Asperlactone

Details

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Internal ID 51a9e66d-8843-461d-a78f-46eb118ea063
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (2R)-2-[(1S)-1-hydroxyethyl]-4-[(2S,3S)-3-methyloxiran-2-yl]-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12O4/c1-4(10)7-3-6(9(11)13-7)8-5(2)12-8/h3-5,7-8,10H,1-2H3/t4-,5-,7+,8+/m0/s1
InChI Key VMLNPJDEXLLCQG-DGCAKLBHSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O4
Molecular Weight 184.19 g/mol
Exact Mass 184.07355886 g/mol
Topological Polar Surface Area (TPSA) 59.10 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.01
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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76375-62-7
2(5H)-Furanone, 5-((1S)-1-hydroxyethyl)-3-((2S,3S)-3-methyloxiranyl)-, (5R)-
DTXSID00227215
(5R)-5-[(1S)-1-hydroxyethyl]-3-[(2S,3S)-3-methyloxiran-2-yl]-2,5-dihydrofuran-2-one
CHEBI:156386
HB3775
AKOS040755981
HY-126603
CS-0105855
(5R)-5-[(1S)-1-hydroxyethyl]-3-[(2S,3S)-3-methyloxiran-2-yl]furan-2(5H)-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Asperlactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9744 97.44%
Caco-2 - 0.6890 68.90%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7527 75.27%
OATP2B1 inhibitior - 0.8620 86.20%
OATP1B1 inhibitior + 0.9253 92.53%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9713 97.13%
P-glycoprotein inhibitior - 0.9034 90.34%
P-glycoprotein substrate - 0.9510 95.10%
CYP3A4 substrate - 0.6648 66.48%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate - 0.8792 87.92%
CYP3A4 inhibition - 0.9127 91.27%
CYP2C9 inhibition - 0.8255 82.55%
CYP2C19 inhibition - 0.6507 65.07%
CYP2D6 inhibition - 0.9362 93.62%
CYP1A2 inhibition - 0.7456 74.56%
CYP2C8 inhibition - 0.9928 99.28%
CYP inhibitory promiscuity - 0.7156 71.56%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8928 89.28%
Carcinogenicity (trinary) Danger 0.5013 50.13%
Eye corrosion - 0.9197 91.97%
Eye irritation - 0.8599 85.99%
Skin irritation - 0.6034 60.34%
Skin corrosion - 0.9001 90.01%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8144 81.44%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.7476 74.76%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6158 61.58%
Acute Oral Toxicity (c) III 0.4699 46.99%
Estrogen receptor binding - 0.8394 83.94%
Androgen receptor binding - 0.7933 79.33%
Thyroid receptor binding - 0.7447 74.47%
Glucocorticoid receptor binding - 0.8644 86.44%
Aromatase binding - 0.8218 82.18%
PPAR gamma - 0.8161 81.61%
Honey bee toxicity - 0.9030 90.30%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.7871 78.71%

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 91.61% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.19% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 88.10% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.96% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.42% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.53% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.38% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.95% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.80% 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 156698
LOTUS LTS0064871
wikiData Q44275049