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  • DC Chemicals Limited
  • China
  • Product Name: Serelaxin
  • Price: $Inquiry/250mg $Inquiry/100mg $Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

99489-94-8

99489-94-8 structure
99489-94-8 structure
  • Name: Relaxin H2 (human) trifluoroacetate salt
  • Chemical Name: Serelaxin
  • CAS Number: 99489-94-8
  • Molecular Formula:
  • Molecular Weight:
  • Catalog: Research Areas Cardiovascular Disease
  • Create Date: 2020-08-11 16:09:08
  • Modify Date: 2024-01-07 17:08:00
  • Serelaxin (RLX-030), a recombinant form of human gene-2 relaxin targeting the RLN receptor, is a vasoactive peptide hormone with an antifibrotic activity[1][2][3].

Name Serelaxin
Description Serelaxin (RLX-030), a recombinant form of human gene-2 relaxin targeting the RLN receptor, is a vasoactive peptide hormone with an antifibrotic activity[1][2][3].
Related Catalog
In Vivo Serelaxin (0.5 mg/kg per day, subcutaneous administration) produces 20 to 40 ng/mL of circulating hormone, which successfully prevents and reduces fibrosis progression in various experimental models of injury. The doses do not exhibit significant toxicity[1]. Serelaxin restores endothelial function by increasing nitric oxide (NO)-mediated relaxation but not endothelium-derived hyperpolarisation (EDH)[2]. Animal Model: Six- to 8-week-old male mice (on a 129sv or 129sv×C57B6J background, which were equally sensitive to tissue injury and fibrosis)[1]. Dosage: 0.5 mg/kg. Administration: Subcutaneous administration per day for 7 days. Result: Produced 20 to 40 ng/mL of circulating hormone.
References

[1]. Chrishan S Samuel, et al. Serelaxin Is a More Efficacious Antifibrotic Than Enalapril in an Experimental Model of Heart Disease. Hypertension. 2014 Aug;64(2):315-22.

[2]. Hooi Hooi Ng, et al. Serelaxin Treatment Reverses Vascular Dysfunction and Left Ventricular Hypertrophy in a Mouse Model of Type 1 Diabetes. Sci Rep. 2017 Jan 9;7:39604.

[3]. Serelaxin.

No Any Chemical & Physical Properties