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261901-57-9

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261901-57-9 Usage

Description

SB269970 HCl, also known as SB-269970, is a potent and selective 5-HT7 receptor antagonist. It is an analogue of SB-258719 and demonstrates high potency both in vivo and in vitro. SB269970 HCl is characterized by its ability to induce functional desensitization of the 5-HT7 receptor system, which may contribute to its rapid antidepressant-like effects in animal models. It exhibits high selectivity for the 5-HT7 receptor, with at least 100-fold selectivity over other 5-HT receptor subtypes except the human 5-HT5A receptor.

Uses

Used in Pharmaceutical Research:
SB269970 HCl is used as a research tool for studying the role of the 5-HT7 receptor in various neurobehavioral effects. Its high selectivity and potency make it a valuable compound for investigating the mechanisms underlying conditions such as schizophrenia, depression, and other cognitive deficits.
Used in Antidepressant Drug Development:
SB269970 HCl is used as a lead compound in the development of new antidepressant medications. Its rapid antidepressant-like effects in animal models suggest that it may be a promising candidate for the development of novel treatments for depression.
Used in Schizophrenia Research:
SB269970 HCl is used as a selective 5-HT7 receptor antagonist in the study of schizophrenia-like cognitive deficits. Its ability to target the 5-HT7 receptor may provide insights into the underlying causes of cognitive impairments associated with schizophrenia and contribute to the development of more effective treatments.
Used in Neuropharmacology:
SB269970 HCl is used as a pharmacological agent in the field of neuropharmacology to explore the interactions between serotonin and its various receptor subtypes. This can help researchers better understand the complex roles of serotonin in the central nervous system and develop more targeted therapies for a range of neurological and psychiatric disorders.

Biochem/physiol Actions

Primary Target5-HT

references

[1] hagan j j, price g w, jeffrey p, et al. characterization of sb-269970-a, a selective 5-ht7 receptor antagonist. british journal of pharmacology, 2000, 130(3): 539-548.

Check Digit Verification of cas no

The CAS Registry Mumber 261901-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,9,0 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 261901-57:
(8*2)+(7*6)+(6*1)+(5*9)+(4*0)+(3*1)+(2*5)+(1*7)=129
129 % 10 = 9
So 261901-57-9 is a valid CAS Registry Number.

261901-57-9 Well-known Company Product Price

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  • Sigma

  • (S7389)  SB-269970 hydrochloride  powder, ≥98% (HPLC)

  • 261901-57-9

  • S7389-5MG

  • 3,006.90CNY

  • Detail
  • Sigma

  • (S7389)  SB-269970 hydrochloride  powder, ≥98% (HPLC)

  • 261901-57-9

  • S7389-25MG

  • 10,570.95CNY

  • Detail

261901-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-3-((2-(2-(4-Methylpiperidin-1-yl)ethyl)pyrrolidin-1-yl)sulfonyl)phenol hydrochloride

1.2 Other means of identification

Product number -
Other names (R)-3-[2-[2-(4-Methylpiperidin-1-yl)ethyl]pyrrolidine-1-sulfonyl]phenol hydrochloride SB 269970A

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:261901-57-9 SDS

261901-57-9Downstream Products

261901-57-9Relevant articles and documents

Efficient Arndt-Eistert synthesis of selective 5-HT7 receptor antagonist SB-269970

Schjoth-Eskesen, Christina,Jensen, Henrik Helligso

, p. 3243 - 3253 (2009)

This contribution describes a novel Arndt-Eistert approach for the efficient synthesis of the potent and selective 5-HT7-antagonist, (R)-3-(2-(2-(4-methylpiperidin-1-yl)-ethyl)pyrrolidine-1-sulfonyl)phenol (SB-269970), from D-proline. The synthesis was ca

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