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1,2-Dihydro-N-[(3-endo)-8-[(2R)-2-hydroxy-3-[methyl(methylsulfonyl)amino]propyl]-8-azabicyclo[3.2.1]oct-3-yl]-1-(1-methylethyl)-2-oxo-3-quinolinecarboxamide is a complex organic compound characterized by a quinoline ring, an amide group, and a bicyclic structure. It is a derivative of quinoline, featuring a nitrogen-containing heterocyclic ring and an amide functional group. 1,2-Dihydro-N-[(3-endo)-8-[(2R)-2-hydroxy-3-[methyl(methylsulfonyl)amino]propyl]-8-azabicyclo[3.2.1]oct-3-yl]-1-(1-methylethyl)-2-oxo-3-quinolinecarboxamide's intricate molecular structure endows it with potential biological activity, making it a promising candidate for applications in medicinal chemistry and drug development.

866933-46-2

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  • 1,2-Dihydro-N-[(3-endo)-8-[(2R)-2-hydroxy-3-[methyl(methylsulfonyl)amino]propyl]-8-azabicyclo[3.2.1]oct-3-yl]-1-(1-methylethyl)-2-oxo-3-quinolinecarboxamide

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  • 1,2-Dihydro-N-[(3-endo)-8-[(2R)-2-hydroxy-3-[methyl(methylsulfonyl)amino]propyl]-8-azabicyclo[3.2.1]oCt-3-yl]-1-(1-methylethyl)-2-oxo-3-quinolinecarboxamide

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  • 1,2-DIHYDRO-N-[(3-ENDO)-8-[(2R)-2-HYDROXY-3-[METHYL(METHYLSULFONYL)AMINO]PROPYL]-8-AZABICYCLO[3.2.1]OCT-3-YL]-1-(1-METHYLETHYL)-2-OXO-3-QUINOLINECARBOXAMIDE

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866933-46-2 Usage

Uses

Used in Medicinal Chemistry:
1,2-Dihydro-N-[(3-endo)-8-[(2R)-2-hydroxy-3-[methyl(methylsulfonyl)amino]propyl]-8-azabicyclo[3.2.1]oct-3-yl]-1-(1-methylethyl)-2-oxo-3-quinolinecarboxamide is used as a compound with potential biological activity for the development of new drugs. Its unique structure, including the quinoline ring and amide group, may contribute to its interaction with biological targets, offering opportunities for the treatment of various diseases.
Used in Drug Development:
In the pharmaceutical industry, 1,2-Dihydro-N-[(3-endo)-8-[(2R)-2-hydroxy-3-[methyl(methylsulfonyl)amino]propyl]-8-azabicyclo[3.2.1]oct-3-yl]-1-(1-methylethyl)-2-oxo-3-quinolinecarboxamide is utilized as a starting point for the design and synthesis of novel therapeutic agents. Its complex molecular architecture allows for modifications and optimizations to enhance its pharmacological properties, such as potency, selectivity, and bioavailability, ultimately leading to the creation of effective medications.

Check Digit Verification of cas no

The CAS Registry Mumber 866933-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,9,3 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 866933-46:
(8*8)+(7*6)+(6*6)+(5*9)+(4*3)+(3*3)+(2*4)+(1*6)=222
222 % 10 = 2
So 866933-46-2 is a valid CAS Registry Number.

866933-46-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[8-[(2R)-2-hydroxy-3-[methyl(methylsulfonyl)amino]propyl]-8-azabicyclo[3.2.1]octan-3-yl]-2-oxo-1-propan-2-ylquinoline-3-carboxamide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:866933-46-2 SDS

866933-46-2Downstream Products

866933-46-2Relevant articles and documents

Discovery, oral pharmacokinetics and in vivo efficacy of velusetrag, a highly selective 5-HT4 receptor agonist that has achieved proof-of-concept in patients with chronic idiopathic constipation

Long, Daniel D.,Armstrong, Scott R.,Beattie, David T.,Choi, Seok-Ki,Fatheree, Paul R.,Gendron, Roland A.L.,Genov, Daniel,Goldblum, Adam A.,Humphrey, Patrick P.,Jiang, Lan,Marquess, Daniel G.,Shaw, Jeng-Pyng,Smith, Jacqueline A.M.,Turner, S. Derek,Vickery, Ross G.

, p. 6048 - 6052 (2012/10/29)

Utilization of Theravance's multivalent approach to drug discovery towards 5-HT4 receptor agonists with a focus on identification of neutral (non-charged at physiological pH) secondary binding groups is described. Optimization of a quinolone-tr

Prokinetic agent for bowel preparation

-

, (2008/12/09)

The invention provides methods of bowel preparation before a diagnostic, surgical or therapeutic procedure, in particular, bowel preparation before a colonoscopy procedure, using a 5-HT4 receptor agonist as a prokinetic agent.

Crystalline form of a quinolinone-carboxamide compound

-

Page/Page column 10, (2010/11/24)

The invention provides a crystalline hydrochloride salt of 1-isopropyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acid {(1S,3R,5R)-8-[(R)-2-hydroxy-3-(methanesulfonyl-methyl-amino)propyl]-8-azabicyclo[3.2.1]oct-3-yl}amide or a solvate thereof. The invention also provides pharmaceutical compositions comprising such crystalline salt forms, methods of using such crystalline salt forms to treat diseases associated with 5-HT4 receptor activity, and processes useful for preparing such crystalline salt forms.

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