找到约 54 条 “T-peptide” 相关结果 (用时 0.058 秒)
目录号 | 产品名称 | 中文名称 | 靶点 |
---|---|---|---|
M2007
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Romidepsin (FK228) | 罗米地辛;罗米地新 | HDAC |
FK228; ISTODAX; Depsipeptide; FR 901228; NSC 630176 | |||
Romidepsin (FK228, Depsipeptide, FR 901228, NSC 630176) 是一种大环缩肽化合物,也是一种组蛋白去乙酰化酶 (HDAC) 抑制剂,可抑制HDAC1,HDAC2,HDAC4 和 HDAC6,IC50 值分别为 36 nM,47 nM,510 nM 和 1.4 μM。Romidepsin可诱导肿瘤细胞周期的停滞和凋亡。 | |||
M1261
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NFAT Inhibitor-1 (VIVIT peptide) | NFAT Inhibitor-1 (VIVIT peptide) | NFAT |
VIVIT peptide; NFAT Inhibitor; ABM-7733 | |||
NFAT Inhibitor-1 (VIVIT peptide) 是一种 NFAT 的细胞渗透性肽抑制剂,在抑制细胞提取物中钙调神经磷酸酶介导的NFAT1、NFAT2和NFAT4去磷酸化方面表现优异。 | |||
M9071
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Amyloid beta-peptide(25-35) | Amyloid beta-peptide(25-35) | Amyloid |
Aβ25-35; β-Amyloid peptide(25-35) | |||
Amyloid beta-peptide(25-35) 是一个阿尔茨海默氏淀粉样蛋白β肽的Aβ(25-35) 片段,在培养细胞中显示出神经毒性活性。 | |||
M9419
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Bax inhibitor peptide V5 | Bax inhibitor peptide V5 | Bcl-2 |
BAX Inhibiting Peptide V5; BIP-V5 | |||
Bax inhibitor peptide V5(BIP-V5)是一种细胞膜渗透性的抑制Bax蛋白易位到线粒体中的肽类抑制剂。 | |||
M9771
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TRAP-6 | TRAP-6 | Peptides |
Thrombin Receptor Activator Peptide 6; PAR-1 agonist peptide | |||
TRAP-6 (Thrombin Receptor Activator Peptide 6) 是一种凝血酶受体激活肽,也是选择性的蛋白酶激活受体 1 (PAR1) 激动剂,TRAP-6 可以通过 PAR 1受体激活血小板并刺激血小板聚集。 | |||
M9857
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TRP-14 | 凝血酶受体激动剂;凝血酶受体活化因子肽 | Peptides |
TRAP; SFLLRNPNDKYEPF; ThroMbin Receptor Agonist Peptide | |||
Ser-Phe-Leu-Leu-Arg-Asn-Pro-Asn-Asp-Lys-Tyr-Glu-Pro-Phe is a synthetic thrombin receptor agonist peptide. | |||
M10059
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Prolactin-Releasing Peptide (1-31) (human) | Prolactin-Releasing Peptide (1-31) (human) | Peptides |
Prolactin-Releasing Peptide (1-31) (human) is a high affinity GPR10 ligand. | |||
M21525
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Recombinant Mouse S100A11 (E.coli , N-6His) | 重组小鼠S100A11蛋白 (E.coli , N-6His) | Cytokines and Growth Factors |
Protein S100-A11; Calgizzarin; Endothelial monocyte-activating polypeptide | |||
重组小鼠蛋白S100-A11由大肠杆菌表达系统产生,目的基因Met1-Ile98在n端带有6His标记表达。蛋白编号:P50543。 | |||
M10203
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ACE-031 | 肌抑素抑制肽7 | Peptides |
Myostatin inhibitory peptide 7 | |||
ACE-031 (Myostatin inhibitory peptide 7) 是活化素受体型IIB (ActRIIB)的可溶形式,同时也是肌生成抑制素(myostatin)的抑制剂,能通过结合肌肉生长抑制素和其他肌肉的负性调节因子来促进肌肉生长,可用于Duchenne型肌营养不良症(DMD)的相关研究。 | |||
M10207
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HIV-1 TAT Peptide TFA | HIV-1 TAT Peptide TFA | HIV Protease |
HIV-1 tat Protein (47-57) | |||
TAT TFA是一种细胞穿透肽,来源于人类免疫缺陷病毒(HIV-1)的转录反激活因子(TAT)。 | |||
M10235
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SLIGRL-NH2 | 蛋白酶激活的受体-2激活肽 | PAR |
Protease-Activated Receptor-2 Activating Peptide | |||
SLIGRL-NH2 (Protease-Activated Receptor-2 Activating Peptide) 是一种蛋白酶激活受体-2 (PAR-2) 的激动剂。 | |||
M10236
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PAR-2 (1-6) (mouse, rat) | H-丝氨酰亮氨酰异亮氨酰甘氨酰精氨酰亮氨酰-OH | PAR |
PAR-2 AGONIST PEPTIDE (SLIGRL), MOUSE | |||
PAR-2 (1-6) (mouse, rat) 是一种 PAR2 的激活剂,它可以用于探索细胞中 PAR2 的信号传导。 | |||
M10247
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Nesiritide acetate | 醋酸奈西立肽;醋酸奈西利肽 | Peptides |
natriureticpeptide; BNP-32; 124584-08-3 | |||
Nesiritide acetate(醋酸奈西立肽,醋酸奈西利肽)是含有32个氨基酸的多肽,同时也是 一种大环类化合物,可作为心房钠尿肽受体(NPR)的激动剂,其对 NPR-A 和 NPR-C 的Kd值分别为 7.3和13 pM。 | |||
M10358
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C-Type Natriuretic Peptide (CNP) (1-22), human | C-型利尿钠肽 1-22 | Angiotensin Receptor |
CNP-22, human | |||
C-Type Natriuretic Peptide (CNP) (1-22), human人是C-型利尿钠肽的1-22片段,其参与维持电解质-液体平衡和血管张力。 CNP抑制血管紧张素I的血管收缩效应,但不抑制血管紧张素II的效应。 | |||
M11207
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GLP-1(7-37) | 人胰高血糖素样肽-1 | GLP Receptor |
Insulinotropin (human);Peptide GLP-1 (human glucose-lowering peptide-1) | |||
GLP-1(7-37) 是一种肠道胰岛素激素,可以增强葡萄糖诱导的胰岛素分泌。 | |||
M13495
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Aviptadil | 阿肽地尔 | Others |
Vasoactive Intestinal Peptide (human, rat, mouse, rabbit, canine, porcine) | |||
Aviptadil 是一种血管活性肠多肽 (VIP) 类似物,具有强的血管舒张 (vasodilatory) 作用。Aviptadil 诱导肺血管扩张,抑制血管 SMCs 增殖、血小板聚集。Aviptadil 可用于肺纤维化、肺动脉高压 (PAH)、SARS-CoV-2 引起呼吸衰竭等的研究。 | |||
M13496
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Aviptadil acetate | 醋酸阿肽地尔 | Others |
Vasoactive Intestinal Peptide acetate salt (human, rat, mouse, rabbit, canine, porcine) | |||
Aviptadil acetate 是一种模拟血管活性肠多肽 (VIP) 类似物,具有强的血管舒张 (vasodilatory) 效应。。Aviptadil acetate 诱导肺血管扩张,抑制血管 SMCs 增殖、血小板聚集。Aviptadil acetate 可用于肺纤维化、肺动脉高压 (PAH)、SARS-CoV-2 引起呼吸衰竭等的研究。 | |||
M13750
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α2β1 Integrin Ligand Peptide TFA | α2β1 Integrin Ligand Peptide TFA | Integrin |
α2β1 Integrin Ligand Peptide TFA 在细胞膜表面与 α2β1 整合素受体相互作用,进入细胞介导细胞外信号。α2β1 Integrin Ligand Peptide是一种潜在的胶原受体拮抗剂。 | |||
M13751
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Arg-Gly-Asp-Ser | Arg-Gly-Asp-Ser | Integrin |
RGDS peptide; Fibronectin tetrapeptide | |||
Arg-Gly-Asp-Ser 是整联蛋白结合序列,抑制整联蛋白受体 (integrin receptor) 功能。Arg-Gly-Asp-Ser 直接并特异性地结合 pro-caspase-8,pro-caspase-9 和 pro-caspase-3,但不与 pro-caspase-1 结合。 | |||
M13758 | MLCK inhibitor peptide 18 | MLCK抑制肽18 | Myosin |
MLCK inhibitor peptide 18 是一种有效的 MLCK 抑制剂,IC50 值为 50 nM,同时较弱抑制 CaM kinase II 的活性。 | |||
M13931
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Calcitonin Gene Related Peptide (CGRP) (83-119), rat TFA | Calcitonin Gene Related Peptide (CGRP) (83-119), rat TFA | CGRP Receptor |
Calcitonin Gene Related Peptide (CGRP) (83-119), rat (TFA) 是一种由 37 个氨基酸组成的降钙素家族神经肽,通过 (CRLR) 起作用。 | |||
M13957
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Carperitide acetate | Carperitide acetate | Endothelin Receptor |
Atrial Natriuretic Peptide (ANP) (1-28), human, porcine acetate | |||
Carperitide acetate (Atrial Natriuretic Peptide (ANP) (1-28), human, porcine acetate) 是一种含 28 个氨基酸的激素,由心脏产生并分泌,以响应心脏损伤和机械拉伸。Carperitide acetate 抑制内皮素-1 (endothelin-1) 分泌。 | |||
M14049 | PAR-4 Agonist Peptide, amide TFA | PAR-4 Agonist Peptide, amide TFA | PAR |
PAR-4-AP TFA; AY-NH2 TFA | |||
PAR-4 Agonist Peptide, amide TFA (PAR-4-AP TFA; AY-NH2 TFA) 是一种蛋白酶激活受体-4 (PAR-4) 激动剂,对 PAR-1 或 PAR-2 都没有作用,且其作用会被 PAR-4 拮抗剂阻断。 | |||
M14073 | ATWLPPR Peptide TFA | ATWLPPR Peptide TFA | Complement System |
ATWLPPR Peptide TFA 是一种选择性的 neuropilin-1 (NRP-1) 抑制剂,能够抑制 VEGF165 与 NRP-1 结合,可用于血管生成的研究。ATWLPPR Peptide TFA 能够减轻糖尿病引起的早期视网膜损伤。 | |||
M14360
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Copper tripeptide | Copper tripeptide | Metabolite/Endogenous Metabolite |
GHK-Cu | |||
Copper tripeptide (GHK-Cu) 是一种天然存在的三肽,可以通过蛋白水解从现有的细胞外蛋白质中除去,并且用作炎性和内皮细胞的化学引诱物。Copper tripeptide 可以增加成纤维细胞中胶原蛋白,弹性蛋白,蛋白多糖和糖胺聚糖中信使 RNA 的产生。Copper tripeptide 是皮肤再生中多种细胞途径的天然调节剂。 | |||
M14556 | Autocamtide-2-related inhibitory peptide TFA | Autocamtide-2-related inhibitory peptide TFA | CaMK |
Autocamtide-2-related inhibitory peptide (TFA) 是高度特异性的、CaMKII 的有效抑制剂,其 IC50 值为 40 nM。 | |||
M14808 | (Arg)9 TFA | (Arg)9 TFA | Peptides |
Nona-L-arginine TFA; Peptide R9 TFA | |||
(Arg)9 TFA (Nona-L-arginine TFA)是可渗透细胞的多肽,在谷氨酸模型实验模型中保护神经的IC50值为0.78 μM。 | |||
M14814
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HA Peptide | 流感病毒血凝素(HA)肽 | Peptides |
Influenza Hemagglutinin (HA) Peptide | |||
HA Peptide (HA tag) 是来自人类流感血凝素 (HA) 的由九个氨基酸组成的多肽。HA Peptide 广泛用于细胞生物学和生物化学中分离,纯化,检测和追踪目标蛋白。 | |||
M14818
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Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat TFA | Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat TFA | Peptides |
MOG (35-55) (TFA) | |||
Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat (TFA) 是中枢神经鞘的一个次要成分。Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat (TFA)引发复发缓解性神经系统疾病,伴有广泛的斑块样脱髓鞘。还能诱导强效的 T细胞和 B 细胞反应,同时是高度脑源性的。 | |||
M14825
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Sincalide ammonium | Sincalide ammonium | Peptides |
Cholecystokinin octapeptide ammonium; CCK-8 ammonium; SQ19844 ammonium | |||
Sincalide ammonium (Cholecystokinin octapeptide ammonium) 是一种速效的胆囊收缩素 (CCK) 的氨基酸多肽激素类似物,可在胆囊造影术中静脉使用。Sincalide ammonium 是一种通过注射促进胆囊收缩并帮助诊断胆囊和胰腺疾病的物质。Sincalide ammonium 的肝胆生理作用是增加胆汁的分泌,使胆囊收缩并使 Oddi 的括约肌松弛,从而使胆汁排入十二指肠。 | |||
M5243
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EED226 | EED226 | PRC2/EED |
EED226是一种首创(first-in-Class)的,有效的、选择性的、具有口服活性的Polycomb repressive complex 2 (PRC2)抑制剂,以H3K27me0 peptide为底物时,IC50=23.4 nM; 以单核小体为底物时,IC50=53.5 nM。 EED226是具有强大抗癌功效的胚胎外胚层发育(EED)抑制剂。 | |||
M40855
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Recombinant Human Siglec-7 Protein (HEK293, C-6His) | 重组人Siglec-7蛋白 (HEK293, C-6His) | Receptor Proteins |
sialic acid binding Ig-like lectin 7; CD328 antigen; p75/AIRM1; QA79 | |||
Human Siglec-7 encodes a 467 amino acid (aa) polypeptide with a hydrophobic signal peptide, an N-terminal Ig-like V-type domain, two Ig-like C2-type domains, a transmembrane region and a cytoplasmic tail. It binds equally well to both alpha 2,3- and alpha 2,6-linked sialic acid. | |||
M11232
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Recombinant Mouse Beta-NGF Protein (110AA, E. coli) | 重组小鼠β-NGF蛋白 (110AA, E. coli) | Cytokines and Growth Factors |
β-NGF; NGFB | |||
Mouse beta -NGF is a homodimer of two 120 amino acid polypeptides. β-NGF acts as a growth and differentiation factor for B lymphocytes, and enhances B-cell survival. | |||
M6709 | EMD 66684 | EMD 66684 | Others |
EMD 66684 is a potent, selective non-peptide AT 1 antagonist. | |||
M7014 | Naltrindole hydrochloride | 纳曲吲哚盐酸盐 | Others |
Naltrindole hydrochloride is a selective non-peptide δ antagonist. | |||
M7257 | SB 222200 | SB 222200 | Others |
SB 222200 is a potent, selective non-peptide NK 3 antagonist. Brain penetrant. | |||
M7263
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SB 334867 | SB 334867 | OX Receptor |
SB334867A free base | |||
SB 334867 is a selective non-peptide OX 1 antagonist. | |||
M7268 | SB 674042 | SB 674042 | Others |
SB 674042 is a potent and selective non-peptide OX 1 antagonist. | |||
M7283 | SDM25N hydrochloride | SDM25N hydrochloride | Others |
SDM25N hydrochloride is a potent, selective non-peptide δ antagonist; also inhibits dengue virus replication. | |||
M7501 | YM 022 | YM 022 | Others |
YM 022 is a highly potent, selective non-peptide CCK 2 antagonist. | |||
M7629
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BIBP3226 TFA | BIBP3226 TFA | Neuropeptide Receptor |
BIBP3226 TFA是第一个选择性的,有效的 Neuropeptide Y (神经肽Y) Y1 (NPY Y1) 受体拮抗剂,对 rNPY Y1,hNPFF2,rNPFF的Ki分别为1.1、79、108 nM。可用于心血管的相关研究。 | |||
M7735
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CP-96345 | CP-96345 | Neurokinin Receptor |
CP96345 | |||
CP-96345 is a highly potent and selective, orally active tachykinin and substance P receptor non-peptide inhibitor. | |||
M7912 | Mastoparan-7 | Mastoparan-7 | Others |
Mastoparan 7 | |||
G protein activator via Gαi and Gαo stimulation, similar to G protein-coupled receptors; peptide originally isolated from wasp venom. | |||
M7974 | Netropsin dihydrochloride | 水合纺锤菌素氟安定 | Others |
Netropsin is an unusual n-methylpyrrole-containin |
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M8150 | SB-668875 | SB-668875 | Others |
SB-668875 is a novel, selective peptide agonist at OX2 orexin receptors. | |||
M8210 | FR-171113 | FR-171113 | Others |
FR171113 was the first non-peptide antagonist of the Protease Activated Receptor-1 (PAR1), also termed thrombin receptor. | |||
M8276
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Pleuromutilin | 泰妙菌素 | Antibiotic |
Drosophilin B; Mutilin 14-glycolate | |||
Pleuromutilin is an antibiotic natural product that inhibits bacterial protein synthesis by binding to bacterial ribosomes in the peptidyl transferase center and inhibiting peptide bond formation. | |||
M8432 | CYM50769 | CYM50769 | Neuropeptide Receptor |
CYM50769 is a potent, specific antagonist of the Neuropeptide B and Neuropeptide W receptor, NPBWR1 (IC50 = 120 nM). | |||
M8491 | Nap-FF | Nap-FF | Others |
Nap-FF (2-Naa-FF) is a cell penetrant dipeptide that self-assembly and adopt the β-sheet structures to form prion-like nanofibrils of small molecules (PriSM). | |||
M8539 | G3335 | G3335 | Others |
G3335 ( L-tryptophyl-L-glutamic acid) is a cell-permeable dipeptide that acts as a selective and reversible PPARγ antagonist with a Kd value of 8. | |||
M8814 | Trap-101 hydrochloride | Trap-101 hydrochloride | Others |
Trap-101 Hydrochloride is a nociceptin/orphanin FQ peptide (NOP) receptor blocker. | |||
M9064
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Oxytocin acetate | 醋酸催产素;醋酸缩宫素 | Oxytocin Receptor |
Orasthin; Ossitocina | |||
Oxytocin acetate是一种哺乳动物神经垂体激素,是一种多效的下丘脑肽 (hypothalamic peptide),有助于分娩、哺乳和亲社会行为。Oxytocin acetate 可以作为一种压力应对分子,具有抗炎、抗氧化剂和保护作用。 | |||
M9190
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Lixisenatide | 利西拉肽;利司那肽 | GLP Receptor |
Lyxumia; Adlyxin; ZP10A peptide | |||
Lixisenatide(Lyxumia, Adlyxin, ZP10A peptide)是一种glucagon-like peptide-1 (GLP-1) receptor激动剂(GLP-1RA),其对人源GLP-1受体的IC50值为1.4 nM。 | |||
M9835
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3X FLAG peptide TFA | 3X FLAG peptide TFA | Peptides |
3X FLAG peptide TFA is a synthetic peptide with a 3-time repeated DYKXXD motif. |