ChemicalBook--->CAS DataBase List--->20324-87-2

20324-87-2

20324-87-2 Structure

20324-87-2 Structure
IdentificationBack Directory
[Name]

Disodium 7,7'-(carbonyldiimino)bis(4-hydroxynaphthalene-2-sulphonate)
[CAS]

20324-87-2
[Synonyms]

AMI-1;AMI 1;AMI1
AMI-1 disodium salt
AMI-1 - AMI-1 sodium salt
J acid urea,disodiuM salt 70%
Disodium 6,6'-ureylenebis[1-naphthol-3-sulfonate]
Sodium 6,6'-(1,3-ureylene) bis(1-naphthol-3-sulfonate)
SODIUM 6,6'-(1,3-UREYLENE) BIS(1,1'-NAPHTHOL)-3,3'-SULFONATE
Disodium 7,7'-(carbonyldiimino)bis(4-hydroxynaphthalene-2-sulphonate)
7,7'-(carbonyldiimino)bis(4-hydroxy-2-naphthalenesulfonic acid) disodium salt
4-hydroxy-7-[(5-hydroxy-7-sulfonatonaphthalen-2-yl)carbamoylamino]naphthalene-2-sulfonate
disodium 4-hydroxy-7-[(5-hydroxy-7-sulfonato-2-naphthyl)carbamoylamino]naphthalene-2-sulfonate
disodium 4-hydroxy-7-[(5-hydroxy-7-sulfonatonaphthalen-2-yl)carbamoylamino]naphthalene-2-sulfonate
disodium 4-hydroxy-7-[(5-hydroxy-7-sulfonato-naphthalen-2-yl)carbamoylamino]naphthalene-2-sulfonate
[EINECS(EC#)]

243-735-4
[Molecular Formula]

C21H14N2Na2O9S2
[MDL Number]

MFCD00068249
[MOL File]

20324-87-2.mol
[Molecular Weight]

548.45
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

insoluble in EtOH; insoluble in DMSO; ≥19.1 mg/mL in H2O
[form ]

Brown solid.
[color ]

Light brown to brown
[EPA Substance Registry System]

2-Naphthalenesulfonic acid, 7,7'-(carbonyldiimino)bis[4-hydroxy-, disodium salt (20324-87-2)
Safety DataBack Directory
[TSCA ]

TSCA listed
[REACH Registrations]

Active
Hazard InformationBack Directory
[Chemical Properties]

Light grey paste. Soluble in water and easily soluble in alkaline solution.
[Uses]

AMI-1 is a Histone Methyltransferase (HMT) inhibitor.
[Biological Activity]

potent, cell permeable and specific protein arginine n-methyltransferase 1 (prmt1) inhibitor (ic50 = 8, 8 μm), does not compete for the adomet (s-adenosyl-l-methionine, sam) binding site, blocks peptide substrate binding, hiv-1 rt polymerase inhibitor (ic50 = 5, 0 μm).
[in vivo]

AMI-1 (0.5 mg; intratumorally; daily; for 7 days) inhibits S180 viability in vivo[4].
? AMI-1 (0.5 mg; intratumorally; daily; for 7 days) downregulates PRMT5 but does not regulate the expression of PRMT7 in a tumor xenograft model[4].
? AMI-1 (0.5 mg; intratumorally; daily; for 7 days) decreases the levels of H4R3me2s and H3R8me2s in a tumor xenograft model[4].

Animal Model:6-7 weeks old male Kunming mice (18-22 g), with S180 cells xenograft[4]
Dosage:0.5 mg
Administration:Intratumorally, daily, for 7 days
Result:Decreased tumor weight.
[IC 50]

PRMT1
Spectrum DetailBack Directory
[Spectrum Detail]

Disodium 7,7'-(carbonyldiimino)bis(4-hydroxynaphthalene-2-sulphonate)(20324-87-2)1HNMR
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