Adenylosuccinic acid tetraammonium

• CAT Number: I043587
• Molecular Formula: C14H30N9O11P
• Molecular Weight: 531.42
• Purity: ≥95%
• Synonyms: azane;(2S)-2-[[9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(phosphonooxymethyl)oxolan-2-yl]purin-6-yl]amino]butanedioic acid
• InChI: InChI=1S/C14H18N5O11P.4H3N/c20-7(21)1-5(14(24)25)18-11-8-12(16-3-15-11)19(4-17-8)13-10(23)9(22)6(30-13)2-29-31(26,27)28;;;;/h3-6,9-10,13,22-23H,1-2H2,(H,20,21)(H,24,25)(H,15,16,18)(H2,26,27,28);4*1H3/t5-,6+,9+,10+,13+;;;;/m0..../s1
• InChIKey: XCLZBEXZAOLWGA-BFHDGDRYSA-N
• SMILES: C1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)N[C@@H](CC(=O)O)C(=O)O.N.N.N.N

Adenylosuccinic acid tetraammonium（Cat No.:I043587）is a salt form of adenosuccinic acid, which is a derivative of purine metabolism. It contains four ammonium ions that enhance its solubility in aqueous solutions, making it suitable for various biochemical studies. Adenylosuccinic acid plays a role in the biosynthesis of purine nucleotides and is involved in cellular energy metabolism. The tetraammonium form is typically used in laboratory research to explore its interactions with enzymes or receptors involved in nucleotide metabolism, energy transfer, and cellular signaling, with potential applications in drug development and metabolic disorder studies.