ChemicalBook > CAS DataBase List > R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT

R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT

Product Name
R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT
CAS No.
266359-93-7
Chemical Name
R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT
Synonyms
Reparixin L-lysine;REPERTAXIN L-LYSINE SALT;Reparixin (L-lysine salt);Reparixin L-lysine salt (Repertaxin L-lysine salt);R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT;Repertaxin,CXCR,inhibit,Reparixin Llysine salt,Reparixin L lysine salt,Inhibitor,Reparixin,CXC chemokine receptors
CBNumber
CB7461888
Molecular Formula
C20H35N3O5S
Formula Weight
429.58
MOL File
266359-93-7.mol
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R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT Property

storage temp. 
2-8°C
solubility 
H2O: 52 mg/mL
form 
lyophilized powder
color 
Off-white to light yellow
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Safety

WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
21492
Product name
Reparixin (L-Lysine salt)
Purity
≥95%
Packaging
1mg
Price
$26
Updated
2024/03/01
Cayman Chemical
Product number
21492
Product name
Reparixin (L-Lysine salt)
Purity
≥95%
Packaging
5mg
Price
$51
Updated
2024/03/01
Cayman Chemical
Product number
21492
Product name
Reparixin (L-Lysine salt)
Purity
≥95%
Packaging
10mg
Price
$90
Updated
2024/03/01
Cayman Chemical
Product number
21492
Product name
Reparixin (L-Lysine salt)
Purity
≥95%
Packaging
25mg
Price
$192
Updated
2024/03/01
TRC
Product number
R144565
Product name
ReparixinL-lysineSalt
Packaging
2.5mg
Price
$305
Updated
2021/12/16
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R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT Chemical Properties,Usage,Production

Uses

Reparixin is an inhibitor of CXCR1 and CXCR2 chemokine receptors. Functions as an agent that blocks a range of activities including leukocyte recruitment and IL-8 signaling.

Biological Activity

reparixin l-lysine salt is an inhibitor of interleukin 8 receptor alpha (cxcr1) and beta (cxcr2) with ic50 value of 5.6 nm and 80 nm respectively [1].cxcr1 and 2 belong to class a of 7-transmembrane g protein coupled receptor, and they share 78% amino acid identity. they are specific receptors for interleukin-8 which is a chemokine. they are mainly expressed in the neutrophils, where they mediate neutrophil migration to the site of inflammation. in addition, they are also involved in tumor aggressive growth and metastasis of human malignant melanoma.structural and biochemical study identified that reparixin l-lysine salt had non-competitive allosteric interaction with cxcr1 and 2, by which blocking cxcr1 and cxr2 in an inactive conformation, and thus suppressed receptor-induced intracellular signaling cascade and cellular response [2]. when cxcr1 were expressed in l1.2 cells, cell migration induced by 10 nm cxc8 was significantly inhibited by reparixin l-lysine salt [1].in mouse model, treatment of reparixin l-lysine salt after introduction of injury significantly (15 mg/ kg/ day for 7 days) suppressed secondary degeneration by reducing cxc8-dependent oligodendrocyte apoptosis, migration to the injury site of neutrophils and ed-1-positive cells. additionally, the level of macrophage-inflammatory protein-2, tumor necrosis factor alpha, interleukin (il)-6, and il-1 beta was also reduced, and the proliferation of glial fibrillary acidic protein-positive cells was significantly reduced [2].in mouse ischemia model, pre-treatment with reparixin reduced the motor deficits, myeloperoxidase activity and il-1b level. furthermore, ischemic injury was also attenuated [3].

storage

Store at -20°C

References

[1] moriconi a et al. , design of noncompetitive interleukin-8 inhibitors acting on cxcr1 and cxcr2. j med chem. 2007, 50(17): 3984-4002.
[2] gorio a, madaschi l, zadra g, reparixin, an inhibitor of cxcr2 function, attenuates inflammatory responses and promotes recovery of functionafter traumatic lesion to the spinal cord. j pharmacol exp ther. 2007, 322(3): 973-981.
[3] sousa l f, coelho f m, rodrigues d h, blockade of cxcr1/2 chemokine receptors protects against brain damage in ischemic stroke in mice. clinics (sao paulo). 2013, 68(3): 391-394.

R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT Preparation Products And Raw materials

Raw materials

Preparation Products

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R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT Suppliers

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266359-93-7, R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALTRelated Search:


  • R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT
  • REPERTAXIN L-LYSINE SALT
  • Reparixin (L-lysine salt)
  • Reparixin L-lysine
  • Reparixin L-lysine salt (Repertaxin L-lysine salt)
  • Repertaxin,CXCR,inhibit,Reparixin Llysine salt,Reparixin L lysine salt,Inhibitor,Reparixin,CXC chemokine receptors
  • 266359-93-7
  • C20H35N3O5S
  • C14H21NO3SC6H14N2O2