2-(5-Ethyl-5-methyltetrahydrofuran-2-yl)propan-2-ol

Details

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Internal ID 3f0b683e-98b9-4019-9b8b-9050db552d88
Taxonomy Organoheterocyclic compounds > Oxolanes
IUPAC Name 2-(5-ethyl-5-methyloxolan-2-yl)propan-2-ol
SMILES (Canonical) CCC1(CCC(O1)C(C)(C)O)C
SMILES (Isomeric) CCC1(CCC(O1)C(C)(C)O)C
InChI InChI=1S/C10H20O2/c1-5-10(4)7-6-8(12-10)9(2,3)11/h8,11H,5-7H2,1-4H3
InChI Key ZSIHHIBGUWREKL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20O2
Molecular Weight 172.26 g/mol
Exact Mass 172.146329876 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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2-(5-ethyl-5-methyloxolan-2-yl)propan-2-ol
SCHEMBL4747639
2-(5-ethyl-5-methyltetrahydrofuran-2-yl)propan-2-ol

2D Structure

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2D Structure of 2-(5-Ethyl-5-methyltetrahydrofuran-2-yl)propan-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9880 98.80%
Caco-2 + 0.8722 87.22%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5304 53.04%
OATP2B1 inhibitior - 0.8414 84.14%
OATP1B1 inhibitior + 0.9328 93.28%
OATP1B3 inhibitior + 0.9272 92.72%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9644 96.44%
P-glycoprotein inhibitior - 0.9747 97.47%
P-glycoprotein substrate - 0.9209 92.09%
CYP3A4 substrate - 0.5337 53.37%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7423 74.23%
CYP3A4 inhibition - 0.7474 74.74%
CYP2C9 inhibition - 0.6412 64.12%
CYP2C19 inhibition - 0.6374 63.74%
CYP2D6 inhibition - 0.8959 89.59%
CYP1A2 inhibition - 0.6357 63.57%
CYP2C8 inhibition - 0.8521 85.21%
CYP inhibitory promiscuity - 0.7304 73.04%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.6082 60.82%
Eye corrosion - 0.7653 76.53%
Eye irritation + 0.9298 92.98%
Skin irritation - 0.6628 66.28%
Skin corrosion - 0.9358 93.58%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5399 53.99%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6682 66.82%
skin sensitisation + 0.7619 76.19%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6837 68.37%
Acute Oral Toxicity (c) III 0.7666 76.66%
Estrogen receptor binding - 0.8290 82.90%
Androgen receptor binding - 0.8261 82.61%
Thyroid receptor binding - 0.7215 72.15%
Glucocorticoid receptor binding - 0.8772 87.72%
Aromatase binding - 0.8294 82.94%
PPAR gamma - 0.8230 82.30%
Honey bee toxicity - 0.9422 94.22%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.7135 71.35%

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 99.24% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 93.06% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.37% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.46% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.96% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.84% 92.62%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.26% 93.04%
CHEMBL259 P32245 Melanocortin receptor 4 84.39% 95.38%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 84.10% 89.05%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 83.83% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.32% 96.77%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.21% 95.50%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.78% 97.50%
CHEMBL1871 P10275 Androgen Receptor 81.42% 96.43%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 80.99% 92.88%
CHEMBL233 P35372 Mu opioid receptor 80.41% 97.93%

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.
Conioselinum anthriscoides
Prunus armeniaca

Cross-Links

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PubChem 5317140
NPASS NPC256816