2-(5-Methyl-5-(oxiran-2-yl)-tetrahydrofuran-2-yl)propan-1-ol

Details

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Internal ID 9b8f956d-10b3-419b-9578-7663cf998f61
Taxonomy Organoheterocyclic compounds > Oxolanes
IUPAC Name 2-[5-methyl-5-(oxiran-2-yl)oxolan-2-yl]propan-1-ol
SMILES (Canonical) CC(CO)C1CCC(O1)(C)C2CO2
SMILES (Isomeric) CC(CO)C1CCC(O1)(C)C2CO2
InChI InChI=1S/C10H18O3/c1-7(5-11)8-3-4-10(2,13-8)9-6-12-9/h7-9,11H,3-6H2,1-2H3
InChI Key XZDUDSXRVQCEKT-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O3
Molecular Weight 186.25 g/mol
Exact Mass 186.125594432 g/mol
Topological Polar Surface Area (TPSA) 42.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.95
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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XZDUDSXRVQCEKT-UHFFFAOYSA-N
2-(5-methyl-5-(oxiran-2-yl)-tetrahydrofuran-2-yl)propan-1-ol

2D Structure

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2D Structure of 2-(5-Methyl-5-(oxiran-2-yl)-tetrahydrofuran-2-yl)propan-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9274 92.74%
Caco-2 + 0.6965 69.65%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6403 64.03%
OATP2B1 inhibitior - 0.8483 84.83%
OATP1B1 inhibitior + 0.9554 95.54%
OATP1B3 inhibitior + 0.9359 93.59%
MATE1 inhibitior - 0.9412 94.12%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9546 95.46%
P-glycoprotein inhibitior - 0.9458 94.58%
P-glycoprotein substrate - 0.8612 86.12%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7599 75.99%
CYP3A4 inhibition - 0.8931 89.31%
CYP2C9 inhibition - 0.7007 70.07%
CYP2C19 inhibition - 0.7726 77.26%
CYP2D6 inhibition - 0.9112 91.12%
CYP1A2 inhibition - 0.8175 81.75%
CYP2C8 inhibition - 0.9249 92.49%
CYP inhibitory promiscuity - 0.8767 87.67%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5422 54.22%
Eye corrosion - 0.9325 93.25%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.7131 71.31%
Skin corrosion - 0.9326 93.26%
Ames mutagenesis + 0.5130 51.30%
Human Ether-a-go-go-Related Gene inhibition - 0.6705 67.05%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.6769 67.69%
skin sensitisation - 0.7405 74.05%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.4804 48.04%
Acute Oral Toxicity (c) III 0.5374 53.74%
Estrogen receptor binding - 0.7401 74.01%
Androgen receptor binding - 0.6613 66.13%
Thyroid receptor binding - 0.7124 71.24%
Glucocorticoid receptor binding - 0.7620 76.20%
Aromatase binding - 0.8254 82.54%
PPAR gamma - 0.7922 79.22%
Honey bee toxicity - 0.8879 88.79%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity - 0.6396 63.96%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.48% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.46% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 94.25% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.69% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 88.59% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.71% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 84.15% 90.17%
CHEMBL2094135 Q96BI3 Gamma-secretase 83.08% 98.05%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.15% 100.00%
CHEMBL2581 P07339 Cathepsin D 81.46% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.44% 92.62%
CHEMBL237 P41145 Kappa opioid receptor 81.10% 98.10%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 80.85% 89.05%

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.
Actinidia arguta

Cross-Links

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PubChem 91264076
LOTUS LTS0146346
wikiData Q105344856