c) III 0.6917 69.17%
Estrogen receptor binding - 0.9638 96.38%
Androgen receptor binding - 0.7771 77.71%
Thyroid receptor binding - 0.8769 87.69%
Glucocorticoid receptor binding - 0.9106 91.06%
Aromatase binding - 0.7588 75.88%
PPAR gamma - 0.8314 83.14%
Honey bee toxicity - 0.9095 90.95%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.6298 62.98%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.24% 95.56%
CHEMBL3012 Q13946 Phosphodiesterase 7A 86.51% 99.29%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.75% 97.25%
CHEMBL2581 P07339 Cathepsin D 84.70% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.05% 93.04%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 83.86% 96.38%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.55% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.39% 94.45%

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.
Pinellia ternata

Cross-Links

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PubChem 557153
NPASS NPC60502