4,6-Dihydroxy-3-(6-hydroxy-1-oxo-3-pentylisochromen-8-yl)oxy-2-(2-oxoheptyl)benzoic acid

Details

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Internal ID c99eb696-81b0-492b-8272-817e5896e56b
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 4,6-dihydroxy-3-(6-hydroxy-1-oxo-3-pentylisochromen-8-yl)oxy-2-(2-oxoheptyl)benzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H32O9/c1-3-5-7-9-17(29)13-20-25(27(33)34)21(31)15-22(32)26(20)37-23-14-18(30)11-16-12-19(10-8-6-4-2)36-28(35)24(16)23/h11-12,14-15,30-32H,3-10,13H2,1-2H3,(H,33,34)
InChI Key BMZVKRNQSCUIKZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H32O9
Molecular Weight 512.50 g/mol
Exact Mass 512.20463259 g/mol
Topological Polar Surface Area (TPSA) 151.00 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.82
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,6-Dihydroxy-3-(6-hydroxy-1-oxo-3-pentylisochromen-8-yl)oxy-2-(2-oxoheptyl)benzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7712 77.12%
Caco-2 - 0.7863 78.63%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6575 65.75%
OATP2B1 inhibitior - 0.5644 56.44%
OATP1B1 inhibitior + 0.8097 80.97%
OATP1B3 inhibitior + 0.8237 82.37%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7821 78.21%
BSEP inhibitior + 0.6697 66.97%
P-glycoprotein inhibitior + 0.6499 64.99%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6084 60.84%
CYP2C9 substrate + 0.8398 83.98%
CYP2D6 substrate - 0.8767 87.67%
CYP3A4 inhibition - 0.5497 54.97%
CYP2C9 inhibition - 0.8001 80.01%
CYP2C19 inhibition - 0.5609 56.09%
CYP2D6 inhibition - 0.8825 88.25%
CYP1A2 inhibition + 0.5752 57.52%
CYP2C8 inhibition + 0.8365 83.65%
CYP inhibitory promiscuity - 0.6848 68.48%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7758 77.58%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.6327 63.27%
Skin irritation - 0.7453 74.53%
Skin corrosion - 0.9149 91.49%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6779 67.79%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5824 58.24%
skin sensitisation - 0.8871 88.71%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5942 59.42%
Acute Oral Toxicity (c) III 0.4504 45.04%
Estrogen receptor binding + 0.7363 73.63%
Androgen receptor binding + 0.7622 76.22%
Thyroid receptor binding - 0.5917 59.17%
Glucocorticoid receptor binding + 0.6446 64.46%
Aromatase binding - 0.4887 48.87%
PPAR gamma + 0.7044 70.44%
Honey bee toxicity - 0.8898 88.98%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5960 59.60%
Fish aquatic toxicity + 0.9966 99.66%

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
CHEMBL230 P35354 Cyclooxygenase-2 98.38% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.34% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.80% 99.17%
CHEMBL2581 P07339 Cathepsin D 96.11% 98.95%
CHEMBL240 Q12809 HERG 95.79% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.91% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 94.01% 96.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.77% 92.08%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 91.86% 95.17%
CHEMBL3401 O75469 Pregnane X receptor 91.81% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.73% 99.23%
CHEMBL3194 P02766 Transthyretin 89.42% 90.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 89.41% 94.42%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.56% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.18% 94.45%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.76% 97.21%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.76% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.01% 94.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.37% 93.56%
CHEMBL1811 P34995 Prostanoid EP1 receptor 80.07% 95.71%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163036440
LOTUS LTS0001541
wikiData Q104938698