ethyl (2Z)-2-hydroxyimino-3-pyrimidin-4-ylpropanoate

Details

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Internal ID 53c76286-37d7-41d2-97d7-bd87520213bf
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl (2Z)-2-hydroxyimino-3-pyrimidin-4-ylpropanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H11N3O3/c1-2-15-9(13)8(12-14)5-7-3-4-10-6-11-7/h3-4,6,14H,2,5H2,1H3/b12-8-
InChI Key DTOCWZKRROVNGQ-WQLSENKSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H11N3O3
Molecular Weight 209.20 g/mol
Exact Mass 209.08004122 g/mol
Topological Polar Surface Area (TPSA) 84.70 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.41
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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90559-55-0
NSC-88413

2D Structure

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2D Structure of ethyl (2Z)-2-hydroxyimino-3-pyrimidin-4-ylpropanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9780 97.80%
Caco-2 + 0.5101 51.01%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.7420 74.20%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.9492 94.92%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6319 63.19%
P-glycoprotein inhibitior - 0.9841 98.41%
P-glycoprotein substrate - 0.9332 93.32%
CYP3A4 substrate - 0.5464 54.64%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate - 0.8982 89.82%
CYP3A4 inhibition - 0.8726 87.26%
CYP2C9 inhibition - 0.7601 76.01%
CYP2C19 inhibition - 0.6969 69.69%
CYP2D6 inhibition - 0.8900 89.00%
CYP1A2 inhibition + 0.5365 53.65%
CYP2C8 inhibition + 0.4516 45.16%
CYP inhibitory promiscuity - 0.9235 92.35%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7239 72.39%
Carcinogenicity (trinary) Non-required 0.6120 61.20%
Eye corrosion - 0.9755 97.55%
Eye irritation + 0.8046 80.46%
Skin irritation - 0.7000 70.00%
Skin corrosion - 0.9180 91.80%
Ames mutagenesis - 0.5854 58.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6663 66.63%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.7034 70.34%
skin sensitisation - 0.8351 83.51%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6646 66.46%
Acute Oral Toxicity (c) III 0.6844 68.44%
Estrogen receptor binding - 0.6798 67.98%
Androgen receptor binding - 0.7422 74.22%
Thyroid receptor binding - 0.5750 57.50%
Glucocorticoid receptor binding + 0.5835 58.35%
Aromatase binding - 0.5766 57.66%
PPAR gamma - 0.5758 57.58%
Honey bee toxicity - 0.9383 93.83%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity - 0.6684 66.84%

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 95.99% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 90.71% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 90.41% 93.65%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 89.56% 93.10%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.42% 86.33%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 88.00% 96.47%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.43% 99.17%
CHEMBL2581 P07339 Cathepsin D 85.73% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.33% 96.00%
CHEMBL4208 P20618 Proteasome component C5 83.68% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.24% 94.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.76% 81.11%

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.
Embelia ribes

Cross-Links

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PubChem 9552087
NPASS NPC310870