17
1
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6594 |
MNS
|
Syk; Src; p97 | Angiogenesis; Tyrosine Kinase/Adaptors; Ubiquitination |
MNS 是一种酪氨酸激酶抑制剂和广谱抗血小板药物,是一种 β-硝基苯乙烯衍生物。它完全抑制 U46619 (IC50:2.1 μM)、ADP (IC50:4.1 μM)、花生四烯酸 (IC50:5.8 μM)、胶原 (IC50:7.0 μM)和凝血酶 (IC50:12.7 μM)诱导的血小板聚集,并抑制 Src (IC50:27.3 μM)、Syk (IC50:2.8 μM) 和 FAK (IC50:97.6 μM)。 | |||
TP1060 |
GPRP acetate (67869-62-9 free base)
Pefabloc FG,Pefa 6003,GPRP acetate |
Others | Others |
GPRP acetate (Pefabloc FG) 是纤维蛋白聚合抑制剂,可抑制纤维蛋白原与血小板膜糖蛋白 Ⅱb/IIIa 复合物(糖蛋白 IIb/IIIa 受体)之间的相互作用。 | |||
T6182 |
Tirofiban
L700462,Aggrastat,替罗非班,MK383 |
Integrin | Cytoskeletal Signaling |
Tirofiban (L700462) 是一种非肽类选择性 GPIIb/IIIa 拮抗剂,IC50 为 9 nM,可抑制血小板聚集。 | |||
T27250 |
Elarofiban
RWJ-53308,RWJ 53308,RWJ53308 |
Integrin | Cytoskeletal Signaling |
Elarofiban(RWJ-53308) 是一种新型且具有口服活性的 GPIIb/IIIa 拮抗剂。 | |||
T27250L |
Elarofiban TFA
Elarofiban TFA(198958-88-2 Free base),RWJ-53308 TFA |
Integrin | Cytoskeletal Signaling |
Elarofiban TFA (RWJ-53308 TFA) 是一种新型且具有口服活性和选择性的 GPIIb/IIIa 拮抗剂,可用于研究心血管疾病。 | |||
T61345L |
Orbofiban TFA
Orbofiban TFA(163250-90-6 Free base) |
Integrin | Cytoskeletal Signaling |
Orbofiban TFA 是一种具有口服活性的GPIIb/IIIa血小板受体拮抗剂,对血小板聚集有抑制作用,可用于研究不稳定冠状动脉综合征。 | |||
T2238 |
Cariporide
卡立泊来德,HOE-642 |
Sodium Channel | Membrane transporter/Ion channel |
Cariporide (HOE-642) 是一种选择性的Na+/H+交换抑制剂。 | |||
T22807 |
GR 144053 trihydrochloride
|
Others | Others |
platelet fibrinogen receptor glycoprotein IIb/IIIa (GpIIb/IIIa) antagonist | |||
T24732 |
roxifiban
DMP-754,DMP754,DMP 754 |
||
Roxifiban 是XV459的前药,是一种抗血小板剂,对血小板糖蛋白IIb/IIIa 复合物(GPIIb/IIIa)受体具有高亲和力和特异性。 | |||
T25608 |
Lamifiban trifluoroacetate
Lamifiban trifluoroacetate salt |
||
Lamifiban trifluoroacetate is an antagonist of the nonpeptide platelet fibrinogen receptor (GPIIb/IIIa). | |||
T61345 |
Orbofiban
|
||
Orbofiban 是一种口服活性血小板膜糖蛋白IIb/IIIa 拮抗剂,抑制血小板聚集。 | |||
T76287 |
KGDS
|
||
KGDS 是一种合成肽,靶向于人活化血小板细胞膜上的整合素 GPIIb-IIIa。氨基酸序列:Lys-Gly-Asp-Ser。 | |||
TP2098 |
Echistatin
Echistatin, α1 isoform |
||
Potent irreversible αVβ3 integrin antagonist (Ki = 0.27 nM). Disrupts attachment of osteoclasts to bone and inhibits bone reabsorption (IC50 = 0.1 nM). Prevents ADP-induced platelet aggregation via inhibition of glycoprotein IIb/IIIa (GpIIb/IIIa, αIIbβ3) | |||
T73643 |
Orbofiban acetate
|
||
Orbofiban acetate 是一种口服活性血小板膜糖蛋白IIb/IIIa 拮抗剂,抑制血小板聚集。 | |||
T71254 |
Clopidogrel HCl
|
||
Clopidogrel HCl is the salt form of Clopidogrel (free base), an inhibitor of ADP-induced platelet aggregation acting by direct inhibition of adenosine diphosphate (ADP) binding to its receptor and of the subsequent ADP-mediated activation of the glycoprotein GPIIb/IIIa complex. | |||
T29073 |
UR-2922
UR 2922 |
||
UR-2922 is an oral antagonist of platelet GPIIb/IIIa. UR-2922 possessed a high affinity for the human platelet receptor (K(d) <1 nM) and a slow dissociation rate (k(off)= 90 min) in vitro. UR-2922 induced no ligand-induced binding sites (LIBS) expression | |||
T29074 |
UR-3216
|
||
UR-3216, a prodrug, is a selective and orally active platelet surface glycoprotein (GPIIb/IIIa) receptor antagonist. UR-3216 is the very tight binding of its active metabolite to platelets (Ki for resting platelets is < 1 nM). UR-2992, the active form of |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN5221 | (-)-Variabilin | ||
Variabilin, a novel inhibitor of human platelet aggregation, it is a potent RGD (Arg-Gly-Asp)-containing antagonist of the fibrinogen receptor glycoprotein IIb-IIIa (GPIIb-IIIa; αIIbβ3) and the vitronectin receptor αvβ3.Variabilin is also an antimicrobial furanosesterterpene. Variabilin is an inhibitor of human secretory and cytosolic phospholipase A2 (PLA2) activities that controls eicosanoid production in vitro and in vivo, inhibits neutrophil degranulation and superoxide generation in vitro a... |