Terrelactone A

Details

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Internal ID 0191ecb7-4fff-4581-b8f7-58d9cdb7da66
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name methyl (2R)-4-hydroxy-2-[[4-hydroxy-3-methoxy-5-(3-methylbut-2-enyl)phenyl]methyl]-3-(4-methoxyphenyl)-5-oxofuran-2-carboxylate
SMILES (Canonical) CC(=CCC1=C(C(=CC(=C1)CC2(C(=C(C(=O)O2)O)C3=CC=C(C=C3)OC)C(=O)OC)OC)O)C
SMILES (Isomeric) CC(=CCC1=C(C(=CC(=C1)C[C@@]2(C(=C(C(=O)O2)O)C3=CC=C(C=C3)OC)C(=O)OC)OC)O)C
InChI InChI=1S/C26H28O8/c1-15(2)6-7-18-12-16(13-20(32-4)22(18)27)14-26(25(30)33-5)21(23(28)24(29)34-26)17-8-10-19(31-3)11-9-17/h6,8-13,27-28H,7,14H2,1-5H3/t26-/m1/s1
InChI Key OUVRGNVUVNCMKG-AREMUKBSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H28O8
Molecular Weight 468.50 g/mol
Exact Mass 468.17841785 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Terrelactone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9809 98.09%
Caco-2 + 0.5198 51.98%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7952 79.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8576 85.76%
OATP1B3 inhibitior - 0.3218 32.18%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9233 92.33%
P-glycoprotein inhibitior + 0.8180 81.80%
P-glycoprotein substrate - 0.5968 59.68%
CYP3A4 substrate + 0.6537 65.37%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8542 85.42%
CYP3A4 inhibition - 0.7438 74.38%
CYP2C9 inhibition + 0.6612 66.12%
CYP2C19 inhibition + 0.6869 68.69%
CYP2D6 inhibition - 0.8753 87.53%
CYP1A2 inhibition - 0.5869 58.69%
CYP2C8 inhibition + 0.8132 81.32%
CYP inhibitory promiscuity + 0.6936 69.36%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9328 93.28%
Carcinogenicity (trinary) Non-required 0.5404 54.04%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.8374 83.74%
Skin irritation - 0.7990 79.90%
Skin corrosion - 0.9490 94.90%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6141 61.41%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.7927 79.27%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7060 70.60%
Acute Oral Toxicity (c) III 0.3107 31.07%
Estrogen receptor binding + 0.9025 90.25%
Androgen receptor binding + 0.7453 74.53%
Thyroid receptor binding + 0.7167 71.67%
Glucocorticoid receptor binding + 0.8779 87.79%
Aromatase binding + 0.6284 62.84%
PPAR gamma + 0.7246 72.46%
Honey bee toxicity - 0.8139 81.39%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 1.0000 100.00%

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 99.71% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.58% 85.14%
CHEMBL2581 P07339 Cathepsin D 96.95% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 96.81% 95.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.24% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.46% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.40% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.04% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 93.38% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.50% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.79% 95.50%
CHEMBL4208 P20618 Proteasome component C5 89.18% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 89.03% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.27% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.07% 99.15%
CHEMBL221 P23219 Cyclooxygenase-1 86.71% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.17% 96.00%
CHEMBL2535 P11166 Glucose transporter 84.93% 98.75%
CHEMBL340 P08684 Cytochrome P450 3A4 83.35% 91.19%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.08% 97.28%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.68% 91.07%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.06% 95.89%

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 139587983
LOTUS LTS0218701
wikiData Q105200467