Vaccine Lab / Alfa Chemistry
Transfectam

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Transfectam

Catalog Number ACM124050777-1
CAS 124050-77-7
Structure
Synonyms Dioctadecylamidoglycylspermine
IUPAC Name (2S)-2,5-Bis(3-aminopropylamino)-N-[2-(dioctadecylamino)acetyl]pentanamide
Molecular Weight 807.4
Molecular Formula C49H102N6O2
Canonical SMILES CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)CC(=O)NC(=O)C(CCCNCCCN)NCCCN
InChI InChI=1S/C49H102N6O2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-44-55(45-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)46-48(56)54-49(57)47(53-43-37-40-51)38-35-41-52-42-36-39-50/h47,52-53H,3-46,50-51H2,1-2H3,(H,54,56,57)/t47-/m0/s1
InChI Key OPCHFPHZPIURNA-MFERNQICSA-N
Purity 98%+
Complexity 779
Covalently-Bonded Unit Count 1
Defined Atom Stereocenter Count 1
Exact Mass 806.80642652
Heavy Atom Count 57
Hydrogen Bond Acceptor Count 7
Hydrogen Bond Donor Count 5
Isomeric SMILES CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)CC(=O)NC(=O)[C@H](CCCNCCCN)NCCCN
Monoisotopic Mass 806.80642652
Physical State Solid
Rotatable Bond Count 48
Storage Conditions -20 °C
Topological Polar Surface Area 126 Ų
Knowledge & Learning Case Study Q&A

Common Cationic Lipids and Their Applications in Vaccines

Messenger RNA (mRNA) vaccines have emerged as a groundbreaking tool in the realm of vaccine development. Unlike traditional vaccines, mRNA vaccines work by introducing genetic material encoding a specific antigen into cells, prompting the cells to produce the antigen themselves. This approach stimulates an immune response as the body identifies the antigen as foreign and generates antibodies to combat it. One of the key benefits of mRNA vaccines is their agility in design and production, allowing for rapid response to emerging threats such as viral outbreaks or mutations. Get more information on:

  • Role of mRNA in Vaccine Development
  • Importance of Cationic Lipids in mRNA Delivery
  • Cationic Lipids in mRNA Vaccine Formulations
  • Popular Cationic Lipids from Alfa Chemistry
  • Examples of Cationic Lipids Utilized in Vaccines

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