(3,4,5-Trihydroxy-6-methyloxan-2-yl) 3-methylbutanoate

Details

Top
Internal ID c6411c36-beac-416c-899f-8842cb395b4d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Hexoses
IUPAC Name (3,4,5-trihydroxy-6-methyloxan-2-yl) 3-methylbutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H20O6/c1-5(2)4-7(12)17-11-10(15)9(14)8(13)6(3)16-11/h5-6,8-11,13-15H,4H2,1-3H3
InChI Key MBGJKCOJAAXZCG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H20O6
Molecular Weight 248.27 g/mol
Exact Mass 248.12598835 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.60
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3,4,5-Trihydroxy-6-methyloxan-2-yl) 3-methylbutanoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5782 57.82%
Caco-2 - 0.6289 62.89%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.7877 78.77%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9224 92.24%
OATP1B3 inhibitior + 0.9191 91.91%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9611 96.11%
P-glycoprotein inhibitior - 0.9195 91.95%
P-glycoprotein substrate - 0.9300 93.00%
CYP3A4 substrate - 0.5505 55.05%
CYP2C9 substrate - 0.7985 79.85%
CYP2D6 substrate - 0.8718 87.18%
CYP3A4 inhibition - 0.8794 87.94%
CYP2C9 inhibition - 0.9287 92.87%
CYP2C19 inhibition - 0.9271 92.71%
CYP2D6 inhibition - 0.9124 91.24%
CYP1A2 inhibition - 0.9430 94.30%
CYP2C8 inhibition - 0.9691 96.91%
CYP inhibitory promiscuity - 0.9600 96.00%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6899 68.99%
Eye corrosion - 0.9618 96.18%
Eye irritation - 0.9314 93.14%
Skin irritation - 0.7969 79.69%
Skin corrosion - 0.9454 94.54%
Ames mutagenesis - 0.6354 63.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7626 76.26%
Micronuclear - 0.6200 62.00%
Hepatotoxicity - 0.6866 68.66%
skin sensitisation - 0.8186 81.86%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.6813 68.13%
Acute Oral Toxicity (c) III 0.6493 64.93%
Estrogen receptor binding - 0.6976 69.76%
Androgen receptor binding - 0.8443 84.43%
Thyroid receptor binding + 0.5811 58.11%
Glucocorticoid receptor binding - 0.4724 47.24%
Aromatase binding - 0.6992 69.92%
PPAR gamma - 0.7544 75.44%
Honey bee toxicity - 0.8618 86.18%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7555 75.55%
Fish aquatic toxicity - 0.4921 49.21%

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 96.00% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.22% 98.95%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 89.09% 96.47%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.00% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 84.52% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.46% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.83% 95.89%

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.
There are no matching plants.

Cross-Links

Top
PubChem 73236374
LOTUS LTS0022971
wikiData Q104171529