methyl 4'-(4-hydroxy-3-methoxybenzoyl)-5'-oxo-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[4a,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-furan]-4-carboxylate

Details

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Internal ID 4408ce37-1379-4a05-bd42-8f05af7f50b6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Iridoid O-glycosides
IUPAC Name methyl 4'-(4-hydroxy-3-methoxybenzoyl)-5'-oxo-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[4a,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-furan]-4-carboxylate
SMILES (Canonical) COC1=C(C=CC(=C1)C(=O)C2=CC3(C=CC4C3C(OC=C4C(=O)OC)OC5C(C(C(C(O5)CO)O)O)O)OC2=O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C(=O)C2=CC3(C=CC4C3C(OC=C4C(=O)OC)OC5C(C(C(C(O5)CO)O)O)O)OC2=O)O
InChI InChI=1S/C27H28O14/c1-36-16-7-11(3-4-15(16)29)19(30)13-8-27(41-24(13)35)6-5-12-14(23(34)37-2)10-38-25(18(12)27)40-26-22(33)21(32)20(31)17(9-28)39-26/h3-8,10,12,17-18,20-22,25-26,28-29,31-33H,9H2,1-2H3
InChI Key RIDIXCFHWOHPTF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H28O14
Molecular Weight 576.50 g/mol
Exact Mass 576.14790556 g/mol
Topological Polar Surface Area (TPSA) 208.00 Ų
XlogP -0.10
Atomic LogP (AlogP) -1.16
H-Bond Acceptor 14
H-Bond Donor 5
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl 4'-(4-hydroxy-3-methoxybenzoyl)-5'-oxo-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[4a,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-furan]-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 + 0.7698 76.98%
Caco-2 - 0.9042 90.42%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.6499 64.99%
OATP2B1 inhibitior - 0.7102 71.02%
OATP1B1 inhibitior + 0.7857 78.57%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8269 82.69%
P-glycoprotein inhibitior + 0.6410 64.10%
P-glycoprotein substrate + 0.5251 52.51%
CYP3A4 substrate + 0.6786 67.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8567 85.67%
CYP3A4 inhibition - 0.7935 79.35%
CYP2C9 inhibition - 0.7288 72.88%
CYP2C19 inhibition - 0.7128 71.28%
CYP2D6 inhibition - 0.8916 89.16%
CYP1A2 inhibition - 0.8234 82.34%
CYP2C8 inhibition + 0.8087 80.87%
CYP inhibitory promiscuity - 0.5685 56.85%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5850 58.50%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.9207 92.07%
Skin irritation - 0.7702 77.02%
Skin corrosion - 0.9379 93.79%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3882 38.82%
Micronuclear + 0.5833 58.33%
Hepatotoxicity - 0.6155 61.55%
skin sensitisation - 0.7908 79.08%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.6487 64.87%
Acute Oral Toxicity (c) III 0.4882 48.82%
Estrogen receptor binding + 0.7915 79.15%
Androgen receptor binding + 0.6703 67.03%
Thyroid receptor binding + 0.5525 55.25%
Glucocorticoid receptor binding + 0.7430 74.30%
Aromatase binding - 0.5693 56.93%
PPAR gamma + 0.7306 73.06%
Honey bee toxicity - 0.8299 82.99%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.8908 89.08%

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 99.23% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.21% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.81% 86.33%
CHEMBL4208 P20618 Proteasome component C5 94.97% 90.00%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 92.25% 95.83%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.57% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.33% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.28% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.10% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.98% 94.00%
CHEMBL2535 P11166 Glucose transporter 85.75% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.29% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.84% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.71% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.11% 92.94%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.05% 91.07%
CHEMBL3401 O75469 Pregnane X receptor 83.56% 94.73%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.17% 96.21%

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.
Morinda citrifolia
Morinda morindoides

Cross-Links

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PubChem 72749379
LOTUS LTS0001212
wikiData Q105236771