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A9232

AMI-1 sodium salt hydrate

≥98% (HPLC)

Synonym(e):

7,7′-Carbonylbis(azanediyl)bis(4-hydroxynaphthalene-2-sulfonic acid) sodium salt hydrate

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5 MG

€ 156,00

25 MG

€ 575,00

€ 156,00


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Über diesen Artikel

Empirische Formel (Hill-System):
C21H16N2O9S2 · xNa+ · yH2O
Molekulargewicht:
504.49 (anhydrous free acid basis)
NACRES:
NA.77
UNSPSC Code:
12352200

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Produktname

AMI-1 sodium salt hydrate, ≥98% (HPLC)

assay

≥98% (HPLC)

form

powder

storage condition

desiccated
protect from light

color

purple

solubility

H2O: >10 mg/mL

storage temp.

2-8°C

Quality Level

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Dieser Artikel
P0039S1825M3935
form

powder

form

solid

form

powder

form

powder

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

room temp

solubility

H2O: >10 mg/mL

solubility

DMSO: 10 mg/mL, clear (warmed)

solubility

H2O: ≥10 mg/mL

solubility

DMSO: 5 mg/mL, clear

storage condition

desiccated, protect from light

storage condition

desiccated

storage condition

desiccated

storage condition

-

Biochem/physiol Actions

AMI-1 inhibits arginine, but not lysine, methyltransferase activity in vitro, while not interacting with S-adenosyl methionine (AdoMet), unlike most methyltransferase inhibitors which compete for the AdoMet binding site.
Protein arginine N-methyltransferases (PRMTs) are involved in post-translational modification implicated in protein trafficking, signal transduction, and transcriptional regulation. AMI-1 does not inhibit lysine methyltransferase activity and does not interact with S-adenosylmethionine (AdoMet), unlike most methyltransferase inhibitors which compete for the AdoMet binding site. AMI-1 can modulate nuclear receptor-regulated transcription from estrogen and androgen response elements; and is a HIV-1 reverse transcriptase inhibitor. AMI-1 is a potent antagonist of NADPH-oxidase-derived superoxide production, but acts as a direct antioxidant rather than indirectly through methyltransferase inhibition.

Features and Benefits

This compound is a featured product for Gene Regulation research. Click here to discover more featured Gene Regulation products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

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Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Cingulate protein arginine methyltransferases 1 regulates peripheral hypersensitivity via fragile X messenger ribonucleoprotein.
Wu, et al.
Frontiers in Molecular Neuroscience, 16, 1153870-1153870 (2023)
Kirti Lathoria et al.
Autophagy, 19(7), 1997-2014 (2023-01-18)
Mutations in the Krebs cycle enzyme IDH1 (isocitrate dehydrogenase (NADP(+)) 1) are associated with better prognosis in gliomas. Though IDH1 mutant (IDH1R132H) tumors are characterized by their antiproliferative signatures maintained through hypermethylation of DNA and chromatin, mechanisms affecting cell death
Wenya Hou et al.
Developmental cell, 45(2), 262-275 (2018-04-25)
The complex architecture of neuronal networks in the brain requires tight control of the actin cytoskeleton. The actin nucleator Cobl is critical for neuronal morphogenesis. Here we reveal that Cobl is controlled by arginine methylation. Coprecipitations, coimmunoprecipitations, cellular reconstitutions, and in vitro

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