A metabolite of bradykinin
Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Bradykinin Fragment (1-5) (trifluoroacetate salt)

Item No. 35302

Technical Information
Synonyms
  • Arg-Pro-Pro-Gly-Phe
  • BK Fragment 1-5
  • RPPGF
Molecular Formula
C27H40N8O6 • XCF3COOH
Formula Weight
Purity
≥98%
A solid
DMF: 10 mg/mlDMSO: 10 mg/mlEthanol: 3 mg/mlPBS (pH 7.2): 5 mg/ml
SMILES
N=C(N)NCCC[C@H](N)C(N1[C@H](C(N2[C@H](C(NCC(N[C@@H](CC3=CC=CC=C3)C(O)=O)=O)=O)CCC2)=O)CCC1)=O.OC(C(F)(F)F)=O
InChi Code
InChI=1S/C27H40N8O6.C2HF3O2/c28-18(9-4-12-31-27(29)30)24(38)35-14-6-11-21(35)25(39)34-13-5-10-20(34)23(37)32-16-22(36)33-19(26(40)41)15-17-7-2-1-3-8-17;3-2(4,5)1(6)7/h1-3,7-8,18-21H,4-6,9-16,28H2,(H,32,37)(H,33,36)(H,40,41)(H4,29,30,31);(H,6,7)/t18-,19-,20-,21-;/m0./s1
InChi Key
LAPYOHFGOBOFAC-NCEXEODOSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Add

    Cayman Chemical
    Neutrophil Biology Wall Poster

    Explore how neutrophils shape the immune response in health and disease. This poster highlights neutrophil pathogen defense mechanisms, including phagocytosis, degranulation, and NETosis, as well as neutrophil roles in inflammation and NET-associated pathologies.

    DOWNLOAD NOW
    Product Description

    Bradykinin fragment (1-5) is a metabolite of the endogenous vasodilator bradykinin (Item No. 37408).1 It is formed from bradykinin by angiotensin-converting enzyme (ACE). Bradykinin fragment (1-5) (100 nM) increases the production of nitric oxide (NO) in neonatal rat cardiomyocytes.2 It inhibits α-thrombin-induced platelet aggregation of washed isolated platelets (IC50 = 0.5 mM).3 Bradykinin fragment (1-5) prevents decreases in mean arterial blood pressure and heart rate and increases survival in a rat model of LPS-induced septicemia.4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Bujak-Giżycka, B., Olszanecki, R., Madej, J., et alMetabolism of bradykinin in aorta of hypertensive rats. Acta Biochim. Pol. 58(2), 199-202 (2011).

    2. Souza-Silva, I.M., de Paula, C.A., Bolais-Amos, L., et alPeptide fragments of bradykinin show unexpected biological activity not mediated by B1 or B2 receptors. Br. J. Pharmacol. 179(12), 3061-3077 (2022).

    3. Hasan, A.A.K., Amenta, S., and Schmaier, A.H. Bradykinin and its metabolite, Arg-Pro-Pro-Gly-Phe, are selective inhibitors of α-thrombin-induced platelet activation. Circulation 94(3), 517-528 (1996).

    4. Morinelli, T.A., Webb, J.G., Jaffa, A.A., et alA metabolic fragment of bradykinin, Arg-Pro-Pro-Gly-Phe, protects against the deleterious effects of lipopolysaccharide in rats. J. Pharmacol. Exp. Ther. 296(1), 71-76 (2001).