Alloxantin

Details

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Internal ID 26be1461-ff3e-468c-b597-1b51e86f3ae1
Taxonomy Organoheterocyclic compounds > Diazines > Pyrimidines and pyrimidine derivatives > Pyrimidones > Barbituric acid derivatives
IUPAC Name 5-hydroxy-5-(5-hydroxy-2,4,6-trioxo-1,3-diazinan-5-yl)-1,3-diazinane-2,4,6-trione
SMILES (Canonical) C1(=O)C(C(=O)NC(=O)N1)(C2(C(=O)NC(=O)NC2=O)O)O
SMILES (Isomeric) C1(=O)C(C(=O)NC(=O)N1)(C2(C(=O)NC(=O)NC2=O)O)O
InChI InChI=1S/C8H6N4O8/c13-1-7(19,2(14)10-5(17)9-1)8(20)3(15)11-6(18)12-4(8)16/h19-20H,(H2,9,10,13,14,17)(H2,11,12,15,16,18)
InChI Key IWDDXZKCDHOOSF-UHFFFAOYSA-N
Popularity 128 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6N4O8
Molecular Weight 286.16 g/mol
Exact Mass 286.01856316 g/mol
Topological Polar Surface Area (TPSA) 191.00 Ų
XlogP -4.00
Atomic LogP (AlogP) -4.82
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 1

Synonyms

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Uroxine
Uroxin
76-24-4
LTL3CDV62U
5-hydroxy-5-(5-hydroxy-2,4,6-trioxo-1,3-diazinan-5-yl)-1,3-diazinane-2,4,6-trione
5,5'-Bibarbituric acid, 5,5'-dihydroxy-
NSC-7634
5,5'-Dihydroxy-5,5'-bibarbituric acid
DTXSID3058795
[5,5'-Bipyrimidine]-2,2',4,4',6,6'(1H,1'H,3H,3'H,5H,5'H)-hexone, 5,5'-dihydroxy-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Alloxantin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6238 62.38%
Caco-2 - 0.8530 85.30%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.9000 90.00%
Subcellular localzation Mitochondria 0.7561 75.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9726 97.26%
OATP1B3 inhibitior + 0.9512 95.12%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9738 97.38%
P-glycoprotein inhibitior - 0.9003 90.03%
P-glycoprotein substrate - 0.9890 98.90%
CYP3A4 substrate - 0.7584 75.84%
CYP2C9 substrate + 0.6092 60.92%
CYP2D6 substrate - 0.8543 85.43%
CYP3A4 inhibition - 0.9144 91.44%
CYP2C9 inhibition - 0.9093 90.93%
CYP2C19 inhibition - 0.8784 87.84%
CYP2D6 inhibition - 0.9445 94.45%
CYP1A2 inhibition - 0.8633 86.33%
CYP2C8 inhibition - 0.9953 99.53%
CYP inhibitory promiscuity - 0.9709 97.09%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.7399 73.99%
Eye corrosion - 0.9903 99.03%
Eye irritation + 0.6448 64.48%
Skin irritation - 0.7876 78.76%
Skin corrosion - 0.9476 94.76%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7208 72.08%
Micronuclear + 0.9300 93.00%
Hepatotoxicity + 0.8231 82.31%
skin sensitisation - 0.8753 87.53%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.5911 59.11%
Acute Oral Toxicity (c) III 0.5102 51.02%
Estrogen receptor binding + 0.6275 62.75%
Androgen receptor binding - 0.5772 57.72%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.5219 52.19%
Aromatase binding - 0.5679 56.79%
PPAR gamma + 0.5826 58.26%
Honey bee toxicity - 0.9443 94.43%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.9160 91.60%

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 91.96% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 87.26% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.74% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.36% 95.56%
CHEMBL4208 P20618 Proteasome component C5 83.43% 90.00%

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 6435
LOTUS LTS0260961
wikiData Q27283170