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Merck

SML0294

ABL127

≥98% (HPLC)

Synonyme(s) :

(3R)-1,2-Dicarboxylic acid, 3-cyclopentyl-4-oxo-3-phenyl-1,2-diazetidine 1,2-dimethyl ester, (3R)-Dimethyl 3-cyclopentyl-4-oxo-3-phenyl-1,2-diazetidine-1,2-dicarboxylate, CID24856225

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A propos de cet article

Formule empirique (notation de Hill) :
C17H20N2O5
Numéro CAS:
1073529-41-5
Poids moléculaire :
332.35
NACRES:
NA.77
PubChem Substance ID:
329825301
UNSPSC Code:
12352200
MDL number:
MFCD28053514
Assay:
≥98% (HPLC)
Form:
film
Quality level:
100

Principaux documents

Voir toute la documentation
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Nom du produit

ABL127, ≥98% (HPLC)

InChI

1S/C17H20N2O5/c1-23-15(21)18-14(20)17(13-10-6-7-11-13,19(18)16(22)24-2)12-8-4-3-5-9-12/h3-5,8-9,13H,6-7,10-11H2,1-2H3/t17-/m0/s1

SMILES string

O=C1[C@](C2=CC=CC=C2)(C3CCCC3)N(C(OC)=O)N1C(OC)=O

InChI key

ZRHWCAFAIHTQKD-KRWDZBQOSA-N

assay

≥98% (HPLC)

form

film

color

colorless

solubility

DMSO: ≥5 mg/mL

storage temp.

2-8°C

Quality Level

100

Catégories apparentées

Biochem/physiol Actions

ABL127 is a potent and selective inhibitor of Protein phosphatase methylesterase-1 (PME-1 or PPME-1).
ABL127 is a potent and selective inhibitor of Protein phosphatase methylesterase-1 (PME-1 or PPME-1). IC50 values were 11.1 nM and 6.4 nM in MDA-MB-231 and HEK 293T cells with no activity detected against >50 other serine hydrolases. PME-1 regulates the methylesterification state of protein phosphatase 2A (PP2A) and is implicated in cancer and neurodegeneration.

Classe de stockage

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number
0000273481
0000273482
0000266777
0000273482
0000273481

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Shunta Ikeda et al.
Journal of biochemistry, 168(6), 643-650 (2020-07-15)
Bone marrow-derived mesenchymal stem cells (BM-MSCs) are multipotent stem cells with ability to self-replicate and differentiate into mesodermal derivatives, such as adipocytes and osteoblasts. BM-MSCs are a critical component of the tumour microenvironment. They support tumour progression by recruiting additional
Bin Wu et al.
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 17(4), 1878-1896 (2020-09-23)
The molecular mechanism of Alzheimer-like cognitive impairment induced by manganese (Mn) exposure has not yet been fully clarified, and there are currently no effective interventions to treat neurodegenerative lesions related to manganism. Protein phosphatase 2 A (PP2A) is a major
Ryotaro Yabe et al.
FEBS open bio, 8(9), 1486-1496 (2018-09-07)
Reversible methyl-esterification (methylation) of Leu309 in the protein phosphatase 2A catalytic subunit (PP2Ac) is essential for proper biogenesis of the PP2A holoenzyme. Accumulating evidence links PP2Ac methylation to diseases, including cancer and neurodegenerative disorders. Protein phosphatase methyl-esterase (PME-1) specifically catalyzes
Sydney A Labuzan et al.
Gene, 739, 144515-144515 (2020-03-01)
Protein phosphatase methylesterase 1 has been identified as a novel gene in skeletal muscle that is upregulated in response to neurogenic atrophy in mice. Western blot analysis confirms that Ppme1 is expressed during both muscle cell proliferation and differentiation. Additionally
Ling Meng et al.
Frontiers in immunology, 12, 648913-648913 (2021-04-30)
The excessive M1 polarization of macrophages drives the occurrence and development of inflammatory diseases. The reprogramming of macrophages from M1 to M2 can be achieved by targeting metabolic events. Taurine promotes for the balance of energy metabolism and the repair

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