Zinnimide

Details

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Internal ID 14fae9a1-f41a-4da8-bf7e-b7fba4d27291
Taxonomy Organoheterocyclic compounds > Isoindoles and derivatives > Isoindolines > Isoindolones > Phthalimides
IUPAC Name 4-methoxy-5-methyl-6-(3-methylbut-2-enoxy)isoindole-1,3-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H17NO4/c1-8(2)5-6-20-11-7-10-12(13(19-4)9(11)3)15(18)16-14(10)17/h5,7H,6H2,1-4H3,(H,16,17,18)
InChI Key ZSSDQYBHZQJKGP-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C15H17NO4
Molecular Weight 275.30 g/mol
Exact Mass 275.11575802 g/mol
Topological Polar Surface Area (TPSA) 64.60 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.23
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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1199799-26-2
4-methoxy-5-methyl-6-(3-methylbut-2-enoxy)isoindole-1,3-dione
CHEBI:181542
ZXB79926
NCGC00380986-01
NCGC00380986-01_C15H17NO4_

2D Structure

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2D Structure of Zinnimide

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 + 0.8621 86.21%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7872 78.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9108 91.08%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6360 63.60%
P-glycoprotein inhibitior - 0.7889 78.89%
P-glycoprotein substrate - 0.8152 81.52%
CYP3A4 substrate + 0.5387 53.87%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8469 84.69%
CYP3A4 inhibition - 0.5715 57.15%
CYP2C9 inhibition + 0.5351 53.51%
CYP2C19 inhibition - 0.6620 66.20%
CYP2D6 inhibition - 0.9095 90.95%
CYP1A2 inhibition + 0.8750 87.50%
CYP2C8 inhibition - 0.7335 73.35%
CYP inhibitory promiscuity + 0.5736 57.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6234 62.34%
Eye corrosion - 0.9871 98.71%
Eye irritation + 0.6497 64.97%
Skin irritation - 0.8301 83.01%
Skin corrosion - 0.9477 94.77%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4028 40.28%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.6927 69.27%
skin sensitisation - 0.8493 84.93%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.5918 59.18%
Acute Oral Toxicity (c) III 0.6186 61.86%
Estrogen receptor binding + 0.6465 64.65%
Androgen receptor binding - 0.6042 60.42%
Thyroid receptor binding - 0.5725 57.25%
Glucocorticoid receptor binding - 0.5497 54.97%
Aromatase binding + 0.7221 72.21%
PPAR gamma - 0.5296 52.96%
Honey bee toxicity - 0.9084 90.84%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9441 94.41%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.21% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 94.62% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.60% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.79% 94.00%
CHEMBL4208 P20618 Proteasome component C5 91.37% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.51% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.17% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.12% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.81% 97.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.56% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.95% 99.17%
CHEMBL2581 P07339 Cathepsin D 85.87% 98.95%
CHEMBL2535 P11166 Glucose transporter 84.83% 98.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.78% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.31% 85.14%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.18% 90.24%
CHEMBL3401 O75469 Pregnane X receptor 83.56% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.39% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.67% 89.00%

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 100641860
LOTUS LTS0097098
wikiData Q77563585