Thelephantin H

Details

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Internal ID e3044f39-3eb7-4feb-b7aa-940e3107edef
Taxonomy Organoheterocyclic compounds > Benzofurans > Phenylbenzofurans
IUPAC Name [2,7,8-trihydroxy-3-(4-hydroxyphenyl)-1-(2-phenylacetyl)oxydibenzofuran-4-yl] 4-hydroxybenzoate
SMILES (Canonical) C1=CC=C(C=C1)CC(=O)OC2=C(C(=C(C3=C2C4=CC(=C(C=C4O3)O)O)OC(=O)C5=CC=C(C=C5)O)C6=CC=C(C=C6)O)O
SMILES (Isomeric) C1=CC=C(C=C1)CC(=O)OC2=C(C(=C(C3=C2C4=CC(=C(C=C4O3)O)O)OC(=O)C5=CC=C(C=C5)O)C6=CC=C(C=C6)O)O
InChI InChI=1S/C33H22O10/c34-20-10-6-18(7-11-20)27-29(39)30(42-26(38)14-17-4-2-1-3-5-17)28-22-15-23(36)24(37)16-25(22)41-32(28)31(27)43-33(40)19-8-12-21(35)13-9-19/h1-13,15-16,34-37,39H,14H2
InChI Key IHUAUKNDLWICHA-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C33H22O10
Molecular Weight 578.50 g/mol
Exact Mass 578.12129689 g/mol
Topological Polar Surface Area (TPSA) 167.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 6.15
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Thelephantin H

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9507 95.07%
Caco-2 - 0.9174 91.74%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7601 76.01%
OATP2B1 inhibitior + 0.5786 57.86%
OATP1B1 inhibitior + 0.8458 84.58%
OATP1B3 inhibitior + 0.8811 88.11%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8979 89.79%
P-glycoprotein inhibitior + 0.7821 78.21%
P-glycoprotein substrate - 0.6524 65.24%
CYP3A4 substrate + 0.6181 61.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8155 81.55%
CYP3A4 inhibition - 0.8808 88.08%
CYP2C9 inhibition + 0.6383 63.83%
CYP2C19 inhibition - 0.6447 64.47%
CYP2D6 inhibition - 0.9371 93.71%
CYP1A2 inhibition - 0.7129 71.29%
CYP2C8 inhibition + 0.9650 96.50%
CYP inhibitory promiscuity - 0.6827 68.27%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9443 94.43%
Carcinogenicity (trinary) Non-required 0.4687 46.87%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.6943 69.43%
Skin irritation - 0.7277 72.77%
Skin corrosion - 0.9578 95.78%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3944 39.44%
Micronuclear + 0.8518 85.18%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8522 85.22%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.9039 90.39%
Acute Oral Toxicity (c) III 0.4145 41.45%
Estrogen receptor binding + 0.8615 86.15%
Androgen receptor binding + 0.9157 91.57%
Thyroid receptor binding + 0.5634 56.34%
Glucocorticoid receptor binding + 0.5863 58.63%
Aromatase binding - 0.6217 62.17%
PPAR gamma + 0.7197 71.97%
Honey bee toxicity - 0.7518 75.18%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9825 98.25%

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 97.90% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.90% 98.95%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 96.06% 91.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.59% 99.17%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 93.97% 95.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.64% 86.33%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 93.37% 92.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.33% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.41% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.93% 95.50%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 90.69% 95.64%
CHEMBL242 Q92731 Estrogen receptor beta 86.00% 98.35%
CHEMBL3401 O75469 Pregnane X receptor 85.03% 94.73%
CHEMBL3194 P02766 Transthyretin 84.43% 90.71%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.95% 94.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.84% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.11% 95.56%
CHEMBL3891 P07384 Calpain 1 82.67% 93.04%
CHEMBL2535 P11166 Glucose transporter 82.20% 98.75%

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 101260624
LOTUS LTS0275556
wikiData Q77374628