Thielavin Z2

Details

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Internal ID 12c37d65-68d2-4c13-b465-790123847211
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 4-[4-(2,4-dihydroxy-3,6-dimethylbenzoyl)oxy-2-methoxy-3,6-dimethylbenzoyl]oxy-2-hydroxy-3,5,6-trimethylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H30O10/c1-11-9-18(30)15(5)23(31)20(11)28(35)38-19-10-12(2)21(26(37-8)16(19)6)29(36)39-25-14(4)13(3)22(27(33)34)24(32)17(25)7/h9-10,30-32H,1-8H3,(H,33,34)
InChI Key FICWTOJSIXNNIZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C29H30O10
Molecular Weight 538.50 g/mol
Exact Mass 538.18389715 g/mol
Topological Polar Surface Area (TPSA) 160.00 Ų
XlogP 6.80
Atomic LogP (AlogP) 5.11
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Thielavin Z2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9450 94.50%
Caco-2 - 0.6707 67.07%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8663 86.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9263 92.63%
OATP1B3 inhibitior - 0.5698 56.98%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6291 62.91%
P-glycoprotein inhibitior + 0.6634 66.34%
P-glycoprotein substrate - 0.8200 82.00%
CYP3A4 substrate + 0.5229 52.29%
CYP2C9 substrate - 0.6089 60.89%
CYP2D6 substrate - 0.8933 89.33%
CYP3A4 inhibition - 0.8310 83.10%
CYP2C9 inhibition - 0.7343 73.43%
CYP2C19 inhibition - 0.8817 88.17%
CYP2D6 inhibition - 0.8907 89.07%
CYP1A2 inhibition - 0.6138 61.38%
CYP2C8 inhibition + 0.5429 54.29%
CYP inhibitory promiscuity - 0.6980 69.80%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7156 71.56%
Carcinogenicity (trinary) Non-required 0.7193 71.93%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.7404 74.04%
Skin irritation - 0.8241 82.41%
Skin corrosion - 0.9491 94.91%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7773 77.73%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.9583 95.83%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.6059 60.59%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.8391 83.91%
Acute Oral Toxicity (c) II 0.6323 63.23%
Estrogen receptor binding + 0.8362 83.62%
Androgen receptor binding + 0.6066 60.66%
Thyroid receptor binding + 0.5784 57.84%
Glucocorticoid receptor binding + 0.7539 75.39%
Aromatase binding + 0.7361 73.61%
PPAR gamma + 0.7153 71.53%
Honey bee toxicity - 0.8380 83.80%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9878 98.78%

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 91.82% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.64% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.03% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.83% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.31% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.30% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.11% 94.42%
CHEMBL2581 P07339 Cathepsin D 85.35% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.82% 86.33%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 84.64% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.63% 99.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.56% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.44% 96.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.43% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.17% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.02% 89.00%

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 139590467
LOTUS LTS0180745
wikiData Q103819024