Thielavin Y

Details

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Internal ID 39e67aae-ffd2-489a-bf06-f99dfb589e1b
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 4-[4-(2,4-dihydroxy-3,6-dimethylbenzoyl)oxy-2-methoxy-3,5,6-trimethylbenzoyl]oxy-2-hydroxy-6-methylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H28O10/c1-11-8-17(10-19(30)20(11)26(32)33)37-28(35)22-13(3)14(4)24(16(6)25(22)36-7)38-27(34)21-12(2)9-18(29)15(5)23(21)31/h8-10,29-31H,1-7H3,(H,32,33)
InChI Key SURHXVKEMTXENB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H28O10
Molecular Weight 524.50 g/mol
Exact Mass 524.16824709 g/mol
Topological Polar Surface Area (TPSA) 160.00 Ų
XlogP 6.50
Atomic LogP (AlogP) 4.80
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 Y

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 - 0.6146 61.46%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8663 86.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8980 89.80%
OATP1B3 inhibitior - 0.5698 56.98%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8433 84.33%
P-glycoprotein inhibitior + 0.6660 66.60%
P-glycoprotein substrate - 0.8615 86.15%
CYP3A4 substrate + 0.5468 54.68%
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 + 0.5062 50.62%
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 - 0.7475 74.75%
Skin irritation - 0.8241 82.41%
Skin corrosion - 0.9491 94.91%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7303 73.03%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.5285 52.85%
skin sensitisation - 0.9583 95.83%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.6059 60.59%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7680 76.80%
Acute Oral Toxicity (c) II 0.6323 63.23%
Estrogen receptor binding + 0.8540 85.40%
Androgen receptor binding + 0.6486 64.86%
Thyroid receptor binding + 0.5955 59.55%
Glucocorticoid receptor binding + 0.7671 76.71%
Aromatase binding + 0.7322 73.22%
PPAR gamma + 0.7425 74.25%
Honey bee toxicity - 0.8282 82.82%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5900 59.00%
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
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.25% 99.15%
CHEMBL3194 P02766 Transthyretin 90.60% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.81% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.48% 94.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.17% 94.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.21% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.64% 99.17%
CHEMBL4208 P20618 Proteasome component C5 85.26% 90.00%
CHEMBL2581 P07339 Cathepsin D 85.13% 98.95%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.88% 91.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.62% 96.09%

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 139590464
LOTUS LTS0169360
wikiData Q104197675