fibrinogen chain

SC-52012 是一种新型有效的纤维蛋白原受体 (fibrinogen receptor) 拮抗剂，是一种 RGD 模拟物，对血小板聚集有抑制作用。

Sucralfate (Sucrose octasulfate–aluminum complex) 是一种口服活性胃保护剂。它抑制消化性活性，并与黏膜损伤时暴露的带负电荷的上皮下蛋白结合，形成一层粘性层，保护血管床和增殖区。它可用于预防和治疗胃肠道疾病。

Angstrom6 (A-6 peptide) 是一种从单链尿激酶纤溶酶原激活剂(scuPA)中提取的 8 肽，它能干扰 uPA uPAR 级联反应并抑制下游效应。Angstrom6 具有抗肿瘤活性，能通过与 CD44 结合并调节 CD44 介导的细胞信号传导，抑制肿瘤细胞的迁移、侵袭和转移。

H-D-Phe-Pip-Arg-pNA (S-2238) acetate is a chromogenic substrate designed based on the N-terminal fragment of the A alpha chain of fibrinogen, which is the physiological target of thrombin. As a specific indicator of thrombin activity, H-D-Phe-Pip-Arg-pNA acetate is utilized to quantify. This assay, utilizing H-D-Phe-Pip-Arg-pNA acetate, ensures high sensitivity, accuracy, and ease of execution.

H-D-Phe-Pip-Arg-pNA hydrochloride, a chromogenic substrate, mimics the N-terminal segment of the A alpha chain of fibrinogen, the native substrate of thrombin. It displays specificity towards thrombin and is employed for quantifying antithrombin-heparin cofactor (AT-III). The utilization of H-D-Phe-Pip-Arg-pNA hydrochloride in the AT-III assay enables a sensitive, accurate, and straightforward measurement process.

H-D-Phe-Pip-Arg-pNA dihydrochloride (S-2238 dihydrochloride )是一种显色底物，模仿了纤维蛋白原Aα链N端片段，即凝血酶的天然底物。H-D-Phe-Pip-Arg-pNA dihydrochloride 专为凝血酶检测而设计，用于抗凝血酶-肝素辅因子(AT-III)的定量。利用该底物的AT-III检测方法以其灵敏度、准确性和实施的便捷性而特别闻名。

Lys-Gln-Ala-Gly-Asp-Val (KQAGDV), 纤维蛋白原γ链(fibrinogen γ-chain)末端六个氨基酸组成，是细胞粘附肽。通过α2bβ3整合素，介导细胞粘附，对平滑肌细胞(SMCs)具有有效粘附配体功能。

Fibrinogen Binding Inhibitor Peptide, a synthetic dodecapeptide, represents the specific platelet receptor recognition site of the human fibrinogen g-chain (residues 400-411).

[Glu1]-Fibrinopeptide B, a derivative of fibrinopeptide B amino acid residues 1-14, originates from human fibrinopeptide B (hFpB). hFpB is a proteolytic cleavage product of the fibrinogen B beta-chain, specifically generated by thrombin, which plays a significant role in activating neutrophils (PMN), monocytes, and fibroblasts.