1. GPCR/G Protein PI3K/Akt/mTOR Stem Cell/Wnt MAPK/ERK Pathway Immunology/Inflammation NF-κB Metabolic Enzyme/Protease Neuronal Signaling
  2. Chemerin Receptor Akt ERK Reactive Oxygen Species Amyloid-β
  3. Chemerin-9 (149-157)

Chemerin-9 (149-157) is a potent agonist of chemokine-like receptor 1 (CMKLR1) . Chemerin-9 (149-157) has anti-inflammatory activity. Chemerin-9 (149-157) stimulates phosphorylation of Akt and ERK as well as ROS production. Chemerin-9 (149-157) ameliorates Aβ1-42-induced memory impairmen. Chemerin-9 (149-157) regulates immune responses, adipocyte differentiation, and glucose metabolism.

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Chemerin-9 (149-157) Chemical Structure

Chemerin-9 (149-157) Chemical Structure

CAS No. : 676367-27-4

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Description

Chemerin-9 (149-157) is a potent agonist of chemokine-like receptor 1 (CMKLR1) . Chemerin-9 (149-157) has anti-inflammatory activity. Chemerin-9 (149-157) stimulates phosphorylation of Akt and ERK as well as ROS production. Chemerin-9 (149-157) ameliorates Aβ1-42-induced memory impairmen. Chemerin-9 (149-157) regulates immune responses, adipocyte differentiation, and glucose metabolism[1][2][3][4].

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[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[4]

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[1].
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[2].
Chemerin-9 (149-157) (8 μg/kg; ICV; daily; for 14 d; male Kunming mice) ameliorates Aβ1-42-induced memory impairment[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: PDM mice[1]
Dosage: 0.2 mg/kg
Administration: Intraperitoneal injection; daily, for 42 days
Result: 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[2]
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[2]
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[3]
Dosage: 8 μg/kg
Administration: Intracerebroventrical injection; daily; for 14 days
Result: Increased in the levels of pro-inflammatory cytokines such as interleukin-1β (IL-1β), tumor necrosis factor (TNF-α) and interleukin-6 (IL-6) in the hippocampus.
Molecular Weight

1063.16

Formula

C54H66N10O13

CAS No.
Unlabeled CAS

Sequence Shortening

YFPGQFAFS

SMILES

OC[C@@H](C(O)=O)NC([C@H](CC1=CC=CC=C1)NC([C@H](C)NC([C@H](CC2=CC=CC=C2)NC([C@H](CCC(N)=O)NC(CNC([C@H]3N(C([C@H](CC4=CC=CC=C4)NC([C@H](CC5=CC=C(O)C=C5)N)=O)=O)CCC3)=O)=O)=O)=O)=O)=O

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Please store the product under the recommended conditions in the Certificate of Analysis.

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Chemerin-9 (149-157)
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