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GSK-1605786, also known as Vercirnon, is an orally bioavailable antagonist of chemokine receptor 9 (CCR9) with high selectivity and potency. It exhibits an IC50 value of 5.4 nM for inhibiting CCL25-induced calcium mobilization in Molt-4 cells and demonstrates allosteric binding to the intracellular side of CCR9, preventing G protein coupling.

698394-73-9

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698394-73-9 Usage

Uses

Used in Pharmaceutical Industry:
GSK-1605786 is used as a therapeutic agent for the treatment of autoimmune and inflammatory diseases, particularly for conditions involving the chemokine receptor CCR9. Its high selectivity and potency make it a promising candidate for targeted therapies.
Used in Cancer Research:
GSK-1605786 is used as a research tool for studying the role of CCR9 in cancer progression and metastasis. Its ability to inhibit CCL25-induced chemotaxis in various cell types, including human T cells and mouse and rat thymocytes, makes it valuable for investigating the mechanisms underlying CCR9-mediated cell migration and invasion in cancer.
Used in Drug Discovery:
GSK-1605786 serves as a lead compound for the development of novel CCR9 antagonists with improved pharmacological properties and therapeutic potential. Its allosteric binding mechanism and selectivity over other chemokine receptors provide a foundation for designing more effective and targeted drugs for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 698394-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,8,3,9 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 698394-73:
(8*6)+(7*9)+(6*8)+(5*3)+(4*9)+(3*4)+(2*7)+(1*3)=239
239 % 10 = 9
So 698394-73-9 is a valid CAS Registry Number.

698394-73-9Relevant academic research and scientific papers

Evaluation of tert-butyl isosteres: Case studies of physicochemical and pharmacokinetic properties, efficacies, and activities

Westphal, Matthias V.,Wolfst?dter, Bernd T.,Plancher, Jean-Marc,Gatfield, John,Carreira, Erick M.

, p. 461 - 469 (2015/03/13)

The tert-butyl group is a common motif in medicinal chemistry. Its incorporation into bioactive compounds is often accompanied by unwanted property modulation, such as increased lipophilicity and decreased metabolic stability. Several alternative substituents are available for the drug discovery process. Herein, physicochemical data of two series of drug analogues of bosentan and vercirnon are documented as part of a comparative study of tert-butyl, pentafluorosulfanyl, trifluoromethyl, bicyclo[1.1.1]pentanyl, and cyclopropyl-trifluoromethyl substituents.

PROPHYLACTIC OR THERAPEUTIC METHOD FOR SJOGREN'S SYNDROME

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Paragraph 0118; 0123; 0124, (2014/06/23)

The present invention provides a prophylactic or therapeutic agent and a prophylactic or therapeutic method superior in the prophylaxis or treatment of Sjogren's syndrome. Provided are a prophylactic or therapeutic agent for Sjogren's syndrome, containing

A CRYSTALLINE FORM OF THE SODIUM SALT OF 4-TERT-BUTYL-N-[4-CHLORO-2-(1-OXY-PYRIDINE-4-CARBONYL)-PHENYL]-BENZENE SULFONAMIDE

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Page/Page column 13; 14, (2013/03/26)

A novel crystalline form of the sodium salt of 4-tert-butyl-N-[4-chloro-2-(1- oxy-pyridine-4-carbonyl)-phenyl]-benzenesulfonamide and pharmaceutical compositions containing the same are disclosed. Processes for the preparation thereof and methods for use

ARYL SULFONAMIDES

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Page/Page column 158-159; 180-181, (2010/02/14)

The present invention relates to compounds that modulate various chemokine receptors. These compounds are useful for treating inflammatory and immune diseases.

ARYL SULFONAMIDES

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Page 63-64, (2008/06/13)

Compounds are provided that act as potent antagonists of the CCR9 receptor, and which have been further confirmed in animal testing for inflammation, one of the hallmark disease states for CCR9. The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR9-mediated diseases, and as controls in assays for the identification of CCR9 antagonists.

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