(2R,3R,4R,5R,6S)-2-butoxy-6-methyloxane-3,4,5-triol

Details

Top
Internal ID fac29561-a8b9-4255-95b3-700c4a22813b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl glycosides > Fatty acyl glycosides of mono- and disaccharides
IUPAC Name (2R,3R,4R,5R,6S)-2-butoxy-6-methyloxane-3,4,5-triol
SMILES (Canonical) CCCCOC1C(C(C(C(O1)C)O)O)O
SMILES (Isomeric) CCCCO[C@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)C)O)O)O
InChI InChI=1S/C10H20O5/c1-3-4-5-14-10-9(13)8(12)7(11)6(2)15-10/h6-13H,3-5H2,1-2H3/t6-,7-,8+,9+,10+/m0/s1
InChI Key SMKNLYABELUZSL-SRQGCSHVSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H20O5
Molecular Weight 220.26 g/mol
Exact Mass 220.13107373 g/mol
Topological Polar Surface Area (TPSA) 79.20 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.37
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (2R,3R,4R,5R,6S)-2-butoxy-6-methyloxane-3,4,5-triol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7457 74.57%
Caco-2 - 0.5158 51.58%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7690 76.90%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9191 91.91%
OATP1B3 inhibitior + 0.9383 93.83%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9628 96.28%
P-glycoprotein inhibitior - 0.9528 95.28%
P-glycoprotein substrate - 0.9194 91.94%
CYP3A4 substrate - 0.5406 54.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8247 82.47%
CYP3A4 inhibition - 0.7939 79.39%
CYP2C9 inhibition - 0.8628 86.28%
CYP2C19 inhibition - 0.8146 81.46%
CYP2D6 inhibition - 0.9204 92.04%
CYP1A2 inhibition - 0.8667 86.67%
CYP2C8 inhibition - 0.8093 80.93%
CYP inhibitory promiscuity - 0.8769 87.69%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7272 72.72%
Eye corrosion - 0.9769 97.69%
Eye irritation - 0.9628 96.28%
Skin irritation - 0.7656 76.56%
Skin corrosion - 0.9422 94.22%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6584 65.84%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.7447 74.47%
skin sensitisation - 0.8335 83.35%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.6053 60.53%
Acute Oral Toxicity (c) III 0.7145 71.45%
Estrogen receptor binding - 0.7715 77.15%
Androgen receptor binding - 0.8694 86.94%
Thyroid receptor binding + 0.5302 53.02%
Glucocorticoid receptor binding - 0.6928 69.28%
Aromatase binding - 0.8371 83.71%
PPAR gamma - 0.7166 71.66%
Honey bee toxicity - 0.9650 96.50%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.5249 52.49%

Targets

Top

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 94.01% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.85% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.00% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.98% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.49% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.46% 86.33%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.09% 97.36%
CHEMBL3401 O75469 Pregnane X receptor 82.76% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 80.91% 91.49%

Plants that contains it

Top
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.
Bellis perennis
Euphorbia hirta

Cross-Links

Top
PubChem 13059943
LOTUS LTS0206174
wikiData Q105255987