2-Ethyl-2,4,5-trimethyl-1,3-dioxolane

Details

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Internal ID 21dd1d9a-51de-4cb2-8add-4fa09acfef94
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals > Ketals
IUPAC Name 2-ethyl-2,4,5-trimethyl-1,3-dioxolane
SMILES (Canonical) CCC1(OC(C(O1)C)C)C
SMILES (Isomeric) CCC1(OC(C(O1)C)C)C
InChI InChI=1S/C8H16O2/c1-5-8(4)9-6(2)7(3)10-8/h6-7H,5H2,1-4H3
InChI Key ZRKDAOBWBAZESR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C8H16O2
Molecular Weight 144.21 g/mol
Exact Mass 144.115029749 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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4359-51-7
DTXSID00278303
RefChem:260465
DTXCID50229461
NSC6985
SCHEMBL10045672
ZRKDAOBWBAZESR-UHFFFAOYSA-N
NSC-6985
2,4,5-trimethyl-2-ethyl-1,3-dioxolane
1,3-Dioxolane, 2-ethyl-2,4,5-trimethyl-
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-2,4,5-trimethyl-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 + 0.9699 96.99%
Caco-2 + 0.7955 79.55%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5192 51.92%
OATP2B1 inhibitior - 0.8614 86.14%
OATP1B1 inhibitior + 0.9146 91.46%
OATP1B3 inhibitior + 0.9354 93.54%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9401 94.01%
P-glycoprotein inhibitior - 0.9458 94.58%
P-glycoprotein substrate - 0.9465 94.65%
CYP3A4 substrate - 0.6584 65.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7706 77.06%
CYP3A4 inhibition - 0.8820 88.20%
CYP2C9 inhibition - 0.8143 81.43%
CYP2C19 inhibition - 0.7355 73.55%
CYP2D6 inhibition - 0.9360 93.60%
CYP1A2 inhibition - 0.6994 69.94%
CYP2C8 inhibition - 0.9381 93.81%
CYP inhibitory promiscuity - 0.6861 68.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Warning 0.4127 41.27%
Eye corrosion - 0.7569 75.69%
Eye irritation + 0.7763 77.63%
Skin irritation - 0.5461 54.61%
Skin corrosion - 0.9281 92.81%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7788 77.88%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5959 59.59%
skin sensitisation + 0.6869 68.69%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5476 54.76%
Acute Oral Toxicity (c) III 0.7753 77.53%
Estrogen receptor binding - 0.8819 88.19%
Androgen receptor binding - 0.6617 66.17%
Thyroid receptor binding - 0.8096 80.96%
Glucocorticoid receptor binding - 0.9461 94.61%
Aromatase binding - 0.7888 78.88%
PPAR gamma - 0.8292 82.92%
Honey bee toxicity - 0.8445 84.45%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.6395 63.95%

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
CHEMBL233 P35372 Mu opioid receptor 86.21% 97.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.98% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.70% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 81.91% 90.17%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.49% 96.61%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.79% 91.11%

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 221881
NPASS NPC38902