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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10811 |
Chymase-IN-1
|
Others | Others |
Chymase-IN-1 是一个有效的,有选择性的,口服有活性的人肥大细胞糜蛋白酶抑制剂,IC50 为 29 nM。 | |||
T12450 | Chymase-IN-2 | Others | Others |
Chymase-IN-2 is a modulator of chymase. | |||
TP1012 |
CH 5450
Z-Ile-Glu-Pro-Phe-Ome |
Others | Others |
CH 5450 (Z-Ile-Glu-Pro-Phe-Ome) 是一种人心脏糜酶 chymase 的短肽类抑制剂。 | |||
TQ0035 |
Fulacimstat
BAY1142524 |
Others | Others |
Fulacimstat (BAY1142524) 是可口服的糜酶抑制剂,能够作用于人糜酶(IC50:4 nM)和仓鼠糜酶(IC50:3 nM)。 | |||
T17186 |
TY-51469
|
Others | Others |
TY-51469是糜蛋白酶 (chymase) 抑制剂,在类人猿和人糜蛋白酶的 IC50 值分别为0.4和7.0 nM。 | |||
T0577 |
Chlorobenzothiazolinone
|
Others | Others |
通过荧光测定,Chlorobenzothiazolinone 在 1 小时后使用 bis(succinoyl-L-alanyl-L-prolyl-L-phenylalanylamide)作为底物抑制重组人糜酶,活性值为 90 μM。 | |||
T28177 |
NK3201
NK-3201,NK 3201 |
||
NK3201, a specific chymase inhibitor, suppresses bleomycin-induced pulmonary fibrosis in hamsters. | |||
T27660 |
JNJ-10311795
|
||
JNJ-10311795, a dual inhibitor of the leukocyte Proteases Cathepsin G and Chymase, has therapeutic efficacy in animals models of inflammation. | |||
T78063 |
Endothelin-1 (1-31) (Human) TFA
|
ERK | MAPK |
Endothelin-1 (1-31) (Human) TFA 是源自chymase对大ET-1选择性水解的一种有效血管收缩剂和血压升高剂。 | |||
T76564 |
Endothelin-1 (1-31) (Human)
|
||
Endothelin-1 (1-31) (Human) 是源于chymase对大ET-1选择性水解而来的有效血管收缩剂和血压升高剂。 | |||
T23233 |
RETF-4NA
|
Others | Others |
chymase substrate peptide | |||
T76564L |
Endothelin-1 (1-31) (Human) acetate
|
||
Endothelin-1 (1-31) (Human) acetate,源自于chymase对大ET-1的选择性水解,是一种有效的血管收缩剂和血压升高剂。 | |||
T11864 |
Iptacopan
LNP023 |
Others | Others |
Iptacopan (LNP023) 是一种与factor B 亲和力较高的抑制剂。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1931 |
Methyllinderone
|
Antifection | Microbiology/Virology |
Methyllinderone is a human chymase inhibitor, it has antioxidant property, it also shows moderate to weak antifungal activities against various pathogenic fungi. |