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

Details

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Internal ID af33bdf7-d66a-4dc6-92e9-7624b591fd0e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides > Hexoses
IUPAC Name (4,5,6-trihydroxy-2-methyloxan-3-yl) 3-(4-methoxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H20O7/c1-9-15(13(18)14(19)16(20)22-9)23-12(17)8-5-10-3-6-11(21-2)7-4-10/h3-9,13-16,18-20H,1-2H3
InChI Key OIVQXJWRPCWLAI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O7
Molecular Weight 324.32 g/mol
Exact Mass 324.12090297 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.08
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6999 69.99%
Caco-2 - 0.5924 59.24%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.5913 59.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8985 89.85%
OATP1B3 inhibitior + 0.9553 95.53%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8725 87.25%
P-glycoprotein inhibitior - 0.8352 83.52%
P-glycoprotein substrate - 0.9267 92.67%
CYP3A4 substrate + 0.5372 53.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8630 86.30%
CYP3A4 inhibition + 0.5061 50.61%
CYP2C9 inhibition - 0.9187 91.87%
CYP2C19 inhibition - 0.8390 83.90%
CYP2D6 inhibition - 0.9085 90.85%
CYP1A2 inhibition - 0.8638 86.38%
CYP2C8 inhibition - 0.7744 77.44%
CYP inhibitory promiscuity + 0.5251 52.51%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9211 92.11%
Carcinogenicity (trinary) Non-required 0.5078 50.78%
Eye corrosion - 0.9640 96.40%
Eye irritation - 0.9406 94.06%
Skin irritation - 0.6344 63.44%
Skin corrosion - 0.9393 93.93%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5937 59.37%
Micronuclear + 0.7600 76.00%
Hepatotoxicity - 0.6057 60.57%
skin sensitisation - 0.8266 82.66%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.8286 82.86%
Acute Oral Toxicity (c) III 0.6606 66.06%
Estrogen receptor binding + 0.5892 58.92%
Androgen receptor binding - 0.6352 63.52%
Thyroid receptor binding - 0.5174 51.74%
Glucocorticoid receptor binding - 0.6204 62.04%
Aromatase binding - 0.5346 53.46%
PPAR gamma - 0.6956 69.56%
Honey bee toxicity - 0.8450 84.50%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8819 88.19%

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 95.74% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.31% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.26% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.18% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.29% 95.56%
CHEMBL4208 P20618 Proteasome component C5 89.00% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.62% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 85.49% 90.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.56% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 81.75% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.41% 97.09%

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.
Buddleja asiatica
Scrophularia buergeriana

Cross-Links

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PubChem 85101415
LOTUS LTS0014590
wikiData Q105192879