4,5-Dimethyl-1,3-dioxolan-2-one

Details

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Internal ID 2b1fb105-68fb-4adf-8c92-a2661e6253fc
Taxonomy Organic acids and derivatives > Organic carbonic acids and derivatives > Carbonic acid diesters
IUPAC Name 4,5-dimethyl-1,3-dioxolan-2-one
SMILES (Canonical) CC1C(OC(=O)O1)C
SMILES (Isomeric) CC1C(OC(=O)O1)C
InChI InChI=1S/C5H8O3/c1-3-4(2)8-5(6)7-3/h3-4H,1-2H3
InChI Key LWLOKSXSAUHTJO-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8O3
Molecular Weight 116.11 g/mol
Exact Mass 116.047344113 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.93
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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4437-70-1
Carbonic acid 2,3-butanediyl
2,3-butylene carbonate
Carbonic acid, cyclic 1,2-dimethylethylene ester
1,3-Dioxolan-2-one, 4,5-dimethyl-
trans-4,5-dimethyl-1,3-dioxolan-2-one
65941-76-6
SCHEMBL137875
1,2-Dimethylethylene carbonate
2,3-Butanediol cyclic carbonate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4,5-Dimethyl-1,3-dioxolan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9893 98.93%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7941 79.41%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9549 95.49%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9563 95.63%
P-glycoprotein inhibitior - 0.9664 96.64%
P-glycoprotein substrate - 0.9895 98.95%
CYP3A4 substrate - 0.7551 75.51%
CYP2C9 substrate - 0.7560 75.60%
CYP2D6 substrate - 0.7912 79.12%
CYP3A4 inhibition - 0.9557 95.57%
CYP2C9 inhibition - 0.9495 94.95%
CYP2C19 inhibition - 0.7973 79.73%
CYP2D6 inhibition - 0.9425 94.25%
CYP1A2 inhibition - 0.7579 75.79%
CYP2C8 inhibition - 0.9979 99.79%
CYP inhibitory promiscuity - 0.8522 85.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9217 92.17%
Carcinogenicity (trinary) Non-required 0.5620 56.20%
Eye corrosion + 0.5217 52.17%
Eye irritation + 0.9604 96.04%
Skin irritation - 0.6616 66.16%
Skin corrosion - 0.9206 92.06%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8532 85.32%
Micronuclear - 0.5100 51.00%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation - 0.7573 75.73%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6992 69.92%
Acute Oral Toxicity (c) III 0.4674 46.74%
Estrogen receptor binding - 0.8507 85.07%
Androgen receptor binding - 0.8274 82.74%
Thyroid receptor binding - 0.8635 86.35%
Glucocorticoid receptor binding - 0.9043 90.43%
Aromatase binding - 0.7558 75.58%
PPAR gamma - 0.9179 91.79%
Honey bee toxicity - 0.8742 87.42%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.5000 50.00%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.78% 95.56%

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.
Elsholtzia ciliata
Mosla chinensis

Cross-Links

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PubChem 536113
NPASS NPC200692