9
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T22106 |
MLS-573151
|
CDK; Ras | Cell Cycle/Checkpoint; GPCR/G Protein; MAPK |
MLS-573151 是 GTPase Cdc42 的选择性抑制剂,EC50 为 2 μM。它通过阻止 GTP 与 Cdc42 的结合来发挥作用。 | |||
T81135 |
Sodium caseinates
|
||
Sodium caseinates,作为主要乳蛋白,能诱导粒细胞增殖与活化,同时提高关键细胞因子GM-CSF与G-CSF的血清浓度。该化合物还可引起小鼠粒细胞的生成。 | |||
TP1597L |
Secretoneurin, rat acetate
Secretoneurin, rat acetate(149146-12-3 Free base) |
Others | Others |
Secretoneurin, rat acetate 是一种 33 个氨基酸的多肽,由分泌粒蛋白 II (SgII) 的蛋白水解加工产生。它在体内和体外诱导大鼠纹状体中的多巴胺释放,它对单核细胞和嗜酸性粒细胞有很强的趋化作用,但对粒细胞没有。 | |||
T27408 |
Gea 3162
Gea3162,Gea-3162 |
||
Gea 3162 is a potent inhibitor of ADP-induced platelet aggregation in platelet rich plasma (PRP). GEA 3162 stimulates cGMP production in granulocytes, platelets, and polymorphonuclear leukocytes. | |||
T39009 |
CAP18 (rabbit)
CAP18 (rabbit) |
||
CAP18 (rabbit) is a 37 amino acid antimicrobial peptide derived from rabbit granulocytes. It exhibits extensive antimicrobial activity against both Gram-positive (IC50, 130-200 nM) and Gram-negative (IC50, 20-100 nM) bacteria. Thus, CAP18 (rabbit) holds promise for the study and advancement of bacterial sepsis research. | |||
T79597 |
LUF7690
|
||
LUF7690(Compound 9)是一种针对人A3AR(hA3AR)的可点击、基于共价亲和力的探针(AfBP)。该探针被应用于识别和表征粒细胞及其他细胞中的hA3AR。 | |||
T35541 |
Lipoxygenin
|
||
Lipoxygenin is an inhibitor of 5-lipoxygenase (5-LO) with an IC50value of 5 μM for inhibition of 5-LO product synthesis in isolated human granulocytes stimulated with the cation ionophore A23187 .1It inhibits hedgehog-dependent signaling in Shh-LIGHT2 cells and TGF-β-, activin A-, bone morphogenic protein (BMP)-, or Wnt-dependent signaling in HEK293T cells (IC50s = 9.3, 3.2, 8.2, 9.6, and 3.7 μM, respectively, in luciferase reporter assays). Lipoxygenin (5 and 10 μM) increases levels of troponin... | |||
T38309 |
LL-37 amide (trifluoroacetate salt)
|
||
LL-37 is a cationic and α-helical antimicrobial peptide expressed in human bone marrow, testis, granulocytes, and gingival epithelium and is upregulated in psoriatic lesions. It inhibits growth of Gram-positive E. coli D21 and Gram-negative B. megatarium in a concentration-dependent manner and LL-37 expression is induced in A549 epithelial cells, alveolar macrophages, neutrophils, and monocyte-derived macrophages following M. tuberculosis infection. LL-37 binds sheep erythrocytes coated with S. ... | |||
T14210 |
Amelubant
BIIL 284 |
LTR | Immunology/Inflammation |
Amelubant (BIIL 284) is a prodrug of active metabolites BIIL 260 and BIIL 315. Anti-inflammatory activity[1]. Amelubant (BIIL 284) is a potent, oral and long acting LTB4 receptor antagonist, negligibly binds to LTB4 receptor, with Kis of 221 nM and 230 nM |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN6057 |
1-Methyl-2-[(Z)-6-undecenyl]-4(1H)-quinolone
(Z)-1-Methyl-2-(undec-6-enyl)quinolin-4(1H)-one |
||
(Z)-1-Methyl-2-(undec-6-enyl)quinolin-4(1H)-one shows strong inhibitory activity on leukotriene biosynthesis in human polymorphonuclear granulocytes, and it is very effective against mycobacteria. | |||
TN2552 | 1-Methyl-2-nonylquinolin-4(1H)-one | Others | Others |
1-Methyl-2-nonylquinolin-4(1H)-one has anti-inflammatory activity, it exhibits inhibitory activity on leukotriene biosynthesis in a bioassay using human polymorphonuclear granulocytes, with IC50 values of 12.1 microM. |