pinafide

structure

Also Known As:

5-nitro-2-(2-(1-pyrrolidine)ethyl)-benzo(de)isoquinoline-1,3-dione; M 12210; M-12210; N-(2-(N-pyrrolidinyl)ethyl)-3-nitronaphthalimide; 5-nitro-2-(2-(1-pyrrolidinyl)ethyl)-1H-benz(de)isoquinoline-1,3(2H)-dione

Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Heterocyclic Compounds: 198
- Fused-Ring Heterocyclic Compounds
  - 2-Ring Heterocyclic Compounds
    - Isoquinolines: 34
      - pinafide: 2

Experts

1.	Bak, Andrzej: 1 article (03/2021)
2.	Fedoruk-Wyszomirska, Agnieszka: 1 article (03/2021)
3.	Giel-Pietraszuk, Małgorzata: 1 article (03/2021)
4.	Gurda-Woźna, Dorota: 1 article (03/2021)
5.	Kiliszek, Agnieszka: 1 article (03/2021)
6.	Kowalczyk, Aleksandra: 1 article (03/2021)
7.	Olejniczak, Agnieszka B: 1 article (03/2021)
8.	Orlicka-Płocka, Marta: 1 article (03/2021)
9.	Rykowski, Sebastian: 1 article (03/2021)
10.	Rypniewski, Wojciech: 1 article (03/2021)

Related Diseases

1.	Neoplasms (Cancer) 03/09/2021 - "We synthesized a series of novel 3-carboranyl-1,8-naphthalimide derivatives, mitonafide and pinafide analogs, using click chemistry, reductive amination and amidation reactions and investigated their in vitro effects on cytotoxicity, cell death, cell cycle, and the production of reactive oxygen species in a HepG2 cancer cell line. "
2.	Carcinoma (Carcinomatosis) 01/01/1980 - "Two of the most active compounds, M-4212 and M-12210, prevented the development of mouse Ehrlich ascites and rat Yoshida carcinoma. "
3.	Ascites 01/01/1980 - "Two of the most active compounds, M-4212 and M-12210, prevented the development of mouse Ehrlich ascites and rat Yoshida carcinoma. "

Related Drugs and Biologics

1.	mitonafide
2.	Reactive Oxygen Species (Oxygen Radicals)