6-(1,3-Dihydroxypentyl)-4-methoxypyran-2-one

Details

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Internal ID 790072c9-ea8b-4822-88de-5e293d6ef314
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 6-(1,3-dihydroxypentyl)-4-methoxypyran-2-one
SMILES (Canonical) CCC(CC(C1=CC(=CC(=O)O1)OC)O)O
SMILES (Isomeric) CCC(CC(C1=CC(=CC(=O)O1)OC)O)O
InChI InChI=1S/C11H16O5/c1-3-7(12)4-9(13)10-5-8(15-2)6-11(14)16-10/h5-7,9,12-13H,3-4H2,1-2H3
InChI Key AWQOSUDFARWYOX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O5
Molecular Weight 228.24 g/mol
Exact Mass 228.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.84
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(1,3-Dihydroxypentyl)-4-methoxypyran-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 + 0.7899 78.99%
Caco-2 + 0.7049 70.49%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6404 64.04%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.9093 90.93%
OATP1B3 inhibitior + 0.9163 91.63%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7831 78.31%
P-glycoprotein inhibitior - 0.9212 92.12%
P-glycoprotein substrate - 0.8790 87.90%
CYP3A4 substrate - 0.6313 63.13%
CYP2C9 substrate - 0.5903 59.03%
CYP2D6 substrate - 0.8349 83.49%
CYP3A4 inhibition - 0.7498 74.98%
CYP2C9 inhibition - 0.8897 88.97%
CYP2C19 inhibition - 0.7766 77.66%
CYP2D6 inhibition - 0.7971 79.71%
CYP1A2 inhibition - 0.9012 90.12%
CYP2C8 inhibition - 0.8914 89.14%
CYP inhibitory promiscuity - 0.8103 81.03%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9019 90.19%
Carcinogenicity (trinary) Non-required 0.7178 71.78%
Eye corrosion - 0.9617 96.17%
Eye irritation - 0.7262 72.62%
Skin irritation - 0.6323 63.23%
Skin corrosion - 0.9295 92.95%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4587 45.87%
Micronuclear - 0.6023 60.23%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8551 85.51%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.8151 81.51%
Acute Oral Toxicity (c) III 0.7501 75.01%
Estrogen receptor binding - 0.5363 53.63%
Androgen receptor binding + 0.6212 62.12%
Thyroid receptor binding - 0.6952 69.52%
Glucocorticoid receptor binding + 0.5870 58.70%
Aromatase binding - 0.8220 82.20%
PPAR gamma + 0.7865 78.65%
Honey bee toxicity - 0.9232 92.32%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.5912 59.12%

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 96.28% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.26% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.80% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.37% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.58% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.80% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.67% 99.17%
CHEMBL4208 P20618 Proteasome component C5 87.14% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 85.40% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.30% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.61% 96.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.43% 90.24%
CHEMBL2535 P11166 Glucose transporter 81.22% 98.75%

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 163016824
LOTUS LTS0182099
wikiData Q104085917