CAS 460738-38-9 Ecallantide

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CAS 460738-38-9 Ecallantide
Details
CAS: 460738-38-9
Sequence: Thr-Asp-Phe-Cys-Asn-Leu-Pro-Pro-Tyr-Thr-Gly-Pro-Cys-Val-Ala-Phe-Phe-Asp-Ile-Ala-Gly-Lys-Cys-Gln-Phe-Lys-Tyr-Asn-Gly-Glu-Gln-Asn-Arg-Phe-Tyr-Ser-Ala-Trp-Gly-Cys-Asp-Gly-Arg-Gly-Asn-Asn-Phe-Val-Tyr-Gly-Gly-Cys-Asp-Arg-Pro-Asn-Thr-Ser-Glu-Glu-Cys-Leu-Arg-Thr-Ala-Cys (Disulfide bridges: Cys4-Cys52, Cys13-Cys38, Cys23-Cys59)
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Related documents
COA/MS/HPLC Report
Peptide Dissolution and Storage Guide
Category
Pharmaceutical Peptides
Category
Pharmaceutical Peptides
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Description

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Product name CAS 460738-38-9 Ecallantide
Sequence Thr-Asp-Phe-Cys-Asn-Leu-Pro-Pro-Tyr-Thr-Gly-Pro-Cys-Val-Ala-Phe-Phe-Asp-Ile-Ala-Gly-Lys-Cys-Gln-Phe-Lys-Tyr-Asn-Gly-Glu-Gln-Asn-Arg-Phe-Tyr-Ser-Ala-Trp-Gly-Cys-Asp-Gly-Arg-Gly-Asn-Asn-Phe-Val-Tyr-Gly-Gly-Cys-Asp-Arg-Pro-Asn-Thr-Ser-Glu-Glu-Cys-Leu-Arg-Thr-Ala-Cys (Disulfide bridges: Cys4-Cys52, Cys13-Cys38, Cys23-Cys59)
Three letter sequence H-Thr-Asp-Phe-Cys-Asn-Leu-Pro-Pro-Tyr-Thr-Gly-Pro-Cys-Val-Ala-Phe-Phe-Asp-Ile-Ala-Gly-Lys-Cys-Gln-Phe-Lys-Tyr-Asn-Gly-Glu-Gln-Asn-Arg-Phe-Tyr-Ser-Ala-Trp-Gly-Cys-Asp-Gly-Arg-Gly-Asn-Asn-Phe-Val-Tyr-Gly-Gly-Cys-Asp-Arg-Pro-Asn-Thr-Ser-Glu-Glu-Cys-Leu-Arg-Thr-Ala-Cys-OH
Peptide purity (HPLC, %) 95%/98%/99%
Molecular formula C₃₀₈H₄₇₈N₈₆O₉₄S₆
Molecular weight (Da) 7059.97

 

Product Basic Information Table

 

Product Standard English Name Product Abbreviation / Alias Function Tags (comma-separated) Amino Acid Full Name Sequence Molecular Formula Exact Molecular Weight (Da) Average Molecular Weight (Da) N-terminal Modification C-terminal Modification Sequence Length (aa)
Ecallantide Ecallantide; DX-88; Kalbitor; CAS 460738-38-9; Plasma kallikrein inhibitor Plasma kallikrein inhibitor,Bradykinin production inhibition,Hereditary angioedema therapy,Serine protease inhibitor,Inflammation regulation research Thr-Asp-Phe-Cys-Asn-Leu-Pro-Pro-Tyr-Thr-Gly-Pro-Cys-Val-Ala-Phe-Phe-Asp-Ile-Ala-Gly-Lys-Cys-Gln-Phe-Lys-Tyr-Asn-Gly-Glu-Gln-Asn-Arg-Phe-Tyr-Ser-Ala-Trp-Gly-Cys-Asp-Gly-Arg-Gly-Asn-Asn-Phe-Val-Tyr-Gly-Gly-Cys-Asp-Arg-Pro-Asn-Thr-Ser-Glu-Glu-Cys-Leu-Arg-Thr-Ala-Cys (3 disulfide bridges for globular conformation) C₃₀₈H₄₇₈N₈₆O₉₄S₆ 7055.42 7059.97 Free amine, unmodified Free carboxyl, unmodified 60

 

Physicochemical Solubility & Storage Parameters

 

Product Code Appearance Long-term Storage Conditions Short-term Storage Conditions Liquid Stability Solid Powder Stability
PEP-ECA001 white powder Store at -20℃, protected from light, sealed and dry, aliquoted; avoid repeated freeze-thaw cycles and reducing agents Solid powder stable for 2 years sealed and dry at 2-8℃; prepare aqueous solutions freshly before use, aliquots stable for 1 month at -20℃ Stable for 72 h at 4℃; disulfide bonds sensitive to reducing agents and high temperature, avoid prolonged room temperature exposure Stable for 3 years at -20℃ under dry & dark conditions

 

Functional Description

Product Code Frontend Short Summary (for search list display) Detailed Biological Function Description Applicable Research Areas (comma-separated) Target / Receptor
PEP-ECA001 Highly selective reversible plasma kallikrein inhibitor that blocks bradykinin production, applied in hereditary angioedema attack and inflammation mechanism research Ecallantide (development code DX-88) is a potent, highly selective plasma kallikrein inhibitor engineered from the Kunitz-type serine protease inhibitor scaffold. Its compact globular structure precisely fits into the active pocket of plasma kallikrein, competitively inhibiting the cleavage of high-molecular-weight kininogen and reducing bradykinin generation at the source. Bradykinin is the core mediator of increased vascular permeability, tissue edema, pain and inflammatory responses, so Ecallantide effectively relieves acute edematous attacks in patients with hereditary angioedema (HAE). Compared with C1 esterase inhibitor replacement therapy, it has a more direct target, smaller molecular weight, stronger tissue penetration, and does not interfere with other coagulation cascade pathways. Approved by the FDA for acute HAE attacks, it serves as a core tool molecule for inflammatory pharmacology, kallikrein-kinin system research and peptide enzyme inhibitor drug development. Inflammation pharmacology research,Hereditary angioedema research,Kallikrein-kinin system research,Peptide enzyme inhibitor development,Vascular permeability regulation research Plasma kallikrein; Bradykinin production pathway

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