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SML1720

Sigma-Aldrich

ATI-2341 trifluoroacetate salt

≥95% (HPLC)

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Synonym(s):
ATI 2341 trifluoroacetate salt, N-(1-Ohexadecyl)-L-methionylglycyl-L-tyrosyl-L-glutaminyl-L-lysyl-L-lysyl-L-leucyl-L-arginyl-L-seryl-L-methionyl-L-threonyl-L-α-aspartyl-L-lysyl-L-tyrosyl-L-arginyl- L-leucine, Pal-MGYQKKLRSMTDKYRL, Pal-Met-Gly-Tyr-Gln-Lys-Lys-Leu-Arg-Ser-Met-Thr-Asp-Lys-Tyr-Arg-Leu
Empirical Formula (Hill Notation):
C104H178N26O25S2 · xC2HF3O2
CAS Number:
Molecular Weight:
2256.82 (free base basis)

Quality Level

assay

≥95% (HPLC)

form

film

color

colorless

shipped in

wet ice

storage temp.

−20°C

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SML1720

ATI-2341 trifluoroacetate salt

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SML1472

TNIIIA2 trifluoroacetate salt

vibrant-m

SML2319

TAT-Gap19 trifluoroacetate salt

vibrant-m

SML2899

Humanin Trifluoroacetate

assay

≥95% (HPLC)

assay

≥95% (HPLC)

assay

≥95% (HPLC)

assay

≥95% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

-

Quality Level

100

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

color

colorless

color

colorless

color

white to off-white

color

white to beige

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

shipped in

-

Biochem/physiol Actions

ATI-2341 is a potent and selective allosteric agonist of chemokine CXC-type receptor 4 (CXCR4) that functions as a biased ligand, favoring Gαi activation over Gα13. ATI-2341 does not promote β-arrestin recruitment. ATI-2341 promotes the mobilization of PMNs and HSPCs in the peripheral circulation of both mice and monkeys.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Jesús M Planesas et al.
Journal of molecular graphics & modelling, 60, 1-14 (2015-06-17)
Several examples of allosteric modulators of GPCRs have been reported recently in the literature, but understanding their molecular mechanism presents a new challenge for medicinal chemistry. For the specific case of the cellular receptor CXCR4, it is known that pepducins
Julie Quoyer et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(52), E5088-E5097 (2013-12-07)
Short lipidated peptide sequences derived from various intracellular loop regions of G protein-coupled receptors (GPCRs) are named pepducins and act as allosteric modulators of a number of GPCRs. Recently, a pepducin selectively targeting the C-X-C chemokine receptor type 4 (CXCR4)
Boris Tchernychev et al.
Proceedings of the National Academy of Sciences of the United States of America, 107(51), 22255-22259 (2010-12-09)
The G protein-coupled receptor (GPCR), chemokine CXC-type receptor 4 (CXCR4), and its ligand, CXCL12, mediate the retention of polymorphonuclear neutrophils (PMNs) and hematopoietic stem and progenitor cells (HSPCs) in the bone marrow. Agents that disrupt CXCL12-mediated chemoattraction of CXCR4-expressing cells
Serap Erdogmus et al.
Nature communications, 10(1), 5784-5784 (2019-12-21)
G-protein coupled receptors (GPCRs) are versatile cellular sensors for chemical stimuli, but also serve as mechanosensors involved in various (patho)physiological settings like vascular regulation, cardiac hypertrophy and preeclampsia. However, the molecular mechanisms underlying mechanically induced GPCR activation have remained elusive.

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