Basic information Safety Supplier Related

2,3,5,6,7,8-HEXAHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE

Basic information Safety Supplier Related

2,3,5,6,7,8-HEXAHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE Basic information

Product Name:
2,3,5,6,7,8-HEXAHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE
Synonyms:
  • 9-Amino-2,3,5,6,7,8-hexahydro-1H-cyclopenta(b)quinoline monohydrochloride
  • MFCD11052605
  • 1H,2H,3H,5H,6H,7H,8H-Cyclopenta[b]quinolin-9-amine
  • CBI-BB ZERO/005050
  • AURORA KA-7699
  • 2,3,5,6,7,8-HEXAHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE
  • 9-AMINO-2,3,5,6,7,8-HEXAHYDRO-1H-CYCLOPENTA[B]QUINOLINE
  • AKOS MSC-0106
CAS:
62732-44-9
MF:
C12H16N2
MW:
188.27
EINECS:
676-166-9
Mol File:
62732-44-9.mol
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2,3,5,6,7,8-HEXAHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE Chemical Properties

Melting point:
202-203 °C(Solv: methanol (67-56-1); water (7732-18-5))
Boiling point:
368.0±42.0 °C(Predicted)
Density 
1.170±0.06 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
DMF: 25 mg/ml,DMSO: 25 mg/ml,DMSO:PBS (pH 7.2) (1:3): 0.25 mg/ml
form 
A solid
pka
10.88±0.20(Predicted)
color 
White to off-white
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
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2,3,5,6,7,8-HEXAHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE Usage And Synthesis

Uses

Ipidacrine is used in biological studies as a possible treatment of toxic cognitive disorders.

Definition

ChEBI: 2,3,5,6,7,8-hexahydro-1H-cyclopenta[b]quinolin-9-amine is an aminoquinoline.

in vivo

Ipidacrine (1 mg/kg, p.o., repeated and a single dose for 5 days) by repeated administration has more potent antiamnesic effects than by single administration in induced by nucleus basalis of meynert (NBM) induced rats[1].
Ipidacrine (10 mg/kg p.o., a single dose) significantly decreases spontaneous movements, which is more selective as an antiamnesic than either Tacrine (HY-111338) and E-2020 (HY-B0034) in rats[1].
Ipidacrine (6.7 mg/kg, intragastrically, daily for 14 days) leads to statistically more efficient evolving of intracavernous pressure (ICPmax)/maxipressure (MAP) compared with control group in Streptozotocin (STZ) (HY-13753)-induced diabetic rats[3].

Animal Model:Rats[1]
Dosage:1 mg/kg
Administration:p.o., repeated and a single dose for 5 days
Result:The repeated administration of ipidacrine improved amnesia induced by nucleus basalis of meynert (NBM) lesions in the passive avoidance task in rats.
Animal Model:Rats[1]
Dosage:3, 10, 30 mg/kg
Administration:p.o., a single dose
Result:Decreased pupil size and increased salivation at 3 mg/kg, decreased spontaneous movements at 10 mg/kg and decreased body temperature and induced tremor at 30 mg/kg in rats.
Animal Model:Rats with streptozotocin (STZ) (HY-13753) induced diabetes mellitus-induced erectile dysfunction (DMED)[1]
Dosage:6.7 mg/kg
Administration:crushed, suspended in 1% starch solution and administered intragastrically daily for 14 days
Result:Ipidacrine was as effective as sildenafil and could significantly improve DMED symptoms.

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