2-Hydroxyethyl prop-2-en-1-yl carbonate

Details

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Internal ID 55395c9c-9440-4603-9829-81fd999ea9a0
Taxonomy Organic acids and derivatives > Organic carbonic acids and derivatives > Carbonic acid diesters
IUPAC Name 2-hydroxyethyl prop-2-enyl carbonate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H10O4/c1-2-4-9-6(8)10-5-3-7/h2,7H,1,3-5H2
InChI Key RHZWMHZZJLEPBC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O4
Molecular Weight 146.14 g/mol
Exact Mass 146.05790880 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.32
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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NSC-2300
2-hydroxyethyl prop-2-en-1-yl carbonate
2-hydroxyethyl prop-2-enyl carbonate
NSC2300
29VG9FA9KD
SCHEMBL1407204
DTXSID90277421
2-HYDROXYETHYL 2-PROPEN-1-YL CARBONATE
CARBONIC ACID, ALLYL 2-HYDROXYETHYL ESTER
CARBONIC ACID, 2-HYDROXYETHYL 2-PROPENYL ESTER
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-Hydroxyethyl prop-2-en-1-yl carbonate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9219 92.19%
Caco-2 + 0.6543 65.43%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7600 76.00%
OATP2B1 inhibitior - 0.8492 84.92%
OATP1B1 inhibitior + 0.9188 91.88%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9550 95.50%
P-glycoprotein inhibitior - 0.9887 98.87%
P-glycoprotein substrate - 0.9848 98.48%
CYP3A4 substrate - 0.6267 62.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7704 77.04%
CYP3A4 inhibition - 0.8257 82.57%
CYP2C9 inhibition - 0.8977 89.77%
CYP2C19 inhibition - 0.8599 85.99%
CYP2D6 inhibition - 0.9450 94.50%
CYP1A2 inhibition - 0.8624 86.24%
CYP2C8 inhibition - 0.9119 91.19%
CYP inhibitory promiscuity - 0.9476 94.76%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.7383 73.83%
Eye corrosion + 0.7837 78.37%
Eye irritation + 0.9924 99.24%
Skin irritation + 0.5346 53.46%
Skin corrosion - 0.8409 84.09%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7502 75.02%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.6428 64.28%
skin sensitisation + 0.6962 69.62%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.8667 86.67%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.7569 75.69%
Acute Oral Toxicity (c) III 0.6661 66.61%
Estrogen receptor binding - 0.9175 91.75%
Androgen receptor binding - 0.8039 80.39%
Thyroid receptor binding - 0.8510 85.10%
Glucocorticoid receptor binding - 0.8663 86.63%
Aromatase binding - 0.8393 83.93%
PPAR gamma - 0.8690 86.90%
Honey bee toxicity - 0.8103 81.03%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.9400 94.00%
Fish aquatic toxicity - 0.4638 46.38%

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 86.31% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.02% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.35% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.47% 86.92%
CHEMBL2885 P07451 Carbonic anhydrase III 81.32% 87.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.84% 91.07%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.56% 89.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.37% 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.
Calotropis procera

Cross-Links

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PubChem 220059
LOTUS LTS0189346
wikiData Q82008565