Ethyl 3-nitropropanoate

Details

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Internal ID 3b21b142-62f4-4127-87a8-83da9a90d52f
Taxonomy Organic 1,3-dipolar compounds > Allyl-type 1,3-dipolar organic compounds > Organic nitro compounds > C-nitro compounds
IUPAC Name ethyl 3-nitropropanoate
SMILES (Canonical) CCOC(=O)CC[N+](=O)[O-]
SMILES (Isomeric) CCOC(=O)CC[N+](=O)[O-]
InChI InChI=1S/C5H9NO4/c1-2-10-5(7)3-4-6(8)9/h2-4H2,1H3
InChI Key IIJLLHGPEZBIIT-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C5H9NO4
Molecular Weight 147.13 g/mol
Exact Mass 147.05315777 g/mol
Topological Polar Surface Area (TPSA) 72.10 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.22
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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RefChem:921263
Ethyl 3-nitropropanoate
3590-37-2
MFCD00096267
Propanoic acid,3-nitro-, ethyl ester
Propanoic acid, 3-nitro-, ethyl ester
ethyl beta-nitropropanoate
SCHEMBL1029123
SCHEMBL8371814
DTXSID40473017
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 3-nitropropanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9126 91.26%
Caco-2 + 0.7173 71.73%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6675 66.75%
OATP2B1 inhibitior - 0.8446 84.46%
OATP1B1 inhibitior + 0.9422 94.22%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9627 96.27%
P-glycoprotein inhibitior - 0.9818 98.18%
P-glycoprotein substrate - 0.9922 99.22%
CYP3A4 substrate - 0.5627 56.27%
CYP2C9 substrate - 0.8070 80.70%
CYP2D6 substrate - 0.8826 88.26%
CYP3A4 inhibition - 0.9525 95.25%
CYP2C9 inhibition - 0.7678 76.78%
CYP2C19 inhibition - 0.7240 72.40%
CYP2D6 inhibition - 0.8173 81.73%
CYP1A2 inhibition - 0.6485 64.85%
CYP2C8 inhibition - 0.9404 94.04%
CYP inhibitory promiscuity - 0.6784 67.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.6169 61.69%
Eye corrosion - 0.9357 93.57%
Eye irritation + 0.9409 94.09%
Skin irritation - 0.7371 73.71%
Skin corrosion - 0.9151 91.51%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7189 71.89%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8314 83.14%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.5507 55.07%
Acute Oral Toxicity (c) III 0.5900 59.00%
Estrogen receptor binding - 0.9354 93.54%
Androgen receptor binding - 0.9734 97.34%
Thyroid receptor binding - 0.9250 92.50%
Glucocorticoid receptor binding - 0.8196 81.96%
Aromatase binding - 0.8849 88.49%
PPAR gamma - 0.8698 86.98%
Honey bee toxicity - 0.8955 89.55%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.7849 78.49%

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 90.59% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.92% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.36% 86.33%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.91% 97.21%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 84.35% 91.24%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.86% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 83.14% 94.73%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.84% 94.33%

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.
Linum usitatissimum

Cross-Links

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PubChem 11804910
NPASS NPC151517