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65043-22-3

65043-22-3 Structure

65043-22-3 Structure
IdentificationBack Directory
[Name]

Indeloxazine hydrochloride
[CAS]

65043-22-3
[Synonyms]

Elen
Noin
CI 874
CI874l
CI-874l
YM 08054
YM 08054-1
Indeloxazine HCl
Indeloxazine hydrochloride
Indeloxadine hydrochloride
Indeloxazine hydrochloride USP/EP/BP
Indeloxazine Hydrochloride: Indeloxazine HCl
2-(3H-Inden-4-yloxymethyl)morpholine hydrochloride
MORPHOLINE, 2-[(1H-INDEN-7-YLOXY)METHYL]-, HYDROCHLORIDE
(±)-2-[(1H-Inden-7-yloxy)methyl]morpholine hydrochloride
Morpholine,2-[(1H-inden-7-yloxy)Methyl]-, hydrochloride (1:1)
[Molecular Formula]

C14H18ClNO2
[MDL Number]

MFCD00875849
[MOL File]

65043-22-3.mol
[Molecular Weight]

267.75
Chemical PropertiesBack Directory
[Melting point ]

169-170°; mp 155-156°
[storage temp. ]

Sealed in dry,Room Temperature
Safety DataBack Directory
[RIDADR ]

3249
[HazardClass ]

6.1(b)
[PackingGroup ]

III
[Toxicity]

LD50 in mice (mg/kg): 47 i.v. (Tachikawa)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Magnesium sulfate-->Isopropyl alcohol-->Indene-->2-AMINOETHYL HYDROGEN SULFATE-->Expoxide
Hazard InformationBack Directory
[Description]

Indeloxazine hydrochloride is a nootropic indicated for the treatment of senile dementia. In animal models indeloxazine reportedly enhances brain energy metabolism and monoamine content; its claimed protective effect on ischemia-induced amnesia is supported by the prolonged step-through latency in passive avoidance tests.
[Chemical Properties]

Polymorphic Forms: Pale yellow needle-shaped crystals obtained from methanol, melting point 169-170°C; colorless acicular crystals obtained from acetone, melting point 155-156°C. Acute toxicity LD50 in mice (mg/kg): 47 mg/kg by intravenous injection. (+)-Form: Crystals obtained from ethanol, melting point 112-113°C. [α]D21 + 4.9° (C = 5, methanol). (-)-Form: Crystals obtained from isopropanol, melting point 142-142.5°C. [α]D20 - 4.9° (C = 5, methanol).
[Originator]

Yamanouchi (Japan)
[Uses]

Antidepressant.
[Brand name]

Elen
[Metabolic pathway]

After oral administration of indeloxazine hydrochloride to rats, two conjugates, which are labile to a- glucosidase hydrolysis but refractory to b-glucosidase, are isolated from the urine and identified as a-D- glucopyranosides of trans-4-(2-morpholinylmethoxy)- 1,2-indandiol and trans-6-[[(1,2-dihydroxy-4- indanyl)oxy]-methyl]-3-morpholinone.
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