Picrasidine V

Details

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Internal ID f365c3a1-a5e7-48d1-a0e2-c21de0ed5a3e
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Beta carbolines
IUPAC Name 8-methoxy-9H-pyrido[3,4-b]indole-1,3,4-trione
SMILES (Canonical) COC1=CC=CC2=C1NC3=C2C(=O)C(=O)NC3=O
SMILES (Isomeric) COC1=CC=CC2=C1NC3=C2C(=O)C(=O)NC3=O
InChI InChI=1S/C12H8N2O4/c1-18-6-4-2-3-5-7-9(13-8(5)6)11(16)14-12(17)10(7)15/h2-4,13H,1H3,(H,14,16,17)
InChI Key VELKHFGMMALQQU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H8N2O4
Molecular Weight 244.20 g/mol
Exact Mass 244.04840674 g/mol
Topological Polar Surface Area (TPSA) 88.30 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.63
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEMBL2229715

2D Structure

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2D Structure of Picrasidine V

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9650 96.50%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7751 77.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9508 95.08%
OATP1B3 inhibitior + 0.9645 96.45%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7863 78.63%
P-glycoprotein inhibitior - 0.9387 93.87%
P-glycoprotein substrate - 0.8463 84.63%
CYP3A4 substrate + 0.5797 57.97%
CYP2C9 substrate + 0.6091 60.91%
CYP2D6 substrate - 0.8649 86.49%
CYP3A4 inhibition - 0.7111 71.11%
CYP2C9 inhibition - 0.8569 85.69%
CYP2C19 inhibition - 0.8415 84.15%
CYP2D6 inhibition - 0.9241 92.41%
CYP1A2 inhibition + 0.8391 83.91%
CYP2C8 inhibition - 0.7880 78.80%
CYP inhibitory promiscuity - 0.6014 60.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6030 60.30%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.7870 78.70%
Skin irritation - 0.8748 87.48%
Skin corrosion - 0.9630 96.30%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6680 66.80%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.6678 66.78%
skin sensitisation - 0.9454 94.54%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5983 59.83%
Acute Oral Toxicity (c) III 0.6710 67.10%
Estrogen receptor binding + 0.7113 71.13%
Androgen receptor binding + 0.6749 67.49%
Thyroid receptor binding - 0.5193 51.93%
Glucocorticoid receptor binding + 0.6458 64.58%
Aromatase binding + 0.7633 76.33%
PPAR gamma - 0.4920 49.20%
Honey bee toxicity - 0.8261 82.61%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.5661 56.61%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.37% 95.56%
CHEMBL2581 P07339 Cathepsin D 96.75% 98.95%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 93.71% 95.72%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.42% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.62% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.51% 96.09%
CHEMBL2535 P11166 Glucose transporter 91.39% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.70% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 88.95% 94.75%
CHEMBL1255126 O15151 Protein Mdm4 88.00% 90.20%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.53% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.31% 93.99%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.50% 96.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.96% 85.14%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.93% 85.49%
CHEMBL1907 P15144 Aminopeptidase N 81.76% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.18% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.09% 96.67%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 80.11% 92.38%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.10% 94.03%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Picrasma quassioides

Cross-Links

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PubChem 5320565
NPASS NPC288987
LOTUS LTS0005963
wikiData Q105284668