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P6258

Sigma-Aldrich

Phe-Pro

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About This Item

Empirical Formula (Hill Notation):
C14H18N2O3
CAS Number:
7669-65-0
Molecular Weight:
262.30
MDL number:
MFCD00020833
UNSPSC Code:
12352202
PubChem Substance ID:
24898749
NACRES:
NA.26

Assay

≥98% (TLC)

form

powder

color

white

storage temp.

−20°C

SMILES string

O=C(N1CCC[C@H]1C(O)=O)[C@@H](N)CC2=CC=CC=C2

InChI

1S/C14H18N2O3/c15-11(9-10-5-2-1-3-6-10)13(17)16-8-4-7-12(16)14(18)19/h1-3,5-6,11-12H,4,7-9,15H2,(H,18,19)

InChI key

WEQJQNWXCSUVMA-UHFFFAOYSA-N

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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The recognition of pathogen-derived ligands by pattern recognition receptors activates the innate immune response, but the potential interaction of quorum-sensing (QS) signaling molecules with host anti-viral defenses remains largely unknown. Here we show that the Vibrio vulnificus QS molecule cyclo(Phe-Pro)
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Dipeptidyl peptidase IV (DPP-IV) inhibition to modulate the incretin effect is a proven strategy to treat type 2 diabetes mellitus. The present study describes the pharmacological profile of a novel DPP-IV inhibitor RBx-0128, as an antidiabetic agent. DPP-IV assay was
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