(2E)-2-ethylidene-4-propan-2-ylcyclopent-4-ene-1,3-dione

Details

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Internal ID f0812a57-5452-4572-bfaf-538c5ffcd5e5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name (2E)-2-ethylidene-4-propan-2-ylcyclopent-4-ene-1,3-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H12O2/c1-4-7-9(11)5-8(6(2)3)10(7)12/h4-6H,1-3H3/b7-4+
InChI Key HDHWQBUJRLQQMJ-QPJJXVBHSA-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) 34.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.67
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E)-2-ethylidene-4-propan-2-ylcyclopent-4-ene-1,3-dione

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 + 0.5472 54.72%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7307 73.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.9630 96.30%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9279 92.79%
P-glycoprotein inhibitior - 0.9744 97.44%
P-glycoprotein substrate - 0.9616 96.16%
CYP3A4 substrate - 0.6435 64.35%
CYP2C9 substrate - 0.7739 77.39%
CYP2D6 substrate - 0.8868 88.68%
CYP3A4 inhibition - 0.9400 94.00%
CYP2C9 inhibition - 0.8430 84.30%
CYP2C19 inhibition - 0.8127 81.27%
CYP2D6 inhibition - 0.9142 91.42%
CYP1A2 inhibition - 0.7753 77.53%
CYP2C8 inhibition - 0.9965 99.65%
CYP inhibitory promiscuity - 0.7270 72.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7454 74.54%
Carcinogenicity (trinary) Non-required 0.5289 52.89%
Eye corrosion + 0.5319 53.19%
Eye irritation + 0.9007 90.07%
Skin irritation + 0.6409 64.09%
Skin corrosion - 0.7195 71.95%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7522 75.22%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.7055 70.55%
skin sensitisation + 0.8369 83.69%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6480 64.80%
Acute Oral Toxicity (c) II 0.5040 50.40%
Estrogen receptor binding - 0.9630 96.30%
Androgen receptor binding - 0.6923 69.23%
Thyroid receptor binding - 0.7207 72.07%
Glucocorticoid receptor binding - 0.9195 91.95%
Aromatase binding - 0.9354 93.54%
PPAR gamma - 0.9308 93.08%
Honey bee toxicity - 0.8657 86.57%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8244 82.44%

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 93.85% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.77% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.42% 90.71%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.62% 89.34%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.60% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 80.39% 94.75%

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.
Coleus amboinicus

Cross-Links

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PubChem 76310416
NPASS NPC471751
ChEMBL CHEMBL3113340
LOTUS LTS0253907
wikiData Q105026362