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  2. 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 .

  3. Benzamide - Wikipedia

    en.wikipedia.org/wiki/Benzamide

    55-21-0 3D model ... 1.341 g/cm 3: Melting point: 127 to 130 °C (261 to 266 °F; 400 to 403 K) ... Benzamide is an organic compound with the chemical formula of C 7 ...

  4. Lisaftoclax - Wikipedia

    en.wikipedia.org/wiki/Lisaftoclax

    Lisaftoclax is an investigational new drug being developed by Ascentage Pharma for the treatment of hematological malignancies, particularly chronic lymphocytic leukemia (CLL) and small lymphocytic lymphoma (SLL).

  5. Benzamidine - Wikipedia

    en.wikipedia.org/wiki/Benzamidine

    Benzamidine is an organic compound with the formula C 6 H 5 C(NH)NH 2. It is the simplest aryl amidine. The compound is a white solid that is slightly soluble in water. It is usually handled as the hydrochloride salt, a white, water-soluble solid. [2]

  6. Category:Benzamides - Wikipedia

    en.wikipedia.org/wiki/Category:Benzamides

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  7. 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.

  8. Sulfabenzamide - Wikipedia

    en.wikipedia.org/wiki/Sulfabenzamide

    This systemic antibiotic -related article is a stub. You can help Wikipedia by expanding it.

  9. Trimethobenzamide - Wikipedia

    en.wikipedia.org/wiki/Trimethobenzamide

    Alkylation of the sodium salt of p-hydroxybenzaldehyde (1) with 2-dimethylaminoethyl chloride affords the ether (2). Reductive amination of the aldehyde in the presence of ammonia gives diamine (3). Acylation of that product with 3,4,5-trimethoxybenzoyl chloride affords trimethobenzamide (4).