(3R)-5-hydroxy-3-methoxy-6-methyl-2,3-dihydropyran-4-one

Details

Top
Internal ID 0bdea6f8-6387-4e55-b6e1-21c8a408d0f5
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name (3R)-5-hydroxy-3-methoxy-6-methyl-2,3-dihydropyran-4-one
SMILES (Canonical) CC1=C(C(=O)C(CO1)OC)O
SMILES (Isomeric) CC1=C(C(=O)[C@@H](CO1)OC)O
InChI InChI=1S/C7H10O4/c1-4-6(8)7(9)5(10-2)3-11-4/h5,8H,3H2,1-2H3/t5-/m1/s1
InChI Key ZGECCQQKESGSNL-RXMQYKEDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H10O4
Molecular Weight 158.15 g/mol
Exact Mass 158.05790880 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.39
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3R)-5-hydroxy-3-methoxy-6-methyl-2,3-dihydropyran-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9201 92.01%
Caco-2 - 0.7510 75.10%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8225 82.25%
OATP2B1 inhibitior - 0.8477 84.77%
OATP1B1 inhibitior + 0.9491 94.91%
OATP1B3 inhibitior + 0.9755 97.55%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8716 87.16%
P-glycoprotein inhibitior - 0.9753 97.53%
P-glycoprotein substrate - 0.9669 96.69%
CYP3A4 substrate - 0.5715 57.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8805 88.05%
CYP3A4 inhibition - 0.8969 89.69%
CYP2C9 inhibition - 0.9720 97.20%
CYP2C19 inhibition - 0.7932 79.32%
CYP2D6 inhibition - 0.9044 90.44%
CYP1A2 inhibition - 0.7928 79.28%
CYP2C8 inhibition - 0.9711 97.11%
CYP inhibitory promiscuity - 0.8519 85.19%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8928 89.28%
Carcinogenicity (trinary) Non-required 0.7520 75.20%
Eye corrosion - 0.9393 93.93%
Eye irritation + 0.9056 90.56%
Skin irritation - 0.6229 62.29%
Skin corrosion - 0.9586 95.86%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7658 76.58%
Micronuclear - 0.6641 66.41%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8420 84.20%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.7055 70.55%
Acute Oral Toxicity (c) III 0.4779 47.79%
Estrogen receptor binding - 0.8793 87.93%
Androgen receptor binding - 0.6983 69.83%
Thyroid receptor binding - 0.8327 83.27%
Glucocorticoid receptor binding - 0.8785 87.85%
Aromatase binding - 0.8787 87.87%
PPAR gamma - 0.8623 86.23%
Honey bee toxicity - 0.9004 90.04%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.6637 66.37%

Targets

Top

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 89.77% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.92% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.21% 95.56%
CHEMBL2581 P07339 Cathepsin D 85.63% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.03% 94.00%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 81.83% 95.55%
CHEMBL4040 P28482 MAP kinase ERK2 80.13% 83.82%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

Top
PubChem 163061157
LOTUS LTS0239704
wikiData Q105375118