Chemerin-9 (149-157)

CAS No. 676367-27-4

Chemerin-9 (149-157)( —— )

Catalog No. M30316 CAS No. 676367-27-4

The nonapeptide 149,YFPGQFAFS157 (chemerin-9), corresponding to the C terminus of processed chemerin, retained most of the activity of the full-size protein, with regard to agonism toward the chemerinR.the natural ligand of ChemR23 (chemerinR).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Chemerin-9 (149-157)
  • Note
    Research use only, not for human use.
  • Brief Description
    The nonapeptide 149,YFPGQFAFS157 (chemerin-9), corresponding to the C terminus of processed chemerin, retained most of the activity of the full-size protein, with regard to agonism toward the chemerinR.the natural ligand of ChemR23 (chemerinR).
  • Description
    The nonapeptide 149,YFPGQFAFS157 (chemerin-9), corresponding to the C terminus of processed chemerin, retained most of the activity of the full-size protein, with regard to agonism toward the chemerinR.the natural ligand of ChemR23 (chemerinR).
  • In Vitro
    Chemerin-9 (149-157) (0.1 nM; 24 h; cardiac fibroblasts) stimulates migration in cardiac fibroblasts and stimulates phosphorylation of Akt and ERK as well as ROS production. Western Blot Analysis Cell Line:Cardiac fibroblasts Concentration:0.1 nM Incubation Time:24 hours Result:Stimulated phosphorylation of Akt and ERK.
  • In Vivo
    Chemerin-9 (149-157) (0.2 mg/kg; i.p.; daily, for 42 days) alleviates glucose intolerance and IR in PDM mice.Chemerin-9 (149-157) (7.7? μg /kg; i.h.; daily, for 28 days) has anti-inflammatory and anti-angiogenic effects in ApoE-/- mice and protects the abdominal aorta from MMP damage.Chemerin-9 (149-157) (8 μg/kg; ICV; daily; for 14 d; male Kunming mice) ameliorates Aβ1-42-induced memory impairment. Animal Model:PDM mice Dosage:0.2 mg/kg Administration:Intraperitoneal injection; daily, for 42 daysResult:Increased expression of chemerin, GLUT2, and PDX1, which led to the alleviation of glucose intolerance and IR in PDM model mice. Animal Model: ApoE-/- mice Dosage:7.7 μg /kg Administration:Subcutaneous injection; daily, for 28 days Result:Suppressed the enlargement of abdominal aorta and reversed the SMC loss.Animal Model:ApoE-/- mice Dosage:7.7 μg/kg Administration:Subcutaneous injection; daily, for 28 days Result:Down-regulated MMP2 and MMP-9 expression and decreased the levels of chemerin and CMKLR1.Animal Model:Male Kunming mice Dosage:8 μg/kg Administration:Intracerebroventrical injection; daily; for 14 days Result:Increased in the levels of pro-in?ammatory cytokines such as interleukin-1β (IL-1β), tumor necrosis factor (TNF-α) and interleukin-6 (IL-6) in the hippocampus.
  • Synonyms
    ——
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Beta Amyloid
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    676367-27-4
  • Formula Weight
    1063.16
  • Molecular Formula
    C54H66N10O13
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ——
  • Chemical Name
    Sequence:{Tyr}{Phe}{Pro}{Gly}{Gln}{Phe}{Ala}{Phe}{Ser}

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

Wittamer V, et al. The C-terminal nonapeptide of mature chemerin activates the chemerin receptor with low nanomolar potency. J Biol Chem. 2004 Mar 12;279(11):9956-62.
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