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SML1773

Sigma-Aldrich

TYFAVLM trifluoroacetate salt

≥98% (HPLC)

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Synonym(s):
P7, Thr-Tyr-Phe-Ala-Val-Leu-Met trifluoroacetate salt, synthetic P7 peptide agonist trifluoroacetate salt
Empirical Formula (Hill Notation):
C41H61N7O10S · xC2HF3O2
Molecular Weight:
844.03 (free base basis)

Quality Level

assay

≥98% (HPLC)

form

lyophilized powder

storage condition

protect from light

color

white

shipped in

wet ice

storage temp.

−20°C

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Sigma-Aldrich

SML1773

TYFAVLM trifluoroacetate salt

TFLLR-NH2 trifluoroacetate salt >98% (HPLC)

T7830

TFLLR-NH2 trifluoroacetate salt

WKYMVdM trifluoroacetate salt ≥98% (HPLC), powder

W3020

WKYMVdM trifluoroacetate salt

Sigma-Aldrich

SML1370

A-779 trifluoroacetate salt

assay

≥98% (HPLC)

assay

>98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

Quality Level

100

Quality Level

-

Quality Level

-

Quality Level

100

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage condition

protect from light

storage condition

-

storage condition

-

storage condition

-

shipped in

wet ice

shipped in

-

shipped in

-

shipped in

wet ice

Biochem/physiol Actions

TYFAVLM/P7, a synthetic peptides comprising adhesion GPR56 β-strand-13 stalk, is a potent and selective agonist of GPR56. TYFAVLM activates GPR56 in cells.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Oladapo E Olaniru et al.
Molecular metabolism, 53, 101285-101285 (2021-07-06)
Members of the adhesion G protein-coupled receptor (aGPCR) subfamily are important actors in metabolic processes, with GPR56 (ADGRG1) emerging as a possible target for type 2 diabetes therapy. GPR56 can be activated by collagen III, its endogenous ligand, and by

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