Penicimutatin

Details

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Internal ID 377d94c7-1bd8-410e-8868-b0bd1505eb10
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > N-alkylindoles
IUPAC Name (3S,6S)-3-benzyl-6-[[1-(3-methylbut-2-enyl)indol-3-yl]methyl]piperazine-2,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H27N3O2/c1-17(2)12-13-28-16-19(20-10-6-7-11-23(20)28)15-22-25(30)26-21(24(29)27-22)14-18-8-4-3-5-9-18/h3-12,16,21-22H,13-15H2,1-2H3,(H,26,30)(H,27,29)/t21-,22-/m0/s1
InChI Key NYJNVRXNQRYYHW-VXKWHMMOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H27N3O2
Molecular Weight 401.50 g/mol
Exact Mass 401.21032711 g/mol
Topological Polar Surface Area (TPSA) 63.10 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.38
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Penicimutatin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 - 0.6769 67.69%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5281 52.81%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.9066 90.66%
OATP1B3 inhibitior + 0.9334 93.34%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7649 76.49%
BSEP inhibitior + 0.9771 97.71%
P-glycoprotein inhibitior + 0.6929 69.29%
P-glycoprotein substrate - 0.5274 52.74%
CYP3A4 substrate + 0.5602 56.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8381 83.81%
CYP3A4 inhibition + 0.6703 67.03%
CYP2C9 inhibition - 0.5127 51.27%
CYP2C19 inhibition - 0.5427 54.27%
CYP2D6 inhibition - 0.8347 83.47%
CYP1A2 inhibition - 0.6208 62.08%
CYP2C8 inhibition - 0.7644 76.44%
CYP inhibitory promiscuity + 0.7215 72.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6477 64.77%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9848 98.48%
Skin irritation - 0.7788 77.88%
Skin corrosion - 0.9310 93.10%
Ames mutagenesis + 0.5692 56.92%
Human Ether-a-go-go-Related Gene inhibition + 0.9181 91.81%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8726 87.26%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.6907 69.07%
Acute Oral Toxicity (c) III 0.5637 56.37%
Estrogen receptor binding + 0.6879 68.79%
Androgen receptor binding + 0.5579 55.79%
Thyroid receptor binding + 0.5427 54.27%
Glucocorticoid receptor binding + 0.6649 66.49%
Aromatase binding + 0.5444 54.44%
PPAR gamma + 0.6742 67.42%
Honey bee toxicity - 0.9213 92.13%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9268 92.68%

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
CHEMBL2581 P07339 Cathepsin D 97.29% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.88% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.44% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 96.18% 90.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.97% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.54% 94.45%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.91% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.32% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.25% 97.25%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 88.75% 97.64%
CHEMBL1937 Q92769 Histone deacetylase 2 88.46% 94.75%
CHEMBL3401 O75469 Pregnane X receptor 87.44% 94.73%
CHEMBL2327 P21452 Neurokinin 2 receptor 85.69% 98.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.13% 89.00%
CHEMBL255 P29275 Adenosine A2b receptor 84.68% 98.59%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.25% 93.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.05% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.66% 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 139587760
LOTUS LTS0026341
wikiData Q77573408