Thielavin Z6

Details

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Internal ID 39c21da4-9179-4209-884d-187b33efa329
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 4-[4-(5-chloro-2,4-dihydroxy-3,6-dimethylbenzoyl)oxy-2-methoxy-3,5,6-trimethylbenzoyl]oxy-2-hydroxy-3,5,6-trimethylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H31ClO10/c1-10-12(3)25(16(7)23(33)18(10)28(35)36)40-30(38)20-11(2)13(4)26(17(8)27(20)39-9)41-29(37)19-14(5)21(31)24(34)15(6)22(19)32/h32-34H,1-9H3,(H,35,36)
InChI Key MJZHMSVXOFMDTF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H31ClO10
Molecular Weight 587.00 g/mol
Exact Mass 586.1605749 g/mol
Topological Polar Surface Area (TPSA) 160.00 Ų
XlogP 7.80
Atomic LogP (AlogP) 6.07
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 Z6

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9535 95.35%
Caco-2 - 0.7140 71.40%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8535 85.35%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.7826 78.26%
OATP1B3 inhibitior - 0.3945 39.45%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5623 56.23%
P-glycoprotein inhibitior + 0.5750 57.50%
P-glycoprotein substrate - 0.8923 89.23%
CYP3A4 substrate + 0.5302 53.02%
CYP2C9 substrate - 0.6178 61.78%
CYP2D6 substrate - 0.8982 89.82%
CYP3A4 inhibition - 0.8940 89.40%
CYP2C9 inhibition - 0.6563 65.63%
CYP2C19 inhibition - 0.8031 80.31%
CYP2D6 inhibition - 0.9020 90.20%
CYP1A2 inhibition - 0.5946 59.46%
CYP2C8 inhibition - 0.6061 60.61%
CYP inhibitory promiscuity - 0.6173 61.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6364 63.64%
Carcinogenicity (trinary) Non-required 0.4978 49.78%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.7701 77.01%
Skin irritation - 0.7254 72.54%
Skin corrosion - 0.9030 90.30%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7455 74.55%
Micronuclear + 0.6274 62.74%
Hepatotoxicity + 0.6159 61.59%
skin sensitisation - 0.8792 87.92%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) II 0.4685 46.85%
Estrogen receptor binding + 0.8749 87.49%
Androgen receptor binding - 0.6110 61.10%
Thyroid receptor binding + 0.5635 56.35%
Glucocorticoid receptor binding + 0.7438 74.38%
Aromatase binding + 0.7845 78.45%
PPAR gamma + 0.6410 64.10%
Honey bee toxicity - 0.8919 89.19%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9964 99.64%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.68% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.19% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.63% 91.11%
CHEMBL3194 P02766 Transthyretin 85.54% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.95% 95.56%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.67% 98.75%
CHEMBL2581 P07339 Cathepsin D 82.25% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.08% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.17% 94.00%

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 139590460
LOTUS LTS0133614
wikiData Q104171765