Lumazine

Details

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Internal ID de1c0518-db8d-4a08-b757-87f2888bbe5f
Taxonomy Organoheterocyclic compounds > Pteridines and derivatives
IUPAC Name 1H-pteridine-2,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H4N4O2/c11-5-3-4(8-2-1-7-3)9-6(12)10-5/h1-2H,(H2,8,9,10,11,12)
InChI Key UYEUUXMDVNYCAM-UHFFFAOYSA-N
Popularity 368 references in papers

Physical and Chemical Properties

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Molecular Formula C6H4N4O2
Molecular Weight 164.12 g/mol
Exact Mass 164.03342538 g/mol
Topological Polar Surface Area (TPSA) 84.00 Ų
XlogP -1.00
Atomic LogP (AlogP) -0.99
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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487-21-8
2,4-DIHYDROXYPTERIDINE
2,4-Pteridinediol
2,4(1H,3H)-Pteridinedione
pteridine-2,4(1H,3H)-dione
Lumazin
pteridine-2,4-diol
1H-pteridine-2,4-dione
Pteridine-2,4-dione
2,4(3H,8H)-Pteridinedione
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Lumazine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 - 0.8991 89.91%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.5526 55.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9731 97.31%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8598 85.98%
P-glycoprotein inhibitior - 0.9881 98.81%
P-glycoprotein substrate - 0.9504 95.04%
CYP3A4 substrate - 0.7325 73.25%
CYP2C9 substrate - 0.6203 62.03%
CYP2D6 substrate - 0.8687 86.87%
CYP3A4 inhibition - 0.9594 95.94%
CYP2C9 inhibition - 0.9070 90.70%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9479 94.79%
CYP1A2 inhibition + 0.9107 91.07%
CYP2C8 inhibition - 0.9665 96.65%
CYP inhibitory promiscuity - 0.9778 97.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8923 89.23%
Carcinogenicity (trinary) Non-required 0.6830 68.30%
Eye corrosion - 0.9882 98.82%
Eye irritation + 0.5365 53.65%
Skin irritation - 0.8898 88.98%
Skin corrosion - 0.9712 97.12%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6998 69.98%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.8250 82.50%
skin sensitisation - 0.9298 92.98%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.7038 70.38%
Acute Oral Toxicity (c) III 0.6271 62.71%
Estrogen receptor binding - 0.8753 87.53%
Androgen receptor binding - 0.7352 73.52%
Thyroid receptor binding - 0.6232 62.32%
Glucocorticoid receptor binding - 0.8810 88.10%
Aromatase binding - 0.4858 48.58%
PPAR gamma - 0.6932 69.32%
Honey bee toxicity - 0.9051 90.51%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity - 0.8570 85.70%

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
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 98.26% 95.72%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.92% 94.45%
CHEMBL255 P29275 Adenosine A2b receptor 91.52% 98.59%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 90.28% 89.34%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.84% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.66% 99.23%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 85.60% 85.30%
CHEMBL308 P06493 Cyclin-dependent kinase 1 84.34% 91.73%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 84.27% 91.67%
CHEMBL2424504 P29375 Lysine-specific demethylase 5A 83.25% 99.23%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 83.06% 88.84%
CHEMBL1937 Q92769 Histone deacetylase 2 82.98% 94.75%
CHEMBL3038469 P24941 CDK2/Cyclin A 82.70% 91.38%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 82.14% 92.88%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.88% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.59% 94.00%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 80.88% 93.24%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 80.76% 96.47%
CHEMBL2535 P11166 Glucose transporter 80.69% 98.75%

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 10250
LOTUS LTS0182033
wikiData Q17189420