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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)

Quality Level

200

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

Certificates of Analysis (COA)

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Dynamic capillary electrophoresis (DCE) and computer simulation of the elution profiles with the stochastic model has been applied to determine the isomerization barriers of the angiotensin converting enzyme inhibitor enalaprilat. The separation of the rotational cis-trans isomeric drug has been
R Gurunath et al.
Biochemical and biophysical research communications, 202(1), 241-245 (1994-07-15)
Non protein amino acids with strong secondary structure preferences are potentially useful in peptide design. alpha-Aminoisobutyric acid (Aib) is a powerful 'stereochemical director' of polypeptide chain folding, stabilizing helical conformations in diverse oligopeptide sequences. In an approach to the de
Wooseong Lee et al.
Nature communications, 9(1), 1606-1606 (2018-04-25)
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)
Joseph A Davis et al.
Indian journal of pharmacology, 44(6), 759-764 (2012-12-19)
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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