(DL-Isoser1)-TRAP-6 trifluoroacetate salt

(DL-Isoser1)-TRAP-6 trifluoroacetate salt contains a stereochemically modified N-terminal residue that influences backbone geometry in the TRAP-6 motif. The peptide still engages receptor-binding sequences, enabling analysis of stereochemical effects. Its salt form enhances solubility in aqueous media. Researchers employ it in analog comparison, conformational studies, and receptor-activation profiling.

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

CAT No: C0127

CAS No:150242-29-8

Synonyms/Alias:150242-29-8;H-DL-Isoser-Phe-Leu-Leu-Arg-Asn-OH;iso-TRAP-6;(2S)-4-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[(3-amino-2-hydroxypropanoyl)amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]-4-methylpentanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-4-oxobutanoic acid;(DL-Isoser1)-TRAP-6;DL-Isoser-Phe-Leu-Leu-Arg-Asn;(DL-Isoser1)-TRAP-6 trifluoroacetate salt;HY-P5001;DA-48730;FI108559;CS-0675638;(DL-Isoser 1)-TRAP-6 trifluoroacetate salt;(2S,5S,8S,11S,14S)-18-amino-2-(2-amino-2-oxoethyl)-14-benzyl-5-(3-guanidinopropyl)-17-hydroxy-8,11-diisobutyl-4,7,10,13,16-pentaoxo-3,6,9,12,15-pentaazaoctadecan-1-oic acid;

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cGMP Peptide
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  • Drug master files (DMF) filing
M.F/Formula
C34H56N10O9
M.W/Mr.
748.9
Sequence
One Letter Code:XFLLRN
Three Letter Code:H-bAla(2-OH)-Phe-Leu-Leu-Arg-Asn-OH
Source#
Synthetic
InChI
InChI=1S/C34H56N10O9/c1-18(2)13-22(29(48)40-21(11-8-12-39-34(37)38)28(47)44-25(33(52)53)16-27(36)46)41-30(49)23(14-19(3)4)42-31(50)24(43-32(51)26(45)17-35)15-20-9-6-5-7-10-20/h5-7,9-10,18-19,21-26,45H,8,11-17,35H2,1-4H3,(H2,36,46)(H,40,48)(H,41,49)(H,42,50)(H,43,51)(H,44,47)(H,52,53)(H4,37,38,39)/t21-,22-,23-,24-,25-,26?/m0/s1
InChI Key
YYJYQAMJNGSSQH-BKJSQPKXSA-N

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