Methyl 5-O-feruloylquinate

Details

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Internal ID 8e2ffb0f-e4db-44b2-a5ae-4b13a7895ab8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclitols and derivatives > Quinic acids and derivatives
IUPAC Name methyl (1R,3R,4S,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxycyclohexane-1-carboxylate
SMILES (Canonical) COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2O)O)(C(=O)OC)O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)/C=C/C(=O)O[C@@H]2C[C@](C[C@H]([C@@H]2O)O)(C(=O)OC)O)O
InChI InChI=1S/C18H22O9/c1-25-13-7-10(3-5-11(13)19)4-6-15(21)27-14-9-18(24,17(23)26-2)8-12(20)16(14)22/h3-7,12,14,16,19-20,22,24H,8-9H2,1-2H3/b6-4+/t12-,14-,16+,18-/m1/s1
InChI Key CPYDMLXRLHYXSV-JZAYIOOCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H22O9
Molecular Weight 382.40 g/mol
Exact Mass 382.12638228 g/mol
Topological Polar Surface Area (TPSA) 143.00 Ų
XlogP 0.20
Atomic LogP (AlogP) -0.25
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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154461-64-0
methyl (1R,3R,4S,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxycyclohexane-1-carboxylate
(1R,3R,4S,5R)-Methyl 1,3,4-trihydroxy-5-(((E)-3-(4-hydroxy-3-methoxyphenyl)acryloyl)oxy)cyclohexanecarboxylate
AKOS040762046

2D Structure

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2D Structure of Methyl 5-O-feruloylquinate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8807 88.07%
Caco-2 - 0.8137 81.37%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6812 68.12%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.9513 95.13%
OATP1B3 inhibitior + 0.9319 93.19%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8088 80.88%
BSEP inhibitior + 0.6720 67.20%
P-glycoprotein inhibitior - 0.7562 75.62%
P-glycoprotein substrate - 0.6775 67.75%
CYP3A4 substrate + 0.6041 60.41%
CYP2C9 substrate - 0.7985 79.85%
CYP2D6 substrate - 0.8266 82.66%
CYP3A4 inhibition - 0.8535 85.35%
CYP2C9 inhibition - 0.8540 85.40%
CYP2C19 inhibition - 0.8798 87.98%
CYP2D6 inhibition - 0.9181 91.81%
CYP1A2 inhibition - 0.7159 71.59%
CYP2C8 inhibition + 0.5580 55.80%
CYP inhibitory promiscuity - 0.9609 96.09%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9343 93.43%
Carcinogenicity (trinary) Non-required 0.6568 65.68%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9516 95.16%
Skin irritation - 0.6941 69.41%
Skin corrosion - 0.8933 89.33%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4295 42.95%
Micronuclear + 0.5700 57.00%
Hepatotoxicity + 0.6269 62.69%
skin sensitisation - 0.7402 74.02%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.9318 93.18%
Acute Oral Toxicity (c) III 0.6134 61.34%
Estrogen receptor binding + 0.7623 76.23%
Androgen receptor binding + 0.6440 64.40%
Thyroid receptor binding + 0.5945 59.45%
Glucocorticoid receptor binding + 0.6732 67.32%
Aromatase binding + 0.5321 53.21%
PPAR gamma - 0.5472 54.72%
Honey bee toxicity - 0.8570 85.70%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9782 97.82%

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 99.73% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.54% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.55% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.27% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.69% 94.45%
CHEMBL2179 P04062 Beta-glucocerebrosidase 91.41% 85.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.23% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.18% 85.14%
CHEMBL4208 P20618 Proteasome component C5 91.01% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.70% 89.00%
CHEMBL2535 P11166 Glucose transporter 89.08% 98.75%
CHEMBL4040 P28482 MAP kinase ERK2 88.15% 83.82%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.22% 95.50%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.18% 89.62%
CHEMBL3194 P02766 Transthyretin 86.66% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.07% 95.89%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 84.00% 91.03%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.46% 91.07%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.23% 97.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.30% 92.62%
CHEMBL340 P08684 Cytochrome P450 3A4 81.17% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.04% 97.09%
CHEMBL3788 O00444 Serine/threonine-protein kinase PLK4 80.98% 83.65%

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.
Coptis chinensis
Coptis deltoidea
Coptis japonica
Coptis teeta
Phellodendron amurense

Cross-Links

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PubChem 102004731
NPASS NPC294100
LOTUS LTS0228653
wikiData Q104967841