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PHI90004

D-Glu-(17)-Liraglutide

GLP-1 Agonist Impurity, analytical standard, Numbering in the name as per API

Sinónimos:

D-Glu-(23)-Liraglutide, H-His-Ala-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-D-Glu-Ala-Ala-Lys (γ-Glu-Palmitoyl)-Glu-Phe-Ile-Ala-Trp-Leu-Val-Arg-Gly-Arg-Gly-OH

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Acerca de este artículo

Fórmula empírica (notación de Hill):
C172H264N42O52
Peso molecular:
3752.19
UNSPSC Code:
41116107
eCl@ss:
25140904
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grade

analytical standard

Quality Segment

API family

liraglutide, liraglutide, liraglutide, liraglutide

form

powder

technique(s)

HPLC: suitable, LC/MS: suitable, liquid chromatography (LC): suitable, mass spectrometry (MS): suitable

color

white to off-white

format

neat

storage temp.

−20°C

SMILES string

OC[C@@H](C(N[C@@H](CC1=CC=C(O)C=C1)C(N[C@@H](CC(C)C)C(N[C@@H](CC C(O)=O)C(NCC(N[C@H](CCC(O)=O)C(N[C@@H](C)C(N[C@@H](C)C(N[C@@H](CCCCNC(CC [C@@H](C(O)=O)NC(CCCCCCCCCCCCCCC)=O)=O)C(N[C@H](C(N[C@H](C(N [C@@H]([C@@H](C)CC)C(N[C@H](C(N[C@@H](CC2=CNC3=CC=CC=C23)C(N[C@@H](CC(C) C)C(N[C@@H](C(C)C)C(N[C@H](C(NCC(N[C@H](C(NCC(O)=O)=O)CCCNC( N)=N)=O)=O)CCCNC(N)=N)=O)=O)=O)=O)C)=O)=O)CC4=CC=CC=C4)=O)CCC(O)=O)=O)=O )=O)=O)=O)=O)=O)=O)=O)NC([C@H](CO)NC([C@H](C(C)C)NC([C@H](CC (O)=O)NC([C@H](CO)NC([C@H]([C@H](O)C)NC([C@H](CC5=CC=CC=C5)N C([C@H]([C@H](O)C)NC(CNC([C@H](CCC(O)=O)NC([C@H](C)NC([C@H](CC6=CNC=N6)N )=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O

General description

D-Glu(17)-Liraglutide is a stereoisomeric impurity of Liraglutide characterised by the replacement of L-Glutamic acid at position 17 (API numbering; position 17 in GLP-1 numbering) with its D-enantiomer (D-Glu). Position 17 resides within the central α-helical domain of the peptide, and its stereoinversion may perturb helix stability and receptor contact surface. The impurity is otherwise structurally identical to Liraglutide, retaining the palmitoyl–γGlu–Lys26 fatty acid conjugate. Racemisation at Glu residues during SPPS, particularly under prolonged activation or elevated temperature, is a recognised source of this impurity type.

Application

Used as an analytical standard for the identification and semi-quantification of the D-Glu17 diastereomeric impurity in Liraglutide API by reversed-phase HPLC, chiral chromatography, and LC-MS/MS methods.

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Este artículo
PHI90001PHI90002SML3925
description

GLP-1 Agonist Impurity, analytical standard, Numbering in the name as per API

description

GLP-1 Agonist Impurity, analytical standard, Numbering in the name as per API

description

GLP-1 Agonist Impurity, analytical standard, Numbering in the name as per API

description

≥95% (HPLC)

technique(s)

HPLC: suitable, liquid chromatography (LC): suitable, mass spectrometry (MS): suitable, LC/MS: suitable

technique(s)

LC/MS: suitable, liquid chromatography (LC): suitable, mass spectrometry (MS): suitable, HPLC: suitable

technique(s)

HPLC: suitable, liquid chromatography (LC): suitable, LC/MS: suitable, mass spectrometry (MS): suitable

technique(s)

-

format

neat

format

neat

format

neat

format

-

grade

analytical standard

grade

analytical standard

grade

analytical standard

grade

-

color

white to off-white

color

white to off-white

color

-

color

white to off-white

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

powder

form

solid, powder

form

solid

form

(Powder or Lyophilized powder or film)


Clase de almacenamiento

11 - Combustible Solids

Punto de inflamación (°F)

Not applicable

Punto de inflamación (°C)

Not applicable



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