>>Signaling Pathways>> Proteases>> Cathepsin>>Cathepsin C-IN-5

Cathepsin C-IN-5

Catalog No.GC65998

Cathepsin C-IN-5(화합물 SF38)는 IC50이 59.9 nM, 4.26 μM, >5 μM, >5 μM, >5 &858888인 강력하고 선택적인 경구 활성 Cathepsin C 억제제입니다. 821d96072c2d58d8970e76f526b0f6b8Cat C, Cat L, Cat S, Cat B, Cat K. 821d96072c2d58d8970e76f526b0f6b8Cathepsin C-IN-5는 골수와 혈액에서 Cat C 활성을 억제합니다. 821d96072c2d58d8970e76f526b0f6b8Cathepsin C-IN-5는 NSP(호중구 세린 프로테아제)의 활성화를 감소시킵니다. 821d96072c2d58d8970e76f526b0f6b8Cathepsin C-IN-5는 항염 작용을 나타냅니다.821d96072c2d58d8970e76f526b0f6b8

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Cathepsin C-IN-5 Chemical Structure

Cas No.: 2825567-97-1

Size 가격 재고 수량
10mg
US$360.00
재고 있음
25mg
US$765.00
재고 있음
50mg
US$1,215.00
재고 있음

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

Cathepsin C-IN-5 (compound SF38) is a potent, selective and orally active Cathepsin C inhibitor with IC50s of 59.9 nM, 4.26 µM, >5 µM, >5 µM, >5 µM for Cat C, Cat L, Cat S, Cat B, Cat K, respectively. Cathepsin C-IN-5 inhibits the Cat C activity in bone marrow and blood. Cathepsin C-IN-5 decreases the activation of NSPs (neutrophil serine proteases). Cathepsin C-IN-5 shows anti-inflammatory activity[1].

Cathepsin C-IN-5 (compound SF38) shows inhibition in THP-1 and U937 cells with IC50s of 115.4, 70.2 nM, respectively[1].

Cathepsin C-IN-5 (1500 mg/kg) shows no significant weight loss or toxic reaction within 7 days after the administration in ICR mice[1].
Cathepsin C-IN-5 (10 mg/kg for p.o.; 2 mg/kg for i.v.) shows good bioavailability with F=42.07%[1].
Cathepsin C-IN-5 (2, 10, 50 mg/kg; p.o.) shows effective antiinflammatory activity and potential protective effect in an animal model of ALI[1].

Animal Model: C57BL/6 male mice (acute lung injury (ALI) mice model)[1]
Dosage: 2, 10, 50 mg/kg (one hour after administration, received LPS (20 mg/kg))
Administration: P.o.
Result: Decreased the levels of proinflammatory cytokines (TNF-a, IL-6, and GM-CSF) and increased the the concentration of the anti-inflammatory cytokine (IL-10) in a dose-dependent manner.

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