BPP 9a

BPP 9a is a proline-rich sequence with characteristic structural rigidity enabling stable conformational states. The motif supports receptor-interface modeling and surface-binding analysis. Its physicochemical properties lend themselves to biophysical characterization. Applications include inhibitory motif studies, peptide folding evaluation, and ligand-target exploration.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
BPP 9a(CAS 35115-60-7)

CAT No: B08011

CAS No:35115-60-7

Synonyms/Alias:TEPROTIDE;35115-60-7;Angiotensin Converting Enzyme Inhibitor;Tepromide;Teprotido;Teprotidum;teprotida;angiotensin-converting enzyme inhibitor;Teprotidum [INN-Latin];SQ 20881;SQ-20881;Teprotido [INN-Spanish];C3E5QBF1R6;Teprotide [USAN:INN:BAN];CCRIS 9333;TEPROTIDE [INN];Teprotide (USAN/INN);TEPROTIDE [USAN];TEPROTIDE [MART.];SO-20881;5-Oxo-L-prolyl-L-tryptophyl-L-prolyl-L-arginyl-L-prolyl-L-glutaminyl-L-isoleucyl-L-prolyl-L-proline;CHEBI:9444;CHEMBL408983;(2S)-1-[(2S)-1-[(2S,3S)-2-[[(2S)-5-amino-2-[[(2S)-1-[(2S)-5-(diaminomethylideneamino)-2-[[(2S)-1-[(2S)-3-(1H-indol-3-yl)-2-[[(2S)-5-oxopyrrolidine-2-carbonyl]amino]propanoyl]pyrrolidine-2-carbonyl]amino]pentanoyl]pyrrolidine-2-carbonyl]amino]-5-oxopentanoyl]amino]-3-methylpentanoyl]pyrrolidine-2-carbonyl]pyrrolidine-2-carboxylic acid;DTXSID301029698;SO 20881;Teprotidum (INN-Latin);Teprotido (INN-Spanish);TEPROTIDE (MART.);Bradykinin potentiator B, 2-L-tryptophan-3-de-L-leucine-4-de-L-proline-8-L-glutamine-;Pyr-Trp-Pro-Arg-Pro-Gln-Ile-Pro-Pro;(2S)-1-[(2S)-1-[(2S,3S)-2-[[(2S)-5-amino-2-[[(2S)-1-[(2S)-5-guanidino-2-[[(2S)-1-[(2S)-3-(1H-indol-3-yl)-2-[[(2S)-5-oxopyrrolidine-2-carbonyl]amino]propanoyl]pyrrolidine-2-carbonyl]amino]pentanoyl]pyrrolidine-2-carbonyl]amino]-5-oxo-pentanoyl]amino]-3-methyl-pentanoyl]pyrrolidine-2-carbonyl]pyrrolidine-2-carboxylic acid;BPP-9a;AC1L9EJT;UNII-C3E5QBF1R6;Bradykinin Potentiating Peptide 9a;Bradykinin-Potentiating Peptide 9a;(2S)-1-((2S)-1-((2S,3S)-2-(((2S)-5-amino-2-(((2S)-1-((2S)-5-guanidino-2-(((2S)-1-((2S)-3-(1H-indol-3-yl)-2-(((2S)-5-oxopyrrolidine-2-carbonyl)amino)propanoyl)pyrrolidine-2-carbonyl)amino)pentanoyl)pyrrolidine-2-carbonyl)amino)-5-oxo-pentanoyl)amino)-3-methyl-pentanoyl)pyrrolidine-2-carbonyl)pyrrolidine-2-carboxylic acid;Peptide 9a, Bradykinin-Potentiating;Nonapeptide Converting Enzyme Inhibitor;Nonapeptide-Converting Enzyme Inhibitor;Enzyme Inhibitor, Nonapeptide-Converting;SCHEMBL613757;SCHEMBL11855843;DTXCID601514903;HY-P2366;MFCD00076208;FB108627;CS-0133127;NS00125817;D06076;G77853;BPP 9a Pyr-Trp-Pro-Arg-Pro-Gln-Ile-Pro-Pro-OH;Q7701390;Angiotensin Converting Enzyme Inhibitor, >=95% (TLC);Pyroglutamyl-tryptophyl-prolyl-arginyl-prolyl-glutaminyl-isoleucyl-prolyl-proline;L-Pyroglutamyl-L-tryptophyl-L-prolyl-L-arginyl-L-prolyl-L-glutaminyl-L-isoleucyl-L-prolyl-L-proline;

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
C53H76N14O12
M.W/Mr.
1101.3
Sequence
One Letter Code:XWPRPQIPP
Three Letter Code:H-Pyr-Trp-Pro-Arg-Pro-Gln-Ile-Pro-Pro-OH
Source#
Synthetic
InChI
InChI=1S/C53H76N14O12/c1-3-29(2)43(51(77)66-25-9-16-39(66)50(76)67-26-10-17-40(67)52(78)79)63-45(71)34(18-20-41(54)68)60-46(72)37-14-7-23-64(37)48(74)35(13-6-22-57-53(55)56)61-47(73)38-15-8-24-65(38)49(75)36(62-44(70)33-19-21-42(69)59-33)27-30-28-58-32-12-5-4-11-31(30)32/h4-5,11-12,28-29,33-40,43,58H,3,6-10,13-27H2,1-2H3,(H2,54,68)(H,59,69)(H,60,72)(H,61,73)(H,62,70)(H,63,71)(H,78,79)(H4,55,56,57)/t29-,33-,34-,35-,36-,37-,38-,39-,40-,43-/m0/s1
InChI Key
UUUHXMGGBIUAPW-CSCXCSGISA-N

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