Fmoc-mephe(4-I)-OH

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Fmoc-mephe(4-I)-OH(CAS 2642726-17-6)

CAT No: CP27874

CAS No: 2642726-17-6

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cGMP Peptide

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IND and NDA support Drug master files (DMF) filing

Synonyms/AliasFMOC-MEPHE(4-I)-OH;SCHEMBL25182931;AT41544;2642726-17-6;
M.F/FormulaC25H22INO4
M.W/Mr.527.3
SequenceThree Letter Code:Fmoc-N(Me)Phe(4-I)-OH
InChIInChI=1S/C25H22INO4/c1-27(23(24(28)29)14-16-10-12-17(26)13-11-16)25(30)31-15-22-20-8-4-2-6-18(20)19-7-3-5-9-21(19)22/h2-13,22-23H,14-15H2,1H3,(H,28,29)/t23-/m0/s1
InChI KeyPMVKRFFNYNBNES-QHCPKHFHSA-N
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    Teduglutide is a polypeptide consisting of 33 amino acids. It is glucagon-like peptide-2 (GLP-2) analogue that is used for the treatment of short bowel syndrome.

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    Terlipressin is a synthetic triglycyllysine derivative of vasopressin with vasoconstrictive, antihemorrhagic, and antidiuretic properties. Upon intravenous administration, terlipressin, an inactive prodrug, is biotransformed to its active moiety, lysine vasopressin (LVP), a nonselective vasopressin analogue with affinity for vasopressin receptors V1 (V1a), V2 and V3 (V1b). As a V1 agonist, terlipressin increases systemic vascular resistance, particularly in the splanchnic area, resulting in a decrease of portal pressure. V1 binding also promotes platelet aggregation and glycogenolysis, while V3 binding induces adrenocorticotropic hormone (ACTH) secretion. Compared to vasopressin, terlipressin has a minimal effect on V2 receptors, which are responsible for promotion of water reabsorption in the collecting ducts of the kidney via stimulation of cyclic AMP production.

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