1-Aminooxy-1,4,5,6-tetrahydroxyhexane-2,3-dione

Details

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Internal ID 33e244ae-2501-4099-bc05-b9bc290fedbe
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides
IUPAC Name 1-aminooxy-1,4,5,6-tetrahydroxyhexane-2,3-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H11NO7/c7-14-6(13)5(12)4(11)3(10)2(9)1-8/h2-3,6,8-10,13H,1,7H2
InChI Key PXVTUTKRTCSFNM-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11NO7
Molecular Weight 209.15 g/mol
Exact Mass 209.05355169 g/mol
Topological Polar Surface Area (TPSA) 150.00 Ų
XlogP -3.70
Atomic LogP (AlogP) -3.95
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Aminooxy-1,4,5,6-tetrahydroxyhexane-2,3-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5576 55.76%
Caco-2 - 0.9870 98.70%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5696 56.96%
OATP2B1 inhibitior - 0.8568 85.68%
OATP1B1 inhibitior + 0.9742 97.42%
OATP1B3 inhibitior + 0.8968 89.68%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9903 99.03%
P-glycoprotein inhibitior - 0.9633 96.33%
P-glycoprotein substrate - 0.9646 96.46%
CYP3A4 substrate - 0.6682 66.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8285 82.85%
CYP3A4 inhibition - 0.8440 84.40%
CYP2C9 inhibition - 0.8708 87.08%
CYP2C19 inhibition - 0.8559 85.59%
CYP2D6 inhibition - 0.8871 88.71%
CYP1A2 inhibition - 0.8638 86.38%
CYP2C8 inhibition - 0.9777 97.77%
CYP inhibitory promiscuity - 0.9813 98.13%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.6612 66.12%
Eye corrosion - 0.9568 95.68%
Eye irritation - 0.9064 90.64%
Skin irritation - 0.7603 76.03%
Skin corrosion - 0.9248 92.48%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7524 75.24%
Micronuclear + 0.6400 64.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.8943 89.43%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.7045 70.45%
Acute Oral Toxicity (c) III 0.5137 51.37%
Estrogen receptor binding - 0.5258 52.58%
Androgen receptor binding - 0.6579 65.79%
Thyroid receptor binding - 0.5833 58.33%
Glucocorticoid receptor binding + 0.6163 61.63%
Aromatase binding - 0.7279 72.79%
PPAR gamma - 0.8015 80.15%
Honey bee toxicity - 0.9224 92.24%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity - 0.9381 93.81%

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 95.95% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.62% 97.29%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.37% 94.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.14% 86.92%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.51% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.54% 96.00%

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 54213979
LOTUS LTS0241526
wikiData Q105216446