![5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F277394-5h-pyrrolo-34-b-pyridine-57-6h-dione.webp&w=3840&q=75)
CAS 4664-00-0: 5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione
Formula:C7H4N2O2
InChI:InChI=1S/C7H4N2O2/c10-6-4-2-1-3-8-5(4)7(11)9-6/h1-3H,(H,9,10,11)
InChI key:InChIKey=ZRKGTINFVOLLNT-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)N1)=NC=CC2
Synonyms:- 1H-pyrrolo[3,4-c]pyridine-1,3(2H)-dione
- 2,3-Pyridinecarboximide
- 2,3-Pyridinedicarboximide
- 5H-pyrrolo[3,4-b]pyridine-5,7(6H)-dione
- NSC 405554
- Pyrrolo[3,4-b]pyridine-5,7-dione
- Quinolinimide
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Found 5 products.
5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione
CAS:5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dionePurity:95%Molecular weight:148.12g/mol5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:148.12100219726562Quinolinimide
CAS:Quinolinimide is a terpene with a fatty acid side chain and an anilino group. It is synthesized from choline by pyridoxal phosphate-dependent enzyme, quinolinic acid synthetase. Quinolinimide has been shown to be active against the Na+ channel in nerve cells, which is responsible for the passage of ions across the membrane. This results in depolarization of the nerve cell and an increase in acetylcholine release. Quinolinimide blocks the Na+ channel by binding to the terminal residues on its outer surface, which prevents ion flow across the membrane and leads to paralysis.Formula:C7H4N2O2Purity:Min. 95%Color and Shape:PowderMolecular weight:148.12 g/molRef: 3D-FQ27388
Discontinued product5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione
CAS:Formula:C7H4N2O2Purity:98%Color and Shape:SolidMolecular weight:148.1189