2-(Hydroxymethyl)-6-(4-hydroxy-3-methylbut-2-enoxy)oxane-3,4,5-triol

Details

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Internal ID 366cfb5a-6a11-4f29-b18a-0d86c21e0689
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl glycosides > Fatty acyl glycosides of mono- and disaccharides
IUPAC Name 2-(hydroxymethyl)-6-(4-hydroxy-3-methylbut-2-enoxy)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H20O7/c1-6(4-12)2-3-17-11-10(16)9(15)8(14)7(5-13)18-11/h2,7-16H,3-5H2,1H3
InChI Key MTNPSFBFGZMJPZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20O7
Molecular Weight 264.27 g/mol
Exact Mass 264.12090297 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP -1.90
Atomic LogP (AlogP) -2.26
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 2-(Hydroxymethyl)-6-(4-hydroxy-3-methylbut-2-enoxy)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 - 0.7533 75.33%
Caco-2 - 0.8539 85.39%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7700 77.00%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.9140 91.40%
OATP1B3 inhibitior + 0.9552 95.52%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9509 95.09%
P-glycoprotein inhibitior - 0.9529 95.29%
P-glycoprotein substrate - 0.9633 96.33%
CYP3A4 substrate - 0.5161 51.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8494 84.94%
CYP3A4 inhibition - 0.9626 96.26%
CYP2C9 inhibition - 0.9009 90.09%
CYP2C19 inhibition - 0.8228 82.28%
CYP2D6 inhibition - 0.9034 90.34%
CYP1A2 inhibition - 0.8627 86.27%
CYP2C8 inhibition - 0.8996 89.96%
CYP inhibitory promiscuity - 0.8506 85.06%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6784 67.84%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.9787 97.87%
Skin irritation - 0.8121 81.21%
Skin corrosion - 0.9563 95.63%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7589 75.89%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.7949 79.49%
skin sensitisation - 0.8778 87.78%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5267 52.67%
Acute Oral Toxicity (c) III 0.5019 50.19%
Estrogen receptor binding - 0.8968 89.68%
Androgen receptor binding - 0.6503 65.03%
Thyroid receptor binding - 0.5946 59.46%
Glucocorticoid receptor binding - 0.6949 69.49%
Aromatase binding - 0.6876 68.76%
PPAR gamma + 0.5829 58.29%
Honey bee toxicity - 0.8029 80.29%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity + 0.7792 77.92%

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 92.76% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.38% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 88.17% 94.73%
CHEMBL3589 P55263 Adenosine kinase 87.77% 98.05%
CHEMBL2581 P07339 Cathepsin D 84.53% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.35% 99.17%

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.
Vicia hirsuta

Cross-Links

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PubChem 72988325
LOTUS LTS0199310
wikiData Q105171788