Ethyl 4-nitrophenyl P-ethylphosphonate

Details

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Internal ID c7714da2-f9fd-460e-a48d-db9fbe5377d0
Taxonomy Benzenoids > Benzene and substituted derivatives > Nitrobenzenes
IUPAC Name 1-[ethoxy(ethyl)phosphoryl]oxy-4-nitrobenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14NO5P/c1-3-15-17(14,4-2)16-10-7-5-9(6-8-10)11(12)13/h5-8H,3-4H2,1-2H3
InChI Key XXUJMEYKYHETBZ-UHFFFAOYSA-N
Popularity 116 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14NO5P
Molecular Weight 259.20 g/mol
Exact Mass 259.06095954 g/mol
Topological Polar Surface Area (TPSA) 81.40 Ų
XlogP 1.70
Atomic LogP (AlogP) 3.22
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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Armin
Ethyl 4-nitrophenyl ethylphosphonate
Arminum
p-Nitrophenyl-O-ethyl ethylphosphonate
Armin (ester)
546-71-4
Armeen
1-[ethoxy(ethyl)phosphoryl]oxy-4-nitrobenzene
Ethyl p-nitrophenyl ethylphosphonate
H39MRI1X2O
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 4-nitrophenyl P-ethylphosphonate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9559 95.59%
Caco-2 + 0.8702 87.02%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.7241 72.41%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8842 88.42%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7850 78.50%
P-glycoprotein inhibitior - 0.9250 92.50%
P-glycoprotein substrate - 0.9628 96.28%
CYP3A4 substrate + 0.6125 61.25%
CYP2C9 substrate - 0.8207 82.07%
CYP2D6 substrate - 0.8425 84.25%
CYP3A4 inhibition - 0.6716 67.16%
CYP2C9 inhibition - 0.6162 61.62%
CYP2C19 inhibition + 0.5208 52.08%
CYP2D6 inhibition - 0.8706 87.06%
CYP1A2 inhibition + 0.5425 54.25%
CYP2C8 inhibition - 0.7677 76.77%
CYP inhibitory promiscuity - 0.5200 52.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5523 55.23%
Carcinogenicity (trinary) Non-required 0.5502 55.02%
Eye corrosion - 0.9604 96.04%
Eye irritation + 0.8691 86.91%
Skin irritation - 0.7569 75.69%
Skin corrosion - 0.9216 92.16%
Ames mutagenesis + 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6422 64.22%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.6785 67.85%
skin sensitisation - 0.8393 83.93%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity + 0.6503 65.03%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.8969 89.69%
Acute Oral Toxicity (c) I 0.5345 53.45%
Estrogen receptor binding + 0.8919 89.19%
Androgen receptor binding + 0.8695 86.95%
Thyroid receptor binding - 0.6863 68.63%
Glucocorticoid receptor binding - 0.8390 83.90%
Aromatase binding + 0.8685 86.85%
PPAR gamma - 0.5591 55.91%
Honey bee toxicity + 0.7929 79.29%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9709 97.09%

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
CHEMBL3401 O75469 Pregnane X receptor 92.79% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.17% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.28% 95.56%
CHEMBL3902 P09211 Glutathione S-transferase Pi 87.67% 93.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.60% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.47% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 84.19% 83.82%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.56% 96.00%
CHEMBL4208 P20618 Proteasome component C5 82.78% 90.00%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.06% 92.86%
CHEMBL1255126 O15151 Protein Mdm4 81.92% 90.20%
CHEMBL2581 P07339 Cathepsin D 81.39% 98.95%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.20% 95.71%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.84% 94.80%

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.
Artemisia armeniaca

Cross-Links

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PubChem 66067
LOTUS LTS0082085
wikiData Q4069610