methyl (1S,4aR,7aR)-4a-hydroxy-7-[(4-hydroxy-3-methoxybenzoyl)oxymethyl]-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate

Details

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Internal ID 207f350f-55aa-4e62-b811-d2410c28a2c5
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name methyl (1S,4aR,7aR)-4a-hydroxy-7-[(4-hydroxy-3-methoxybenzoyl)oxymethyl]-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H30O14/c1-34-15-7-11(3-4-14(15)27)21(31)36-9-12-5-6-25(33)13(22(32)35-2)10-37-23(17(12)25)39-24-20(30)19(29)18(28)16(8-26)38-24/h3-5,7,10,16-20,23-24,26-30,33H,6,8-9H2,1-2H3/t16-,17+,18-,19+,20-,23+,24+,25+/m1/s1
InChI Key AZLWQZHYZULOEX-BNFWLUPDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H30O14
Molecular Weight 554.50 g/mol
Exact Mass 554.16355563 g/mol
Topological Polar Surface Area (TPSA) 211.00 Ų
XlogP -1.00
Atomic LogP (AlogP) -1.54
H-Bond Acceptor 14
H-Bond Donor 6
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (1S,4aR,7aR)-4a-hydroxy-7-[(4-hydroxy-3-methoxybenzoyl)oxymethyl]-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7403 74.03%
Caco-2 - 0.8924 89.24%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.5985 59.85%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.8405 84.05%
OATP1B3 inhibitior + 0.9619 96.19%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8811 88.11%
P-glycoprotein inhibitior - 0.4307 43.07%
P-glycoprotein substrate - 0.5104 51.04%
CYP3A4 substrate + 0.6778 67.78%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8495 84.95%
CYP3A4 inhibition - 0.8757 87.57%
CYP2C9 inhibition - 0.8887 88.87%
CYP2C19 inhibition - 0.7796 77.96%
CYP2D6 inhibition - 0.8865 88.65%
CYP1A2 inhibition - 0.8388 83.88%
CYP2C8 inhibition + 0.7792 77.92%
CYP inhibitory promiscuity - 0.8896 88.96%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6560 65.60%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9287 92.87%
Skin irritation - 0.7717 77.17%
Skin corrosion - 0.9458 94.58%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7272 72.72%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.6698 66.98%
skin sensitisation - 0.8140 81.40%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6490 64.90%
Acute Oral Toxicity (c) III 0.3947 39.47%
Estrogen receptor binding + 0.8142 81.42%
Androgen receptor binding + 0.6767 67.67%
Thyroid receptor binding + 0.5442 54.42%
Glucocorticoid receptor binding + 0.6885 68.85%
Aromatase binding + 0.5819 58.19%
PPAR gamma + 0.6608 66.08%
Honey bee toxicity - 0.7860 78.60%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6666 66.66%
Fish aquatic toxicity + 0.9370 93.70%

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 99.64% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.86% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.30% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.23% 99.17%
CHEMBL4208 P20618 Proteasome component C5 89.56% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.89% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.92% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.51% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.75% 96.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.33% 89.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.23% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 84.14% 91.19%
CHEMBL2535 P11166 Glucose transporter 83.83% 98.75%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 83.66% 95.83%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.78% 95.89%
CHEMBL2581 P07339 Cathepsin D 82.09% 98.95%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.87% 96.90%
CHEMBL3401 O75469 Pregnane X receptor 80.72% 94.73%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.36% 96.61%

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.
Amphilophium crucigerum

Cross-Links

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PubChem 162863776
LOTUS LTS0183455
wikiData Q104921784