5-(1,2-Dihydroxypropan-2-yl)-4-methoxypyran-2-one

Details

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Internal ID d80d3045-3196-4330-b868-447d857942d9
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 5-(1,2-dihydroxypropan-2-yl)-4-methoxypyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12O5/c1-9(12,5-10)6-4-14-8(11)3-7(6)13-2/h3-4,10,12H,5H2,1-2H3
InChI Key MZHZXCQZVTZSOE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O5
Molecular Weight 200.19 g/mol
Exact Mass 200.06847348 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP -1.30
Atomic LogP (AlogP) -0.15
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(1,2-Dihydroxypropan-2-yl)-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 + 0.7883 78.83%
Caco-2 + 0.8126 81.26%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7871 78.71%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9282 92.82%
OATP1B3 inhibitior + 0.9349 93.49%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9128 91.28%
P-glycoprotein inhibitior - 0.9683 96.83%
P-glycoprotein substrate - 0.9313 93.13%
CYP3A4 substrate - 0.5754 57.54%
CYP2C9 substrate - 0.6437 64.37%
CYP2D6 substrate - 0.8574 85.74%
CYP3A4 inhibition - 0.8885 88.85%
CYP2C9 inhibition - 0.9603 96.03%
CYP2C19 inhibition - 0.9144 91.44%
CYP2D6 inhibition - 0.9365 93.65%
CYP1A2 inhibition - 0.8395 83.95%
CYP2C8 inhibition - 0.8780 87.80%
CYP inhibitory promiscuity - 0.9675 96.75%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6874 68.74%
Eye corrosion - 0.9795 97.95%
Eye irritation + 0.5840 58.40%
Skin irritation - 0.7748 77.48%
Skin corrosion - 0.9491 94.91%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7327 73.27%
Micronuclear - 0.6086 60.86%
Hepatotoxicity - 0.5049 50.49%
skin sensitisation - 0.7213 72.13%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.5734 57.34%
Acute Oral Toxicity (c) III 0.6944 69.44%
Estrogen receptor binding - 0.5763 57.63%
Androgen receptor binding - 0.6459 64.59%
Thyroid receptor binding - 0.6123 61.23%
Glucocorticoid receptor binding - 0.6211 62.11%
Aromatase binding - 0.8034 80.34%
PPAR gamma - 0.7069 70.69%
Honey bee toxicity - 0.9500 95.00%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5849 58.49%
Fish aquatic toxicity - 0.5571 55.71%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.12% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.98% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.23% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.09% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.99% 94.00%
CHEMBL2581 P07339 Cathepsin D 90.53% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.01% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.29% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 86.50% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.24% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 84.29% 83.82%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.05% 86.92%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.18% 91.07%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.10% 93.99%

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 85590814
LOTUS LTS0186130
wikiData Q105175514