4-methyl-2-(4-methyl-5-oxooxolan-3-yl)-2H-furan-5-one

Details

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Internal ID f077b721-0df5-44b9-914a-719bba494333
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 4-methyl-2-(4-methyl-5-oxooxolan-3-yl)-2H-furan-5-one
SMILES (Canonical) CC1C(COC1=O)C2C=C(C(=O)O2)C
SMILES (Isomeric) CC1C(COC1=O)C2C=C(C(=O)O2)C
InChI InChI=1S/C10H12O4/c1-5-3-8(14-9(5)11)7-4-13-10(12)6(7)2/h3,6-8H,4H2,1-2H3
InChI Key BABJXHCBFYMVBG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O4
Molecular Weight 196.20 g/mol
Exact Mass 196.07355886 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.67
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-methyl-2-(4-methyl-5-oxooxolan-3-yl)-2H-furan-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 + 0.6623 66.23%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7331 73.31%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9348 93.48%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9205 92.05%
P-glycoprotein inhibitior - 0.9588 95.88%
P-glycoprotein substrate - 0.8924 89.24%
CYP3A4 substrate - 0.5470 54.70%
CYP2C9 substrate - 0.6352 63.52%
CYP2D6 substrate - 0.9183 91.83%
CYP3A4 inhibition - 0.9398 93.98%
CYP2C9 inhibition - 0.6929 69.29%
CYP2C19 inhibition - 0.7440 74.40%
CYP2D6 inhibition - 0.9354 93.54%
CYP1A2 inhibition + 0.5230 52.30%
CYP2C8 inhibition - 0.9790 97.90%
CYP inhibitory promiscuity - 0.7094 70.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8828 88.28%
Carcinogenicity (trinary) Non-required 0.5950 59.50%
Eye corrosion - 0.9249 92.49%
Eye irritation + 0.9023 90.23%
Skin irritation - 0.5337 53.37%
Skin corrosion - 0.8469 84.69%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6042 60.42%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.7905 79.05%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.4836 48.36%
Acute Oral Toxicity (c) III 0.5980 59.80%
Estrogen receptor binding - 0.6810 68.10%
Androgen receptor binding - 0.7557 75.57%
Thyroid receptor binding - 0.7800 78.00%
Glucocorticoid receptor binding - 0.8886 88.86%
Aromatase binding - 0.8502 85.02%
PPAR gamma - 0.8846 88.46%
Honey bee toxicity - 0.8440 84.40%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9511 95.11%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.46% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.12% 94.80%
CHEMBL2581 P07339 Cathepsin D 83.18% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.99% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.58% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.14% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.34% 89.00%

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 14484621
LOTUS LTS0179936
wikiData Q104922067