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93565-01-6

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93565-01-6 Structure

93565-01-6 Structure
IdentificationBack Directory
[Name]

MDL 72527
[CAS]

93565-01-6
[Synonyms]

CPC-200
MDL727527
MDL 72527
Mdl-72527da
MDL 72527, >=97%
MDL-72527 (MDL72527
MDL 72527 (hydrochloride)
N1,N4-Bis(2,3-butadienyl)putrescine
N,N'-Bis(2,3-butadienyl)-1,4-butanediamine
N1,N4-Di(buta-2,3-dienyl)butane-1,4-diamine
N,N'-Bis(2,3-butanedienyl)-1,4-butanediamine
N,N'-di(buta-2,3-dien-1-yl)butane-1,4-diaMine
N1,N4-Di-2,3-butadienyl-1,4-butanediaminedihydrochloride
N1,N4-bis(2,3-Butadienyl)-1,4-butanediamine hydrochloride
N,N'-bis(2,3-Butadienyl)-1,4-butanediamine dihydrochloride
N1,N4-DI(BUTA-2,3-DIENYL)BUTANE-1,4-DIAMINE DIHYDROCHLORIDE
N1,N4-Di(buta-2,3-dien-1-yl)butane-1,4-diaMine dihydrochloride
[Molecular Formula]

C12H20N2.2HCl
[MDL Number]

MFCD13152261
[MOL File]

93565-01-6.mol
Chemical PropertiesBack Directory
[Melting point ]

236-237 °C (decomp)(Solv: ethanol (64-17-5); ethyl acetate (141-78-6))
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

H2O: soluble15mg/mL, clear
[form ]

powder
[color ]

light yellow to light brown
[Water Solubility ]

H2O: 15mg/mL, clear
[InChI]

1S/C12H20N2.2ClH/c1-3-5-9-13-11-7-8-12-14-10-6-4-2;;/h5-6,13-14H,1-2,7-12H2;2*1H
[InChIKey]

ITVRWVVFVHINOH-UHFFFAOYSA-N
[SMILES]

Cl.Cl.C=C=CCNCCCCNCC=C=C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

MDL 72527 is a lysosomotropic polyamineoxidase inhibitor.
[Biological Activity]

Polyamine oxidase (POA) inhibitor. Does not inhibit monoamine oxidase or D-Amino acid oxidase. Displays anticancer and neuroprotective activity in vivo .
[in vivo]

MDL 72527 (100 mg/kg; i.p.; once) shows neuroprotective against neuronal cell damage after temporary focal cerebral ischemia[1].

Animal Model:250-300 g, Male spontaneously hypertensive rats (SHRs)[1]
Dosage:100 mg/kg
Administration:I.p.; after the induction of ischemia
Result:Significantly reduced meanarterial blood pressure, changed the brain edema formation from 85.7 ± 0.3 to 84.5 ± 0.9% in cortex and from 79.9 ± 1.7 to 78.4 ± 2.0% in subcortex (difference not significant), reduced ischemic injury volume by 22% in the cortex and 17% in the subcortex.
Spectrum DetailBack Directory
[Spectrum Detail]

MDL 72527(93565-01-6)1HNMR
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