Methyl (2,5-dihydroxy-3-nitrophenyl) acetate

Details

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Internal ID ec102847-84c5-4de7-ae80-974012bdbeff
Taxonomy Benzenoids > Phenols > Nitrophenols
IUPAC Name methyl 2-(2,5-dihydroxy-3-nitrophenyl)acetate
SMILES (Canonical) COC(=O)CC1=C(C(=CC(=C1)O)[N+](=O)[O-])O
SMILES (Isomeric) COC(=O)CC1=C(C(=CC(=C1)O)[N+](=O)[O-])O
InChI InChI=1S/C9H9NO6/c1-16-8(12)3-5-2-6(11)4-7(9(5)13)10(14)15/h2,4,11,13H,3H2,1H3
InChI Key NBFISYVVWKCRKR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H9NO6
Molecular Weight 227.17 g/mol
Exact Mass 227.04298701 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 1.40
Atomic LogP (AlogP) 0.72
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl (2,5-dihydroxy-3-nitrophenyl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8148 81.48%
Caco-2 - 0.7013 70.13%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7522 75.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7677 76.77%
OATP1B3 inhibitior + 0.9368 93.68%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9187 91.87%
P-glycoprotein inhibitior - 0.9678 96.78%
P-glycoprotein substrate - 0.8980 89.80%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.8705 87.05%
CYP3A4 inhibition - 0.8835 88.35%
CYP2C9 inhibition - 0.6896 68.96%
CYP2C19 inhibition - 0.7649 76.49%
CYP2D6 inhibition - 0.9134 91.34%
CYP1A2 inhibition - 0.7564 75.64%
CYP2C8 inhibition - 0.5681 56.81%
CYP inhibitory promiscuity - 0.8101 81.01%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5946 59.46%
Carcinogenicity (trinary) Non-required 0.5537 55.37%
Eye corrosion - 0.9818 98.18%
Eye irritation + 0.6995 69.95%
Skin irritation - 0.7925 79.25%
Skin corrosion - 0.9444 94.44%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7177 71.77%
Micronuclear + 0.9400 94.00%
Hepatotoxicity + 0.8034 80.34%
skin sensitisation - 0.9070 90.70%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5947 59.47%
Nephrotoxicity + 0.5491 54.91%
Acute Oral Toxicity (c) III 0.6899 68.99%
Estrogen receptor binding + 0.5580 55.80%
Androgen receptor binding + 0.6044 60.44%
Thyroid receptor binding - 0.7510 75.10%
Glucocorticoid receptor binding + 0.6889 68.89%
Aromatase binding - 0.7101 71.01%
PPAR gamma - 0.5526 55.26%
Honey bee toxicity - 0.9625 96.25%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9482 94.82%

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 93.49% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.16% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.96% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.99% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.15% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 87.43% 94.73%
CHEMBL4208 P20618 Proteasome component C5 87.03% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.56% 96.95%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 85.01% 92.88%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.82% 94.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.89% 95.56%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.86% 91.07%
CHEMBL1255126 O15151 Protein Mdm4 81.24% 90.20%

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.
Ainsliaea cordifolia
Dictamnus dasycarpus

Cross-Links

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PubChem 85672025
LOTUS LTS0145261
wikiData Q105144882