Penidienone

Details

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Internal ID e8213ca5-6538-4a27-a5c1-679293590b44
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Quinomethanes > O-quinomethanes
IUPAC Name 5-[(1E,3E)-hepta-1,3-dienyl]-6-methylidenecyclohex-2-en-1-one
SMILES (Canonical) CCCC=CC=CC1CC=CC(=O)C1=C
SMILES (Isomeric) CCC/C=C/C=C/C1CC=CC(=O)C1=C
InChI InChI=1S/C14H18O/c1-3-4-5-6-7-9-13-10-8-11-14(15)12(13)2/h5-9,11,13H,2-4,10H2,1H3/b6-5+,9-7+
InChI Key JNFGTEZBSNFLIN-SBIWHPGTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O
Molecular Weight 202.29 g/mol
Exact Mass 202.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.60
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Penidienone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.7192 71.92%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.5271 52.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9039 90.39%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5951 59.51%
P-glycoprotein inhibitior - 0.9604 96.04%
P-glycoprotein substrate - 0.8057 80.57%
CYP3A4 substrate - 0.5172 51.72%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate - 0.8756 87.56%
CYP3A4 inhibition - 0.9372 93.72%
CYP2C9 inhibition - 0.8809 88.09%
CYP2C19 inhibition - 0.7622 76.22%
CYP2D6 inhibition - 0.8822 88.22%
CYP1A2 inhibition - 0.5632 56.32%
CYP2C8 inhibition - 0.8965 89.65%
CYP inhibitory promiscuity - 0.5070 50.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7110 71.10%
Carcinogenicity (trinary) Non-required 0.5297 52.97%
Eye corrosion + 0.6643 66.43%
Eye irritation + 0.7132 71.32%
Skin irritation + 0.6423 64.23%
Skin corrosion - 0.9343 93.43%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5296 52.96%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.9368 93.68%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.6087 60.87%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6537 65.37%
Acute Oral Toxicity (c) III 0.8051 80.51%
Estrogen receptor binding - 0.8192 81.92%
Androgen receptor binding - 0.7226 72.26%
Thyroid receptor binding - 0.7485 74.85%
Glucocorticoid receptor binding - 0.6871 68.71%
Aromatase binding - 0.6672 66.72%
PPAR gamma + 0.6549 65.49%
Honey bee toxicity - 0.9183 91.83%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9473 94.73%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.36% 97.25%
CHEMBL2581 P07339 Cathepsin D 91.63% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.60% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.59% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.85% 96.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10679626
LOTUS LTS0115636
wikiData Q77573673