4-Hydroxy-6-methyloxan-2-one

Details

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Internal ID 9a07e7b5-4994-4088-a916-9a3d3179fa18
Taxonomy Organoheterocyclic compounds > Lactones > Delta valerolactones
IUPAC Name 4-hydroxy-6-methyloxan-2-one
SMILES (Canonical) CC1CC(CC(=O)O1)O
SMILES (Isomeric) CC1CC(CC(=O)O1)O
InChI InChI=1S/C6H10O3/c1-4-2-5(7)3-6(8)9-4/h4-5,7H,2-3H2,1H3
InChI Key KKZQBMBBMJKIRQ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O3
Molecular Weight 130.14 g/mol
Exact Mass 130.062994177 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.07
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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27751-97-9
(4S,6S)-3,4,5,6-Tetrahydro-4-hydroxy-6-methyl-2H-pyran-2-one
NSC48106
SCHEMBL2686685
DTXSID70950442
CHEBI:173519
KKZQBMBBMJKIRQ-UHFFFAOYSA-N
NSC-48106
4-hydroxy-6-methyltetrahydropyran-2-one

2D Structure

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2D Structure of 4-Hydroxy-6-methyloxan-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 + 0.9789 97.89%
Caco-2 + 0.6795 67.95%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6891 68.91%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.9047 90.47%
OATP1B3 inhibitior + 0.9722 97.22%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9569 95.69%
P-glycoprotein inhibitior - 0.9806 98.06%
P-glycoprotein substrate - 0.9389 93.89%
CYP3A4 substrate - 0.6766 67.66%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.8423 84.23%
CYP3A4 inhibition - 0.9694 96.94%
CYP2C9 inhibition - 0.9682 96.82%
CYP2C19 inhibition - 0.9218 92.18%
CYP2D6 inhibition - 0.9755 97.55%
CYP1A2 inhibition - 0.9062 90.62%
CYP2C8 inhibition - 0.9913 99.13%
CYP inhibitory promiscuity - 0.9931 99.31%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8047 80.47%
Carcinogenicity (trinary) Non-required 0.6500 65.00%
Eye corrosion - 0.6446 64.46%
Eye irritation + 0.9724 97.24%
Skin irritation + 0.7061 70.61%
Skin corrosion - 0.6709 67.09%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8111 81.11%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.7093 70.93%
skin sensitisation - 0.8546 85.46%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7248 72.48%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.6555 65.55%
Acute Oral Toxicity (c) III 0.7022 70.22%
Estrogen receptor binding - 0.9377 93.77%
Androgen receptor binding - 0.7833 78.33%
Thyroid receptor binding - 0.8685 86.85%
Glucocorticoid receptor binding - 0.8575 85.75%
Aromatase binding - 0.8352 83.52%
PPAR gamma - 0.8786 87.86%
Honey bee toxicity - 0.9319 93.19%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.7601 76.01%

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 87.90% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.14% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.65% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.40% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.89% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.33% 95.56%

Plants that contains it

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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.
Garcinia atroviridis

Cross-Links

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PubChem 241025
LOTUS LTS0022940
wikiData Q82928509