nc

NC-1300-B 抑制 H（+）-K（+）-ATP 酶，可用于研究胃溃疡。

SIAIS630121-NC 是 SIAIS630121 的阴性对照，SIAIS630121 是 NAMPT (烟酰胺磷酸核糖基转移酶) 的降解物。

SIAIS630120-NC 为 SIAIS630120 的阴性对照，其为 NAMPT(烟酰胺磷酸核糖基转移酶)的降解物。

NC 1100 is a calcium channel antagonist.

NC1153 is a blocker of IL-2-induced activation of JAK3 and its downstream substrates STAT5a/b. It promotes long-term allograft survival and sparing the recipient from multiple toxicities.

NC182 is a topo II inhibitor that shows selective and potent topo II inhibition on the induction of topo II-dependent DNA fragmentation.

NC190 is an inhibitor of topoisomerase II that inhibited the growth of FM3A cells in clinical trials. NC-190 strongly inhibited the growth of FM3A cells when cultured with NC-190 for 48 h (IC50: 0.019 μg/ml). NC-190 potently suppressed DNA synthesis with

NC00075159 is an opener of human KCNQ4 (Kv7.4) potassium channel.

NC043 is an inhibitor of Wnt/β-catenin signaling, it forms a covalent bond with the Cys-516 residue of CARF.

NC-174 is a trisubstituted guanidine high potency synthetic sweetener.

Primordazine NC-6364997 is a negative control for Primordazine A and Primordazine B.

NC1 is a novel highly active allosteric inhibitor of protein tyrosine phosphatase, non-receptor type 22 (PTPN22) which is a lymphoid-specific tyrosine phosphatase (LYP).

NC-2100 is an aperoxisome proliferator-activated receptor-gamma (PPARgamma) activator.

NC03 is a PI4K2A inhibitor which decreases the PI4P pools in Golgi and endosomes.

NC-III-49-1 是一种有效的二价 BET（bivalent bromodomain and extraterminal domain (BET)）抑制剂。NC-III-49-1 显示与 BRD4-1、BRD4-2、BRD4-T、BRDT-1、BRDT-2、BRDT-T 的结合潜力，Kd 值分别为 0.095、0.32、0.29、0.089 、5.5、0.058 nM。NC-III-49-1 显示出抗增殖活性。NC-III-49-1 降低 c-Myc 的表达。

NC-R17是一种衍生自RSL3的非共价GPX4降解剂，涉及铁死亡(Ferroptosis)过程。该化合物展现出抗肿瘤活性，用于非共价GPX4 PROTAC的设计。

NC318 是一种靶向 Siglec-15/CD33L3的人源化抗体，可用于研究非小细胞肺癌。

NC9 is an irreversible inhibitor of transglutaminase 2 (TG2) and also inhibits Factor XIIIA (FXIIIA).

UCSF924NC is the recommended negative control compound for the high-affinity dopamine D4 receptor (DRD4) partial agonist UCSF924. UCSF924NC exhibits a 1/2500-fold reduced D4 affinity when compared with that of UCSF924.

NC762 是一种人源化 IgG1κ 单克隆抗体，靶向人类 B7-H4 (B7 同源物 4)。该化合物的 Fc 区域具有三个点突变 (S239D/A330L/I332E; DLE)，这增强了其与 CD16a (FcγRIIIa) 的结合能力，从而表现出更高的抗体依赖性细胞毒作用 (ADCC)。通过结合在肿瘤上表达的 B7-H4，NC762 能够抑制体内肿瘤的生长，适用于晚期或转移性实体瘤等癌症的研究。

Eprodisate disodium (NC-503) 是一种带负电荷的磺化类的原纤维形成抑制剂，是口服具有活力的 Eprodisate 二钠盐形式，可用于研究淀粉样蛋白A(AA) 淀粉样变性病。

Vecuronium bromide (ORG NC 45) 是一种合成的中效单季铵盐类固醇和非去极化神经肌肉阻滞剂，具有肌肉松弛活性。

Neotame (HSDB 7965) 是阿斯巴甜的衍生物，是低热量、高效的人造甜味剂，非营养性甜味剂和增味剂，其甜度是糖的 7000-13,000 倍，可用于多种食品。

Ipenoxazone is an effective and centrally acting muscle relaxant.