| 名称 | Enfuvirtide (T-20) | 
		 
		| 别名 | ENF | 
		 
		| 序列(单字母缩写) | Ac-YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF-NH2 | 
		
		
		 
		| 序列(三字母缩写) | Ac-{TYR}{THR}{SER}{LEU}{ILE}{HIS}{SER}{LEU}{ILE}{GLU}{GLU}{SER}{GLN}{ASN}{GLN}{GLN}{GLU}{LYS}{ASN}{GLU}{GLN}{GLU}{LEU}{LEU}{GLU}{LEU}{ASP}{LYS}{TRP}{ALA}{SER}{LEU}{TRP}{ASN}{TRP}{PHE}-NH2 | 
		 
		| C-端 | NH2 | 
		 
		| 基本描述 | 36 residue synthetic peptide that inhibits HIV-1 fusion with CD4 cells. N-terminal acetylated, C-terminal amide. Enfuvirtide is the first in this class to reach market approval. Fusion inhibitors block the last step in the three-step viral entry process consisting of attachment, co-receptor binding and fusion, thereby preventing viral capsid entry into the host cell. Enfuvirtide has a unique mechanism of action and  viral target specificity, and in clinical trials has been shown to exhibit both  efficacy and low toxicity. Enfuvirtide is a peptide mimetic of an essential region within viral envelope glycoprotein gp41 that functions by blocking gp41 structural rearrangements at a transitional pre-fusion conformation. | 
		 
		| 分子量 | 4491.880 | 
		 
		| 化学式 | C204H301N51O64 | 
		 
		| 纯度 | > 95% | 
		 
		| N-端 | Ac | 
		 
		| 存储条件 | Store at -20°C. Keep tightly closed. Store in a cool dry place. | 
		 
		| 注释 | HIV-I TAT Protein Peptide | 
		
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		| Reference | Mink M, Mosier SM et al. Impact of human immunodeficiency virus type 1 gp41 amino acid substitutions selected during enfuvirtide treatment on gp41 binding and antiviral potency of enfuvirtide in vitro. J Virol. Oct 2005;79(19):12447-54. |