t peptide

Highly neurotoxic cell-permeable analog of PHF6. Induces aggregation of Tau peptides.

Peptide T acetate(106362-32-7 free base) 是一种来自 HIV-1 gp120 V2 区域的八肽。它是一种合成八肽，其可能的作用机制是 gp120 对 CD4 受体的竞争性抑制以及与血管肠肽受体的结合和抑制细胞因子作用。

HIV Peptide T（Peptide T），这种合成的八肽是HIV感染治疗中的一种抗病毒药物，其主要通过竞争性抑制gp120（HIV表面蛋白）与CD4受体的相互作用，同时与血管肠肽（vasointestinal peptide, VIP）受体同源结合并且阻断细胞因子的产生与作用来发挥功效。

This peptide, a nuclear localization signal DNA tagged to this peptide efficiently translocates into the cell nucleus.

SV40 T-Ag-derived NLS peptide acetate (SV40 T-Ag-derived NLS peptide acetate)(105425-98-7 free base) 是一种核定位信号肽。用这种肽标记的 DNA 可以有效地转移到细胞核中。

Peptide T is an octapeptide from the V2 region of HIV-1 gp120. This synthetic octapeptide potentially functions through competitive inhibition of gp120 binding to the CD4 receptor, as well as interaction with vasointestinal peptide (VIP) receptors.

Peptide T (TFA) is an octapeptide derived from the V2 region of HIV-1 gp120. It serves as a ligand for the CD4 receptor, effectively inhibiting the binding of HIV to the CD4 receptor.

Peptide T amide is an octapeptide segment of HIV envelope gp120 and is used in AIDS therapy.

EGF-R (661-681) T669 Peptide 是一种 MAPK 底物，可用于测量 MAPK 催化活性。

T9 peptide (SKTFNTHPQSTP) 是一种特定肌肉靶向的肽.它与 C2C12 成肌细胞具有高度结合能力.当T9 peptide 与寡核苷酸结合时,其对心脏和股四头肌的靶向特异性得到增强,但对肾、肝和膈肌的靶向作用不明显.

Thrombin receptor agonist peptide (TRAP-14) is a 14-amino acid peptide agonist of the α-thrombin receptor. It induces aggregation of washed platelets as well as platelets in citrated and hirudin plasma. TRAP-14 (100 μM) increases the cytosolic calcium concentration in isolated guinea pig pulmonary smooth muscle cells 5-fold over baseline. It increases pulmonary arterial pressure in isolated guinea pig lung when used at a concentration of 1 μM, which is comparable to the effect induced by 10 nM α-thrombin. TRAP-14 also induces contraction of isolated rat aortic rings and increases endothelin-1 (ET-1) levels in a dose-dependent manner, an effect that is reversed by the ETA antagonist BQ-123 and the nitric oxide synthase (NOS) inhibitor L-NNA .

TAT peptide (TFA) 是一种可渗透细胞的肽 (GRKKRRQRRRPQ)，来自HIV-1反转录激活因子 (Tat)。

PAR-4 Agonist Peptide, amide (AY-NH2) 是蛋白酶激活受体 4 (PAR-4) 的激动剂，对 PAR-1 或 PAR-2 均无影响，其作用可被 PAR-4 拮抗剂阻断。

PAR-4 Agonist Peptide, amide acetate 是蛋白酶激活受体 4 (PAR-4) 的激动剂。

C5aR1 antagonist peptide 是一种源自C5a (趋化因子补体片段5过敏毒素) C末端的生物活性线性肽。它能在人和大鼠的C5a受体上阻断C5a的结合，对于细胞免疫反应的触发起着关键作用。C5a的过度表达与多种免疫炎性疾病如关节炎、阿尔茨海默病、囊性纤维化和系统性红斑狼疮等有着密切关联。

PAR-4 Agonist Peptide, amide TFA (PAR-4-AP (TFA)) 是一种蛋白酶激活受体 4 (PAR-4) 激动剂，对 PAR-1 或 PAR-2 均无影响，其作用可被 PAR-4 拮抗剂阻断。

TAT peptide corresponds to the polycationic aa49-57 region of TAT protein. TAT peptide is a cell-penetrating peptide (CPP) used to cargo larger molecules through the lipophilic barrier of the cellular membranes to deliver them inside the cells with intact

This peptide is a scrambled sequence of NADPH oxidase assembly peptide inhibitor gp91 ds-tat. It is used as a control peptide. It is two amino acid residues shorter at the N-terminus compared to the scrambled gp91 ds-tat.

Antioxidant peptide A is a short peptide, which contains alternative aromatic or sulfur-containing amino acid.

Antioxidant peptide A acetate (159147-88-3 free base) 是一种短肽，它含有替代的芳香族或含硫氨基酸。

Substance P-related peptide that inhibits binding of G proteins to their receptors. Competitively and reversibly inhibits M2 muscarinic receptor activation of Gi or Go and inhibits Gs activation by β-adrenoceptors.

G-Protein antagonist peptide acetate 是一种 substance P 相关肽，可抑制 G 蛋白与其受体的结合。G-Protein antagonist peptide acetate 竞争性和可逆性地抑制毒蕈碱型乙酰胆碱受体 M2 (M2 muscarinic receptor) 对 Gi 或 Go 的激活，并通过 β-肾上腺素受体抑制 Gs 的激活。

Receptor for advanced glycation end products (RAGE) antagonist. Blocks S100P, S100A4 and HMGB-1 mediated RAGE activation in vitro and in vivo. Inhibits growth and metastasis of rat glioma tumors. Reduces cell growth and RAGE-mediated NF-κB activity in hum

RAGE antagonist peptide acetate 是一种高级的糖基化终产物 (RAGE) 拮抗剂。 它具有抗肿瘤和抗炎活性。 它可防止 RAGE 与其几个重要的配体结合，包括 HMGB-1、S100P 和 S100A4。