(2S,3S,4R,5R,6S)-2-(2-hydroxybut-3-enoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID 308dd940-232b-4f81-bcf4-75cb6dc15ee1
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl glycosides > Fatty acyl glycosides of mono- and disaccharides
IUPAC Name (2S,3S,4R,5R,6S)-2-(2-hydroxybut-3-enoxy)-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O7/c1-2-5(12)4-16-10-9(15)8(14)7(13)6(3-11)17-10/h2,5-15H,1,3-4H2/t5?,6-,7-,8+,9-,10-/m0/s1
InChI Key JIMWXFWXOSWLSG-HSDFISHXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O7
Molecular Weight 250.25 g/mol
Exact Mass 250.10525291 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP -2.10
Atomic LogP (AlogP) -2.65
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9196 91.96%
Caco-2 - 0.8622 86.22%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.6424 64.24%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.9146 91.46%
OATP1B3 inhibitior + 0.9609 96.09%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9734 97.34%
P-glycoprotein inhibitior - 0.9384 93.84%
P-glycoprotein substrate - 0.9794 97.94%
CYP3A4 substrate - 0.5649 56.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8382 83.82%
CYP3A4 inhibition - 0.9130 91.30%
CYP2C9 inhibition - 0.9584 95.84%
CYP2C19 inhibition - 0.9089 90.89%
CYP2D6 inhibition - 0.9313 93.13%
CYP1A2 inhibition - 0.9517 95.17%
CYP2C8 inhibition - 0.9226 92.26%
CYP inhibitory promiscuity - 0.9560 95.60%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7278 72.78%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.9606 96.06%
Skin irritation - 0.8431 84.31%
Skin corrosion - 0.9470 94.70%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5423 54.23%
Micronuclear - 0.8441 84.41%
Hepatotoxicity - 0.7699 76.99%
skin sensitisation - 0.8586 85.86%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6571 65.71%
Acute Oral Toxicity (c) III 0.4596 45.96%
Estrogen receptor binding - 0.7636 76.36%
Androgen receptor binding - 0.8228 82.28%
Thyroid receptor binding - 0.5180 51.80%
Glucocorticoid receptor binding + 0.6475 64.75%
Aromatase binding - 0.7334 73.34%
PPAR gamma - 0.5334 53.34%
Honey bee toxicity - 0.5727 57.27%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.7599 75.99%

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 95.85% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.47% 96.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.18% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.74% 99.17%
CHEMBL3589 P55263 Adenosine kinase 88.64% 98.05%
CHEMBL3401 O75469 Pregnane X receptor 83.96% 94.73%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 82.22% 97.34%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Moricandia arvensis

Cross-Links

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PubChem 163098006
LOTUS LTS0160758
wikiData Q105129201