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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766173Generated: October 25, 2026

NADPH → HCID 178513078, compound

https://huagongshe.com/reaction/1766173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNADPHHCID 5884—
ReactantUdp-glucuronic acidHCID 17473—
ReactantMagnesium ChlorideHCID 5360315—
ReactantHCID 178513073HCID 178513073—
SolventAcetonitrileHCID 6342—
ProductHCID 178513078HCID 178513078—

Reaction Steps

4.8 mg of N-(1-quinolin-4-yl-1H-pyrrolo[2,3-b]pyridine-3-carbonyl)-guanidine were dissolved using 150 ml of an aqueous solution containing 381 mg MgCl2, 1.3 mM NADPH (Dihydronicotinamide adenine dinucleotide phosphate, Calbiochem product number: 481973; Shen, A. L., et al. 1989. J. Biol. Chem. 264, 7584; Yamano, S., et al. 1989. Mol. Pharmacol. 36, 83.), 300 mg of human S9 fraction and 2.5 mM UDPGA (Uridine 5′-diphosphoglucuronic acid trisodium salt, Sigma catalog number U6751). The mixture was incubated for 120 minutes at 37° C. Then, 40 ml of acetonitrile were added, proteins centrifuged and decanted. This solution was concentrated to 100 ml and chromatographed using the system described below. The solvents were removed under reduced pressure to yield 0.9 mg of N-[1-(2-hydroxy-quinolin-4-yl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-guanidine as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230007B2
Source datasetuspto-grants-2007_06
ORD IDord-b68fa4f6388441388165def11d5c1e30
Source noteuspto-grants-2007_06