3-Methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enenitrile

Details

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Internal ID 96123142-c08e-49ab-b994-692a18c6173c
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl glycosides > Fatty acyl glycosides of mono- and disaccharides
IUPAC Name 3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enenitrile
SMILES (Canonical) CC(=CC#N)COC1C(C(C(C(O1)CO)O)O)O
SMILES (Isomeric) CC(=CC#N)COC1C(C(C(C(O1)CO)O)O)O
InChI InChI=1S/C11H17NO6/c1-6(2-3-12)5-17-11-10(16)9(15)8(14)7(4-13)18-11/h2,7-11,13-16H,4-5H2,1H3
InChI Key DAVUWBZDLSJMFA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H17NO6
Molecular Weight 259.26 g/mol
Exact Mass 259.10558726 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP -1.60
Atomic LogP (AlogP) -1.73
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enenitrile

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8557 85.57%
Caco-2 - 0.8418 84.18%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6865 68.65%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.9064 90.64%
OATP1B3 inhibitior + 0.9585 95.85%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9035 90.35%
P-glycoprotein inhibitior - 0.9353 93.53%
P-glycoprotein substrate - 0.9618 96.18%
CYP3A4 substrate + 0.5101 51.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8520 85.20%
CYP3A4 inhibition - 0.9157 91.57%
CYP2C9 inhibition - 0.8480 84.80%
CYP2C19 inhibition - 0.8464 84.64%
CYP2D6 inhibition - 0.9116 91.16%
CYP1A2 inhibition - 0.8561 85.61%
CYP2C8 inhibition - 0.8534 85.34%
CYP inhibitory promiscuity - 0.7519 75.19%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6834 68.34%
Eye corrosion - 0.9847 98.47%
Eye irritation - 0.9872 98.72%
Skin irritation - 0.8360 83.60%
Skin corrosion - 0.9571 95.71%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5997 59.97%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.7864 78.64%
skin sensitisation - 0.8777 87.77%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.6198 61.98%
Acute Oral Toxicity (c) III 0.4982 49.82%
Estrogen receptor binding - 0.7907 79.07%
Androgen receptor binding - 0.6449 64.49%
Thyroid receptor binding - 0.5132 51.32%
Glucocorticoid receptor binding - 0.5387 53.87%
Aromatase binding - 0.7038 70.38%
PPAR gamma - 0.6304 63.04%
Honey bee toxicity - 0.5496 54.96%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.7243 72.43%

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 94.43% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.70% 91.11%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.43% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 85.85% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.53% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.23% 96.00%
CHEMBL3589 P55263 Adenosine kinase 82.77% 98.05%

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.
Hordeum vulgare
Oemleria cerasiformis

Cross-Links

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PubChem 85373987
LOTUS LTS0019481
wikiData Q104974025