Erinacerin T

Details

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Internal ID 16394374-a72a-4c3c-b2c5-80ffbb5e8227
Taxonomy Organoheterocyclic compounds > Isoindoles and derivatives > Isoindolines > Isoindolones
IUPAC Name methyl 6-(4,6-dihydroxy-1,3-dioxoisoindol-5-yl)-4-methylhex-4-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H17NO6/c1-8(4-6-12(19)23-2)3-5-9-11(18)7-10-13(14(9)20)16(22)17-15(10)21/h3,7,18,20H,4-6H2,1-2H3,(H,17,21,22)
InChI Key MOBXTHUEHJFZOU-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H17NO6
Molecular Weight 319.31 g/mol
Exact Mass 319.10558726 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.42
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Erinacerin T

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9864 98.64%
Caco-2 - 0.6322 63.22%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6672 66.72%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.8140 81.40%
OATP1B3 inhibitior + 0.9057 90.57%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7822 78.22%
BSEP inhibitior - 0.7747 77.47%
P-glycoprotein inhibitior - 0.8481 84.81%
P-glycoprotein substrate - 0.7295 72.95%
CYP3A4 substrate + 0.5718 57.18%
CYP2C9 substrate + 0.5959 59.59%
CYP2D6 substrate - 0.8711 87.11%
CYP3A4 inhibition - 0.6737 67.37%
CYP2C9 inhibition - 0.8085 80.85%
CYP2C19 inhibition - 0.7416 74.16%
CYP2D6 inhibition - 0.9042 90.42%
CYP1A2 inhibition + 0.5591 55.91%
CYP2C8 inhibition - 0.6217 62.17%
CYP inhibitory promiscuity - 0.6712 67.12%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6247 62.47%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.7080 70.80%
Skin irritation - 0.8090 80.90%
Skin corrosion - 0.9463 94.63%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6289 62.89%
Micronuclear + 0.6400 64.00%
Hepatotoxicity - 0.5790 57.90%
skin sensitisation - 0.8553 85.53%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7639 76.39%
Acute Oral Toxicity (c) III 0.5272 52.72%
Estrogen receptor binding + 0.6080 60.80%
Androgen receptor binding - 0.5382 53.82%
Thyroid receptor binding - 0.5855 58.55%
Glucocorticoid receptor binding + 0.7009 70.09%
Aromatase binding - 0.5427 54.27%
PPAR gamma + 0.8560 85.60%
Honey bee toxicity - 0.8753 87.53%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9791 97.91%

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 99.62% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.25% 94.45%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 94.28% 95.64%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.82% 85.14%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 92.13% 89.34%
CHEMBL2581 P07339 Cathepsin D 92.01% 98.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 90.53% 91.07%
CHEMBL4208 P20618 Proteasome component C5 90.41% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.60% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 87.76% 94.73%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.20% 85.30%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.57% 99.17%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 85.80% 80.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.94% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.13% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 83.78% 91.19%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.67% 93.03%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.31% 95.17%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 83.02% 96.90%
CHEMBL1951 P21397 Monoamine oxidase A 82.77% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.55% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 81.42% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.65% 89.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.04% 97.21%

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 139584511
LOTUS LTS0237054
wikiData Q77370614