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

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
Molecular Weight:
429.58
MDL Number:
MFCD07772189
MOL File:
266359-93-7.mol
MSDS File:
SDS
Last updated:2023-06-30 15:45:59

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

storage temp. 2-8°C
solubility H2O: 52 mg/mL
form lyophilized powder
FDA UNII 4RZ9P05120

SAFETY

Risk and Safety Statements

WGK Germany  3

R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 21492 Reparixin (L-Lysine salt) ≥95% 266359-93-7 1mg $26 2024-03-01 Buy
Cayman Chemical 21492 Reparixin (L-Lysine salt) ≥95% 266359-93-7 5mg $51 2024-03-01 Buy
Cayman Chemical 21492 Reparixin (L-Lysine salt) ≥95% 266359-93-7 10mg $90 2024-03-01 Buy
Cayman Chemical 21492 Reparixin (L-Lysine salt) ≥95% 266359-93-7 25mg $192 2024-03-01 Buy
TRC R144565 ReparixinL-lysineSalt 266359-93-7 2.5mg $305 2021-12-16 Buy
Product number Packaging Price Buy
21492 1mg $26 Buy
21492 5mg $51 Buy
21492 10mg $90 Buy
21492 25mg $192 Buy
R144565 2.5mg $305 Buy

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

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

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TargetMol Chemicals Inc.
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Haoyuan Chemexpress Co., Ltd. 021-58950125 info@chemexpress.com China 7553 61
SPIRO PHARMA eric_feng1954@126.com China 9254 55
Guangzhou QiYun Biotechnology Co., Ltd. 020-61288194 61288195 505721671@qq.com China 3868 58
ChengDu TongChuangYuan Pharmaceutical Co.Ltd 028-83379370 13880556291 tcy@tcypharm.com China 5503 58

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

266359-93-7(R-(-)-2-(4-ISOBUTYLPHENYL)PROPIONYL METHANSULPHONAMIDE, LYSINE SALT)Related 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 C14H21NO3SC6H14N2O2 C20H35N3O5S