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Molecules of Korolchuk IP-NFT (VITA-FAST) Price Live Chart
Molecules of Korolchuk IP-NFT (VITA-FAST) Price Today
Der heutige Preis von Molecules of Korolchuk IP-NFT (VITA-FAST) beträgt $4.92, bei einem 24-Stunden-Handelsvolumen von $7.26K und somit hat Molecules of Korolchuk IP-NFT (VITA-FAST) eine Marktkapitalisierung von $4.92M, was ihm eine Marktdominanz von +0% verleiht. Der Preis von Molecules of Korolchuk IP-NFT (VITA-FAST) hat sich in den letzten 24 Stunden um +1.37% geändert.
VITA-FAST Price Data
- 24-Stunden-Volumen$7.26K
- Allzeithoch(ATH)$31.21
- 24 Stunden hoch$5.17
- Allzeittief (ATL)$2.14
- 24-Stunden-Tief$4.8
VITA-FAST Market Cap Infos
- Marktkapitalisierung$4.92M
- Vollständig verwässert Bewertung$4.92M
- Marktkapitalisierung/FDV100%
- Grundstimmung des MarktesNeutral
VITA-FAST Versorgung
- Umlaufende Versorgung1M VITA-FAST
- Gesamtes Angebot1M VITA-FAST
- Max. Supply1M VITA-FAST
Über Molecules of Korolchuk IP-NFT (VITA-FAST)
Contract

0x6034e0d...6a1d33d36
Explorer
etherscan.io
Website
vitadao.com
What is the project about?
VitaDAO, a decentralized autonomous organization, introduces VITA-FAST, an innovative funding model for longevity research. Leveraging the Ethereum blockchain, VITA-FAST are ERC-20 tokens, signifying fractional ownership of the Intellectual Property Non-Fungible Token (IP-NFT) from longevity research conducted at the Korolchuk Lab, Newcastle University. VITA-FAST token holders gain governance rights over the IP, democratizing the decision-making processes in scientific research.
1. What is the project about?
The project is focused on discovering and developing therapeutic compounds that can reactivate autophagy in Npc1 -/- cells. This involves screening bioactive and commercial small molecules in cell survival assays to identify potential autophagy activators that are not cytotoxic. The project uses advanced techniques like luciferase-p6 clearance and Halo-GFP-LC3 orthogonal assays for this purpose.
2. What makes your project unique?
The project's uniqueness lies in its approach to identifying novel compounds that can induce autophagy in NPC1 -/- cells, a crucial process for treating Niemann-Pick Type C disease. Unlike existing treatments, this project employs high-throughput screening methods and innovative assays to discover compounds with high chemical variability and no similarity to existing autophagy inducers, opening up possibilities for new iIP.
3. History of your project.
The project, led by Dr. Korolchuk and his team at Newcastle University, has progressed from generating data on thousands of compounds using advanced screening assays to identifying lead compounds with potential autophagic properties. It has evolved to include the synthesis of derivatives of these compounds and is now moving towards drug translation processes, including pharmacokinetics and scalability studies.
4. What’s next for your project?
The next steps involve screening third-generation compounds, conducting in vitro and in vivo mo