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  2. Serdexmethylphenidate - Wikipedia

    en.wikipedia.org/wiki/Serdexmethylphenidate

    Serdexmethylphenidate is a prodrug of dexmethylphenidate created by the pharmaceutical company KemPharm (now Zevra Therapeutics). The compound was first approved by the FDA as one of the active ingredients in Azstarys for the treatment of attention deficit hyperactivity disorder (ADHD) in children, adolescents, and adults in March 2021.

  3. α-Pyrrolidinohexiophenone - Wikipedia

    en.wikipedia.org/wiki/Α-Pyrrolidinohexiophenone

    α-Pyrrolidinohexiophenone is a longer chain homologue of α-PVP, having an extra carbon on the alkyl side chain.Regarding the potency of alpha-PHP in the brain, chemist Michael H. Baumann of the Designer Drug Research Unit (established by Baumann [8]) of the National Institute on Drug Abuse stated: "alpha-PHP might be even more potent than alpha-PVP"; this statement is based on laboratory ...

  4. Serdexmethylphenidate/dexmethylphenidate - Wikipedia

    en.wikipedia.org/wiki/Serdexmethylphenidate/dex...

    This page was last edited on 16 October 2024, at 16:04 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  5. Prodrug - Wikipedia

    en.wikipedia.org/wiki/Prodrug

    A prodrug is a pharmacologically inactive medication or compound that, after intake, is metabolized (i.e., converted within the body) into a pharmacologically active drug. [1] [2] Instead of administering a drug directly, a corresponding prodrug can be used to improve how the drug is absorbed, distributed, metabolized, and excreted . [3] [4]

  6. α-PHiP - Wikipedia

    en.wikipedia.org/wiki/Α-PHiP

    In July 2016 α-PiHP was first identified as a designer drug [2] when it was reported to the EMCDDA by a forensic laboratory in Slovenia. [3] [4] It is a positional isomer of pyrovalerone, with the methyl group shifted from the 4-position of the aromatic ring to the 4-position of the acyl chain. Similarly to other cathinones, use of α-PiHP can ...

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  8. DEPT (medicine) - Wikipedia

    en.wikipedia.org/wiki/DEPT_(medicine)

    In CDEPT, a prodrug-converting enzyme expressed by a clostridial expression plasmid converts a prodrug into an active drug form within the tumor. While the prodrug is the inactive form and can be administrated to the blood, the products of the prodrug cleavage are highly cytotoxic and show their effect only in the vicinity of tumor cells.

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