Dehydronepetalactone

Details

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Internal ID f7fbf0e9-efdd-4a26-9372-ef5617cdb406
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 4,7-dimethyl-6,7-dihydro-5H-cyclopenta[c]pyran-1-one
SMILES (Canonical) CC1CCC2=C1C(=O)OC=C2C
SMILES (Isomeric) CC1CCC2=C1C(=O)OC=C2C
InChI InChI=1S/C10H12O2/c1-6-3-4-8-7(2)5-12-10(11)9(6)8/h5-6H,3-4H2,1-2H3
InChI Key JRMIDKPHJPTJMM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O2
Molecular Weight 164.20 g/mol
Exact Mass 164.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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JRMIDKPHJPTJMM-UHFFFAOYSA-N

2D Structure

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2D Structure of Dehydronepetalactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.6239 62.39%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4447 44.47%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9663 96.63%
OATP1B3 inhibitior + 0.9671 96.71%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8921 89.21%
P-glycoprotein inhibitior - 0.9615 96.15%
P-glycoprotein substrate - 0.9599 95.99%
CYP3A4 substrate - 0.5445 54.45%
CYP2C9 substrate + 0.5861 58.61%
CYP2D6 substrate - 0.8534 85.34%
CYP3A4 inhibition - 0.9405 94.05%
CYP2C9 inhibition - 0.8112 81.12%
CYP2C19 inhibition - 0.7582 75.82%
CYP2D6 inhibition - 0.9038 90.38%
CYP1A2 inhibition + 0.8422 84.22%
CYP2C8 inhibition - 0.9391 93.91%
CYP inhibitory promiscuity - 0.9557 95.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5938 59.38%
Eye corrosion - 0.7875 78.75%
Eye irritation + 0.5757 57.57%
Skin irritation + 0.6331 63.31%
Skin corrosion - 0.8243 82.43%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6030 60.30%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.6477 64.77%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.7830 78.30%
Acute Oral Toxicity (c) III 0.7345 73.45%
Estrogen receptor binding - 0.9600 96.00%
Androgen receptor binding - 0.6176 61.76%
Thyroid receptor binding - 0.8205 82.05%
Glucocorticoid receptor binding - 0.8821 88.21%
Aromatase binding - 0.8307 83.07%
PPAR gamma - 0.7345 73.45%
Honey bee toxicity - 0.9421 94.21%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9103 91.03%

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 91.37% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.07% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.02% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.22% 97.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 86.84% 86.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.16% 93.40%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.72% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.44% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.88% 94.80%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.33% 93.65%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.24% 90.71%

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 nepetella
Nepeta nuda

Cross-Links

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PubChem 528332
LOTUS LTS0013178
wikiData Q104253260