coumaroyl(-4)Rha(a1-6)Glc(b)-O-Bn

Details

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Internal ID 81a361db-a2ee-48fe-90d7-4f682a9c05ec
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Hydroxycinnamic acid esters > Coumaric acid esters
IUPAC Name [(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-phenylmethoxyoxan-2-yl]methoxy]oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H34O12/c1-15-26(40-20(30)12-9-16-7-10-18(29)11-8-16)23(33)25(35)27(38-15)37-14-19-21(31)22(32)24(34)28(39-19)36-13-17-5-3-2-4-6-17/h2-12,15,19,21-29,31-35H,13-14H2,1H3/b12-9+/t15-,19+,21+,22-,23-,24+,25+,26-,27+,28+/m0/s1
InChI Key GTALKGZJYFBKJM-NQPYHCKISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H34O12
Molecular Weight 562.60 g/mol
Exact Mass 562.20502652 g/mol
Topological Polar Surface Area (TPSA) 185.00 Ų
XlogP 0.10
Atomic LogP (AlogP) -0.18
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of coumaroyl(-4)Rha(a1-6)Glc(b)-O-Bn

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7467 74.67%
Caco-2 - 0.8948 89.48%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.8857 88.57%
Subcellular localzation Mitochondria 0.7602 76.02%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.8388 83.88%
OATP1B3 inhibitior + 0.9573 95.73%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6310 63.10%
P-glycoprotein inhibitior - 0.6112 61.12%
P-glycoprotein substrate - 0.7602 76.02%
CYP3A4 substrate + 0.6084 60.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8771 87.71%
CYP3A4 inhibition - 0.9411 94.11%
CYP2C9 inhibition - 0.9053 90.53%
CYP2C19 inhibition - 0.9154 91.54%
CYP2D6 inhibition - 0.9261 92.61%
CYP1A2 inhibition - 0.9319 93.19%
CYP2C8 inhibition + 0.7462 74.62%
CYP inhibitory promiscuity - 0.6405 64.05%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5699 56.99%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.9387 93.87%
Skin irritation - 0.8454 84.54%
Skin corrosion - 0.9557 95.57%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7181 71.81%
Micronuclear + 0.5307 53.07%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.8513 85.13%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.8948 89.48%
Acute Oral Toxicity (c) III 0.7433 74.33%
Estrogen receptor binding + 0.7428 74.28%
Androgen receptor binding + 0.5764 57.64%
Thyroid receptor binding + 0.5539 55.39%
Glucocorticoid receptor binding + 0.5758 57.58%
Aromatase binding + 0.5307 53.07%
PPAR gamma + 0.7148 71.48%
Honey bee toxicity - 0.7838 78.38%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5855 58.55%
Fish aquatic toxicity + 0.9027 90.27%

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 97.73% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.27% 86.33%
CHEMBL2581 P07339 Cathepsin D 96.12% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.27% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.54% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 92.32% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.15% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 91.92% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 91.20% 90.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.26% 95.89%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 89.13% 91.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.80% 96.00%
CHEMBL5678 P34947 G protein-coupled receptor kinase 5 85.77% 88.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 84.55% 97.36%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.47% 89.00%

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.
Dracocephalum ruyschiana

Cross-Links

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PubChem 71578499
NPASS NPC138777