Trypethelon-methylether

Details

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Internal ID 341ea2db-e82f-4f21-9e57-6a00fdad7334
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name 7-methoxy-2,3,3,9-tetramethyl-2H-benzo[g][1]benzofuran-4,5-dione
SMILES (Canonical) CC1C(C2=C(O1)C3=C(C=C(C=C3C)OC)C(=O)C2=O)(C)C
SMILES (Isomeric) CC1C(C2=C(O1)C3=C(C=C(C=C3C)OC)C(=O)C2=O)(C)C
InChI InChI=1S/C17H18O4/c1-8-6-10(20-5)7-11-12(8)16-13(15(19)14(11)18)17(3,4)9(2)21-16/h6-7,9H,1-5H3
InChI Key CCLFCEGGIPRBIN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O4
Molecular Weight 286.32 g/mol
Exact Mass 286.12050905 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.93
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Trypethelon-methylether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7870 78.70%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7745 77.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8856 88.56%
OATP1B3 inhibitior + 0.9666 96.66%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6150 61.50%
P-glycoprotein inhibitior - 0.7787 77.87%
P-glycoprotein substrate - 0.8996 89.96%
CYP3A4 substrate + 0.5723 57.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7905 79.05%
CYP3A4 inhibition + 0.6366 63.66%
CYP2C9 inhibition + 0.5956 59.56%
CYP2C19 inhibition + 0.6926 69.26%
CYP2D6 inhibition - 0.8319 83.19%
CYP1A2 inhibition + 0.7946 79.46%
CYP2C8 inhibition - 0.8443 84.43%
CYP inhibitory promiscuity + 0.9186 91.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9743 97.43%
Carcinogenicity (trinary) Danger 0.4383 43.83%
Eye corrosion - 0.9785 97.85%
Eye irritation + 0.8131 81.31%
Skin irritation - 0.7644 76.44%
Skin corrosion - 0.9510 95.10%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5213 52.13%
Micronuclear + 0.5700 57.00%
Hepatotoxicity + 0.5960 59.60%
skin sensitisation - 0.6861 68.61%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.7205 72.05%
Acute Oral Toxicity (c) III 0.5411 54.11%
Estrogen receptor binding + 0.8740 87.40%
Androgen receptor binding + 0.6165 61.65%
Thyroid receptor binding - 0.5280 52.80%
Glucocorticoid receptor binding - 0.5057 50.57%
Aromatase binding + 0.6940 69.40%
PPAR gamma + 0.5565 55.65%
Honey bee toxicity - 0.8275 82.75%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9904 99.04%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.66% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.85% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.44% 93.40%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 89.94% 94.80%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.02% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.75% 85.14%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.86% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.60% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.26% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.89% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.11% 91.07%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.46% 86.33%
CHEMBL2581 P07339 Cathepsin D 83.93% 98.95%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.61% 96.21%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.95% 96.77%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 81.33% 96.09%
CHEMBL4208 P20618 Proteasome component C5 80.53% 90.00%

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 71440283
LOTUS LTS0246886
wikiData Q75067762