(s)-5-Hydroxy-3,4-dimethyl-5-pentylfuran-2(5h)-one

Details

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Internal ID 22cd12f3-b311-4f99-b0e0-a6a45b7bb866
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (5S)-5-hydroxy-3,4-dimethyl-5-pentylfuran-2-one
SMILES (Canonical) CCCCCC1(C(=C(C(=O)O1)C)C)O
SMILES (Isomeric) CCCCC[C@]1(C(=C(C(=O)O1)C)C)O
InChI InChI=1S/C11H18O3/c1-4-5-6-7-11(13)9(3)8(2)10(12)14-11/h13H,4-7H2,1-3H3/t11-/m0/s1
InChI Key VJZWZDQDXPADSE-NSHDSACASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18O3
Molecular Weight 198.26 g/mol
Exact Mass 198.125594432 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.15
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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(s)-5-hydroxy-3,4-dimethyl-5-pentylfuran-2(5h)-one

2D Structure

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2D Structure of (s)-5-Hydroxy-3,4-dimethyl-5-pentylfuran-2(5h)-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9859 98.59%
Caco-2 + 0.9560 95.60%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6436 64.36%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.8937 89.37%
OATP1B3 inhibitior + 0.9572 95.72%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9241 92.41%
P-glycoprotein inhibitior - 0.9515 95.15%
P-glycoprotein substrate - 0.8742 87.42%
CYP3A4 substrate - 0.5467 54.67%
CYP2C9 substrate + 0.5993 59.93%
CYP2D6 substrate - 0.8773 87.73%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.8085 80.85%
CYP2C19 inhibition - 0.5996 59.96%
CYP2D6 inhibition - 0.9403 94.03%
CYP1A2 inhibition - 0.7100 71.00%
CYP2C8 inhibition - 0.9067 90.67%
CYP inhibitory promiscuity - 0.7707 77.07%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5675 56.75%
Eye corrosion - 0.9745 97.45%
Eye irritation + 0.7884 78.84%
Skin irritation + 0.6265 62.65%
Skin corrosion - 0.8511 85.11%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5062 50.62%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5523 55.23%
skin sensitisation - 0.6979 69.79%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.8071 80.71%
Acute Oral Toxicity (c) III 0.5050 50.50%
Estrogen receptor binding - 0.7751 77.51%
Androgen receptor binding - 0.6909 69.09%
Thyroid receptor binding - 0.5556 55.56%
Glucocorticoid receptor binding - 0.7768 77.68%
Aromatase binding - 0.7332 73.32%
PPAR gamma - 0.6823 68.23%
Honey bee toxicity - 0.9832 98.32%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.6562 65.62%
Fish aquatic toxicity + 0.9442 94.42%

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
CHEMBL2581 P07339 Cathepsin D 96.51% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 95.23% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.65% 95.56%
CHEMBL299 P17252 Protein kinase C alpha 90.31% 98.03%
CHEMBL3401 O75469 Pregnane X receptor 87.16% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.19% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.28% 97.25%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 83.93% 85.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.24% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.71% 96.09%

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.
Litsea verticillata
Phleum pratense
Rhaphidophora decursiva

Cross-Links

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PubChem 155551640
LOTUS LTS0020602
wikiData Q105287631