1. MAPK/ERK Pathway Stem Cell/Wnt NF-κB GPCR/G Protein Immunology/Inflammation
  2. ERK NF-κB CCR
  3. Resolvin D5

Resolvin D5 is an anti-inflammatory and analgesic agent produced in M2 macrophages. Resolvin D5 alleviates Paclitaxel (HY-B0015)-induced mechanical allodynia and inflammatory pain by activating the GPR32 receptor, with gender specificity (effective only in male mice) and independence from TRPV1 or TRPA1 channels. Resolvin D5 attenuates LPS-induced ERK phosphorylation and NF-κB nuclear translocation, downregulates proinflammatory mediators such as IL-6 and CCL5, inhibits Th17 cell differentiation and osteoclastogenesis, promotes regulatory T cell differentiation, and shows no cytotoxicity to human monocytes. The level of Resolvin D5 is elevated in arthritic SKG mice, but Resolvin D5 has no effect on dendritic cell differentiation or M1 macrophage polarization, nor does it prevent ZyA-induced arthritis progression. Resolvin D5 is suitable for research related to chemotherapy-induced peripheral neuropathy, inflammatory pain and rheumatoid arthritis.

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Resolvin D5

Resolvin D5 Chemical Structure

CAS No. : 578008-43-2

Size Price Stock Quantity
Solvent
5 μg (277.40 μM * 50 μL in Ethanol) In-stock
Solvent
10 μg (277.40 μM * 100 μL in Ethanol) In-stock
Solvent
25 μg (277.40 μM * 250 μL in Ethanol) In-stock

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Based on 1 publication(s) in Google Scholar

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Description

Resolvin D5 is an anti-inflammatory and analgesic agent produced in M2 macrophages. Resolvin D5 alleviates Paclitaxel (HY-B0015)-induced mechanical allodynia and inflammatory pain by activating the GPR32 receptor, with gender specificity (effective only in male mice) and independence from TRPV1 or TRPA1 channels. Resolvin D5 attenuates LPS-induced ERK phosphorylation and NF-κB nuclear translocation, downregulates proinflammatory mediators such as IL-6 and CCL5, inhibits Th17 cell differentiation and osteoclastogenesis, promotes regulatory T cell differentiation, and shows no cytotoxicity to human monocytes. The level of Resolvin D5 is elevated in arthritic SKG mice, but Resolvin D5 has no effect on dendritic cell differentiation or M1 macrophage polarization, nor does it prevent ZyA-induced arthritis progression. Resolvin D5 is suitable for research related to chemotherapy-induced peripheral neuropathy, inflammatory pain and rheumatoid arthritis[1][2][3].

In Vitro

Resolvin D5 (100, 500 nM; 3-5 days) suppresses Th17 cell differentiation and facilitates Treg differentiation in CD4+ T cells isolated from SKG mouse spleens in a concentration-dependent manner[1].
Resolvin D5 (1-100 nM; 3 days) suppresses the proliferation of CD4+ T cells isolated from SKG mouse spleens in a concentration-dependent manner, with 100 nM inducing a significant reduction in proliferating cells[1].
Resolvin D5 (10-500 nM; 3 days) suppresses RANKL-induced osteoclast differentiation in bone marrow-derived macrophages from SKG mice in a concentration-dependent manner, with 10, 100, and 500 nM concentrations reducing TRAP+ MNC formation and downregulating key osteoclastogenesis-related genes[1].

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

Cell Differentiation Assay[1]

Cell Line: Th17 cell
Concentration: 1, 10, 100, 500 nM
Incubation Time: 3-5 days
Result: Suppressed Th17 cell differentiation and facilitates Treg differentiation in CD4+ T cells isolated from SKG mouse spleens in a concentration-dependent manner (100-500 nM).
In Vivo

Resolvin D5 (1000 ng; i.p.; daily) does not prevent arthritis progression in a chronic persistent SKG mouse model of rheumatoid arthritis[1].
Resolvin D5 (100 ng; i.t.; single dose) produces a transient, male-specific reduction in chemotherapy-induced mechanical allodynia in wild-type, Trpv1 knockout, and Trpa1 knockout mice, with no analgesic effect in female mice[2].
Resolvin D5 (10 ng; i.t.; single dose) produces a male-specific reduction in formalin-induced Phase II inflammatory pain, with no analgesic effect in female mice or on Phase I pain responses[2].

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

Animal Model: CD1 mice with Chemotherapy-induced peripheral neuropathy (male and female, adult, 25-35 g); B6.129X1-Trpv1tm1Jul/J (male and female, Trpv1 knockout); B6;129P-Trpa1tm1Kykw/J (male and female, Trpa1 knockout)[2]
Dosage: 100 ng
Administration: i.t.; single dose
Result: Significantly increased paw withdrawal threshold (reduced mechanical allodynia) in male wild-type, male Trpv1 knockout, and male Trpa1 knockout mice at 1 hour post-injection, with effects diminished by 3 hours post-injection.
Showed no significant change in paw withdrawal threshold in female wild-type, female Trpv1 knockout, or female Trpa1 knockout mice at any time point post-injection.
Animal Model: CD1 mice with Inflammatory pain (male and female, adult, 25-35 g)[2]
Dosage: 10 ng
Administration: i.t.; single dose
Result: Significantly reduced the duration of licking and flinching during the Phase II inflammatory pain response (10-45 minutes post-formalin) in male mice, with no significant effect on Phase I pain behavior (0-10 minutes post-formalin).
Showed no significant change in Phase I or Phase II pain behavior in female mice.
Molecular Weight

360.49

Formula

C22H32O4

CAS No.
Appearance

Liquid

Color

Colorless to light yellow

SMILES

CC/C=C\C[C@H](O)/C=C/C=C\C/C=C\C=C\[C@@H](O)C/C=C\CCC(O)=O

Structure Classification
Initial Source
Shipping

Shipping with dry ice.

Storage

-80°C

Purity & Documentation

Purity: 98.3%

References
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Resolvin D5
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