2-Amino-3,4a,8,8a-tetrahydropteridine-4,7-dione

Details

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Internal ID c8ae1164-ad53-4b98-a05c-97b9814d4f41
Taxonomy Organoheterocyclic compounds > Pteridines and derivatives > Pterins and derivatives
IUPAC Name 2-amino-3,4a,8,8a-tetrahydropteridine-4,7-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H7N5O2/c7-6-10-4-3(5(13)11-6)8-1-2(12)9-4/h1,3-4H,(H,9,12)(H3,7,10,11,13)
InChI Key CMOXKYQQTMHEHE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H7N5O2
Molecular Weight 181.15 g/mol
Exact Mass 181.05997448 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP -2.30
Atomic LogP (AlogP) -2.67
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Amino-3,4a,8,8a-tetrahydropteridine-4,7-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9838 98.38%
Caco-2 - 0.7018 70.18%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.4400 44.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9585 95.85%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9682 96.82%
P-glycoprotein inhibitior - 0.9690 96.90%
P-glycoprotein substrate - 0.8209 82.09%
CYP3A4 substrate - 0.5996 59.96%
CYP2C9 substrate - 0.5928 59.28%
CYP2D6 substrate - 0.8528 85.28%
CYP3A4 inhibition - 0.9815 98.15%
CYP2C9 inhibition - 0.9482 94.82%
CYP2C19 inhibition - 0.9071 90.71%
CYP2D6 inhibition - 0.9393 93.93%
CYP1A2 inhibition - 0.6997 69.97%
CYP2C8 inhibition - 0.8430 84.30%
CYP inhibitory promiscuity - 0.9931 99.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6663 66.63%
Eye corrosion - 0.9849 98.49%
Eye irritation - 0.9288 92.88%
Skin irritation - 0.7515 75.15%
Skin corrosion - 0.9482 94.82%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7543 75.43%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8999 89.99%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.5732 57.32%
Acute Oral Toxicity (c) III 0.6082 60.82%
Estrogen receptor binding - 0.8809 88.09%
Androgen receptor binding - 0.6538 65.38%
Thyroid receptor binding - 0.5346 53.46%
Glucocorticoid receptor binding - 0.6670 66.70%
Aromatase binding + 0.5452 54.52%
PPAR gamma - 0.7833 78.33%
Honey bee toxicity - 0.8401 84.01%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity - 0.9690 96.90%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 88.82% 89.34%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.19% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 84.52% 90.17%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 81.28% 93.40%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.24% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.22% 95.56%

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.
Litsea verticillata
Sophora flavescens

Cross-Links

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PubChem 57336529
NPASS NPC274405