2-Ethyl-1,3-dioxolane

Details

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Internal ID 1a7bf8dd-6eeb-4034-91cf-f5ca0f805fcb
Taxonomy Organoheterocyclic compounds > Dioxolanes > 1,3-dioxolanes
IUPAC Name 2-ethyl-1,3-dioxolane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H10O2/c1-2-5-6-3-4-7-5/h5H,2-4H2,1H3
InChI Key WEBRDDDJKLAXTO-UHFFFAOYSA-N
Popularity 18 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10O2
Molecular Weight 102.13 g/mol
Exact Mass 102.068079557 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.77
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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2568-96-9
1,3-Dioxolane, 2-ethyl-
EINECS 219-910-6
Propanal, cyclic 1,2-ethanediyl acetal
DTXSID80180374
RefChem:86856
DTXCID90102865
219-910-6
WEBRDDDJKLAXTO-UHFFFAOYSA-N
MFCD00792514
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Ethyl-1,3-dioxolane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 + 0.7014 70.14%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4732 47.32%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.9562 95.62%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9606 96.06%
P-glycoprotein inhibitior - 0.9852 98.52%
P-glycoprotein substrate - 0.9755 97.55%
CYP3A4 substrate - 0.7453 74.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7706 77.06%
CYP3A4 inhibition - 0.9661 96.61%
CYP2C9 inhibition - 0.7940 79.40%
CYP2C19 inhibition - 0.7344 73.44%
CYP2D6 inhibition - 0.9028 90.28%
CYP1A2 inhibition - 0.6975 69.75%
CYP2C8 inhibition - 0.9774 97.74%
CYP inhibitory promiscuity - 0.7906 79.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.4360 43.60%
Eye corrosion + 0.7715 77.15%
Eye irritation + 0.9722 97.22%
Skin irritation + 0.4935 49.35%
Skin corrosion - 0.8634 86.34%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6962 69.62%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5873 58.73%
skin sensitisation - 0.8332 83.32%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6724 67.24%
Acute Oral Toxicity (c) III 0.8942 89.42%
Estrogen receptor binding - 0.9006 90.06%
Androgen receptor binding - 0.9298 92.98%
Thyroid receptor binding - 0.8717 87.17%
Glucocorticoid receptor binding - 0.9024 90.24%
Aromatase binding - 0.9023 90.23%
PPAR gamma - 0.8801 88.01%
Honey bee toxicity - 0.9676 96.76%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.5996 59.96%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.21% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.85% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 86.44% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.65% 97.09%

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.
Pterocarpus indicus

Cross-Links

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PubChem 17381
NPASS NPC238339