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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937438Generated: November 2, 2026

Octahydroindolizine-1,2,8-triol → Swainsonine

https://huagongshe.com/reaction/1937438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctahydroindolizine-1,2,8-triolHCID 5363—
Reactant4-Nitrophenyl-alpha-D-mannopyranosideHCID 82579—
ReactantSodium AcetateHCID 517045—
ProductSwainsonineHCID 51683—

Reaction Steps

The test compound swainsonine is prepared by 0.4 serial dilution of a 40 μM stock. Present in each determination is 10 μl diluted test compound, 25 μl of 10 mM paranitrophenyl mannopyranoside, 200 mM sodium acetate, pH 5.6 and 15 μl of purified rat liver Golgi mannosidase II. After incubating the reaction for 60 minutes at 37° C., the reaction is quenched with 50 μl of 0.5 M sodium carbonate. Absorption is read at 405 mn. After subtracting the blank from positive controls and samples, the samples are normalized against the positive control mean using a variable slope, sigmoidal curve fit, with bottom=0, top=100. The signal is proportional to the amount of products from the uninhibited reaction. The calculated IC50 for inhibition of purified Golgi mannosidase II by swainsonine hydrochloride is 0.068±0.021 μM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395745B1
Source datasetuspto-grants-2002_05
ORD IDord-390f28a4e5d1494399de28e0502f3451
Source noteuspto-grants-2002_05