2-Hepta-2,4-dienoxy-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID 4562fde2-0f57-43f6-b679-8d1d1e8e0f3b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl glycosides > Fatty acyl glycosides of mono- and disaccharides
IUPAC Name 2-hepta-2,4-dienoxy-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H22O6/c1-2-3-4-5-6-7-18-13-12(17)11(16)10(15)9(8-14)19-13/h3-6,9-17H,2,7-8H2,1H3
InChI Key TTXIMEBZVOGTTI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H22O6
Molecular Weight 274.31 g/mol
Exact Mass 274.14163842 g/mol
Topological Polar Surface Area (TPSA) 99.40 Ų
XlogP -0.20
Atomic LogP (AlogP) -0.67
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Hepta-2,4-dienoxy-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 - 0.8683 86.83%
Caco-2 - 0.6690 66.90%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7237 72.37%
OATP2B1 inhibitior - 0.8608 86.08%
OATP1B1 inhibitior + 0.8707 87.07%
OATP1B3 inhibitior + 0.9686 96.86%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9387 93.87%
P-glycoprotein inhibitior - 0.9388 93.88%
P-glycoprotein substrate - 0.9657 96.57%
CYP3A4 substrate - 0.5469 54.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8375 83.75%
CYP3A4 inhibition - 0.9600 96.00%
CYP2C9 inhibition - 0.9289 92.89%
CYP2C19 inhibition - 0.8586 85.86%
CYP2D6 inhibition - 0.9441 94.41%
CYP1A2 inhibition - 0.9261 92.61%
CYP2C8 inhibition - 0.8914 89.14%
CYP inhibitory promiscuity - 0.8424 84.24%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6847 68.47%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9593 95.93%
Skin irritation - 0.8575 85.75%
Skin corrosion - 0.9592 95.92%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5684 56.84%
Micronuclear - 0.8441 84.41%
Hepatotoxicity - 0.8449 84.49%
skin sensitisation - 0.9103 91.03%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6445 64.45%
Acute Oral Toxicity (c) III 0.4732 47.32%
Estrogen receptor binding - 0.8697 86.97%
Androgen receptor binding - 0.6602 66.02%
Thyroid receptor binding - 0.5805 58.05%
Glucocorticoid receptor binding - 0.5148 51.48%
Aromatase binding - 0.7369 73.69%
PPAR gamma + 0.5463 54.63%
Honey bee toxicity - 0.8616 86.16%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity - 0.7623 76.23%

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 93.57% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 90.30% 96.61%
CHEMBL226 P30542 Adenosine A1 receptor 90.22% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.89% 91.11%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.81% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.98% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.69% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 83.71% 94.73%
CHEMBL3589 P55263 Adenosine kinase 81.99% 98.05%

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 162816298
LOTUS LTS0038905
wikiData Q104197832