N-hydroxy-N-(1-hydroxypropan-2-yl)nitrous amide

Details

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Internal ID ea8ae5c8-077e-4bdd-b55a-db585501a410
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Organic nitroso compounds > Organic N-nitroso compounds
IUPAC Name N-hydroxy-N-(1-hydroxypropan-2-yl)nitrous amide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C3H8N2O3/c1-3(2-6)5(8)4-7/h3,6,8H,2H2,1H3
InChI Key KBIVZHFFKKKJLT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C3H8N2O3
Molecular Weight 120.11 g/mol
Exact Mass 120.05349212 g/mol
Topological Polar Surface Area (TPSA) 73.10 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.26
H-Bond Acceptor 4
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 N-hydroxy-N-(1-hydroxypropan-2-yl)nitrous amide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8431 84.31%
Caco-2 - 0.5887 58.87%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6599 65.99%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.9473 94.73%
OATP1B3 inhibitior + 0.9367 93.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9079 90.79%
P-glycoprotein inhibitior - 0.9830 98.30%
P-glycoprotein substrate - 0.9834 98.34%
CYP3A4 substrate - 0.6664 66.64%
CYP2C9 substrate - 0.8476 84.76%
CYP2D6 substrate - 0.7503 75.03%
CYP3A4 inhibition - 0.9337 93.37%
CYP2C9 inhibition - 0.8238 82.38%
CYP2C19 inhibition - 0.8058 80.58%
CYP2D6 inhibition - 0.9032 90.32%
CYP1A2 inhibition - 0.7464 74.64%
CYP2C8 inhibition - 0.9939 99.39%
CYP inhibitory promiscuity - 0.9776 97.76%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Danger 0.5433 54.33%
Eye corrosion - 0.9434 94.34%
Eye irritation + 0.9002 90.02%
Skin irritation - 0.6329 63.29%
Skin corrosion - 0.9015 90.15%
Ames mutagenesis + 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7942 79.42%
Micronuclear + 0.9700 97.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.7826 78.26%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.7707 77.07%
Acute Oral Toxicity (c) III 0.5738 57.38%
Estrogen receptor binding - 0.9401 94.01%
Androgen receptor binding - 0.8038 80.38%
Thyroid receptor binding - 0.8240 82.40%
Glucocorticoid receptor binding - 0.8944 89.44%
Aromatase binding - 0.8427 84.27%
PPAR gamma - 0.8937 89.37%
Honey bee toxicity - 0.8831 88.31%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.8661 86.61%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.91% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.36% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.52% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.26% 89.34%
CHEMBL2885 P07451 Carbonic anhydrase III 85.48% 87.45%
CHEMBL3401 O75469 Pregnane X receptor 83.08% 94.73%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.06% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.35% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.09% 97.25%

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 137378
LOTUS LTS0234070
wikiData Q83004184