2-Hydroxy-2,4-dimethyl-5-propan-2-ylfuran-3-one

Details

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Internal ID 3545dadd-4250-4e2c-976f-a3162c94e367
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones
IUPAC Name 2-hydroxy-2,4-dimethyl-5-propan-2-ylfuran-3-one
SMILES (Canonical) CC1=C(OC(C1=O)(C)O)C(C)C
SMILES (Isomeric) CC1=C(OC(C1=O)(C)O)C(C)C
InChI InChI=1S/C9H14O3/c1-5(2)7-6(3)8(10)9(4,11)12-7/h5,11H,1-4H3
InChI Key ZJJMPZKVGDHGBI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O3
Molecular Weight 170.21 g/mol
Exact Mass 170.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.22
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Hydroxy-2,4-dimethyl-5-propan-2-ylfuran-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9745 97.45%
Caco-2 - 0.6481 64.81%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.7543 75.43%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior + 0.9350 93.50%
OATP1B3 inhibitior + 0.9586 95.86%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9404 94.04%
P-glycoprotein inhibitior - 0.9428 94.28%
P-glycoprotein substrate - 0.9765 97.65%
CYP3A4 substrate - 0.5706 57.06%
CYP2C9 substrate - 0.6015 60.15%
CYP2D6 substrate - 0.8704 87.04%
CYP3A4 inhibition - 0.9514 95.14%
CYP2C9 inhibition - 0.9311 93.11%
CYP2C19 inhibition - 0.8844 88.44%
CYP2D6 inhibition - 0.9601 96.01%
CYP1A2 inhibition - 0.8264 82.64%
CYP2C8 inhibition - 0.9764 97.64%
CYP inhibitory promiscuity - 0.7732 77.32%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9128 91.28%
Carcinogenicity (trinary) Non-required 0.4058 40.58%
Eye corrosion - 0.7638 76.38%
Eye irritation - 0.5000 50.00%
Skin irritation + 0.5410 54.10%
Skin corrosion - 0.8582 85.82%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6277 62.77%
Micronuclear - 0.5100 51.00%
Hepatotoxicity + 0.6784 67.84%
skin sensitisation - 0.5341 53.41%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.7592 75.92%
Acute Oral Toxicity (c) III 0.6339 63.39%
Estrogen receptor binding - 0.8729 87.29%
Androgen receptor binding - 0.8245 82.45%
Thyroid receptor binding - 0.6780 67.80%
Glucocorticoid receptor binding - 0.8971 89.71%
Aromatase binding - 0.8420 84.20%
PPAR gamma - 0.8695 86.95%
Honey bee toxicity - 0.9520 95.20%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.7991 79.91%

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 90.53% 91.11%
CHEMBL2581 P07339 Cathepsin D 87.67% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.18% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 86.55% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.31% 94.45%
CHEMBL4072 P07858 Cathepsin B 83.36% 93.67%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.41% 93.56%

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.
Helichrysum zeyheri

Cross-Links

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PubChem 130030957
LOTUS LTS0271751
wikiData Q105377944