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n =35), neopterin ( r =0.5

The molecule has two asymmetric carbons at the 3 and 3 positions on the -ionone rings, giving rise to three optical stereoisomers: (3S,3S), (3R,3R), and the meso form (3R,3S)

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Moreover, understanding differences in sample preparation, such as treatment with glucuronidase or sulfatase, as well as the analytical instrumentation applied are critical