(2R,3S)-2-ethyl-3-heptyloxirane

Details

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Internal ID a9084ef7-d6ba-4da4-b1c5-8b8a6c8a6708
Taxonomy Organoheterocyclic compounds > Epoxides
IUPAC Name (2R,3S)-2-ethyl-3-heptyloxirane
SMILES (Canonical) CCCCCCCC1C(O1)CC
SMILES (Isomeric) CCCCCCC[C@H]1[C@H](O1)CC
InChI InChI=1S/C11H22O/c1-3-5-6-7-8-9-11-10(4-2)12-11/h10-11H,3-9H2,1-2H3/t10-,11+/m1/s1
InChI Key MKEISLUOZPVPJD-MNOVXSKESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H22O
Molecular Weight 170.29 g/mol
Exact Mass 170.167065321 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.52
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3S)-2-ethyl-3-heptyloxirane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 + 0.9090 90.90%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.3696 36.96%
OATP2B1 inhibitior - 0.8431 84.31%
OATP1B1 inhibitior + 0.9272 92.72%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8600 86.00%
P-glycoprotein inhibitior - 0.9450 94.50%
P-glycoprotein substrate - 0.8942 89.42%
CYP3A4 substrate - 0.6393 63.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7350 73.50%
CYP3A4 inhibition - 0.8988 89.88%
CYP2C9 inhibition - 0.7540 75.40%
CYP2C19 inhibition - 0.7239 72.39%
CYP2D6 inhibition - 0.9253 92.53%
CYP1A2 inhibition + 0.5606 56.06%
CYP2C8 inhibition - 0.8998 89.98%
CYP inhibitory promiscuity - 0.8154 81.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.5881 58.81%
Eye corrosion + 0.7209 72.09%
Eye irritation + 0.8575 85.75%
Skin irritation + 0.6942 69.42%
Skin corrosion - 0.9169 91.69%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5966 59.66%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6530 65.30%
skin sensitisation + 0.7761 77.61%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.8533 85.33%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6903 69.03%
Acute Oral Toxicity (c) IV 0.4829 48.29%
Estrogen receptor binding - 0.8265 82.65%
Androgen receptor binding - 0.7933 79.33%
Thyroid receptor binding - 0.7345 73.45%
Glucocorticoid receptor binding - 0.8561 85.61%
Aromatase binding - 0.8385 83.85%
PPAR gamma - 0.8481 84.81%
Honey bee toxicity - 0.9710 97.10%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.7856 78.56%
Fish aquatic toxicity + 0.8304 83.04%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.08% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.68% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.51% 97.25%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 89.82% 90.24%
CHEMBL2996 Q05655 Protein kinase C delta 89.34% 97.79%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.05% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.59% 92.86%
CHEMBL2581 P07339 Cathepsin D 86.29% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 85.89% 89.63%
CHEMBL3401 O75469 Pregnane X receptor 85.70% 94.73%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.66% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.93% 99.17%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 81.83% 80.33%

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.
Niphogeton ternata
Panax ginseng

Cross-Links

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PubChem 131847730
LOTUS LTS0237608
wikiData Q105165866