Pronqodine A

Details

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Internal ID ab64e6d4-ec26-4c3a-bca1-a79ce5a2fd31
Taxonomy Organoheterocyclic compounds > Benzothiazoles
IUPAC Name 5-(methylamino)-1,2-benzothiazole-4,7-dione
SMILES (Canonical) CNC1=CC(=O)C2=C(C1=O)C=NS2
SMILES (Isomeric) CNC1=CC(=O)C2=C(C1=O)C=NS2
InChI InChI=1S/C8H6N2O2S/c1-9-5-2-6(11)8-4(7(5)12)3-10-13-8/h2-3,9H,1H3
InChI Key FIAXOEDOQLZQMW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C8H6N2O2S
Molecular Weight 194.21 g/mol
Exact Mass 194.01499861 g/mol
Topological Polar Surface Area (TPSA) 87.30 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.63
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pronqodine A

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 + 0.5871 58.71%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.6511 65.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9430 94.30%
OATP1B3 inhibitior + 0.9463 94.63%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9668 96.68%
P-glycoprotein inhibitior - 0.9507 95.07%
P-glycoprotein substrate - 0.8669 86.69%
CYP3A4 substrate - 0.5520 55.20%
CYP2C9 substrate - 0.8075 80.75%
CYP2D6 substrate - 0.8455 84.55%
CYP3A4 inhibition - 0.6459 64.59%
CYP2C9 inhibition + 0.5229 52.29%
CYP2C19 inhibition + 0.5976 59.76%
CYP2D6 inhibition - 0.8449 84.49%
CYP1A2 inhibition + 0.7814 78.14%
CYP2C8 inhibition - 0.9521 95.21%
CYP inhibitory promiscuity + 0.7736 77.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8043 80.43%
Carcinogenicity (trinary) Non-required 0.5567 55.67%
Eye corrosion - 0.9799 97.99%
Eye irritation + 0.5326 53.26%
Skin irritation - 0.7442 74.42%
Skin corrosion - 0.8973 89.73%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6367 63.67%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.6927 69.27%
skin sensitisation - 0.7779 77.79%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.7488 74.88%
Acute Oral Toxicity (c) III 0.6124 61.24%
Estrogen receptor binding - 0.7717 77.17%
Androgen receptor binding - 0.4823 48.23%
Thyroid receptor binding - 0.7407 74.07%
Glucocorticoid receptor binding - 0.6326 63.26%
Aromatase binding - 0.5876 58.76%
PPAR gamma - 0.9010 90.10%
Honey bee toxicity - 0.8237 82.37%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.7472 74.72%

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 93.80% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 91.75% 89.34%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.85% 81.11%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 88.63% 96.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.23% 95.56%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 86.91% 85.30%
CHEMBL3055 P50613 Cyclin-dependent kinase 7 85.87% 81.88%
CHEMBL2093869 P05106 Integrin alpha-IIb/beta-3 84.27% 95.42%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 83.86% 96.90%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.83% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.56% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.12% 96.09%

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 71665488
LOTUS LTS0225060
wikiData Q77503040