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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881205Generated: October 26, 2026

Methylene blue cation → 1H-Indolamine

https://huagongshe.com/reaction/881205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylene blue cationHCID 4139—
ReactantD-TryptophanHCID 9060—
ReactantHCID 178519208HCID 178519208—
SolventPotassium Phosphate, TribasicHCID 62657—
Product1H-IndolamineHCID 122074—

Reaction Steps

Human indoleamine 2,3-dioxygenasae (IDO) with an N-terminal His tag was expressed in E. coli and purified to homogeneity. IDO catalyzes the oxidative cleavage of the pyrrole ring of the indole nucleus of tryptophan to yield N′-formylkynurenine. The assays were performed at room temperature as described in the literature using 95 nM IDO and 2 mM D-Trp in the presence of 20 mM ascorbate, 5 μM methylene blue and 0.2 mg/mL catalase in 50 mM potassium phosphate buffer (pH 6.5). The initial reaction rates were recorded by continuously following the absorbance increase at 321 nm due to the formation of N′-formlylkynurenine (See: Sono, M., et al., 1980, J. Biol. Chem. 255, 1339-1345).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993605B2
Source datasetuspto-grants-2015_03
ORD IDord-d0f2b1425b584cc7b84fee160fd8dd07
Source noteuspto-grants-2015_03