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  2. Sonrotoclax - Wikipedia

    en.wikipedia.org/wiki/Sonrotoclax

    Sonrotoclax is an investigational new drug that is being evaluated for the treatment of hematologic malignancies, particularly chronic lymphocytic leukemia (CLL) and small lymphocytic lymphoma (SLL). [1]

  3. Benzamide - Wikipedia

    en.wikipedia.org/wiki/Benzamide

    Benzamide is an organic compound with the chemical formula of C 7 H 7 NO. It is the simplest amide derivative of benzoic acid. In powdered form, it appears as a white solid, while in crystalline form, it appears as colourless crystals. [5] It is slightly soluble in water, [2] and soluble in many organic solvents. [6]

  4. U-77891 - Wikipedia

    en.wikipedia.org/wiki/U-77891

    U-77891 is an opioid analgesic drug that was first synthesized in 1983 by the Upjohn company. [1] It was originally synthesized to prove that the removal of a single methylene spacer of the benzamide would alter a κ-opioid receptor agonist such as U-50488 into an μ-opioid receptor agonist, as well as producing a semi-rigid derivative of U-47700.

  5. GR-55562 - Wikipedia

    en.wikipedia.org/wiki/GR-55562

    The drug is a silent antagonist of the serotonin 5-HT 1B receptor, unlike the related agent GR-127935. [1] [4] GR-55562 has around 10-fold selectivity for the serotonin 5-HT 1B receptor over the serotonin 5-HT 1D receptor and has only weak affinity for a number of other serotonin receptors. [4]

  6. Tucidinostat - Wikipedia

    en.wikipedia.org/wiki/Tucidinostat

    Tucidinostat (INN, also known as chidamide and sold under the brand names Epidaza and Hiyasta) is a histone deacetylase inhibitor (HDI) developed in China. [1] It was also known as HBI-8000 . [ 2 ] It is a benzamide HDI and inhibits Class I HDAC1 , HDAC2 , HDAC3 , as well as Class IIb HDAC10 .

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  8. Sultopride - Wikipedia

    en.wikipedia.org/wiki/Sultopride

    Sultopride (trade names Barnetil, Barnotil, Topral) is an atypical antipsychotic of the benzamide chemical class used in Europe, Japan, and Hong Kong for the treatment of schizophrenia. [2] [3] [4] It was launched by Sanofi-Aventis in 1976. [2] Sultopride acts as a selective D 2 and D 3 receptor antagonist. [5]

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