ChemAbout
© 2026 ChemAbout
Insights|Privacy Policy|Terms of Service|[email protected]
Home/Compounds/Research Reagent/Lipid Membrane Translocating Peptide
C71H127N17O16
1474.9 g/mol
Research Reagent

Lipid Membrane Translocating Peptide

CAS333757-44-1
Category
Research Reagent
Compound Class
Peptide
Primary Use
Research Compound

This compound is a synthetic peptide designed as a research reagent for cell-penetrating applications. It consists of a 15-amino acid sequence rich in hydrophobic residues, enabling membrane translocation for laboratory studies.

Research tool for studying intracellular deliveryLaboratory reagent for membrane-permeation assays

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

Sourcing or supplying this compound?

List your inventory or post a purchase request

CAS 333757-44-1

List This Product
Sign in to publish supply information
Request This Product
Submit a request without registering

Related Compounds

ReferenceSame Category

Spermidine hydrochloride

CAS334-50-9

research compound

ReferenceSame Category

2,3,5,6-Pyrazinetetracarbonitrile

CAS33420-37-0

research compound

ReferenceSame Category

11-Phenylundecanoic acid

CAS3343-24-6

research compound

ReferenceSame Category

Dihydro Uracil-d4

CAS334473-41-5

research compound

Identifiers
IUPAC Name

(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S)-2,6-diaminohexanoyl]amino]hexanoyl]amino]propanoyl]amino]propanoyl]amino]propanoyl]amino]-3-methylbutanoyl]amino]-4-methylpentanoyl]amino]-4-methylpentanoyl]pyrrolidine-2-carbonyl]amino]-3-methylbutanoyl]amino]-4-methylpentanoyl]amino]-4-methylpentanoyl]amino]propanoyl]amino]propanoyl]pyrrolidine-2-carboxylic acid

InChIKey

JWEFWSKWKIEMAL-LQVNOOSUSA-N

SMILES

C[C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N2CCC[C@H]2C(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)N

Synonyms (1)

—