Delmitide acetate

Modify Date: 2025-08-31 16:12:40

Delmitide acetate Structure
Delmitide acetate structure
Common Name Delmitide acetate
CAS Number 501019-16-5 Molecular Weight 1288.62
Density N/A Boiling Point N/A
Molecular Formula C59H105N17O11.C2H4O2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Delmitide acetate


Delmitide (RDP58) acetate is an orally active d-isomer decapeptide with potent anti-inflammatory activity. Delmitide acetate inhibits production of TNF-α, IFN-γ, and interleukin (IL)-12, and up-regulates heme oxygenase 1 activity. Delmitide acetate can be used for the research of ulcerative colitis[1][2].

 Names

Name Delmitide acetate

 Delmitide acetate Biological Activity

Description Delmitide (RDP58) acetate is an orally active d-isomer decapeptide with potent anti-inflammatory activity. Delmitide acetate inhibits production of TNF-α, IFN-γ, and interleukin (IL)-12, and up-regulates heme oxygenase 1 activity. Delmitide acetate can be used for the research of ulcerative colitis[1][2].
Related Catalog
In Vivo Delmitide acetate (oral; 2.5, 5, 10 mg/kg; daily) significantly reduced CPT-11induced diarrhea, mucosal inflammation, and mortality in mice by suppressing the overproduction of proinflammatory cytokines TNF-a, IFN-y, and IL-12 in vivo[2]. Delmitide acetate (oral; 2.5, 5, 10 mg/kg; daily) generates an enhanced tumor response and prolongation of time to relapse without concomitant Gl toxicity in mice[2].
References

[1]. Arthur Kaser, et al. Novel therapeutic targets in the treatment of IBD. Kaser, Arthur; Tilg, Herbert (2008). Expert Opinion on Therapeutic Targets, 12(5), 553–563.

[2]. Jingsong Zhao, et al. Oral RDP58 allows CPT-11 dose intensification for enhanced tumor response by decreasing gastrointestinal toxicity. Clin Cancer Res. 2004 Apr 15;10(8):2851-9.  

 Chemical & Physical Properties

Molecular Formula C59H105N17O11.C2H4O2
Molecular Weight 1288.62
InChIKey LTDMAMSELCSERL-XCQJOGLYSA-N
SMILES CC(=O)O.CCCCC(NC(=O)C(N)CCCN=C(N)N)C(=O)NC(CCCC)C(=O)NC(CCCC)C(=O)NC(CCCN=C(N)N)C(=O)NC(CCCC)C(=O)NC(CCCC)C(=O)NC(CCCC)C(=O)NCC(=O)NC(Cc1ccc(O)cc1)C(N)=O
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