(5-Acetyloxy-4,6-dihydroxy-2-methyloxan-3-yl) 3-(4-methoxyphenyl)prop-2-enoate

Details

Top
Internal ID ef73fed1-c192-49c7-8950-db5e12a6dd23
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Hexoses
IUPAC Name (5-acetyloxy-4,6-dihydroxy-2-methyloxan-3-yl) 3-(4-methoxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H22O8/c1-10-16(15(21)17(18(22)24-10)25-11(2)19)26-14(20)9-6-12-4-7-13(23-3)8-5-12/h4-10,15-18,21-22H,1-3H3
InChI Key GWYPCEPXZGWZNI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H22O8
Molecular Weight 366.40 g/mol
Exact Mass 366.13146766 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.65
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (5-Acetyloxy-4,6-dihydroxy-2-methyloxan-3-yl) 3-(4-methoxyphenyl)prop-2-enoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7582 75.82%
Caco-2 - 0.7198 71.98%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.5614 56.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8944 89.44%
OATP1B3 inhibitior + 0.8589 85.89%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5604 56.04%
P-glycoprotein inhibitior - 0.6580 65.80%
P-glycoprotein substrate - 0.8761 87.61%
CYP3A4 substrate + 0.5715 57.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8651 86.51%
CYP3A4 inhibition - 0.6121 61.21%
CYP2C9 inhibition - 0.9007 90.07%
CYP2C19 inhibition - 0.8722 87.22%
CYP2D6 inhibition - 0.8844 88.44%
CYP1A2 inhibition - 0.9089 90.89%
CYP2C8 inhibition - 0.7564 75.64%
CYP inhibitory promiscuity - 0.5840 58.40%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8939 89.39%
Carcinogenicity (trinary) Danger 0.5494 54.94%
Eye corrosion - 0.9730 97.30%
Eye irritation - 0.9555 95.55%
Skin irritation - 0.7231 72.31%
Skin corrosion - 0.9526 95.26%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5918 59.18%
Micronuclear + 0.7800 78.00%
Hepatotoxicity - 0.6057 60.57%
skin sensitisation - 0.9029 90.29%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.7245 72.45%
Acute Oral Toxicity (c) III 0.5762 57.62%
Estrogen receptor binding + 0.6163 61.63%
Androgen receptor binding - 0.5787 57.87%
Thyroid receptor binding - 0.5435 54.35%
Glucocorticoid receptor binding - 0.6557 65.57%
Aromatase binding - 0.7058 70.58%
PPAR gamma - 0.7132 71.32%
Honey bee toxicity - 0.8491 84.91%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9091 90.91%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.81% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.38% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.87% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.46% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.98% 95.56%
CHEMBL4208 P20618 Proteasome component C5 88.26% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.62% 99.17%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.70% 81.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.60% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 82.19% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 81.96% 90.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.02% 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.
Buddleja asiatica

Cross-Links

Top
PubChem 162924401
LOTUS LTS0233119
wikiData Q105022914