| Weight | 463.296 g/mol |
|---|---|
| Formula | C14H18N5O11P |
| Hydrogen Acceptors | 12 |
| Hydrogen Donors | 7 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 9 |
Adenylsuccinic acid (19240-42-7, 19046-78-7)
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- Adenine succinic acid and adenylsuccinic acid from mammalian liver: isolation and identification. (Biochemical Journal, 1957)
- Nucleotides of microorganisms. II. Isolation of adenylsuccinic acid and adenosinosuccini acid from the mycelium of Penicillium chrysogenum Thom (Annali dell'Istituto Superiore di Sanit, 1961)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=NC2=C(C(=N1)NC(CC(=O)O)C(=O)O)N=CN2C3C(C(C(O3)COP(=O)(O)O)O)O
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InChIKeyOFBHPPMPBOJXRT-UHFFFAOYSA-N
- Pubchem - Adenylsuccinic acid
- Wikipedia - N(6)-(1,2-dicarboxyethyl)-AMP
Adenylosuccinate is an intermediate in the interconversion of purine nucleotides inosine monophosphate (IMP) and adenosine monophosphate (AMP). The enzyme adenylosuccinate synthase carries out the reaction by the addition of aspartate to IMP and requires the input of energy from a phosphoanhydride bond in the form of guanosine triphosphate (GTP). GTP is used instead of adenosine triphosphate (ATP), so the reaction is not dependent on its products.
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