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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T41308L |
Gly-Phe β-naphthylamide acetate
Gly-Phe β-naphthylamide acetate(21438-66-4 Free base) |
Others | Others |
Gly-Phe β-naphthylamide acetate 是 Cathepsin C 的底物,可用于研究组织蛋白酶 C 的功能、溶酶体内水解和溶酶体膜通透性。 | |||
T18308 |
MC-Gly-Gly-Phe
|
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MC-Gly-Gly-Phe 是一种用于抗体-药物偶联物的可切割接头。 | |||
TP1159L |
Boc-Gly-Gly-Phe-Gly-OH acetate
Boc-Gly-Gly-Phe-Gly-OH acetate(187794-49-6 free base),GGFG acetate |
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Boc-Gly-Gly-Phe-Gly-OH acetate (GGFG acetate)(187794-49-6 free base) 是 N 和 C 保护的四肽的自组装体。 | |||
T17953 |
Fmoc-Gly-Gly-Phe-OtBu
|
Others | Others |
Fmoc-Gly-Gly-Phe-OtBu 是一种用于合成抗体偶联药物的 linker,可降解。 | |||
T8667 |
MC-Gly-Gly-Phe-Gly
DSN28369 |
Others | Others |
MC-Gly-Gly-Phe-Gly (DSN28369) 是一种可降解的 ADC linker,是一种异双功能接头,可用于制备抗体药物偶联物。 | |||
T7211 |
Tyr-Gly-Gly-Phe-Met-OH
Methionine enkephalin,蛋氨酸脑啡肽,Met-Enkephalin,[MET5]脑啡肽 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Tyr-Gly-Gly-Phe-Met-OH (Met-Enkephalin) 是天然存在的内源性阿片肽、metenkephalin 和 zeta-和 delta-阿片受体激动剂的合成形式,是 mu-阿片受体激动剂,具有潜在的镇痛、神经调节、免疫调节、抗炎、抗肿瘤作用以及镇痛、抗抑郁和胃肠运动调节活性。 | |||
TP1861L |
Gly-Phe-Arg acetate(121822-47-7 free base)
|
Others | Others |
Gly-Phe-Arg acetate(121822-47-7 free base) 是一种模拟泥蟹抽吸信息素的超强合成三肽。 | |||
T41308 |
Gly-Phe β-naphthylamide
|
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Gly-Phe β-naphthylamide 在生命科学相关研究中具有广泛的应用。 | |||
TP1159 |
Boc-Gly-Gly-Phe-Gly-OH
GGFG |
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Boc-Gly-Gly-Phe-Gly-OH is a self-assembly of N- and C-protected tetrapeptide. | |||
TP1861 |
Gly-Phe-Arg
|
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Gly-Phe-Arg is a highly potent synthetic tripeptide that mimics the pumping pheromone of the mud-crab. | |||
T40257 |
Mc-Gly-Gly-Phe-Gly-PAB-OH
Mc-GGFG-PAB-OH,Mc-Gly-Gly-Phe-Gly-PAB-OH |
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Mc-Gly-Gly-Phe-Gly-PAB-OH, also known as Mc-GGFG-PAB-OH, serves as a cleavable ADC linker exclusively employed in the synthesis of antibody-drug conjugates (ADCs). | |||
T17951 |
Fmoc-Gly-Gly-D-Phe-OtBu
|
Others | Others |
Fmoc-Gly-Gly-D-Phe-OtBu, an ADC cleavable linker, is utilized in the synthesis of antibody-drug conjugates. It is the R-isomer of Fmoc-Gly-Gly-Phe-OtBu [1]. | |||
T39064 |
MC-Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH
MC-Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH |
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MC-Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH is an ADC linker commonly employed in ADC synthesis. This cleavable linker plays a fundamental role in the conjugation process of antibody-drug conjugates (ADCs). | |||
TP1495 |
Boc-Gly-Gly-Phe-Gly-OH TFA(187794-49-6,free)
Boc-Gly-Gly-Phe-Gly-OH TFA |
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Boc-Gly-Gly-Phe-Gly-OH TFA is a self-assembly of N-protected and C-protected tetrapeptides and is a protease cleaved connector for antibody-drug binding (ADC). | |||
T77833 |
Mc-Gly-Gly-Phe-Gly-PAB-OH TFA
Mc-GGFG-PAB-OH TFA |
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Mc-Gly-Gly-Phe-Gly-PAB-OH (Mc-GGFG-PAB-OH) TFA为可降解的ADC linker,适用于抗体偶联活性分子(ADC)的合成。 | |||
T10920 |
Cyclo(Arg-Gly-Asp-D-Phe-Val) TFA
|
Others | Others |
Arg-Gly-Asp-D-Phe-Val (TFA) has anti-tumor activity and is an inhibitor of integrin αvβ3. | |||
T2568L |
Felypressin acetate
2-(L-Phenylalanine)-8-L-lysinevasopressin,醋酸苯赖加压素,PLV2. H-Cys-Phe-Phe-Gln-Asn-Cys-Pro-Lys-Gly-NH2 (Disulfide bond),PLV 2,PLV-2 |
Vasopressin Receptor | GPCR/G Protein |
Felypressin acetate (PLV-2) 是加压素 1 的激动剂,作用于所有精氨酸加压素受体 1AS。 Felypressin acetate 可用于牙科手术。 | |||
T31919 |
Gdpflrfamide
Gly-asp-pro-phe-leu-arg-phe-amide |
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Gdpflrfamide is a neuropeptide that existed in the snail Lymnaea stagnalis. | |||
T83709 |
LIH383 TFA
Phe-Gly-Gly-Phe-Met-Arg-Arg-Lys-NH2 |
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LIH383是一种趋化因子(C-X-C motif) 受体7 (CXCR7)的多肽激动剂,属于趋化因子和阿片肽清除受体。它专一性激活CXCR7 (EC50 = 0.61 nM),在3 µM浓度时,相比μ-、δ-、κ-阿片受体以及诺氨酸阿片肽(NOP)受体的β-arrestin招募实验中表现出高选择性。LIH383(3 µM)通过阻止U87-ACKR3细胞中,由非选择性阿片受体激动剂dynorphin A诱导的CXCR7对阿片肽的摄取,发挥作用。 | |||
T31568 |
DP 432
DP432,beta-Alanyl-Arg-Gly-Phe-Phe-Tyr-NH2,DP-432 |
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DP 432 is an insulin hexapeptide fragment. | |||
TP2376 |
Cholecystokinin pentapeptide
CCK-5,Gly-trp-met-asp-phe-NH2 |
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Cholecystokinin pentapeptide is a peptide hormone of the gastrointestinal system responsible for stimulating the digestion of fat and protein. | |||
T32840 |
Locustakinin
Ala-phe-ser-ser-trp-gly-NH2,Lomk peptide,Locustakinn |
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Locustakinin is a myotropic peptide. | |||
T26198 |
Snf 9007
Snf-9007,Asp-tyr-D-phe-gly-trp-(N-Me)nle-asp-phe-NH2,Snf9007 |
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Snf 9007 is an antagonist of cholecystokinin. | |||
T83720 |
Biotin-Crosstide TFA
Biotin-Gly-Arg-Pro-Arg-Thr-Ser-Ser-Phe-Ala-Glu-Gly-OH |
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Biotin-crosstide是Akt底物crosstide的生物素化形式。 | |||
T25194 |
BW 443C
BW443C,BW-443C,Tyr-arg-gly-(4-nitro-phe)-pro-NH2 |
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BW 443C is a selective agonist of mu-opioid receptor. | |||
T31958 |
Glycine-pentagastrin
Glycine pentagastrin,Boc-gly-trp-met-asp-phe-NH2,Tbgtmap |
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Glycine-pentagastrin can enhance gastric mucosal defence mechanisms against acid and protect the gastric mucosa from experimental injury. | |||
TP2382 |
Gastrin hexapeptide
Tyr-gly-trp-met-asp-phe-NH2,Gastrin C-terminal hexapeptide |
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Gastrin hexapeptide is a hexapeptide from porcine antral mucosa. | |||
T64866 |
Glycyl-L-phenylalanine
Gly-Phe,(S)-2-(2-Aminoacetamido)-3-phenylpropanoic acid |
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Glycyl-L-phenylalanine (Gly-L-Phe)是一种二肽,常当作气管上皮细胞肽转运的模型肽,在粘膜液中会立即降解,可用于皮肤衰老和保湿。 | |||
T25168 |
Boc-ypgflt(O-tbu)
Boc-tyr-pro-gly-phe-leu-thr(O-t-Bu) |
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Boc-ypgflt(O-tbu) is a delta-receptor-selective opioid antagonist. | |||
TP1252 |
N-terminally acetylated Leu-enkephalin acetate
Ac-L-Tyr-Gly-Gly-L-Phe-D-Leu-COOH,N-terminally acetylated Leu-enkephalin |
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N-terminally acetylated Leu-enkephalin is the N-terminally acetylated form of Leu-enkephalin. | |||
T25507 |
HP 228
HP-228,Ac-Nle-gln-his-D-phe-arg-D-trp-gly-NH2,HP228 |
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HP 228 is a heptapeptide by inhibits the induction of nitric oxide synthase. | |||
T83687 |
Mca-RPPGFSAFK(Dnp)-OH TFA
(7-methoxycoumarin-4-yl)acetyl-Arg-Pro-Pro-Gly-Phe-Ser-Ala-Phe-Lys(2,4-dinitrophenyl)-OH |
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Mca-RPPGFSAFK(Dnp)-OH 是 endothelin-converting enzyme-1 (ECE-1) 的一种荧光底物。当 ECE-1 切割该底物时,会释放 7-methoxycoumarin-4-acetyl (Mca),其荧光可以用来量化 ECE-1 的活性。Mca 的激发/发射峰值分别为 328/420 nm。 | |||
T26305 |
U 67827E
N-Ac-Asp-tyr(So3H)-nle-gly-trp-nle-asp-phe-NH2,U-67827E,U67827E |
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U 67827E is a long-lasting cholecystokinin agonist. It acts by decreases food intake. | |||
T30643 |
BW 942C
Tyr-met-O-gly-4-No2-phe-pro-NH2,BW942C,BW-942-C,BW-942C |
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BW 942C is a pentapeptide that is enkephalin-like. | |||
T2568 |
Felypressin
Octapressin,Felypressin Acetate,PLV-2,H-[Cys-Phe-Phe-Gln-Asn-Cys]-Pro-Lys-Gly-NH2,苯赖加压素 |
Vasopressin Receptor | GPCR/G Protein |
Felypressin (Octapressin) 是一种加压素 1 激动剂,也是血管收缩剂,可用于牙科手术中。 | |||
T83666 |
Kisspeptin-10 (zebrafish) TFA
Tyr-Asn-Leu-Asn-Ser-Phe-Gly-Leu-Arg-Tyr-NH2,Kp-10 |
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Kisspeptin-10是一种在斑马鱼的大脑、卵巢和睾丸中表达的神经肽,参与性腺发育和类固醇表达。在10 ng/ml的浓度下使用时,能提高孤立的斑马鱼卵巢滤泡中编码黄体生成素(luteinizing hormone, Lh)受体,以及孕酮受体a (Progestin receptor a, Pra)和Prb的mRNA水平。在0.1和1 µg/g的剂量下给予时,Kisspeptin-10能在雌性金鱼中增加黄体生成素的血清水平,但在雄性金鱼中则不会。 | |||
T83690 |
[Leu144, Arg147]-PLP (139-151) TFA
[Leu144, Arg147] Proteolipid Peptide (139-151),H-His-Ser-Leu-Gly-Lys-Leu-Leu-Gly-Arg-Pro-Asp-Lys-Phe-OH |
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[Leu144,Arg147]-PLP (139-151)是髓鞘脂蛋白(PLP)的一种突变肽段,包含位于144和147位置的色氨酸到亮氨酸以及组氨酸到精氨酸的替换。使用[Leu144, Arg147]-PLP (139-151)(50 µg)乳化于完全弗氏佐剂(CFA)免疫后,能增加小鼠脾脏中的IL-4水平。它在体外抑制Th1细胞激活,但在体内不抑制,其中它诱导调节性T细胞的产生。用[Leu144, Arg147]-PLP (139-151)预免疫可以延迟由脑炎肽PLP (178-191)、髓磷脂少突细胞蛋白(MOG) (92-106)或髓鞘基础蛋白(MBP)在小鼠中诱导的实验性自身免疫性脑炎(EAE)的发病。 | |||
T83774 |
Shepherdin TFA
Lys-His-Ser-Ser-Gly-Cys-Ala-Phe-Leu-OH,Survivin (79-87) |
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Shepherdin是人体survivin的79-87氨基酸对应的合成肽,也是survivin与heat shock protein 90 (Hsp90)之间蛋白质-蛋白质相互作用的抑制剂。它以浓度依赖的方式与Hsp90的N末端结构域结合,并在150 µM的浓度下抑制了在分离的人源网状红细胞提取物中重组人survivin与Hsp90之间的相互作用。结合了穿膜肽penetratin或HIV Tat序列的Shepherdin肽结合物,体内外具有抗癌活性。 | |||
T77904 |
Fomc-Gly-Gly-Phe-Gly-OH
|
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Fomc-Gly-Gly-Phe-Gly-OH(化合物D5)是ADC双药接头合成的中间体,其参与形成ADC双药物连接组装单元的关键步骤。 | |||
T25550 |
Jmv 176
Jmv-176,Jmv176,Boc-tyr(SO3)-nle-psi-(coch2)-gly-trp-nle-asp-phe-NH2 |
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Jmv 176 is a CCK agonist when first given and becomes a cholecystokinin antagonist after 3-4 hours. | |||
T8761 |
[Leu15]-Gastrin I human
Amino Acid Sequence Glp-Gly-Pro-Trp-Leu-Glu-Glu-Glu-Glu-Glu-Ala-Tyr-Gly-Trp-Leu-Asp-Phe-NH2 |
Others | Others |
[Leu15]-Gastrin I human (Amino Acid Sequence Glp-Gly-Pro-Trp-Leu-Glu-Glu-Glu-Glu-Glu-Ala-Tyr-Gly-Trp-Leu-Asp-Phe-NH2) 基因编码人体内的蛋白质 [Leu15]-胃泌素 I。在人类染色体中,GAST 基因定位于 17q21.2。胃窦中的 G 细胞产生 [Leu15]-胃泌素 I 的前体前胃泌素。前胃泌素经过裂解和加工产生胃泌素,它对整个胃肠道上皮细胞具有营养作用。胃泌素对消化系统的生长至关重要,并刺激壁细胞产生胃酸。胃泌素通过称为胆囊收缩素(CCK) 或 CCK-B 受体 (CCK-BR) 的 G 蛋白偶联受体发挥其功能。胃泌素的释放受到食物的刺激,尤其是蛋白质饮食,并受到非常低的 pH 值的抑制。萎缩性胃炎、幽门螺杆菌感染和长期服用质子泵抑制剂感染可能导致胃泌素过度表达。胃腺癌显示高水平的胃泌素。 | |||
T77818 | Fmoc-Gly-Gly-Phe-OH | ||
Fmoc-Gly-Gly-Phe-OH为用于合成抗体药物偶联物(ADCs)的可降解ADC连接子。 | |||
T25913 |
P-113
P 113,Ala-lys-arg-his-his-gly-tyr-lys-arg-lys-phe-his-NH2 |
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P-113 is a peptide with antimicrobial activity. | |||
T36405 |
Pro-Adrenomedullin (153-185), human
Pro-Adrenomedullin (153-185), human,H2N-Ser-Leu-Pro-Glu-Ala-Gly-Pro-Gly-Arg-Thr-Leu-Val-Ser-Ser-Lys-Pro-Gln-Ala-His-Gly-Ala-Pro-Ala-Pro-Pro-Ser-Gly-Ser-Ala-Pro-His-Phe-Leu-OH |
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Pro-Adrenomedullin(153-185),human, (C143H224N42O43), a peptide with the sequence H2N-SLPEAGPGRTLVSSKPQAHGAPAPPSGSAPHFL-OH, MW= 3219.6. Adrenomedullin (AM) is a ubiquitously expressed peptide initially isolated from phaechromyctoma in 19931. AM was initially identified as a vasodilator, some have cited this as the most potent endogenous vasodilatory peptide found in the body2. Differences in opinion regarding the ability of AM to relax vascular tone arises from the differences in the model system... | |||
T77902 |
Boc-Gly-Gly-Phe-Gly-OH TFA
|
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Boc-Gly-Gly-Phe-Gly-OH TFA为一种ADC linker,特性为可降解,适用于抗体偶联活性分子(ADC)的合成。 | |||
T81874 |
Mal-cyclohexane-Gly-Gly-Phe-Gly-Exatecan
|
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Mal-cyclohexane-Gly-Gly-Phe-Gly-Exatecan 是用于合成 ADC 的偶联化合物,合成的 ADC 在体内外均显示出具有良好抗肿瘤活性。 | |||
T82279 |
Gly-Mal-Gly-Gly-Phe-Gly-amide-methylcyclopropane-Exatecan
|
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Gly-Mal-Gly-Gly-Phe-Gly-amide-methylcyclopropane-Exatecan 适合用作抗体药物偶联物(ADC)的合成工艺。 | |||
T77858 |
MC-Gly-Gly-Phe-Gly-Cyclobutanecarboxylic-Exatecan
|
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MC-Gly-Gly-Phe-Gly-Cyclobutanecarboxylic-Exatecan是一个构成抗体药物偶联物(ADC)活性部分的化合物,由ADC连接子(MC-Gly-Gly-Phe-Gly-Cyclobutanecarboxylic)与DNA拓扑异构酶I抑制剂Exatecan通过化学键合形成。此合成ADC主要应用于癌症研究领域。 | |||
T77888 |
Mal-PEG2-Gly-Gly-Phe-Gly-Exatecan
|
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Mal-PEG2-Gly-Gly-Phe-Gly-Exatecan是一个ADC药物-linker偶联物,包含Exatecan和linker。该化合物主要用于ADC合成与癌症研究。 | |||
T83688 |
R 715 TFA
[Ac-Lys-[D-βNal7,Ile8]des-Arg9]-BK,Ac-Lys-Arg-Pro-Pro-Gly-Phe-Ser-D2Nal-Ile-OH |
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R 715是一种布拉迪肾上腺素B1受体拮抗剂。它抑制在表达布拉迪肾上腺素B1受体的孤立人类脐带中由布拉迪肾上腺素引发的收缩(pA2 = 8.49)。R 715(200、400及600 µg/kg)通过尾部闪烁测试减少了由链脲佐菌素(STZ)诱导的糖尿病神经病变小鼠模型中尾部撤回的潜伏期。它还在以髓磷脂少突胶质细胞糖蛋白(MOG)(35-55)(MOG35-55)抗原肽诱导的实验性自体免疫性脑炎(EAE)小鼠模型中,通过每天1 mg/kg的剂量减少了后肢无力和瘫痪的发病率,改善对称步态,并减少脊髓炎症灶点数、神经元脱髓鞘以及病灶单核细胞侵袭。R 715(0.01 nmol/动物,脑室内)能在自发性高血压大鼠中降低平均动脉血压并增加心率。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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TN6682 | Cyclo(Phe-Gly) | ||
Cyclo(Phe-Gly) shows weak antagonistic activity against VEGFR2 -CD, it also shows strong inhibitory activity against human cancer cells(KB,KBv200) with LD50 at 6.5 and 11.2 umol/L,respectively. |