Exotoxin

Details

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Internal ID af6c91dd-61ea-46a3-b468-da12dfcb64ea
Taxonomy Nucleosides, nucleotides, and analogues > Purine nucleosides
IUPAC Name 2-[5-[[5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy]-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-4-phosphonooxyhexanedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H32N5O19P/c23-17-7-18(25-3-24-17)27(4-26-7)19-10(31)8(29)6(43-19)2-42-14-5(1-28)44-22(11(32)9(14)30)45-16(21(37)38)12(33)15(13(34)20(35)36)46-47(39,40)41/h3-6,8-16,19,22,28-34H,1-2H2,(H,35,36)(H,37,38)(H2,23,24,25)(H2,39,40,41)
InChI Key OTLLEIBWKHEHGU-UHFFFAOYSA-N
Popularity 5,164 references in papers

Physical and Chemical Properties

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Molecular Formula C22H32N5O19P
Molecular Weight 701.50 g/mol
Exact Mass 701.14291081 g/mol
Topological Polar Surface Area (TPSA) 390.00 Ų
XlogP -7.00
Atomic LogP (AlogP) -6.39
H-Bond Acceptor 20
H-Bond Donor 12
Rotatable Bonds 14

Synonyms

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23526-02-5
Bacillus thuringiensis B toxin
NSC197177
.beta.-Exotoxin
NSC-197177
CERAPP_20701
SCHEMBL5934015
Bacillus thuringensis B exotoxin
Thuringiensin, calcium technical
CHEMBL1988470
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Exotoxin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6723 67.23%
Caco-2 - 0.8817 88.17%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.3330 33.30%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8963 89.63%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6151 61.51%
P-glycoprotein inhibitior + 0.6060 60.60%
P-glycoprotein substrate + 0.5366 53.66%
CYP3A4 substrate + 0.6518 65.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8748 87.48%
CYP3A4 inhibition - 0.7347 73.47%
CYP2C9 inhibition - 0.8997 89.97%
CYP2C19 inhibition - 0.8904 89.04%
CYP2D6 inhibition - 0.8935 89.35%
CYP1A2 inhibition - 0.8274 82.74%
CYP2C8 inhibition + 0.5829 58.29%
CYP inhibitory promiscuity - 0.9000 90.00%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5475 54.75%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.9180 91.80%
Skin irritation - 0.7590 75.90%
Skin corrosion - 0.9256 92.56%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4161 41.61%
Micronuclear + 1.0000 100.00%
Hepatotoxicity - 0.5968 59.68%
skin sensitisation - 0.8361 83.61%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.8556 85.56%
Acute Oral Toxicity (c) II 0.7380 73.80%
Estrogen receptor binding + 0.7679 76.79%
Androgen receptor binding + 0.5943 59.43%
Thyroid receptor binding + 0.5561 55.61%
Glucocorticoid receptor binding + 0.6151 61.51%
Aromatase binding + 0.6204 62.04%
PPAR gamma + 0.6663 66.63%
Honey bee toxicity - 0.7204 72.04%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.7162 71.62%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.89% 96.09%
CHEMBL3137261 O14744 PRMT5/MEP50 complex 95.09% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.43% 91.11%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 91.51% 86.92%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 89.33% 80.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.79% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.88% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.56% 99.23%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 85.74% 96.47%
CHEMBL3401 O75469 Pregnane X receptor 85.35% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.86% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.70% 96.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 84.02% 97.36%
CHEMBL4523377 Q86WV6 Stimulator of interferon genes protein 83.87% 95.48%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.78% 94.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.73% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.65% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.62% 95.89%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 82.08% 82.50%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.07% 100.00%
CHEMBL5524 Q99873 Protein-arginine N-methyltransferase 1 81.87% 96.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.23% 94.00%
CHEMBL279 P35968 Vascular endothelial growth factor receptor 2 80.57% 95.52%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.47% 100.00%

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.
There are no matching plants.

Cross-Links

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PubChem 304586
LOTUS LTS0028524
wikiData Q105199679