Palmarumycin EG1

Details

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Internal ID 29e5071b-4f42-47e9-b22a-b9450caf82da
Taxonomy Benzenoids > Tetralins
IUPAC Name (5'S)-5'-methoxyspiro[2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene-3,8'-6,7-dihydro-5H-naphthalene]-1',4'-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H18O5/c1-24-15-10-11-21(20-14(23)9-8-13(22)19(15)20)25-16-6-2-4-12-5-3-7-17(26-21)18(12)16/h2-9,15,22-23H,10-11H2,1H3/t15-/m0/s1
InChI Key SXKCUYZQERBLMA-HNNXBMFYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H18O5
Molecular Weight 350.40 g/mol
Exact Mass 350.11542367 g/mol
Topological Polar Surface Area (TPSA) 68.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.36
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Palmarumycin EG1

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8556 85.56%
Caco-2 + 0.5137 51.37%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7447 74.47%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9286 92.86%
OATP1B3 inhibitior + 0.9670 96.70%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6079 60.79%
P-glycoprotein inhibitior - 0.4818 48.18%
P-glycoprotein substrate - 0.8482 84.82%
CYP3A4 substrate + 0.5582 55.82%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate + 0.3613 36.13%
CYP3A4 inhibition - 0.8840 88.40%
CYP2C9 inhibition - 0.7217 72.17%
CYP2C19 inhibition - 0.6009 60.09%
CYP2D6 inhibition - 0.8078 80.78%
CYP1A2 inhibition + 0.6323 63.23%
CYP2C8 inhibition + 0.4682 46.82%
CYP inhibitory promiscuity - 0.7423 74.23%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4861 48.61%
Eye corrosion - 0.9837 98.37%
Eye irritation - 0.5899 58.99%
Skin irritation - 0.6926 69.26%
Skin corrosion - 0.9265 92.65%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4673 46.73%
Micronuclear - 0.6200 62.00%
Hepatotoxicity - 0.5319 53.19%
skin sensitisation - 0.9013 90.13%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.6312 63.12%
Acute Oral Toxicity (c) III 0.5913 59.13%
Estrogen receptor binding + 0.7492 74.92%
Androgen receptor binding + 0.7411 74.11%
Thyroid receptor binding + 0.5452 54.52%
Glucocorticoid receptor binding + 0.6801 68.01%
Aromatase binding - 0.4857 48.57%
PPAR gamma + 0.7835 78.35%
Honey bee toxicity - 0.8301 83.01%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.7196 71.96%

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 98.93% 91.11%
CHEMBL240 Q12809 HERG 96.44% 89.76%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.25% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.94% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.21% 97.09%
CHEMBL1951 P21397 Monoamine oxidase A 89.87% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.07% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.44% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.34% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.19% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.90% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 85.41% 94.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.93% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.54% 95.89%
CHEMBL2581 P07339 Cathepsin D 81.54% 98.95%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 80.66% 91.79%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.45% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.05% 93.99%

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 139584538
LOTUS LTS0199570
wikiData Q77371052