4,5-Diacetamido-3,6-dihydroxyoxane-2-carboxylic acid

Details

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Internal ID 2acc03ff-e11e-4a44-80af-076292e8fb5e
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Amino acids and derivatives > Gamma amino acids and derivatives
IUPAC Name 4,5-diacetamido-3,6-dihydroxyoxane-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16N2O7/c1-3(13)11-5-6(12-4(2)14)10(18)19-8(7(5)15)9(16)17/h5-8,10,15,18H,1-2H3,(H,11,13)(H,12,14)(H,16,17)
InChI Key SOXOUCOZZYMXPU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16N2O7
Molecular Weight 276.24 g/mol
Exact Mass 276.09575085 g/mol
Topological Polar Surface Area (TPSA) 145.00 Ų
XlogP -2.30
Atomic LogP (AlogP) -2.84
H-Bond Acceptor 6
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,5-Diacetamido-3,6-dihydroxyoxane-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9421 94.21%
Caco-2 - 0.9291 92.91%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6190 61.90%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.7668 76.68%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9907 99.07%
P-glycoprotein inhibitior - 0.9368 93.68%
P-glycoprotein substrate - 0.9474 94.74%
CYP3A4 substrate - 0.5766 57.66%
CYP2C9 substrate + 0.5898 58.98%
CYP2D6 substrate - 0.8726 87.26%
CYP3A4 inhibition - 0.9455 94.55%
CYP2C9 inhibition - 0.9679 96.79%
CYP2C19 inhibition - 0.9541 95.41%
CYP2D6 inhibition - 0.9625 96.25%
CYP1A2 inhibition - 0.9759 97.59%
CYP2C8 inhibition - 0.9510 95.10%
CYP inhibitory promiscuity - 0.9858 98.58%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.7488 74.88%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9359 93.59%
Skin irritation - 0.7684 76.84%
Skin corrosion - 0.9614 96.14%
Ames mutagenesis - 0.6347 63.47%
Human Ether-a-go-go-Related Gene inhibition - 0.7888 78.88%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.5085 50.85%
skin sensitisation - 0.9146 91.46%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6929 69.29%
Acute Oral Toxicity (c) III 0.5040 50.40%
Estrogen receptor binding - 0.7734 77.34%
Androgen receptor binding - 0.7971 79.71%
Thyroid receptor binding - 0.5552 55.52%
Glucocorticoid receptor binding - 0.8571 85.71%
Aromatase binding - 0.8461 84.61%
PPAR gamma - 0.7020 70.20%
Honey bee toxicity - 0.8888 88.88%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.8268 82.68%

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 91.46% 83.82%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 86.59% 81.11%
CHEMBL3401 O75469 Pregnane X receptor 85.68% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.36% 85.14%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 85.29% 87.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.36% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 82.93% 91.19%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.88% 99.17%
CHEMBL2581 P07339 Cathepsin D 81.52% 98.95%

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 77518085
LOTUS LTS0044417
wikiData Q105257274