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Merck
CN

H3021

Sigma-Aldrich

Antiflammin-2

≥97% (HPLC)

Synonym(s):

Anti-inflammatory peptide 2, His-Asp-Met-Asn-Lys-Val-Leu-Asp-Leu

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About This Item

Empirical Formula (Hill Notation):
C46H77N13O15S
CAS Number:
Molecular Weight:
1084.25
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
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Assay

≥97% (HPLC)

composition

Peptide content, ~65%

storage temp.

−20°C

SMILES string

CSCCC(NC(=O)C(CC(O)=O)NC(=O)C(N)Cc1cnc[nH]1)C(=O)NC(CC(N)=O)C(=O)NC(CCCCN)C(=O)NC(C(C)C)C(=O)NC(CC(C)C)C(=O)NC(CC(O)=O)C(=O)NC(CC(C)C)C(O)=O

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Wayne B Anderson et al.
Chemical research in toxicology, 17(5), 650-662 (2004-05-18)
Dichloroacetic acid (DCA) is a drinking water contaminant, a therapeutic agent, and a rodent carcinogen. Glutathione transferase zeta (GSTZ1-1) catalyzes the biotransformation of a range of alpha-haloalkanoates and the cis-trans isomerization of maleylacetoacetate. GSTZ1-1 catalyzes the bioactivation of fluorine-lacking dihaloacetates
Degradation of antiflammin 2 in aqueous solution.
J L Wolfe et al.
Journal of pharmaceutical sciences, 83(12), 1762-1764 (1994-12-01)
J M Ye et al.
Journal of pharmaceutical sciences, 85(7), 695-699 (1996-07-01)
Antiflammin 2 (HDMNKVLDL, AF2) is a synthetic peptide derived from the region of highest sequence similarity of lipocortin I and uteroglobin, and is a potent antiinflammatory agent without any known side effects of corticosteroids. The antiinflammatory activity of AF2 has
Ahmad M Kamal et al.
TheScientificWorldJournal, 6, 1375-1384 (2006-10-31)
The anti-inflammatory actions of the nonapeptide antiflammin-2, identified by homology with uteroglobin and annexin-A1 sequences, have been described in some detail, yet its mechanisms of action remain elusive. Since recent data indicate an involvement of the formyl peptide receptor (FPR)-like
K E Rodgers et al.
Journal of investigative surgery : the official journal of the Academy of Surgical Research, 10(1-2), 31-36 (1997-01-01)
Adhesion formation is a major source of postoperative morbidity and mortality. Therefore, the reduction of postoperative adhesion formation would be of clinical benefit. Various modalities have been shown to reduce adhesion formation, including fibrinolytic enzymes, nonsteroidal anti-inflammatory drugs, and barriers

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