(2S,3S,4R,5S,6S)-3-(1-hydroxyethenylamino)-6-(hydroxymethyl)oxane-2,4,5-triol

Details

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Internal ID bc0f5b94-61f3-424e-a75e-bb286e107d16
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Hexoses
IUPAC Name (2S,3S,4R,5S,6S)-3-(1-hydroxyethenylamino)-6-(hydroxymethyl)oxane-2,4,5-triol
SMILES (Canonical) C=C(NC1C(C(C(OC1O)CO)O)O)O
SMILES (Isomeric) C=C(N[C@H]1[C@H]([C@@H]([C@@H](O[C@@H]1O)CO)O)O)O
InChI InChI=1S/C8H15NO6/c1-3(11)9-5-7(13)6(12)4(2-10)15-8(5)14/h4-14H,1-2H2/t4-,5-,6+,7+,8-/m0/s1
InChI Key QWGMMTHILQPIPX-TXXZRHAASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H15NO6
Molecular Weight 221.21 g/mol
Exact Mass 221.08993720 g/mol
Topological Polar Surface Area (TPSA) 122.00 Ų
XlogP -1.40
Atomic LogP (AlogP) -2.59
H-Bond Acceptor 7
H-Bond Donor 6
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,3S,4R,5S,6S)-3-(1-hydroxyethenylamino)-6-(hydroxymethyl)oxane-2,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9086 90.86%
Caco-2 - 0.9402 94.02%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5441 54.41%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.6979 69.79%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9910 99.10%
P-glycoprotein inhibitior - 0.9645 96.45%
P-glycoprotein substrate - 0.9640 96.40%
CYP3A4 substrate - 0.6308 63.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8391 83.91%
CYP3A4 inhibition - 0.9339 93.39%
CYP2C9 inhibition - 0.8610 86.10%
CYP2C19 inhibition - 0.8168 81.68%
CYP2D6 inhibition - 0.9235 92.35%
CYP1A2 inhibition - 0.8499 84.99%
CYP2C8 inhibition - 0.9397 93.97%
CYP inhibitory promiscuity - 0.9360 93.60%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6976 69.76%
Eye corrosion - 0.9844 98.44%
Eye irritation - 0.9844 98.44%
Skin irritation - 0.7799 77.99%
Skin corrosion - 0.9402 94.02%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7181 71.81%
Micronuclear + 0.6600 66.00%
Hepatotoxicity - 0.6575 65.75%
skin sensitisation - 0.8254 82.54%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.6865 68.65%
Acute Oral Toxicity (c) III 0.5360 53.60%
Estrogen receptor binding - 0.6636 66.36%
Androgen receptor binding - 0.8451 84.51%
Thyroid receptor binding - 0.6220 62.20%
Glucocorticoid receptor binding - 0.6212 62.12%
Aromatase binding - 0.7526 75.26%
PPAR gamma - 0.7939 79.39%
Honey bee toxicity - 0.8316 83.16%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.7921 79.21%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.21% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 90.29% 95.93%
CHEMBL3589 P55263 Adenosine kinase 89.00% 98.05%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.10% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 82.48% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.32% 99.17%

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 163105754
LOTUS LTS0249728
wikiData Q105229161