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245080-24-4

245080-24-4 Structure

245080-24-4 Structure
IdentificationBack Directory
[Name]

2-((6S,15S,18S,27S,35S,38S,41S,43aS,48aS)-12-(4-aminobutyl)-35-benzyl-6,41-di((S)-sec-butyl)-21-(3-guanidinopropyl)-15-((R)-1-hydroxyethyl)-9-(hydroxymethyl)-5,8,11,14,17,20,23,26,29,34,37,40,43,48-tetradecaoxohexatetracontahydro-1H,5H-18,38-(methanodithiomethano)tripyrrolo[1,2-a:1',2'-b1:1'',2''-e1][1,4,7,10,13,16,19,22,25,28,31,34,37,40]tetradecaazacyclodotetracontin-27-yl)acetic acid
[CAS]

245080-24-4
[Synonyms]

SFTI-1
Cyclo(L-arginyl-L-cysteinyl-L-threonyl-L-lysyl-L-seryl-L-isoleucyl-L-prolyl-L-prolyl-L-isoleucyl-L-cysteinyl-L-phenylalanyl-L-prolyl-L-α-aspartylglycyl), cyclic (2→10)-disulfide
2-((6S,15S,18S,27S,35S,38S,41S,43aS,48aS)-12-(4-aminobutyl)-35-benzyl-6,41-di((S)-sec-butyl)-21-(3-guanidinopropyl)-15-((R)-1-hydroxyethyl)-9-(hydroxymethyl)-5,8,11,14,17,20,23,26,29,34,37,40,43,48-tetradecaoxohexatetracontahydro-1H,5H-18,38-(methanodithi
2-((6S,15S,18S,27S,35S,38S,41S,43aS,48aS)-12-(4-aminobutyl)-35-benzyl-6,41-di((S)-sec-butyl)-21-(3-guanidinopropyl)-15-((R)-1-hydroxyethyl)-9-(hydroxymethyl)-5,8,11,14,17,20,23,26,29,34,37,40,43,48-tetradecaoxohexatetracontahydro-1H,5H-18,38-(methanodithiomethano)tripyrrolo[1,2-a:1',2'-b1:1'',2''-e1][1,4,7,10,13,16,19,22,25,28,31,34,37,40]tetradecaazacyclodotetracontin-27-yl)acetic acid
[Molecular Formula]

C67H104N18O18S2
[MOL File]

245080-24-4.mol
[Molecular Weight]

1513.78
Chemical PropertiesBack Directory
[density ]

1.53±0.1 g/cm3(Predicted)
[form ]

Solid
[pka]

4.01±0.10(Predicted)
[color ]

White to off-white
[Sequence]

Cyclic(Arg-Cys-Thr-Lys-Ser-Ile-Pro-Pro-Ile-Cys-Phe-Pro-Asp-Gly) (Disulfide bridge: Cys2-Cys10)
Hazard InformationBack Directory
[Uses]

SFTI-1 is a cyclic peptide trypsin inhibitor comprising 14 amino acid residues. SFTI-1 is a potent Bowman-Birk inhibitor.
[References]

[1] M L Korsinczky, et al. Solution structures by 1H NMR of the novel cyclic trypsin inhibitor SFTI-1 from sunflower seeds and an acyclic permutant. J Mol Biol. 2001 Aug 17;311(3):579-91. DOI:10.1006/jmbi.2001.4887
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