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Chemical Structure| 1675-66-7 Chemical Structure| 1675-66-7

Structure of Adelmidrol
CAS No.: 1675-66-7

Chemical Structure| 1675-66-7

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Adelmidrol is an ethanolamide derivative of azelaic acid with anti-inflammatory properties partly dependent on PPARγ, it also markedly reduce pro-inflammatory NF-κB pathway.

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Product Details of Adelmidrol

CAS No. :1675-66-7
Formula : C13H26N2O4
M.W : 274.36
SMILES Code : O=C(NCCO)CCCCCCCC(NCCO)=O
MDL No. :MFCD00868853
InChI Key :PAHZPHDAJQIETD-UHFFFAOYSA-N
Pubchem ID :176874

Safety of Adelmidrol

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of Adelmidrol

PI3K-AKT
pyroptosis

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Caco-2 cells 10 μM 24 h To evaluate the effect of Adelmidrol on PEA levels under inflammatory conditions, results showed Adelmidrol significantly increased PEA production. Metabolites. 2022 May 19;12(5):457

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Male CD1 mice Bleomycin-induced pulmonary fibrosis model Oral 10 mg/kg Daily for 21 days Adelmidrol treatment reduced the infiltration of inflammatory cells, decreased myeloperoxidase (MPO) activity, and downregulated the overexpression of pro-inflammatory cytokines (IL-6, IL-1β, TNF-α, and TGF-1β). Additionally, adelmidrol significantly modulated antioxidant capacity, reduced oxidative burden, decreased nitric oxide production, and regulated the JAK2/STAT3 and IκBα/NF-κB pathways. Histological examination revealed reduced lung tissue injury, mast cell degranulation, chymase activity, and collagen deposition. Antioxidants (Basel). 2020 Jul 9;9(7):601
Rats Β-carrageenin-induced granuloma model Local administration 15, 30, 70 mg/ml Single administration, lasting 96 hours To evaluate the anti-inflammatory effect of Adelmidrol in a chronic inflammation model. Results showed that Adelmidrol significantly reduced granuloma formation, leukocyte infiltration, pro-inflammatory markers (e.g., TNF-α, iNOS, and nitric oxide), and angiogenesis by modulating mast cell degranulation and numbers. J Cell Mol Med. 2009 Jun;13(6):1086-95

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.64mL

0.73mL

0.36mL

18.22mL

3.64mL

1.82mL

36.45mL

7.29mL

3.64mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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