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Catalogue Number |
Product | Order number / Unit |
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6500 | Dimethyl-8-acetyl-hexahydropyrrolo[2,3]indol-1,2-dicarboxylate |
6500.0010: 10 mg per vial
Please inquire for customized filling and bulk quantities. ![]() |
Precursor for α-[11C]Methyl-L-tryptophan
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Molar Mass: 318.32 | ||
C16H18N2O5 | ||
[79465-83-1] | ||
Colourless crystals packaged in dark glass screw cap vials. | ||
Purity: > 95 % | ||
Certificates:
CoA; 1H NMR spectrum |
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Chemical Name: CA index name: Pyrrolo[2,3-b]indole-1,2(2H)-dicarboxylic acid, 8-acetyl-3,3a,8,8a-tetrahydro-, dimethyl ester, (2α,3a beta,8a beta)- |
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Synonymes: Dimethyl-(2S, 3aR, 8aS)-8-acetyl-1,2,3,3a,8a-hexahydropyrrolo[2,3]indol-1,2-dicarboxylate |
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Literature: Shoaf S. et al. The suitability of [11C]-α-methyl-L-tryptophan as a tracer for serotonin synthesis: studies with dual administration of [11C]- and [14C]-labeled tracer. J. Cereb. Blood Flow Metab. 2000, 20, 244-252. |
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Shoaf S. et al. Brain serotonin synthesis rates in rhesus monkeys determined by [11C]-α-methyl-L-tryptophan and positron emission tomography compared to CSF 5-hydroxyindole-3-acetic acid concentrations. Neuropsychopharmacology 1998, 19, 354-353. | ||
Chakraborty P.K. et al. A high-yield and simplified procedure for the synthesis of α-[11C]methyl-L-tryptophan. Nucl. Med. Biol. 1996, 23, 1005-1008. | ||
Mzengeza S. et al. Asymmetric radiosynthesis of α-[11C]methyl-L-tryptophan for PET studies. Nucl. Med. Biol. 1995, 22, 303-307. | ||
date of product catalogue issue: 10 May 2017 |