methyl (3-methyl-5-oxo-4H-imidazol-2-yl) hydrogen phosphate

Details

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Internal ID 0c6bfb89-2744-448e-a90b-925ff5072990
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives
IUPAC Name methyl (3-methyl-5-oxo-4H-imidazol-2-yl) hydrogen phosphate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H9N2O5P/c1-7-3-4(8)6-5(7)12-13(9,10)11-2/h3H2,1-2H3,(H,9,10)
InChI Key WUGCPJPZXRWKQO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C5H9N2O5P
Molecular Weight 208.11 g/mol
Exact Mass 208.02490839 g/mol
Topological Polar Surface Area (TPSA) 88.40 Ų
XlogP -1.30
Atomic LogP (AlogP) -0.42
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (3-methyl-5-oxo-4H-imidazol-2-yl) hydrogen phosphate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4698 46.98%
Caco-2 - 0.7605 76.05%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.5821 58.21%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.9627 96.27%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9095 90.95%
P-glycoprotein inhibitior - 0.9630 96.30%
P-glycoprotein substrate - 0.9083 90.83%
CYP3A4 substrate - 0.5128 51.28%
CYP2C9 substrate - 0.7829 78.29%
CYP2D6 substrate - 0.8648 86.48%
CYP3A4 inhibition - 0.9679 96.79%
CYP2C9 inhibition - 0.8359 83.59%
CYP2C19 inhibition - 0.7852 78.52%
CYP2D6 inhibition - 0.9140 91.40%
CYP1A2 inhibition - 0.8118 81.18%
CYP2C8 inhibition - 0.9805 98.05%
CYP inhibitory promiscuity - 0.9953 99.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.5628 56.28%
Eye corrosion - 0.9611 96.11%
Eye irritation + 0.5992 59.92%
Skin irritation - 0.7383 73.83%
Skin corrosion - 0.9083 90.83%
Ames mutagenesis - 0.7154 71.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7988 79.88%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.5611 56.11%
skin sensitisation - 0.8418 84.18%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.8005 80.05%
Acute Oral Toxicity (c) III 0.4951 49.51%
Estrogen receptor binding - 0.7817 78.17%
Androgen receptor binding - 0.7160 71.60%
Thyroid receptor binding - 0.7340 73.40%
Glucocorticoid receptor binding - 0.9144 91.44%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.7461 74.61%
Honey bee toxicity - 0.4696 46.96%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.8037 80.37%

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 93.61% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.98% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.84% 95.56%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 85.66% 87.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.06% 94.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.92% 81.11%
CHEMBL4208 P20618 Proteasome component C5 80.44% 90.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 101639346
LOTUS LTS0086274
wikiData Q105313029