(2R)-2-[(R)-hydroxy-[(2R,3S)-3-methyloxiran-2-yl]methyl]-4-methyl-2H-furan-5-one

Details

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Internal ID 5bd32d2a-806c-435a-a31b-6920ca565fa5
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (2R)-2-[(R)-hydroxy-[(2R,3S)-3-methyloxiran-2-yl]methyl]-4-methyl-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H12O4/c1-4-3-6(13-9(4)11)7(10)8-5(2)12-8/h3,5-8,10H,1-2H3/t5-,6+,7+,8-/m0/s1
InChI Key HDVUTKZGLKYRBY-OSMVPFSASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O4
Molecular Weight 184.19 g/mol
Exact Mass 184.07355886 g/mol
Topological Polar Surface Area (TPSA) 59.10 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.01
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-2-[(R)-hydroxy-[(2R,3S)-3-methyloxiran-2-yl]methyl]-4-methyl-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 + 0.9677 96.77%
Caco-2 + 0.5987 59.87%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7171 71.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9258 92.58%
OATP1B3 inhibitior + 0.9500 95.00%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9459 94.59%
P-glycoprotein inhibitior - 0.9367 93.67%
P-glycoprotein substrate - 0.9360 93.60%
CYP3A4 substrate - 0.5965 59.65%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate - 0.8792 87.92%
CYP3A4 inhibition - 0.9072 90.72%
CYP2C9 inhibition - 0.8998 89.98%
CYP2C19 inhibition - 0.7016 70.16%
CYP2D6 inhibition - 0.9309 93.09%
CYP1A2 inhibition - 0.7655 76.55%
CYP2C8 inhibition - 0.9844 98.44%
CYP inhibitory promiscuity - 0.7957 79.57%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8928 89.28%
Carcinogenicity (trinary) Danger 0.4883 48.83%
Eye corrosion - 0.8863 88.63%
Eye irritation - 0.5279 52.79%
Skin irritation - 0.5618 56.18%
Skin corrosion - 0.8922 89.22%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8234 82.34%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.7089 70.89%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6262 62.62%
Acute Oral Toxicity (c) III 0.3997 39.97%
Estrogen receptor binding - 0.8952 89.52%
Androgen receptor binding - 0.8925 89.25%
Thyroid receptor binding - 0.6563 65.63%
Glucocorticoid receptor binding - 0.8800 88.00%
Aromatase binding - 0.8155 81.55%
PPAR gamma - 0.7465 74.65%
Honey bee toxicity - 0.8752 87.52%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.7355 73.55%

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 91.97% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 90.54% 94.73%
CHEMBL2581 P07339 Cathepsin D 89.32% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.86% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.46% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.21% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.90% 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 101412323
LOTUS LTS0252068
wikiData Q105026612