Thielavin W

Details

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Internal ID b316f054-78d9-4eb5-91ad-142102502b31
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 4-[4-(2,4-dihydroxy-6-methylbenzoyl)oxy-2-hydroxy-3,5,6-trimethylbenzoyl]oxy-2-hydroxy-3,6-dimethylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H26O10/c1-10-7-16(28)9-17(29)19(10)26(34)37-24-13(4)12(3)21(23(31)15(24)6)27(35)36-18-8-11(2)20(25(32)33)22(30)14(18)5/h7-9,28-31H,1-6H3,(H,32,33)
InChI Key XFPQAQWPFDKAQJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H26O10
Molecular Weight 510.50 g/mol
Exact Mass 510.15259702 g/mol
Topological Polar Surface Area (TPSA) 171.00 Ų
XlogP 6.70
Atomic LogP (AlogP) 4.50
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Thielavin W

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9506 95.06%
Caco-2 - 0.6388 63.88%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8895 88.95%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.9403 94.03%
OATP1B3 inhibitior - 0.5000 50.00%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5537 55.37%
P-glycoprotein inhibitior + 0.6280 62.80%
P-glycoprotein substrate - 0.8389 83.89%
CYP3A4 substrate - 0.5057 50.57%
CYP2C9 substrate - 0.6130 61.30%
CYP2D6 substrate - 0.9089 90.89%
CYP3A4 inhibition - 0.7914 79.14%
CYP2C9 inhibition - 0.5787 57.87%
CYP2C19 inhibition - 0.8708 87.08%
CYP2D6 inhibition - 0.9003 90.03%
CYP1A2 inhibition - 0.6210 62.10%
CYP2C8 inhibition + 0.6847 68.47%
CYP inhibitory promiscuity - 0.6703 67.03%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7356 73.56%
Carcinogenicity (trinary) Non-required 0.7275 72.75%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.6913 69.13%
Skin irritation - 0.8220 82.20%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8915 89.15%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.9158 91.58%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5170 51.70%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6685 66.85%
Acute Oral Toxicity (c) III 0.5364 53.64%
Estrogen receptor binding + 0.8101 81.01%
Androgen receptor binding + 0.7160 71.60%
Thyroid receptor binding + 0.5464 54.64%
Glucocorticoid receptor binding + 0.7333 73.33%
Aromatase binding + 0.6773 67.73%
PPAR gamma + 0.7310 73.10%
Honey bee toxicity - 0.8146 81.46%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9943 99.43%

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
CHEMBL3194 P02766 Transthyretin 94.25% 90.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 90.83% 94.42%
CHEMBL2581 P07339 Cathepsin D 90.38% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.14% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.71% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.88% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.54% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.25% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.07% 99.15%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.06% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.00% 94.45%
CHEMBL4208 P20618 Proteasome component C5 82.45% 90.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.16% 95.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.91% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.66% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 81.08% 94.73%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.29% 97.21%

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 139590462
LOTUS LTS0245650
wikiData Q104200938