5(S)-(1-(1(S)-hydroxybut-2-enyl))-furan-2-one

Details

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Internal ID 81369487-5c03-42bb-ade5-da8d5d8c64b8
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (2S)-2-[(E,1S)-1-hydroxybut-2-enyl]-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H10O3/c1-2-3-6(9)7-4-5-8(10)11-7/h2-7,9H,1H3/b3-2+/t6-,7-/m0/s1
InChI Key SMKPKIFBQCUYGS-VHJVCUAWSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O3
Molecular Weight 154.16 g/mol
Exact Mass 154.062994177 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.40
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5(S)-(1-(1(S)-hydroxybut-2-enyl))-furan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 - 0.5477 54.77%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6848 68.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8777 87.77%
OATP1B3 inhibitior + 0.9591 95.91%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9614 96.14%
P-glycoprotein inhibitior - 0.9806 98.06%
P-glycoprotein substrate - 0.9633 96.33%
CYP3A4 substrate - 0.6198 61.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8993 89.93%
CYP3A4 inhibition - 0.9747 97.47%
CYP2C9 inhibition - 0.9569 95.69%
CYP2C19 inhibition - 0.9229 92.29%
CYP2D6 inhibition - 0.9713 97.13%
CYP1A2 inhibition - 0.8228 82.28%
CYP2C8 inhibition - 0.9790 97.90%
CYP inhibitory promiscuity - 0.9157 91.57%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8444 84.44%
Carcinogenicity (trinary) Non-required 0.4371 43.71%
Eye corrosion + 0.9126 91.26%
Eye irritation + 0.6936 69.36%
Skin irritation + 0.7326 73.26%
Skin corrosion + 0.7589 75.89%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8255 82.55%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.5991 59.91%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.5647 56.47%
Acute Oral Toxicity (c) III 0.5114 51.14%
Estrogen receptor binding - 0.9148 91.48%
Androgen receptor binding - 0.8994 89.94%
Thyroid receptor binding - 0.8281 82.81%
Glucocorticoid receptor binding - 0.7699 76.99%
Aromatase binding - 0.8475 84.75%
PPAR gamma - 0.8344 83.44%
Honey bee toxicity - 0.8603 86.03%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.5756 57.56%

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 90.41% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.98% 85.14%
CHEMBL2581 P07339 Cathepsin D 84.97% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.85% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.38% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.51% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.66% 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 10820768
LOTUS LTS0230919
wikiData Q77384316