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3- (methylamino)- 2- ((methylamino)methyl)propane- 1- thiol

a radioprotective agent; structure in first source
Also Known As:
Prc-210
Networked: 12 relevant articles (5 outcomes, 2 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Fahl, William E: 10 articles (01/2022 - 04/2012)
2. Soref, Cheryl M: 3 articles (07/2013 - 04/2012)
3. Goesch, Torsten R: 2 articles (01/2022 - 01/2021)
4. Dreischmeier, Emma: 2 articles (01/2021 - 01/2020)
5. Verhoven, Bret M: 2 articles (01/2021 - 08/2020)
6. Wilson, Nancy A: 2 articles (01/2021 - 08/2020)
7. Bath, Natalie M: 2 articles (08/2020 - 07/2019)
8. Redfield, Robert R: 2 articles (08/2020 - 07/2019)
9. Back, Susan: 2 articles (01/2020 - 01/2019)
10. Hacker, Timothy A: 2 articles (01/2019 - 04/2012)

Related Diseases

1. Ischemia
2. Carcinogenesis
3. Neoplasms (Cancer)
4. Reperfusion Injury
5. Myocardial Infarction
01/01/2019 - "Significant reduction of ischemia-reperfusion cell death in mouse myocardial infarcts using the immediate-acting PrC-210 ROS-scavenger."
01/01/2021 - "PrC-210 confers 100% survival to mice and rats that received an otherwise 100% lethal radiation dose and 36% reduction of ischemia-reperfusion-induced mouse myocardial infarct damage, and thus is a viable candidate to prevent human ROS-induced ischemia-reperfusion and ionizing radiation toxicities. "
01/01/2019 - "In a series of both in vitro and in vivo experiments, we show that: (a) in vitro, PrC-210 was the most potent and effective ROS-scavenger when functionally compared to eight of the most commonly studied antioxidants in the MI literature, (b) in vitro PrC-210 ROS-scavenging efficacy was both immediate (seconds) and long-lasting (hours), which would make it effective in both (1) real-time (seconds), as post-MI or cardiac surgery hearts are reperfused with PrC-210-containing blood, and (2) long-term (hours), as hearts are bathed with systemic PrC-210 after MI or surgery, (c) systemic PrC-210 caused a significant 36% reduction of mouse cardiac muscle death following a 45-minute cardiac IR insult; in a striking coincidence, the PrC-210 36% reduction in cardiac muscle death equals the 36% of the MI-induced cardiac cell death estimated 6 years ago by Ovize and colleagues to result from "reperfusion injury," (d) hearts in PrC-210-treated mice performed better than controls after heart attacks when functionally analyzed using echocardiography, and (e) the PrC-210 ROS-scavenging mechanism of action was corroborated by its ability to prevent >85% of the direct, H2O2-induced killing of neonate cardiomyocytes in cell culture. "

Related Drugs and Biologics

1. Antioxidants
2. Sulfhydryl Compounds (Thiols)
3. Caspases
4. Reactive Oxygen Species (Oxygen Radicals)
5. DNA (Deoxyribonucleic Acid)
6. University of Wisconsin-lactobionate solution
7. Amifostine (Ethyol)
8. Propylene Glycol (1,2 Propanediol)
9. Cytokines
10. Free Radical Scavengers

Related Therapies and Procedures

1. Transplantation
2. Controlled Hypotension