2-Methoxy-1,3-dioxolane

Details

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Internal ID e6a89442-38a2-4f41-97a9-2eec25123244
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ortho esters
IUPAC Name 2-methoxy-1,3-dioxolane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H8O3/c1-5-4-6-2-3-7-4/h4H,2-3H2,1H3
InChI Key VRAYTNFBRROPJU-UHFFFAOYSA-N
Popularity 15 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8O3
Molecular Weight 104.10 g/mol
Exact Mass 104.047344113 g/mol
Topological Polar Surface Area (TPSA) 27.70 Ų
XlogP -0.20
Atomic LogP (AlogP) -0.04
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1,3-Dioxolane, 2-methoxy-
EINECS 243-229-3
VRAYTNFBRROPJU-UHFFFAOYSA-
DTXSID80173362
RefChem:87794
DTXCID8095853
243-229-3
InChI=1/C4H8O3/c1-5-4-6-2-3-7-4/h4H,2-3H2,1H3
VRAYTNFBRROPJU-UHFFFAOYSA-N
19693-75-5
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-Methoxy-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 + 0.9744 97.44%
Caco-2 + 0.6556 65.56%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6735 67.35%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9733 97.33%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9562 95.62%
P-glycoprotein inhibitior - 0.9821 98.21%
P-glycoprotein substrate - 0.9812 98.12%
CYP3A4 substrate - 0.6380 63.80%
CYP2C9 substrate - 0.8208 82.08%
CYP2D6 substrate - 0.7447 74.47%
CYP3A4 inhibition - 0.9814 98.14%
CYP2C9 inhibition - 0.8925 89.25%
CYP2C19 inhibition - 0.7690 76.90%
CYP2D6 inhibition - 0.9133 91.33%
CYP1A2 inhibition - 0.7049 70.49%
CYP2C8 inhibition - 0.9654 96.54%
CYP inhibitory promiscuity - 0.8659 86.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.4161 41.61%
Eye corrosion - 0.7330 73.30%
Eye irritation + 0.9785 97.85%
Skin irritation - 0.8213 82.13%
Skin corrosion - 0.9711 97.11%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7450 74.50%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5784 57.84%
skin sensitisation - 0.9004 90.04%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.6124 61.24%
Acute Oral Toxicity (c) III 0.4891 48.91%
Estrogen receptor binding - 0.8974 89.74%
Androgen receptor binding - 0.9282 92.82%
Thyroid receptor binding - 0.8623 86.23%
Glucocorticoid receptor binding - 0.8751 87.51%
Aromatase binding - 0.9223 92.23%
PPAR gamma - 0.8713 87.13%
Honey bee toxicity - 0.6915 69.15%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.9263 92.63%

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 89.68% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 86.14% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.32% 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 29744
NPASS NPC74730