Glycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-L-leucyl-L-glutamine | CAS No. 113274-56-9

Glycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-L-leucyl-L-glutamine

Basic Information

CAS Number

113274-56-9

Molecular Formula

C66H93N13O25

Molecular Weight

1468.54 g/mol

AD

Basic Physical Properties

CCC(C)C(C(=O)N1CCCC1C(=O)NC(CCC(=O)O)C(=O)NC(CCC(=O)O)C(=O)NC(CC2=CC=C(C=C2)O)C(=O)NC(CC(C)C)C(=O)NC(CCC(=O)N)C(=O)O)NC(=O)C(CCC(=O)O)NC(=O)C(CCC(=O)O)NC(=O)C(CC3=CC=CC=C3)NC(=O)C(CC(=O)O)NC(=O)CN

InChI

InChI=1S/C66H93N13O25/c1-5-34(4)55(78-59(96)41(21-26-53(89)90)71-56(93)38(18-23-50(83)84)72-61(98)44(29-35-10-7-6-8-11-35)77-63(100)46(31-54(91)92)69-49(82)32-67)65(102)79-27-9-12-47(79)64(101)73-40(20-25-52(87)88)57(94)70-39(19-24-51(85)86)58(95)76-45(30-36-13-15-37(80)16-14-36)62(99)75-43(28-33(2)3)60(97)74-42(66(103)104)17-22-48(68)81/h6-8,10-11,13-16,33-34,38-47,55,80H,5,9,12,17-32,67H2,1-4H3,(H2,68,81)(H,69,82)(H,70,94)(H,71,93)(H,72,98)(H,73,101)(H,74,97)(H,75,99)(H,76,95)(H,77,100)(H,78,96)(H,83,84)(H,85,86)(H,87,88)(H,89,90)(H,91,92)(H,103,104)/t34-,38-,39-,40-,41-,42-,43-,44-,45-,46-,47-,55-/m0/s1

InChIKey

ZNEKMMIWGPUTGR-SQJOKQRMSA-N

LogP

-3.648700000000016

Topological Polar Surface Area

624.4499999999999 Ų

Hydrogen Bond Donor/Acceptor

21 / 38

Complexity

3050

Synonyms & References

English

  • 113274-56-9
  • Hirudin (54-65
  • HY-P1636
  • AKOS025311601
  • CS-0066098
  • CHEMBL411059
  • Hirudin (54-65)
  • Hirudin (54-65) (desulfated)
  • Hirudin(54-65)(desulfated)
  • HIRUDIN (54-65) (DESULFATED)
  • HIRUDIN FRAGMENT 54-65 NON-SULFATED
  • H-GLY-ASP-PHE-GLU-GLU-ILE-PRO-GLU-GLU-TYR-LEU-GLN-OH
  • GLY-ASP-PHE-GLU-GLU-ILE-PRO-GLU-GLU-TYR-LEU-GLN
  • Hirudin
  • Glycyl-alpha-aspartylphenylalanyl-alpha-glutamyl-alpha-glutamylisoleucylprolyl-alpha-glutamyl-alpha-glutamyltyrosylleucylglutamine
  • 5-Amino-2-[[2-[[2-[[2-[[2-[[1-[2-[[2-[[2-[[2-[[2-[(2-aminoacetyl)amino]-3-carboxypropanoyl]amino]-3-
  • Lyophilized hirudin
  • Hirudin (54-65) (desulfated) Trifluoroacetate

MDL Number

MFCD00076563

FAQ

What are the physical and chemical properties of Glycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-L-leucyl-L-glutamine (CAS: 113274-56-9)?

Glycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-L-leucyl-L-glutamine is a complex peptide with a molecular weight of approximately 1475.6 g/mol. It is highly soluble in water and slightly soluble in ethanol. It exhibits moderate reactivity, particularly with nucleophiles. This peptide is stable under mild conditions but can be vulnerable to proteolytic degradation under harsh conditions. It crystallizes in a form that is stable under room temperature conditions.

How is Glycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-L-leucyl-L-glutamine (CAS: 113274-56-9) typically synthesized?

Glycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-L-leucyl-L-glutamine is synthesized through solid-phase peptide synthesis (SPPS) using Fmoc chemistry. The synthesis involves sequential coupling of protected amino acids, followed by cleavage from the resin and purification. The final product is obtained with good yield and high purity, typically using HPLC for purification.

What industries use Glycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-L-leucyl-L-glutamine (CAS: 113274-56-9)?

Glycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-L-leucyl-L-glutamine is primarily used in the pharmaceutical industry for the development of peptides and proteins. It is also utilized in the polymer industry for the modification of polymer properties, in sensor technology for detecting specific biological markers, and in semiconductor applications for specific functional groups.

What precautions should be taken when handling Glycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-L-leucyl-L-glutamine (CAS: 113274-56-9)?

When handling Glycyl-L-alpha-aspartyl-L-phenylalanyl-L-alpha-glutamyl-L-alpha-glutamyl-L-isoleucyl-L-prolyl-L-alpha-glutamyl-L-alpha-glutamyl-L-tyrosyl-L-leucyl-L-glutamine, it is essential to wear appropriate personal protective equipment (PPE) including gloves, goggles, and a lab coat. Work should be conducted in a well-ventilated area or a fume hood. In case of a spill, immediately clean up using appropriate absorbent materials and dispose of waste according to local regulations. Always refer to the safety data sheet (SDS) for detailed handling and emergency instructions.

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