Ethyl hydrogen malonate

Details

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Internal ID 12ec2941-66bc-4d88-b40c-dbbfe534f288
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Dicarboxylic acids and derivatives
IUPAC Name 3-ethoxy-3-oxopropanoic acid
SMILES (Canonical) CCOC(=O)CC(=O)O
SMILES (Isomeric) CCOC(=O)CC(=O)O
InChI InChI=1S/C5H8O4/c1-2-9-5(8)3-4(6)7/h2-3H2,1H3,(H,6,7)
InChI Key HGINADPHJQTSKN-UHFFFAOYSA-N
Popularity 96 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8O4
Molecular Weight 132.11 g/mol
Exact Mass 132.04225873 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.02
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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1071-46-1
3-ethoxy-3-oxopropanoic acid
Monoethyl malonate
monoethyl malonic acid
mono-Ethyl malonate
Monoethyl hydrogen malonate
malonic acid monoethyl ester
(Ethoxycarbonyl)acetic acid
malonic acid monoethylester
EINECS 213-992-7
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl hydrogen malonate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9558 95.58%
Caco-2 - 0.5415 54.15%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.8134 81.34%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.9641 96.41%
OATP1B3 inhibitior + 0.9563 95.63%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9390 93.90%
P-glycoprotein inhibitior - 0.9847 98.47%
P-glycoprotein substrate - 0.9899 98.99%
CYP3A4 substrate - 0.7028 70.28%
CYP2C9 substrate + 0.6168 61.68%
CYP2D6 substrate - 0.8932 89.32%
CYP3A4 inhibition - 0.9163 91.63%
CYP2C9 inhibition - 0.9373 93.73%
CYP2C19 inhibition - 0.9406 94.06%
CYP2D6 inhibition - 0.9435 94.35%
CYP1A2 inhibition - 0.9368 93.68%
CYP2C8 inhibition - 0.9736 97.36%
CYP inhibitory promiscuity - 0.9651 96.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.6732 67.32%
Eye corrosion + 0.8266 82.66%
Eye irritation + 0.9949 99.49%
Skin irritation - 0.5200 52.00%
Skin corrosion + 0.5139 51.39%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7971 79.71%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.5140 51.40%
skin sensitisation - 0.8730 87.30%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5389 53.89%
Acute Oral Toxicity (c) III 0.6518 65.18%
Estrogen receptor binding - 0.9106 91.06%
Androgen receptor binding - 0.9666 96.66%
Thyroid receptor binding - 0.9250 92.50%
Glucocorticoid receptor binding - 0.9133 91.33%
Aromatase binding - 0.9260 92.60%
PPAR gamma - 0.8058 80.58%
Honey bee toxicity - 0.9732 97.32%
Biodegradation + 0.9500 95.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.7152 71.52%

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 92.02% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 89.00% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.19% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 86.11% 89.63%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.64% 96.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.85% 94.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.30% 96.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.53% 97.21%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.29% 85.14%

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.
Sigesbeckia glabrescens
Sigesbeckia pubescens

Cross-Links

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PubChem 70615
NPASS NPC90221