Tubakialactone E

Details

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Internal ID 6d52e120-b533-4f83-ac31-cd608b9b94bb
Taxonomy Organoheterocyclic compounds > Benzofurans > Benzofuranones
IUPAC Name 3-(1-hydroxyethyl)-5,7-dimethoxy-3-methyl-2-benzofuran-1-one
SMILES (Canonical) CC(C1(C2=C(C(=CC(=C2)OC)OC)C(=O)O1)C)O
SMILES (Isomeric) CC(C1(C2=C(C(=CC(=C2)OC)OC)C(=O)O1)C)O
InChI InChI=1S/C13H16O5/c1-7(14)13(2)9-5-8(16-3)6-10(17-4)11(9)12(15)18-13/h5-7,14H,1-4H3
InChI Key VDPWRNYMVKSNST-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O5
Molecular Weight 252.26 g/mol
Exact Mass 252.09977361 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.47
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tubakialactone E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9856 98.56%
Caco-2 + 0.7472 74.72%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6548 65.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9192 91.92%
OATP1B3 inhibitior + 0.8983 89.83%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8614 86.14%
P-glycoprotein inhibitior - 0.8993 89.93%
P-glycoprotein substrate - 0.9319 93.19%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7785 77.85%
CYP3A4 inhibition - 0.6906 69.06%
CYP2C9 inhibition - 0.9333 93.33%
CYP2C19 inhibition - 0.8472 84.72%
CYP2D6 inhibition - 0.9096 90.96%
CYP1A2 inhibition - 0.6097 60.97%
CYP2C8 inhibition - 0.8424 84.24%
CYP inhibitory promiscuity - 0.8128 81.28%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9019 90.19%
Carcinogenicity (trinary) Non-required 0.4121 41.21%
Eye corrosion - 0.9250 92.50%
Eye irritation - 0.6156 61.56%
Skin irritation - 0.7205 72.05%
Skin corrosion - 0.9658 96.58%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7284 72.84%
Micronuclear + 0.6300 63.00%
Hepatotoxicity - 0.6216 62.16%
skin sensitisation - 0.8338 83.38%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.6114 61.14%
Acute Oral Toxicity (c) II 0.6062 60.62%
Estrogen receptor binding - 0.6491 64.91%
Androgen receptor binding - 0.4944 49.44%
Thyroid receptor binding - 0.5518 55.18%
Glucocorticoid receptor binding - 0.5954 59.54%
Aromatase binding + 0.6014 60.14%
PPAR gamma + 0.5942 59.42%
Honey bee toxicity - 0.9101 91.01%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.7961 79.61%

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 98.33% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.51% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.56% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.91% 96.09%
CHEMBL4208 P20618 Proteasome component C5 94.37% 90.00%
CHEMBL4040 P28482 MAP kinase ERK2 94.03% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.07% 94.45%
CHEMBL2581 P07339 Cathepsin D 90.92% 98.95%
CHEMBL2535 P11166 Glucose transporter 88.49% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.95% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.56% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.96% 97.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.71% 99.15%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.27% 91.07%
CHEMBL3401 O75469 Pregnane X receptor 81.50% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.90% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.29% 92.62%

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 132820812
LOTUS LTS0213234
wikiData Q104199264