36408-16-9
Chemical Structure
5-Deaza-FMN
Synonym(s): 5-Deazaflavin mononucleotide
- CAS No.: 36408-16-9
- Formula:C18H22N3O9P
- Molecular Weight:455.36
IUPAC Name: (2R,3S,4S)-5-(7,8-dimethyl-2,4-dioxo-3,4-dihydropyrimido[4,5-b]quinolin-10(2H)-yl)-2,3,4-trihydroxypentyl dihydrogen phosphate
InChIKey: LAWFKZVKVIYTAR-ZNMIVQPWSA-N
SMILES: O=P(O)(O)OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C2=CC(C)=C(C)C=C2C=C3C1=NC(NC3=O)=O
Biological Activity: 5-Deaza-FMN (5-Deazaflavin mononucleotide) is a binder of type II isopentenyl diphosphate: dimethylallyl diphosphate isomerase (IDI-2) with a Kd value of 16 μM. 5-Deaza-FMN acts as a radical generator, forming radicals through photoinduced single-electron transfer of tryptophan. 5-Deaza-FMN finds applications in biocatalysis and photocatalysis[1][2].
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5-Deaza-FMN | 5-Deaza-FMN (5-Deazaflavin mononucleotide) is a binder of type II isopentenyl diphosphate: dimethylallyl diphosphate isomerase (IDI-2) with a Kd value of 16 μM. 5-Deaza-FMN acts as a radical generator, forming radicals through photoinduced single-electron transfer of tryptophan. 5-Deaza-FMN finds applications in biocatalysis and photocatalysis. | |||||||||||||||||||||
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References
- [1]. Kittleman W, et al. Characterization and mechanistic studies of type II isopentenyl diphosphate:dimethylallyl diphosphate isomerase from Staphylococcus aureus. Biochemistry. 2007 Jul 17;46(28):8401-13. [Content Brief]
- [2]. Panter S, et al. Unraveling the 13C Hyperfine Structure of the 5‐Deazaflavin Radical in Solution Using Photo‐CIDNP Spectroscopy. ChemPhotoChem. 2026 Jun;10(6):e202500377.
