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ChemicalBook--->CAS DataBase List--->58142-99-7

58142-99-7

58142-99-7 Structure

58142-99-7 Structure
IdentificationBack Directory
[Name]

Isoquinoline, 5-iodo- (9CI)
[CAS]

58142-99-7
[Synonyms]

Isoquinoline, 5-iodo-
Isoquinoline, 5-iodo- (9CI)
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C9H6IN
[MDL Number]

MFCD11226893
[MOL File]

58142-99-7.mol
[Molecular Weight]

255.06
Chemical PropertiesBack Directory
[Boiling point ]

336.8±15.0 °C(Predicted)
[density ]

1.837±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,2-8°C
[solubility ]

Ethanol:25.51(Max Conc. mg/mL);100.0(Max Conc. mM)
DMSO:25.51(Max Conc. mg/mL);100.0(Max Conc. mM)
[form ]

solid
[pka]

4.48±0.13(Predicted)
[color ]

Yellow to brown
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P280-P301+P312-P362+P364
[HS Code ]

2933491090
Hazard InformationBack Directory
[Biological Activity]

DSRM-3716 is a potent and selective SARM1 NADase inhibitor (NAD+ hydrolysis IC50 = 75 nM using recombinant SARM1 SAM-TIR construct) th at recapitulates the SARM1-/- phenotype and protects axons from degeneration induced by axotomy (EC50 = 2.1/1.9 μM by fragmentation/NfL release using mouse DRG neurons; 81/88% protection by 1/3 μM DSRM-3716 using human iPSC-derived motor neurons) or mitochondrial dysfunction (3-30 μM DSRM-3716 against 25 μM rotenone-induced injury; mouse DRG neurons). MechanisticallyDSRM-3716 undergoes base exchange with the nicotinamide (NAM) moiety of nicotinamide adenine dinucleotide (NAD+) to yield the bona fide inhibitor 1AD.
[storage]

4°C, protect from light
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