Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7625 |
TRAP-6
PAR-1 agonist peptide,Thrombin Receptor Activator Peptide 6,TRAP-6(2TFA) |
Protease-activated Receptor | GPCR/G Protein |
TRAP-6 (Thrombin Receptor Activator Peptide 6) 是一种多肽片段,是选择性的蛋白酶激活受体 1 (PAR1) 激动剂,通过凝血酶受体激活人血小板。 | |||
T7623L |
PAR-4 Agonist Peptide, amide acetate
PAR-4 Agonist Peptide, amide acetate(352017-71-1 free base) |
Protease-activated Receptor | GPCR/G Protein |
PAR-4 Agonist Peptide, amide acetate 是蛋白酶激活受体 4 (PAR-4) 的激动剂。 | |||
T38836L |
Protease-Activated Receptor-1, PAR-1 Agonist acetate
|
Protease-activated Receptor | GPCR/G Protein |
Protease-Activated Receptor-1, PAR-1 Agonist acetate 是一种选择性蛋白酶激活受体 1 (PAR-1) 激动剂肽。 它对应于 PAR1 栓系配体,可以选择性地模拟凝血酶通过该受体的作用。 | |||
TP1065 |
PAR-4 Agonist Peptide, amide TFA
PAR-4-AP (TFA),AY-NH2 (TFA) |
Protease-activated Receptor | GPCR/G Protein |
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。 | |||
T38852L |
TRAP-6 amide acetate
|
Protease-activated Receptor | GPCR/G Protein |
TRAP-6 amide acetate 是一种 PAR-1 凝血酶受体激动剂肽。 | |||
T7623 |
PAR-4 Agonist Peptide, amide
AY-NH2,PAR-4 Agonist Peptide, amide(2TFA),PAR-4-AP |
Protease-activated Receptor | GPCR/G Protein |
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。 | |||
T76650 |
PAR-2 (1-6) (human)
|
||
PAR-2 (1-6) (human) (SLIGKV) 是 PAR-2的多肽激动剂。 | |||
T36288 |
Protease-Activated Receptor-1, PAR-1 Agonist TFA
|
||
Protease-Activated Receptor-1 (PAR-1) Agonist TFA is a selective peptide that acts as an agonist for the proteinase-activated receptor-1 (PAR-1). Corresponding to the tethered ligand of PAR-1, this compound mimics the actions of thrombin through the PAR-1 receptor[1][2]. | |||
T36289 |
Protease-Activated Receptor-3 (PAR-3) (1-6), human TFA
|
||
Protease-Activated Receptor-3 (PAR-3) (1-6), human TFA is a peptide that acts as an agonist for the proteinase-activated receptor (PAR-3)[1]. | |||
T38852 |
TRAP-6 amide
|
||
TRAP-6 amide is a PAR-1 thrombin receptor agonist peptide. | |||
T38887 |
TRAP-6 amide TFA
|
||
TRAP-6 amide TFA is a PAR-1 thrombin receptor agonist peptide. | |||
T80236 |
TFLLRN-NH2
|
||
TFLLRN-NH2 为具备生物活性的肽类化合物,作用为PAR-1激动剂。 | |||
T38836 |
Protease-Activated Receptor-1, PAR-1 Agonist
|
||
Protease-Activated Receptor-1 (PAR-1) Agonist, a selective peptide, activates the PAR-1 receptor by mimicking the specific actions of thrombin. It corresponds to the PAR1 tethered ligand, facilitating selective activation of this receptor. | |||
T75872 |
Parstatin(mouse) TFA
|
||
Parstatin(mouse) TFA 是具有细胞通透性的 PAR-1凝血酶受体的肽类激动剂,是一种有效的血管生成抑制剂。 | |||
T75902 |
SLIGRL-NH2 TFA
Protease-Activated Receptor-2 Activating Peptide TFA |
||
SLIGRL-NH2 TFA(Protease-Activated Receptor-2 Activating Peptide TFA)作为PAR-2(蛋白酶激活受体-2)的激动剂,具有高度特异性。 | |||
T75873 |
Parstatin(human) TFA
|
||
Parstatin(human) TFA 是具有细胞通透性的 PAR-1凝血酶受体的肽类激动剂,是一种有效的血管生成抑制剂。 | |||
T80111 |
TRAP-5 amide
|
||
TRAP-5 amide为蛋白酶激活受体1(PAR1)特异性的激动剂肽。 | |||
T80240 |
Ala-parafluoroPhe-Arg-Cha-Cit-Tyr-NH2
|
||
Ala-parafluoroPhe-Arg-Cha-Cit-Tyr-NH2是一类具有生物活性的肽,作为蛋白酶激活受体1 (PAR-1) 的选择性激动剂,其特异性优于PAR-2。该肽通过HEK293细胞进行的基于细胞的钙信号传导测定确认了其对PAR-1的高特异性,并可用于研究PAR-1在体内的激活。PAR-1除了介导凝血酶的多种细胞作用外,还与PAR-4协作,参与调控凝血酶诱导的被分类为“凝血型”的肝细胞癌。 | |||
T80239 |
TFLLRNPNDK-NH2
|
Thrombin | Proteases/Proteasome |
TFLLRNPNDK-NH2 是具备生物活性的肽类化合物,作为凝血酶受体激活肽(PAR-1 激动剂肽)能够可逆地与 PAR-1 结合,模拟凝血酶对底物蛋白通过水解作用产生的“束缚配体”。同凝血酶的作用相似,此肽能够增加液体与蛋白质的渗透性。 | |||
T80235 |
YFLLRNP
|
||
YFLLRNP 是 PAR-1 部分激动剂,具有生物活性。它在低浓度下选择性地激活 G12/13 信号通路,而不会对 Gq 或 Gi 通路产生影响(60 μM)。 | |||
T35955 |
PAR2 (1-6) amide (human) (trifluoroacetate salt)
PAR2 (1-6) amide (human) (trifluoroacetate salt) |
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PAR2 (1-6) amide is a synthetic peptide agonist of proteinase-activated receptor 2 (PAR2) that corresponds to residues 1-6 of the amino terminal tethered ligand sequence of human PAR2 and residues 37-42 of the full-length sequence.1It binds to NCTC 2544 cells expressing human PAR2 (Ki= 9.64 μM in a radioligand binding assay) and induces calcium mobilization in the same cells (EC50= 0.075 μM).2PAR2 (1-6) amide (100 μM) reduces colony formation of A549 lung cancer cells.1It induces superoxide prod... |