Proteins(蛋白质)

Cat.No. 产品名称 Information

GP26010 BTC Human, HEK BTC Human Recombinant produced in HEK293 cells is a single, glycosylated polypeptide chain (32-111 a

GP26009 proBNP Human Recombinant Human Pro B-type Natriuretic Protein produced in E

GP26008 NT-proBNP Human NT-Pro-B-type Natriuretic Protein Human Recombinant produced in E

GP26007 b NGF Human, HEK BNGFHuman Recombinant produced inHEK293 is a noncovalently disulfide linked homodimer, glycosylated, polypeptide chain (Ser122-Arg239) containing 2 identical 118 amino acids and having a molecular mass of 26

GP26006 Clusterin Mouse Clusterin Mouse Recombinant is a single, glycosylated polypeptide chain containing 433 amino acids (22-448a

GP26005 Clusterin Human, Serum

GP26004 ANGPTL7 Human ANGPTL7 Human Recombinant produced in HEK293 cells is a single, glycosylated polypeptide chain (27-346a

GP26003 Acrp30 Mouse Acrp30 Mouse Recombinant is a single, glycosylated polypeptide chain containing 230 amino acids (18-247a

GP26002 ACVR1 Human ACVR1 produced in Sf9 Baculovirus cells is a single, glycosylated polypeptide chain containing 342 amino acids (21-123a

GP29001 MMP14 Human, His MMP14 Human Recombinant produced in Sf9 Baculovirus cells is a single, non-glycosylated polypeptide chain containing 527 amino acids (21-538a

GC26066 WAY-383487 WAY-383487 is one of the Tat peptide derivatives and inhibits HIV-1 long terminal repeat-activated transcription.

GC25991 tetrathiomolybdate Tetrathiomolybdate (TM) is used in the clinic for the treatment of Wilson's disease by inducing dimerization of the metal-binding domain of the cellular copper efflux protein ATP7B (WLN4) through a unique sulfur-bridged Mo2S6O2 cluster.

GC25940 SNS-314 SNS-314 is a potent and selective inhibitor of Aurora A, Aurora B and Aurora C with IC50 of 9 nM, 31 nM, and 3 nM, respectively. It is less potent to Trk A/B, Flt4, Fms, Axl, c-Raf and DDR2. Phase 1.

GC25935 Simufilam dihydrochloride

PTI-125 dihydrochloride

Simufilam (PTI-125) Dihydrochloride is a small molecule modulator that preferentially binds altered FLNA and restores its native conformation, restoring receptor and synaptic activities and reducing its α7nAChR/TLR4 associations and downstream pathologies.

GC25930 SHP099 HCl SHP099 is a highly potent, selective and orally bioavailable small-molecule SHP2 inhibitor with an IC50 value of 0.071 μM and shows no activity against SHP1.

GC25530 Iso-H7 dihydrochloride Iso-H7 dihydrochloride is an inhibitor of phosphokinase C.

GC25389 Ethyl potassium malonate

Potassium 3-ethoxy-3-oxopropanoate, Malonic Acid Monoethyl Ester Potassium Salt

Ethyl potassium malonate (Potassium 3-ethoxy-3-oxopropanoate) is used as a competitive inhibitor of the enzyme succinate dehydrogenase. It acts as a precursor to produce (trimethylsilyl)ethyl malonate, which is utilized to prepare beta-ketoesters by acylation and serves as an intermediate for the preparation of ethyl tert-butyl malonate.

GC25306 CQ31 CQ31, a small molecule, selectively activates caspase activation and recruitment domain-containing 8 (CARD8).

GC25039 AG-120 (racemic) AG-120 (racemic), the racemic mixture of AG-120, is an orally available inhibitor of isocitrate dehydrogenase type 1 (IDH1) with potential antineoplastic activity.

GC25005 1-Naphthyl phosphate potassium salt

α-Naphthyl acid phosphate monopotassium salt

1-Naphthyl phosphate potassium salt (α-Naphthyl acid phosphate monopotassium salt) is a non-specific phosphatase inhibitor which acts on acid, alkaline, and protein phosphatases.

GC68449 CA inhibitor 1

GS-6207 analog

CA inhibitor 1 (GS-6207 analog) 是一种有效的 HIV 衣壳抑制剂，可用于抑制 HIV。

GC68437 Vimentin-IN-1 Vimentin-IN-1 是 FiVe1 衍生物，是一种口服有效的选择性抗癌剂。FiVe1 能够结合 III 型中间丝蛋白 vimentin (VIM)，诱导 Ser56 过度磷酸化，导致有丝分裂的选择性中断和转化表达 VIM 的间充质癌细胞的多核化。Vimentin-IN-1 比 FiVe1 表现出更好的口服利用度和药代动力学特征。

GC68416 RAD51-IN-3 RAD51-IN-3 是一种 RAD51 抑制剂，详细信息请参考专利 WO2019051465A1 的化合物 Example 66A。

GC68390 α5β1 integrin agonist-1 α5β1 integrin agonist-1 作为 α5β1 integrin 激动剂，能够选择性地将 5-FU 输送到肿瘤细胞中，成功地导致肿瘤细胞死亡。

GC68386 CD73-IN-5 CD73-IN-5 是一种有效且选择性的非核苷酸小分子 CD73 抑制剂（IC50 = 19 nM）。

GC68346 Uliledlimab

TJ004309

Uliledlimab 是一种有效的抗 CD73 人源单克隆抗体。Uliledlimab 抑制胞外单磷酸腺苷 (AMP) 向腺苷的转化。Uliledlimab 可用于癌症的研究。

GC68344 Mupadolimab

CPI-006

Mupadolimab (CPI-006) 是一种 IgG1κ 人源化的 FcγR 结合缺陷抗 CD73 单抗，激活 CD73POS B 细胞。

GC68283 Etrolizumab

rhuMAb Beta7; RG7413; PRO145223

Etrolizumab (rhuMAb Beta7) 是一种肠道选择性抗-β7 整合素单克隆抗体。Etrolizuma b是针对 α4β7 和 αEβ7 整合素的 β7 亚基的特异性靶向药物。Etrolizumab 可用于炎症性肠病 (IBD) 的研究。

GC68147 dAURK-4 hydrochloride dAURK-4 hydrochloride 是 Alisertib 的一种衍生物，是一种有效的选择性 AURKA (Aurora A) 降解剂。dAURK-4 hydrochloride 具有抗癌作用。

GC68023 HIV-1 inhibitor-48 HIV-1 inhibitor-48 (compound 13o) 是一种新型的非核苷逆转录酶抑制剂 (NNRTI)，具有抗 HIV-1 活性。

GC68008 GÜ2602 GÜ2602 是一种有效的、可逆的组织蛋白酶 K (cathepsin K (CatK)) 抑制剂，对成熟 CatK (mCatK) 的 Ki 值为 0.013 nM。GÜ2602 抑制组织蛋白酶 K 酶原的自催化激活。

GC67983 Norathyriol

Mangiferitin

Norathyriol (Mangiferitin) 是芒果苷的天然代谢物。 Norathyriol 以非竞争性方式抑制 α-葡萄糖苷酶 (α-glucosidase )，IC50 为 3.12 μM。Norathyriol 还抑制 PPARα、PPARβ 和 PPARγ，IC50 分别为 92.8 µM、102.4 µM 和 153.5 µM。具有抗氧化、抗癌、抗菌、抗炎、抗菌活性。

GC67947 Triolein 13C3

三油酸甘油酯 13C3

Triolein 13C3 是一种 13C 标记的 Triolein。Triolein 是一种对称三酰甘油，能够减少 MMP-1 的上调，具有很强的抗氧化、抗炎活性。

GC67938 Guaiacin

愈创木素

Guaiacin 是从 Machilus thunbergii SIEB. et ZUCC 的树皮中分离的芳基萘型木质素。Guaiacin 显着增加碱性磷酸酶活性和成骨细胞分化。

GC67908 Calpain-2-IN-1 Calpain-2-IN-1 (Formula 1A) 是一种 calpain-2 亚型特异性的抑制剂，对 calpain-1 和 calpain-2 的 Ki 分别为 181 nM 和 7.8 nM。Calpain-2-IN-1 可用于神经退行性疾病和其他突触功能疾病的研究。

GC67899 Aurora kinase inhibitor-8 Aurora kinase inhibitor-8 是一种高选择性 Aurora 激酶的抑制剂。

GC67888 RAD51-IN-5 RAD51-IN-5 是一种有效的 RAD51 抑制剂。RAD51 是一种真核生物基因。RAD51-IN-5 具有研究线粒体缺陷病症的潜力 (摘自专利 WO2021164746A1，化合物 3)。

GC67798 MLS-0437605 MLS-0437605 是一种选择性双特异性磷酸酶 3 (DUSP3) 抑制剂，IC50 为 3.7 μM。MLS-0437605 对 DUSP3 的选择性比对 DUSP22 和其他蛋白酪氨酸磷酸酶 (PTP) 更具选择性。

GC67778 Sirtuin modulator 3 Sirtuin modulator 3 (compound 129) 是一种 N -苯基苯甲酰胺衍生物，作为 Sirtuin 调制剂。

GC67775 Casein kinase 1δ-IN-3 Casein kinase 1δ-IN-3 (Compound 23a) 是一种酪蛋白激酶 1δ (CK1d) 抑制剂，pIC50 为 6.5376 M。

GC67708 PLN-1474 PLN-1474 (compound 1) 是具有口服活性的，选择性的 avß1 整合素抑制剂，IC50 值 <50 nM。PLN-1474 在肝纤维化小鼠模型中显著降低肝脏 pSMAD3/SMAD3 水平、肝脏胶原蛋白基因表达和肝脏 OHP 浓度。PLN-1474 可用于预防、延缓或治疗纤维化或肝硬化疾病或紊乱的研究。