26308-21-4

Basic information

• Product Name: L-Phenylalaninamide, N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl-L-methionylglycyl-L-tryptophyl-L -methionyl-L-a-aspartyl-
• CAS NO: 26308-21-4
• Molecular Formula: C50H65N9O12S2
• Molecular Weight: 1048.25
• Mol File: 26308-21-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: L-Phenylalaninamide, N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl-L-methionylglycyl-L-tryptophyl-L -methionyl-L-a-aspartyl-(CAS DataBase Reference)
• NIST Chemistry Reference: L-Phenylalaninamide, N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl-L-methionylglycyl-L-tryptophyl-L -methionyl-L-a-aspartyl-(26308-21-4)
• EPA Substance Registry System: L-Phenylalaninamide, N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl-L-methionylglycyl-L-tryptophyl-L -methionyl-L-a-aspartyl-(26308-21-4)

Safety Data

• Hazardous Substances Data: 26308-21-4(Hazardous Substances Data)

Upstream product

• 47710-78-1 Boc-Tyr-Met-Gly-OH 
• 20866-56-2 2,5-dioxopyrrolidin-1-yl N-(tert-butoxycarbonyl)-L-tyrosinate 
• 3845-64-5 tertbutoxycarbonyl-L-methionine N-hydroxysuccinimide ester 
• 23446-03-9 2-((2S)-2-((tert-butoxycarbonyl)amino)-4-(methylthio)butanamido)acetic acid 
• 5609-49-4 L-Tryptophyl-L-methionyl-L-aspartyl-L-phenylalanine amide hydrochloride 
• 109210-41-5 Boc-Tyr-Met-Gly-ONB 
• 92409-86-4 methionyl-glycyl-tryptophyl-methionyl-aspartyl-phenylalanine amide trifluoroacetate 

Downstream Products

• 92410-00-9 Suc-Tyr-Met-Gly-Trp-Met-Asp-Phe-NH₂ 
• 109210-45-9 Suc-Tyr-(OSO₃Na)-Met-Gly-Trp-Met-Asp-Phe-NH₂ 
• 109210-42-6 H-Tyr-Met-Gly-Trp-Met-Asp-Phe-NH₂ 
• 67105-75-3 Boc-Tyr(SO₃Na)-Met-Gly-Trp-Met-Asp-Phe-NH₂ (Boc-CCK-7) 
• 20987-59-1 N-tert-butyloxycarbonyl-O-sulfotyrosyl-methionyl-glycyl-tryptophyl-methionyl-aspartyl-phenylalanine amide 
• 63229-04-9 H-Tyr-Met-Gly-Trp-Met-Asp-Phe-NH₂*TFA 

Relevant articles and documents

SYNTHESIS AND BIOLOGICAL PROPERTIES OF CHOLECYSTOKININ HEPTAPEPTIDE ANALOGUES CONTAINING D- AND L-FORMS OF TERT-LEUCINE OR NEOPENTYLGLYCINE IN POSITION 5

Using solution or solid-phase synthesis we prepared the cholecystokinin fragment Boc-CCK-7 (Boc-Tyr-(SO3-*Na+)-Met-Gly-Trp-Met-Asp-PheNH2) and its four analogues in which the methionine moiety (Met) in the carboxy-terminal part is re

Synthesis of five cholecystokinin-like peptides and determination of their analgesic effects

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