7-O-(4''-O-glucosyl)coumaroyl-loganic acid

Details

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Internal ID 2d9576c0-adda-43c5-ad45-ec4b2b715212
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Iridoid O-glycosides
IUPAC Name (1S,4aS,6S,7R,7aS)-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(E)-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H40O17/c1-12-17(8-15-16(28(41)42)11-43-29(21(12)15)48-31-27(40)25(38)23(36)19(10-33)47-31)45-20(34)7-4-13-2-5-14(6-3-13)44-30-26(39)24(37)22(35)18(9-32)46-30/h2-7,11-12,15,17-19,21-27,29-33,35-40H,8-10H2,1H3,(H,41,42)/b7-4+/t12-,15+,17-,18+,19+,21+,22+,23+,24-,25-,26+,27+,29-,30+,31-/m0/s1
InChI Key IZDNHCQZHNEUGA-PFJQXYNRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H40O17
Molecular Weight 684.60 g/mol
Exact Mass 684.22654980 g/mol
Topological Polar Surface Area (TPSA) 272.00 Ų
XlogP -1.20
Atomic LogP (AlogP) -2.80
H-Bond Acceptor 16
H-Bond Donor 9
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-O-(4''-O-glucosyl)coumaroyl-loganic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6748 67.48%
Caco-2 - 0.8974 89.74%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.8714 87.14%
Subcellular localzation Mitochondria 0.6789 67.89%
OATP2B1 inhibitior - 0.8591 85.91%
OATP1B1 inhibitior + 0.6988 69.88%
OATP1B3 inhibitior + 0.9565 95.65%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7096 70.96%
P-glycoprotein inhibitior - 0.4547 45.47%
P-glycoprotein substrate - 0.6845 68.45%
CYP3A4 substrate + 0.6513 65.13%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8805 88.05%
CYP3A4 inhibition - 0.9374 93.74%
CYP2C9 inhibition - 0.8102 81.02%
CYP2C19 inhibition - 0.7854 78.54%
CYP2D6 inhibition - 0.9046 90.46%
CYP1A2 inhibition - 0.7909 79.09%
CYP2C8 inhibition + 0.6428 64.28%
CYP inhibitory promiscuity - 0.6563 65.63%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6431 64.31%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9215 92.15%
Skin irritation - 0.7630 76.30%
Skin corrosion - 0.9427 94.27%
Ames mutagenesis - 0.5793 57.93%
Human Ether-a-go-go-Related Gene inhibition + 0.7617 76.17%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.7964 79.64%
skin sensitisation - 0.8407 84.07%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8532 85.32%
Acute Oral Toxicity (c) III 0.5079 50.79%
Estrogen receptor binding + 0.8322 83.22%
Androgen receptor binding + 0.5685 56.85%
Thyroid receptor binding - 0.4911 49.11%
Glucocorticoid receptor binding + 0.5998 59.98%
Aromatase binding - 0.5084 50.84%
PPAR gamma + 0.6993 69.93%
Honey bee toxicity - 0.8009 80.09%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9317 93.17%

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 97.46% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.30% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.66% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.27% 96.00%
CHEMBL221 P23219 Cyclooxygenase-1 95.19% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.36% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.69% 95.56%
CHEMBL4208 P20618 Proteasome component C5 91.33% 90.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.69% 86.92%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.66% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.49% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 83.07% 94.73%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.05% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.28% 95.89%
CHEMBL2581 P07339 Cathepsin D 81.49% 98.95%
CHEMBL226 P30542 Adenosine A1 receptor 80.09% 95.93%

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.
Gentiana linearis

Cross-Links

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PubChem 163188097
LOTUS LTS0070355
wikiData Q105123134