Home Other Building Blocks 475086-01-2
475086-01-2,MFCD10567093
Catalog No.:AA00DA84

475086-01-2 | Ns-304

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
98%
in stock  
$17.00   $12.00
- +
2mg
98%
in stock  
$25.00   $18.00
- +
5mg
98%
in stock  
$35.00   $25.00
- +
10mg
98%
in stock  
$50.00   $35.00
- +
100mg
≥98%(HPLC)
in stock  
$411.00   $288.00
- +
500mg
≥98%(HPLC)
in stock  
$1,650.00   $1,155.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00DA84
Chemical Name:
Ns-304
CAS Number:
475086-01-2
Molecular Formula:
C26H32N4O4S
Molecular Weight:
496.6217
MDL Number:
MFCD10567093
SMILES:
O=C(NS(=O)(=O)C)COCCCCN(c1cnc(c(n1)c1ccccc1)c1ccccc1)C(C)C
Properties
Properties
 
Form:
Solid  
MP:
134-138°C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
730  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
35  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
12  
XLogP3:
3.8  

Downstream Synthesis Route
475085-57-5    3144-09-0   
Selexipag 

[1]CurrentPatentAssignee:EASTCHINAPHARMACEUTICALGROUPLIMITEDCOLTD-CN107365275,2017,ALocationinpatent:Paragraph0061;0062;0063;0064;0065;0066-0070

[2]CurrentPatentAssignee:SHANGHAISHIJIBIOLOGICALTECH;SEASONSBIOTECHNOLOGYTAIZHOU;SHANGHAISEASONSBIOTECHNOLOGY-US2018/29998,2018,A1Locationinpatent:Paragraph0076-079

[3]CurrentPatentAssignee:LUPINLIMITED-WO2017/60827,2017,A1Locationinpatent:Page/Pagecolumn12;13

[4]Asaki,Tetsuo;Hamamoto,Taisuke;Sugiyama,Yukiteru;Kuwano,Keiichi;Kuwabara,Kenji[BioorganicandMedicinalChemistry,2007,vol.15,#21,p.6692-6704]

[5]Asaki,Tetsuo;Kuwano,Keiichi;Morrison,Keith;Gatfield,John;Hamamoto,Taisuke;Clozel,Martine[JournalofMedicinalChemistry,2015,vol.58,#18,p.7128-7137]

[6]CurrentPatentAssignee:JIANGSUFANGSHENGPHARMACEUTICAL-CN113480484,2021,ALocationinpatent:Paragraph0027;0029;0030;0032;0033;0035

[7]CurrentPatentAssignee:NANJINGNMGADDS-CN106957269,2017,ALocationinpatent:Paragraph0025;0026

[8]CurrentPatentAssignee:NIPPONSHINYAKUCOLTD-EP1400518,2004,A1Locationinpatent:Page53-54

[9]CurrentPatentAssignee:MEGAFINEPHARMA(P)LTD.-WO2017/42828,2017,A2Locationinpatent:Page/Pagecolumn45-46

[10]CurrentPatentAssignee:HONOURRD-WO2017/168401,2017,A1Locationinpatent:Page/Pagecolumn11

[11]CurrentPatentAssignee:VIATRISINC-WO2018/15974,2018,A1Locationinpatent:Page/Pagecolumn39;40

[12]CurrentPatentAssignee:NANJINGUNIVERSITYOFSCIENCEANDTECHNOLOGY-CN112939877,2021,ALocationinpatent:Paragraph0059-0063;0064-0066;0069-0070

[1]Asaki,Tetsuo;Kuwano,Keiichi;Morrison,Keith;Gatfield,John;Hamamoto,Taisuke;Clozel,Martine[JournalofMedicinalChemistry,2015,vol.58,#18,p.7128-7137]

[2]CurrentPatentAssignee:MEGAFINEPHARMA(P)LTD.-WO2017/42828,2017,A2

[3]CurrentPatentAssignee:MEGAFINEPHARMA(P)LTD.-WO2017/42828,2017,A2

[4]CurrentPatentAssignee:LUPINLIMITED-WO2017/60827,2017,A1

[5]CurrentPatentAssignee:HONOURRD-WO2017/168401,2017,A1

[6]CurrentPatentAssignee:NANJINGNMGADDS-CN106957269,2017,A

[7]CurrentPatentAssignee:VIATRISINC-WO2018/15974,2018,A1

[8]CurrentPatentAssignee:EASTCHINAPHARMACEUTICALGROUPLIMITEDCOLTD-CN107365275,2017,A

[9]CurrentPatentAssignee:SHANGHAISEASONSBIOTECHNOLOGY;SEASONSBIOTECHNOLOGYTAIZHOU;SHANGHAISHIJIBIOLOGICALTECH-US2018/29998,2018,A1

[10]CurrentPatentAssignee:JIANGSUFANGSHENGPHARMACEUTICAL-CN113480484,2021,A

[11]Zhang,Kun;Hu,Kaizhao;Li,Qian;Li,Min;Gao,Ke;Yang,Kecheng;Zhao,Bing;Shi,Xiao-Jing;Zhang,Lirong;Liu,Hong-Min[JournalofMedicinalChemistry,2023,vol.66,#11,p.7221-7242]

[1]Asaki,Tetsuo;Kuwano,Keiichi;Morrison,Keith;Gatfield,John;Hamamoto,Taisuke;Clozel,Martine[JournalofMedicinalChemistry,2015,vol.58,#18,p.7128-7137]

[2]CurrentPatentAssignee:MEGAFINEPHARMA(P)LTD.-WO2017/42828,2017,A2

[3]CurrentPatentAssignee:MEGAFINEPHARMA(P)LTD.-WO2017/42828,2017,A2

[4]CurrentPatentAssignee:HONOURRD-WO2017/168401,2017,A1

[5]CurrentPatentAssignee:VIATRISINC-WO2018/15974,2018,A1

[6]CurrentPatentAssignee:SHANGHAISEASONSBIOTECHNOLOGY;SEASONSBIOTECHNOLOGYTAIZHOU;SHANGHAISHIJIBIOLOGICALTECH-US2018/29998,2018,A1

[7]Zhang,Kun;Hu,Kaizhao;Li,Qian;Li,Min;Gao,Ke;Yang,Kecheng;Zhao,Bing;Shi,Xiao-Jing;Zhang,Lirong;Liu,Hong-Min[JournalofMedicinalChemistry,2023,vol.66,#11,p.7221-7242]

[1]CurrentPatentAssignee:HEBEIUNIVERSITYOFSCIENCESANDTECHNOLOGY-CN106008364,2016,ALocationinpatent:Paragraph0023

[2]CurrentPatentAssignee:TEVAPHARMACEUTICALINDUSTRIESLTD.-WO2017/40872,2017,A1Locationinpatent:Paragraph0097-0098

[3]CurrentPatentAssignee:TEVAPHARMACEUTICALINDUSTRIESLTD.-WO2018/22704,2018,A1Locationinpatent:Paragraph00142-00144

475086-01-2   
CASUnavailable 

[1]CurrentPatentAssignee:LUPINLIMITED-WO2017/42731,2017,A1Locationinpatent:Page/Pagecolumn11;12

Literature

Title: Selexipag for the treatment of pulmonary arterial hypertension.

Journal: Expert review of respiratory medicine 20160101

Title: Pharmacokinetics and Tolerability of the Novel Oral Prostacyclin IP Receptor Agonist Selexipag.

Journal: American journal of cardiovascular drugs : drugs, devices, and other interventions 20150101

Title: Pathways in pulmonary arterial hypertension: the future is here.

Journal: European respiratory review : an official journal of the European Respiratory Society 20121201

Title: Selexipag: a selective prostacyclin receptor agonist that does not affect rat gastric function.

Journal: The Journal of pharmacology and experimental therapeutics 20101001

Title: A long-acting and highly selective prostacyclin receptor agonist prodrug, 2-{4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}-N-(methylsulfonyl)acetamide (NS-304), ameliorates rat pulmonary hypertension with unique relaxant responses of its active form, {4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}acetic acid (MRE-269), on rat pulmonary artery.

Journal: The Journal of pharmacology and experimental therapeutics 20080901

Title: Synthesis and evaluation of N-acylsulfonamide and N-acylsulfonylurea prodrugs of a prostacyclin receptor agonist.

Journal: Bioorganic & medicinal chemistry 20071215

Title: Structure-activity studies on diphenylpyrazine derivatives: a novel class of prostacyclin receptor agonists.

Journal: Bioorganic & medicinal chemistry 20071101

Title: 2-[4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy]-N-(methylsulfonyl)acetamide (NS-304), an orally available and long-acting prostacyclin receptor agonist prodrug.

Journal: The Journal of pharmacology and experimental therapeutics 20070901

Title: Prostanoid receptors and their biological actions.

Journal: Progress in lipid research 19930101

Title: An enzyme isolated from arteries transforms prostaglandin endoperoxides to an unstable substance that inhibits platelet aggregation.

Journal: Nature 19761021

Title: Kuwano K, et al. 2--[(5,6-diphenylpyrazin-2-yl)(isopropyl)aminobutoxy-N-(methylsulfonyl)acetamide (NS-304), an orally available and long-acting prostacyclin receptor agonist prodrug. J Pharmacol Exp Ther. 2007 Sep;322(3):1181-8.

Title: Mous DS, et al. Treatment of rat congenital diaphragmatic hernia with sildenafil and NS-304, selexipag's active compound, at the pseudoglandular stage improves lung vasculature. Am J Physiol Lung Cell Mol Physiol. 2018 May 10.

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