2-(Hydroxymethyl)-6-(3-phenylpropoxy)oxane-3,4,5-triol

Details

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Internal ID ada0a6ce-9a27-4aa3-a612-cf9f345efcc7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl glycosides > Fatty acyl glycosides of mono- and disaccharides
IUPAC Name 2-(hydroxymethyl)-6-(3-phenylpropoxy)oxane-3,4,5-triol
SMILES (Canonical) C1=CC=C(C=C1)CCCOC2C(C(C(C(O2)CO)O)O)O
SMILES (Isomeric) C1=CC=C(C=C1)CCCOC2C(C(C(C(O2)CO)O)O)O
InChI InChI=1S/C15H22O6/c16-9-11-12(17)13(18)14(19)15(21-11)20-8-4-7-10-5-2-1-3-6-10/h1-3,5-6,11-19H,4,7-9H2
InChI Key QHNJVZUXAYIKTA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O6
Molecular Weight 298.33 g/mol
Exact Mass 298.14163842 g/mol
Topological Polar Surface Area (TPSA) 99.40 Ų
XlogP 0.10
Atomic LogP (AlogP) -0.56
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-(Hydroxymethyl)-6-(3-phenylpropoxy)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 - 0.9317 93.17%
Caco-2 - 0.6927 69.27%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7863 78.63%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.8593 85.93%
OATP1B3 inhibitior + 0.9474 94.74%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8885 88.85%
P-glycoprotein inhibitior - 0.9064 90.64%
P-glycoprotein substrate - 0.9404 94.04%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7873 78.73%
CYP3A4 inhibition - 0.9302 93.02%
CYP2C9 inhibition - 0.7456 74.56%
CYP2C19 inhibition - 0.8218 82.18%
CYP2D6 inhibition - 0.9302 93.02%
CYP1A2 inhibition - 0.9374 93.74%
CYP2C8 inhibition + 0.5315 53.15%
CYP inhibitory promiscuity - 0.8253 82.53%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6382 63.82%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.9157 91.57%
Skin irritation - 0.8482 84.82%
Skin corrosion - 0.9681 96.81%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.8141 81.41%
Hepatotoxicity - 0.9019 90.19%
skin sensitisation - 0.9034 90.34%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.7629 76.29%
Acute Oral Toxicity (c) III 0.5478 54.78%
Estrogen receptor binding - 0.7199 71.99%
Androgen receptor binding - 0.6166 61.66%
Thyroid receptor binding - 0.5524 55.24%
Glucocorticoid receptor binding - 0.6849 68.49%
Aromatase binding - 0.6532 65.32%
PPAR gamma - 0.5252 52.52%
Honey bee toxicity - 0.8467 84.67%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.7847 78.47%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 97.38% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.62% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.54% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.66% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.74% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.30% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.19% 99.17%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 83.77% 94.23%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 81.57% 96.37%
CHEMBL3891 P07384 Calpain 1 81.47% 93.04%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.16% 96.25%

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.
Entada rheedii
Rhodiola rosea

Cross-Links

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PubChem 13139865
LOTUS LTS0099317
wikiData Q105221036