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H-Gly-Arg-Ala-Asp-Ser-Pro-OH

H-Gly-Arg-Ala-Asp-Ser-Pro-OH offers a compact motif integrating charged and polar residues useful for substrate-recognition research. Backbone conformation allows investigation of turn-inducing residues. Solubility characteristics assist kinetic analysis in enzymatic assays. Applications include structural modeling, receptor-binding exploration, and synthetic peptide design.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: R04049

CAS No:99896-86-3

Synonyms/Alias:H-Gly-Arg-Ala-Asp-Ser-Pro-OH;Gly-Arg-Ala-Asp-Ser-Pro;99896-86-3;(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[(2-aminoacetyl)amino]-5-(diaminomethylideneamino)pentanoyl]amino]propanoyl]amino]-3-carboxypropanoyl]amino]-3-hydroxypropanoyl]pyrrolidine-2-carboxylic acid;HY-P4232;CS-0653252;

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  • CMC information required for an IND
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  • Drug master files (DMF) filing
M.F/Formula
C23H39N9O10
M.W/Mr.
601.6
Sequence
One Letter Code:GRADSP
Three Letter Code:H-Gly-Arg-Ala-Asp-Ser-Pro-OH
InChI
InChI=1S/C23H39N9O10/c1-11(28-19(38)12(29-16(34)9-24)4-2-6-27-23(25)26)18(37)30-13(8-17(35)36)20(39)31-14(10-33)21(40)32-7-3-5-15(32)22(41)42/h11-15,33H,2-10,24H2,1H3,(H,28,38)(H,29,34)(H,30,37)(H,31,39)(H,35,36)(H,41,42)(H4,25,26,27)/t11-,12-,13-,14-,15-/m0/s1
InChI Key
YCJRGURCDKCPCI-YTFOTSKYSA-N

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