1-Nitro-2-phenylethane

Details

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Internal ID b7592bda-6599-4976-b7a5-14a1260d7c50
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 2-nitroethylbenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H9NO2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-5H,6-7H2
InChI Key XAWCLWKTUKMCMO-UHFFFAOYSA-N
Popularity 145 references in papers

Physical and Chemical Properties

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Molecular Formula C8H9NO2
Molecular Weight 151.16 g/mol
Exact Mass 151.063328530 g/mol
Topological Polar Surface Area (TPSA) 45.80 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.51
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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6125-24-2
2-Nitroethylbenzene
Benzene, (2-nitroethyl)-
1-Nitro-2-phenylethane
1-(PHENYL) 2-NITROETHANE
MFCD00210449
1-(2-nitroethyl)benzene
2-phenylnitroethane
NSC23854
EINECS 228-094-0
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Nitro-2-phenylethane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9696 96.96%
Caco-2 + 0.9381 93.81%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.5774 57.74%
OATP2B1 inhibitior - 0.8707 87.07%
OATP1B1 inhibitior + 0.9356 93.56%
OATP1B3 inhibitior + 0.9387 93.87%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8447 84.47%
P-glycoprotein inhibitior - 0.9909 99.09%
P-glycoprotein substrate - 0.9655 96.55%
CYP3A4 substrate - 0.6592 65.92%
CYP2C9 substrate - 0.8185 81.85%
CYP2D6 substrate - 0.7888 78.88%
CYP3A4 inhibition - 0.8781 87.81%
CYP2C9 inhibition - 0.8360 83.60%
CYP2C19 inhibition - 0.5717 57.17%
CYP2D6 inhibition - 0.8769 87.69%
CYP1A2 inhibition + 0.6129 61.29%
CYP2C8 inhibition - 0.8450 84.50%
CYP inhibitory promiscuity - 0.6614 66.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5009 50.09%
Carcinogenicity (trinary) Non-required 0.6475 64.75%
Eye corrosion + 0.5000 50.00%
Eye irritation + 0.9799 97.99%
Skin irritation - 0.5733 57.33%
Skin corrosion - 0.6011 60.11%
Ames mutagenesis + 0.5321 53.21%
Human Ether-a-go-go-Related Gene inhibition - 0.8093 80.93%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.6677 66.77%
skin sensitisation - 0.6658 66.58%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5103 51.03%
Acute Oral Toxicity (c) III 0.4929 49.29%
Estrogen receptor binding - 0.8929 89.29%
Androgen receptor binding - 0.8383 83.83%
Thyroid receptor binding - 0.8976 89.76%
Glucocorticoid receptor binding - 0.6699 66.99%
Aromatase binding - 0.9136 91.36%
PPAR gamma - 0.7617 76.17%
Honey bee toxicity - 0.8506 85.06%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity - 0.8243 82.43%

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
CHEMBL2581 P07339 Cathepsin D 94.31% 98.95%
CHEMBL3902 P09211 Glutathione S-transferase Pi 90.97% 93.81%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.95% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.16% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.06% 95.56%
CHEMBL5805 Q9NR97 Toll-like receptor 8 86.01% 96.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.46% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 82.64% 90.20%
CHEMBL3401 O75469 Pregnane X receptor 82.00% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 80.87% 90.17%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 80.86% 100.00%

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.
Dennettia tripetala

Cross-Links

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PubChem 80208
LOTUS LTS0121064
wikiData Q83084734