Penochalasin J

Details

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Internal ID e5c8d953-6d4d-428a-801d-a5d819b283ff
Taxonomy Organoheterocyclic compounds > Isoindoles and derivatives > Isoindolines > Isoindolones
IUPAC Name (1S,7E,9S,11E,13S,16S,17R,18S)-18-(1H-indol-3-ylmethyl)-7,9,15,16-tetramethyl-19-azatricyclo[11.7.0.01,17]icosa-7,11,14-triene-2,5,20-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H38N2O3/c1-19-8-7-9-24-16-21(3)22(4)30-28(17-23-18-33-27-11-6-5-10-26(23)27)34-31(37)32(24,30)29(36)13-12-25(35)15-20(2)14-19/h5-7,9-11,14,16,18-19,22,24,28,30,33H,8,12-13,15,17H2,1-4H3,(H,34,37)/b9-7+,20-14+/t19-,22+,24-,28-,30-,32+/m0/s1
InChI Key MYTCOOYZKCVFJE-ZOHYDBOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H38N2O3
Molecular Weight 498.70 g/mol
Exact Mass 498.28824308 g/mol
Topological Polar Surface Area (TPSA) 79.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 5.87
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Penochalasin J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 - 0.7556 75.56%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7517 75.17%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.8936 89.36%
OATP1B3 inhibitior + 0.9329 93.29%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.9956 99.56%
P-glycoprotein inhibitior + 0.8842 88.42%
P-glycoprotein substrate + 0.6262 62.62%
CYP3A4 substrate + 0.7083 70.83%
CYP2C9 substrate - 0.8075 80.75%
CYP2D6 substrate - 0.8301 83.01%
CYP3A4 inhibition + 0.7460 74.60%
CYP2C9 inhibition - 0.5926 59.26%
CYP2C19 inhibition - 0.5224 52.24%
CYP2D6 inhibition - 0.8412 84.12%
CYP1A2 inhibition - 0.5837 58.37%
CYP2C8 inhibition + 0.5452 54.52%
CYP inhibitory promiscuity + 0.8149 81.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4679 46.79%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9771 97.71%
Skin irritation - 0.7844 78.44%
Skin corrosion - 0.9274 92.74%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9203 92.03%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.5376 53.76%
skin sensitisation - 0.8676 86.76%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.7737 77.37%
Acute Oral Toxicity (c) III 0.4625 46.25%
Estrogen receptor binding + 0.7951 79.51%
Androgen receptor binding + 0.6268 62.68%
Thyroid receptor binding + 0.6390 63.90%
Glucocorticoid receptor binding + 0.8354 83.54%
Aromatase binding + 0.5814 58.14%
PPAR gamma + 0.7545 75.45%
Honey bee toxicity - 0.7272 72.72%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9436 94.36%

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 99.41% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.08% 95.56%
CHEMBL2581 P07339 Cathepsin D 96.78% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 94.07% 97.79%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.46% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.03% 85.14%
CHEMBL1937 Q92769 Histone deacetylase 2 92.90% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.55% 99.23%
CHEMBL3310 Q96DB2 Histone deacetylase 11 91.24% 88.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.61% 96.09%
CHEMBL255 P29275 Adenosine A2b receptor 88.86% 98.59%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 88.70% 97.64%
CHEMBL230 P35354 Cyclooxygenase-2 87.91% 89.63%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.80% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.51% 92.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.48% 97.09%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.03% 89.62%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 84.14% 96.39%
CHEMBL1914 P06276 Butyrylcholinesterase 83.67% 95.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.81% 86.33%
CHEMBL4302 P08183 P-glycoprotein 1 81.63% 92.98%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.94% 89.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.71% 96.25%
CHEMBL2535 P11166 Glucose transporter 80.34% 98.75%

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 139590395
LOTUS LTS0070685
wikiData Q105175158