ChemicalBook--->CAS DataBase List--->66611-27-6

66611-27-6

66611-27-6 Structure

66611-27-6 Structure
IdentificationBack Directory
[Name]

Ru 24969
[CAS]

66611-27-6
[Synonyms]

RU 24969 hemisuccinate >=98% (HPLC)
5-Methoxy-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole succinate (2:1)
1H-Indole, 5-methoxy-3-(1,2,3,6-tetrahydro-4-pyridinyl)-, succinate (2:1)
1H-Indole, 5-methoxy-3-(1,2,3,6-tetrahydro-4-pyridinyl)-, butanedioate (2:1)
Butanedioic acid, compd. with 5-methoxy-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (1:2)
Butanedioic acid, compd. with5-methoxy-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (1:2)OTHER CA INDEX NAMES:1H-Indole, 5-methoxy-3-(1,2,3,6-tetrahydro-4-pyridinyl)-, butanedioate(2:1)
[Molecular Formula]

C32H38N4O6
[MDL Number]

MFCD09878262
[MOL File]

66611-27-6.mol
[Molecular Weight]

574.667
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: slightly soluble,DMSO: slightly soluble,Ethanol: slightly soluble,PBS (pH 7.2): 1 mg/ml
[form ]

A crystalline solid
[color ]

yellow to yellow-orange
[Water Solubility ]

H2O: 2mg/mL, clear (warmed)
[InChI]

1S/2C14H16N2O.C4H6O4/c2*1-17-11-2-3-14-12(8-11)13(9-16-14)10-4-6-15-7-5-10;5-3(6)1-2-4(7)8/h2*2-4,8-9,15-16H,5-7H2,1H3;1-2H2,(H,5,6)(H,7,8)
[InChIKey]

BNYJLRQAWCQJOM-UHFFFAOYSA-N
[SMILES]

COC1=CC2=C(NC=C2C3=CCNCC3)C=C1.OC(CCC(O)=O)=O.COC4=CC5=C(NC=C5C6=CCNCC6)C=C4
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

RU 24969 Succinate (2:1), is a SR-1A and SR-1B, and moderate SR-2C agonist. 5-HT1B/1A agonist. Also, it is a well-established substrate for human serotonin transporter (SERT).
[Biological Activity]

RU-24969 is a potent and selective agonist at the 5-HT1A and 5-HT1B receptors.
[in vivo]

RU 24969 (0.03-3.0 mg/kg; s.c.) dose-dependently decreases water consumption in water deprived rats[1].
RU 24969 (0.3-3.0 mg/kg; s.c.) dose-dependently increases forward locomotion[1].

Animal Model:Male Sprague-Dawley rats[1]
Dosage:0.03, 0.3, 1.0, 3.0 mg/kg
Administration:A single s.c.
Result:Decreased water consumption significantly at dose of 0.3, 1.0, and 3.0 mg/kg.
[IC 50]

5-HT1B Receptor: 0.38 nM (Ki); 5-HT1A Receptor: 2.5 nM (Ki)
[storage]

Store at RT
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