Wailupemycin G

Details

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Internal ID 0bce65c9-2a51-465d-8944-45cb1813f26f
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 6-(4,5-dihydroxy-2-phenylnaphthalen-1-yl)-4-hydroxypyran-2-one
SMILES (Canonical) C1=CC=C(C=C1)C2=CC(=C3C(=C2C4=CC(=CC(=O)O4)O)C=CC=C3O)O
SMILES (Isomeric) C1=CC=C(C=C1)C2=CC(=C3C(=C2C4=CC(=CC(=O)O4)O)C=CC=C3O)O
InChI InChI=1S/C21H14O5/c22-13-9-18(26-19(25)10-13)20-14-7-4-8-16(23)21(14)17(24)11-15(20)12-5-2-1-3-6-12/h1-11,22-24H
InChI Key ZZTFZGJHNCTGFE-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H14O5
Molecular Weight 346.30 g/mol
Exact Mass 346.08412354 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.24
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Wailupemycin G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9498 94.98%
Caco-2 - 0.6399 63.99%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7343 73.43%
OATP2B1 inhibitior - 0.6844 68.44%
OATP1B1 inhibitior + 0.9050 90.50%
OATP1B3 inhibitior - 0.7274 72.74%
MATE1 inhibitior - 0.5600 56.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.4884 48.84%
P-glycoprotein inhibitior - 0.7621 76.21%
P-glycoprotein substrate - 0.8698 86.98%
CYP3A4 substrate + 0.5635 56.35%
CYP2C9 substrate + 0.5173 51.73%
CYP2D6 substrate - 0.8799 87.99%
CYP3A4 inhibition + 0.5478 54.78%
CYP2C9 inhibition + 0.7323 73.23%
CYP2C19 inhibition - 0.5797 57.97%
CYP2D6 inhibition - 0.9607 96.07%
CYP1A2 inhibition - 0.6332 63.32%
CYP2C8 inhibition + 0.7638 76.38%
CYP inhibitory promiscuity + 0.5294 52.94%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7006 70.06%
Eye corrosion - 0.9930 99.30%
Eye irritation + 0.8722 87.22%
Skin irritation + 0.6066 60.66%
Skin corrosion - 0.9783 97.83%
Ames mutagenesis + 0.5646 56.46%
Human Ether-a-go-go-Related Gene inhibition - 0.8411 84.11%
Micronuclear + 0.9600 96.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8690 86.90%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6532 65.32%
Acute Oral Toxicity (c) II 0.6059 60.59%
Estrogen receptor binding + 0.8819 88.19%
Androgen receptor binding + 0.8775 87.75%
Thyroid receptor binding + 0.5921 59.21%
Glucocorticoid receptor binding + 0.9011 90.11%
Aromatase binding + 0.7300 73.00%
PPAR gamma + 0.9617 96.17%
Honey bee toxicity - 0.8794 87.94%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5233 52.33%
Fish aquatic toxicity + 0.9542 95.42%

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 99.02% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.14% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.26% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.58% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.82% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.63% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.49% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.40% 95.50%
CHEMBL2083 P15090 Fatty acid binding protein adipocyte 87.75% 95.71%
CHEMBL3401 O75469 Pregnane X receptor 87.46% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.59% 86.33%
CHEMBL1811 P34995 Prostanoid EP1 receptor 85.07% 95.71%
CHEMBL1951 P21397 Monoamine oxidase A 84.11% 91.49%
CHEMBL242 Q92731 Estrogen receptor beta 84.00% 98.35%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.50% 91.71%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.66% 92.08%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.10% 93.99%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.01% 99.17%

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 54712252
LOTUS LTS0005819
wikiData Q105387037