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  4. Baphicacanthus cusia (Nees) Bremek.

Baphicacanthus cusia (Nees) Bremek.

Baphicacanthus cusia (Nees) Bremek. (3):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-W018800
    4(3H)-Quinazolinone 491-36-1 99.91%
    4(3H)-Quinazolinone, oral bioavailability and low clearance, is biologically active nitrogen heterocyclic compounds. 4(3H)-Quinazolinone possesses a wide spectrum of biological properties like antibacterial, antifungal, anticonvulsant, anti-inflammatory, anticancerous and analgesic activities. 4(3H)-Quinazolinone is non-β-lactam antibacterials active against Staphylococcus Aureus (MRSA), which target cell-wall biosynthesis. 4(3H)-Quinazolinone synergized with piperacillin-tazobactam (TZP) can kill MRSA in a bactericidal manner. Additionally, 4(3H)-Quinazolinone shows typical apoptotic morphology and exerts anti-cancer activity through EGFR kinase inhibition in cancer cell lines. 4(3H)-Quinazolinone is a promising candidate for research in bacteria-related diseases and new chemotherapeutic agents
  • HY-N1836
    3-Acetonyl-3-hydroxyoxindole 33417-17-3
    3-Acetonyl-3-hydroxyoxindole (AHO) is a potent systemic acquired resistance (SAR) inducer in plants. 3-Acetonyl-3-hydroxyoxindole induces resistance in tobacco plants against infection with tobacco mosaic virus (TMV) and the fungal pathogen Erysiphe cichoracearum. 3-Acetonyl-3-hydroxyoxindole increases the level of pathogenesis-related gene 1 (PR-1) expression, salicylic acid (SA) accumulation and phenylalanine ammonia-lyase activity.
  • HY-W749874
    Qingdainone 97457-31-3
    Qingdainone is a natural product that can be obtained from Qingdai. Qingdainone has the potential to study cancer and inflammation.