2-Ethyl-4-(2-ethylbutyl)-2-hydroxy-5-pent-2-en-3-ylfuran-3-one

Details

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Internal ID bf1fee06-450e-4c4b-b5bd-b7a8767774f1
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones
IUPAC Name 2-ethyl-4-(2-ethylbutyl)-2-hydroxy-5-pent-2-en-3-ylfuran-3-one
SMILES (Canonical) CCC(CC)CC1=C(OC(C1=O)(CC)O)C(=CC)CC
SMILES (Isomeric) CCC(CC)CC1=C(OC(C1=O)(CC)O)C(=CC)CC
InChI InChI=1S/C17H28O3/c1-6-12(7-2)11-14-15(13(8-3)9-4)20-17(19,10-5)16(14)18/h8,12,19H,6-7,9-11H2,1-5H3
InChI Key IVLRLNXBYCZYPV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H28O3
Molecular Weight 280.40 g/mol
Exact Mass 280.20384475 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.12
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Ethyl-4-(2-ethylbutyl)-2-hydroxy-5-pent-2-en-3-ylfuran-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9820 98.20%
Caco-2 + 0.9444 94.44%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6521 65.21%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9095 90.95%
OATP1B3 inhibitior + 0.9552 95.52%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5469 54.69%
P-glycoprotein inhibitior - 0.9015 90.15%
P-glycoprotein substrate - 0.9147 91.47%
CYP3A4 substrate - 0.5501 55.01%
CYP2C9 substrate - 0.6027 60.27%
CYP2D6 substrate - 0.8467 84.67%
CYP3A4 inhibition - 0.8613 86.13%
CYP2C9 inhibition - 0.8905 89.05%
CYP2C19 inhibition - 0.7005 70.05%
CYP2D6 inhibition - 0.9494 94.94%
CYP1A2 inhibition - 0.8547 85.47%
CYP2C8 inhibition - 0.9126 91.26%
CYP inhibitory promiscuity - 0.8299 82.99%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5785 57.85%
Eye corrosion - 0.9485 94.85%
Eye irritation - 0.5984 59.84%
Skin irritation + 0.5502 55.02%
Skin corrosion - 0.8683 86.83%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6613 66.13%
Micronuclear - 0.7267 72.67%
Hepatotoxicity - 0.6301 63.01%
skin sensitisation - 0.6442 64.42%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.7666 76.66%
Acute Oral Toxicity (c) III 0.6001 60.01%
Estrogen receptor binding - 0.6048 60.48%
Androgen receptor binding + 0.5444 54.44%
Thyroid receptor binding + 0.6617 66.17%
Glucocorticoid receptor binding - 0.4712 47.12%
Aromatase binding - 0.7119 71.19%
PPAR gamma - 0.5083 50.83%
Honey bee toxicity - 0.9375 93.75%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8338 83.38%

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 90.47% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.06% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.41% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 84.39% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.64% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.60% 85.14%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 81.28% 80.00%
CHEMBL3401 O75469 Pregnane X receptor 80.09% 94.73%
CHEMBL4208 P20618 Proteasome component C5 80.01% 90.00%

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 162814934
LOTUS LTS0104987
wikiData Q104169166