2-Amino-4,6-dihydroxypteridine

AlkaPlorer ID: AK054087

Synonym: 2-Amino-1,5-dihydro-4,6-pteridinedione, Xanthopterin, Uropterin

IUPAC Name: 2-amino-3,5-dihydropteridine-4,6-dione

Structure

SMILES: NC1=NC(O)=C2NC(=O)C=NC2=N1

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InChI: InChI=1S/C6H5N5O2/c7-6-10-4-3(5(13)11-6)9-2(12)1-8-4/h1H,(H,9,12)(H3,7,8,10,11,13)

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InChIKey: VURKRJGMSKJIQX-UHFFFAOYSA-N

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Properties Information

Molecule Weight: 179.13899999999998

TPSA: 117.78

MolLogP: -0.9991000000000004

Number of H-Donors: 3

Number of H-Acceptors: 6

RingCount: 2

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Homo sapiens 15-hydroxyprostaglandin dehydrogenase [NAD+] Potency 28183.8 nM None
Homo sapiens Aldehyde dehydrogenase 1A1 Potency 28183.8 nM None
Homo sapiens Endoplasmic reticulum-associated amyloid beta-peptide-binding protein Potency 25118.9 nM None
Homo sapiens Lysine-specific demethylase 4D-like Potency 3548.1 nM None
Homo sapiens Menin/Histone-lysine N-methyltransferase MLL Potency 17782.8 nM None
Homo sapiens Microtubule-associated protein tau Potency 3981.1 nM None
Homo sapiens Solute carrier organic anion transporter family member 1B1 Inhibition 104.4 % 10.1124/mol.112.084152
Homo sapiens Solute carrier organic anion transporter family member 1B3 Inhibition 104.74 % 10.1124/mol.112.084152
Homo sapiens Thyroid hormone receptor beta-1 Potency 35.5 nM None
Homo sapiens Tyrosyl-DNA phosphodiesterase 1 Potency 14581.0 nM None

Metabolism Information

AKRT ID Reaction Reaction Link ID
AKRT016345 N=c1[nH]c(=O)c2[nH]c(=O)cnc2[nH]1>>O=c1cnc2[nH]c(=O)[nH]c(=O)c2[nH]1 enzymemap_79069
AKRT016756 N=c1nc(O)c2[nH]c(=O)cnc2[nH]1>>O=c1cnc2nc(O)nc(O)c2[nH]1 MNXR172124