Epiphorellic acid 2

Details

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Internal ID 8bd4a8e1-06da-4958-a913-4f7a844f1e6c
Taxonomy Benzenoids > Benzene and substituted derivatives > Diphenylethers
IUPAC Name 6-hydroxy-3-[5-hydroxy-2-methoxycarbonyl-3-(3-oxopentyl)phenoxy]-4-methoxy-2-pentylbenzoic acid
SMILES (Canonical) CCCCCC1=C(C(=CC(=C1OC2=CC(=CC(=C2C(=O)OC)CCC(=O)CC)O)OC)O)C(=O)O
SMILES (Isomeric) CCCCCC1=C(C(=CC(=C1OC2=CC(=CC(=C2C(=O)OC)CCC(=O)CC)O)OC)O)C(=O)O
InChI InChI=1S/C26H32O9/c1-5-7-8-9-18-23(25(30)31)19(29)14-21(33-3)24(18)35-20-13-17(28)12-15(10-11-16(27)6-2)22(20)26(32)34-4/h12-14,28-29H,5-11H2,1-4H3,(H,30,31)
InChI Key SGQNLWJQSWFWLJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H32O9
Molecular Weight 488.50 g/mol
Exact Mass 488.20463259 g/mol
Topological Polar Surface Area (TPSA) 140.00 Ų
XlogP 5.50
Atomic LogP (AlogP) 5.03
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Epiphorellic acid 2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9030 90.30%
Caco-2 - 0.5902 59.02%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8403 84.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8217 82.17%
OATP1B3 inhibitior - 0.2885 28.85%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9382 93.82%
P-glycoprotein inhibitior + 0.7684 76.84%
P-glycoprotein substrate + 0.5310 53.10%
CYP3A4 substrate + 0.6313 63.13%
CYP2C9 substrate - 0.5928 59.28%
CYP2D6 substrate - 0.8652 86.52%
CYP3A4 inhibition + 0.5177 51.77%
CYP2C9 inhibition - 0.5554 55.54%
CYP2C19 inhibition - 0.5311 53.11%
CYP2D6 inhibition - 0.7529 75.29%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition + 0.9032 90.32%
CYP inhibitory promiscuity - 0.6924 69.24%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8023 80.23%
Carcinogenicity (trinary) Non-required 0.7314 73.14%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.8311 83.11%
Skin irritation - 0.8076 80.76%
Skin corrosion - 0.9193 91.93%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6990 69.90%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5784 57.84%
skin sensitisation - 0.8722 87.22%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5492 54.92%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5713 57.13%
Acute Oral Toxicity (c) III 0.5335 53.35%
Estrogen receptor binding + 0.7701 77.01%
Androgen receptor binding + 0.6337 63.37%
Thyroid receptor binding - 0.5962 59.62%
Glucocorticoid receptor binding + 0.7600 76.00%
Aromatase binding + 0.5581 55.81%
PPAR gamma + 0.7424 74.24%
Honey bee toxicity - 0.9046 90.46%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5215 52.15%
Fish aquatic toxicity + 0.9962 99.62%

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
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 99.36% 95.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.88% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.75% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.58% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.91% 98.95%
CHEMBL240 Q12809 HERG 93.56% 89.76%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.89% 96.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.84% 92.08%
CHEMBL1255126 O15151 Protein Mdm4 89.67% 90.20%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.12% 97.21%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.88% 96.00%
CHEMBL2535 P11166 Glucose transporter 88.29% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.39% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.96% 94.73%
CHEMBL3194 P02766 Transthyretin 86.64% 90.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 85.54% 94.42%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.06% 90.71%
CHEMBL230 P35354 Cyclooxygenase-2 83.10% 89.63%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 83.04% 91.79%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.00% 95.50%

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 14331493
LOTUS LTS0163615
wikiData Q104375196