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H-Pro-His-Pro-Phe-His-Phe-Phe-Val-Tyr-Lys-OH

H-Pro-His-Pro-Phe-His-Phe-Phe-Val-Tyr-Lys-OH presents a decapeptide enriched in aromatic residues and histidines that influence stacking and metal-binding behavior. Proline residues introduce conformational constraints relevant to turn formation. The sequence is suitable for spectroscopic and folding investigations. Research applications include peptide-metal interaction studies, structural motif analysis, and aggregation behavior evaluation.

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

CAT No: R01010

CAS No:75645-19-1

Synonyms/Alias:75645-19-1;Renin Inhibitor;H-PRO-HIS-PRO-PHE-HIS-PHE-PHE-VAL-TYR-LYS-OH;Pro-His-Pro-His-Phe-Phe-Val-Tyr-Lys;SCHEMBL10658713;FP111016;

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C69H87N15O12
M.W/Mr.
1318.5
Sequence
One Letter Code:PHPFHFFVYK
Three Letter Code:H-DL-Pro-DL-His-DL-Pro-DL-Phe-DL-His-DL-Phe-DL-Phe-DL-Val-DL-Tyr-DL-Lys-OH
Source#
Synthetic
InChI
InChI=1S/C69H87N15O12/c1-42(2)59(67(93)81-54(35-46-25-27-49(85)28-26-46)61(87)76-51(69(95)96)22-12-13-29-70)83-65(91)55(34-45-20-10-5-11-21-45)78-62(88)52(32-43-16-6-3-7-17-43)77-64(90)56(36-47-38-71-40-74-47)79-63(89)53(33-44-18-8-4-9-19-44)80-66(92)58-24-15-31-84(58)68(94)57(37-48-39-72-41-75-48)82-60(86)50-23-14-30-73-50/h3-11,16-21,25-28,38-42,50-59,73,85H,12-15,22-24,29-37,70H2,1-2H3,(H,71,74)(H,72,75)(H,76,87)(H,77,90)(H,78,88)(H,79,89)(H,80,92)(H,81,93)(H,82,86)(H,83,91)(H,95,96)
InChI Key
AIRMFERKNRDUKD-UHFFFAOYSA-N

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