3-But-2-enoyl-4-hydroxy-4,5-dimethyl-2-prop-1-enylcyclopent-2-en-1-one

Details

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Internal ID e9f0ce83-4a47-455d-9c14-ddf443675e22
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 3-but-2-enoyl-4-hydroxy-4,5-dimethyl-2-prop-1-enylcyclopent-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H18O3/c1-5-7-10-12(11(15)8-6-2)14(4,17)9(3)13(10)16/h5-9,17H,1-4H3
InChI Key DWFPYAPCVLPCFN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O3
Molecular Weight 234.29 g/mol
Exact Mass 234.125594432 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.97
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-But-2-enoyl-4-hydroxy-4,5-dimethyl-2-prop-1-enylcyclopent-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 + 0.6881 68.81%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8032 80.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8836 88.36%
OATP1B3 inhibitior + 0.9663 96.63%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6996 69.96%
P-glycoprotein inhibitior - 0.9475 94.75%
P-glycoprotein substrate - 0.9218 92.18%
CYP3A4 substrate - 0.5192 51.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8962 89.62%
CYP3A4 inhibition - 0.9098 90.98%
CYP2C9 inhibition - 0.8924 89.24%
CYP2C19 inhibition - 0.8938 89.38%
CYP2D6 inhibition - 0.9361 93.61%
CYP1A2 inhibition - 0.8803 88.03%
CYP2C8 inhibition - 0.9096 90.96%
CYP inhibitory promiscuity - 0.8950 89.50%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7104 71.04%
Carcinogenicity (trinary) Non-required 0.5042 50.42%
Eye corrosion - 0.7333 73.33%
Eye irritation - 0.8939 89.39%
Skin irritation + 0.7251 72.51%
Skin corrosion - 0.7011 70.11%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5866 58.66%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.6502 65.02%
skin sensitisation + 0.6600 66.00%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.5288 52.88%
Acute Oral Toxicity (c) III 0.5829 58.29%
Estrogen receptor binding - 0.6956 69.56%
Androgen receptor binding - 0.7827 78.27%
Thyroid receptor binding - 0.5350 53.50%
Glucocorticoid receptor binding - 0.8956 89.56%
Aromatase binding - 0.8177 81.77%
PPAR gamma - 0.4841 48.41%
Honey bee toxicity - 0.8833 88.33%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8322 83.22%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.91% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.83% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.61% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 81.91% 91.19%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.74% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.63% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.57% 89.00%

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 162814605
LOTUS LTS0167497
wikiData Q105161191