Linsidomine hydrochloride
Names
[ CAS No. ]:
16142-27-1
[ Name ]:
Linsidomine hydrochloride
[Synonym ]:
3-(4-morpholinyl)-5-sydnone imine hydrochloride
[3-(4-Morpholinyl)-1,2,3-oxadiazol-3-ium-5-yl]azanide hydrochloride (1:1)
3-(4-Morpholinyl)sydnone imine hydrochloride Linsidomine hydrochloride SIN-1 hydrochloride
T6N DOTJ A- AT5KNOYJ DUM &&sydnone
SIN-I HYDROCHLORIDE
LINSIDOMINE HCL
3-(4-morpholinyl)-sydnonimine hydrochloride
[3-(Morpholin-4-yl)-1,2,3-oxadiazol-3-ium-5-yl]azanide hydrochloride (1:1)
MFCD00221615
3-(4-Morpholinyl)sydnone imine hydrochloride
LinsidoMine Chlorhydrate
3-morpholinosydnone imine hydrochloride
1,2,3-Oxadiazolium, 5-amino-3-(4-morpholinyl)-, inner salt, hydrochloride (1:1)
MolsidoMine IMpurity A
SIN-1
SIN-1 CHLORIDE
B-HT 933 dihydrochloride
3-morpholino-sydnonimine hydrochloride
SIN-1 HCL
3-Morpholinosydnonimine hydrochloride
5-Imino-3-(morpholin-4-yl)-5H-1,2,3-oxadiazol-3-ium-2-ide hydrochloride (1:1)
SIN-1 HYDROCHLORIDE
EINECS 247-207-4
LINSIDOMINE
Biological Activity
[Description]:
[Related Catalog]:
[References]
Chemical & Physical Properties
[ Melting Point ]:
186 °C
[ Molecular Formula ]:
C6H11ClN4O2
[ Molecular Weight ]:
206.630
[ Exact Mass ]:
206.057053
[ PSA ]:
67.28000
[ Storage condition ]:
-20°C
[ Water Solubility ]:
soluble
MSDS
Toxicological Information
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- WU7687800
- CHEMICAL NAME :
- Sydnone imine, 3-morpholino-, monohydrochloride
- CAS REGISTRY NUMBER :
- 16142-27-1
- LAST UPDATED :
- 198910
- DATA ITEMS CITED :
- 3
- MOLECULAR FORMULA :
- C6-H10-N4-O2.Cl-H
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 480 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 2,280,1968
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intraperitoneal
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 315 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 2,280,1968
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intravenous
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 260 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- REFERENCE :
- OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 2,280,1968
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Safety Phrases ]:
S24/25
[ RIDADR ]:
NONH for all modes of transport
[ HS Code ]:
2934999090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2934999090
[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles
Cell Death Dis. 5 , e1410, (2014)
Platelet activation is a frontline response to injury, not only essential for clot formation but also important for tissue repair. Indeed, the reparative influence of platelets has long been exploited...
Taurine reduces nitrosative stress and nitric oxide synthase expression in high glucose-exposed human Schwann cells.Exp. Neurol. 233(1) , 154-62, (2012)
The role of taurine in regulating glucose-induced nitrosative stress has been examined in human Schwann cells, a model for understanding the pathogenesis of diabetic neuropathy. Exposure to high gluco...
Comparative kinetics of thiol oxidation in two distinct free-radical generating systems: SIN-1 versus AAPH.Free Radic. Res. 46(10) , 1190-200, (2012)
To study oxidative stress in biological systems, chemical compounds capable of producing free radicals have been widely used. Here, we compared two free-radical generators, 3-morpholinosydnonimine (SI...