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    Home > Pharmaceutical Intermediates > Anticonvulsants (Find 18 items)

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    Anticonvulsants

    L-Leucine

    (61-90-5)
    Leucine (abbreviated as Leu or L; encoded by the six codons UUA, UUG, CUU, CUC, CUA, and CUG) is an α-amino acid used in the biosynthesis of proteins. It contains an α-amino group (which is in the protonated −NH+ 3 form under biological conditions), an α-carboxylic acid group (which is in the deprotonated −COO− form under biological conditions), and an isobutyl side chain, classifying it as a nonpolar (at physiological pH) amino acid. It is essential in humans—meaning the body cannot synthesize it and thus must obtain from the diet.Leucine is a major component of the subunits in ferritin, astacin, and other "buffer" proteins.

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    N-Hydroxysuccinimide

    (6066-82-6)
    Additive used in the carbodiimide method for improved amidations and peptide couplings.

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    L-2-Aminobutanamidehydrochloride

    (7682-20-4)
    Levetiracetam intermediate

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    Oxcarbazepine

    (28721-07-5)
    The keto derivative of Carbamazepine. Used as an anticonvulsant

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    BOC-Glycine

    (4530-20-5)
    Used in the composition of drugs containing Ketoprofen, and Sodium hyaluronate as antiinflammatory agents.

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    Benzyl2-bromoacetate

    (5437-45-6)
    Colorless to light yellow liqui

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    (R)-Benzyloxymethyl-oxirane

    (14618-80-5)
    Used in the preparation of lactone fragments of compadine and lovastatin. 1 Preparation of cis-1,3-polyol, 2 dideoxy nucleoside 3 and spiroacetal cyanohydrin chiral.

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    Ethyl propionylacetate

    (4949-44-4)
    An intermediate of Rosuvastatin.

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    10,11-DIHYDRO-10-HYDROXYCARBAZEPINE

    (29331-92-8)
    10,11-dihydro-10-hydroxy Carbamazepinee is the active metabolite of oxcarbazepine . Oxcarbazepine is rapidly and almost completely converted to 10,11-dihydro-10-hydroxycarbamazepine, which then demonstrates anticonvulsant efficacy by modulating several ion channels and receptors. ?10,11-dihydro-10-hydroxy Carbamazepine is reported to inhibit both voltage-gated Na+ and Ca2+ channels, to potentiate voltage-gated K+ channels, to antagonize adenosine A1 receptors, to increase dopaminergic transmission, and to inhibit glutamate release.

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    2-Pyridylacetic acid hydrochloride

    (16179-97-8)
    Used in nucleophilic substitution

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    Anticonvulsants Intermediates are some key chemical raw materials or products in the synthesis process of anticonvulsant drugs. You can easily find high-quality new anticonvulsants intermediates, products and their manufacturers or suppliers on Echemi. We will continue to track the research and development of new products on anticonvulsant medicine.

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