15
2
1
3
Cat. No. | Product Name | ||
---|---|---|---|
L7810 | 高溶解性多官能团片段化合物库 | 1159 compounds | |
高溶解性多官能团片段库包含1159 种片段分子 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4213 |
NCT-503
NCT 503 |
Dehydrogenase; FLT; TAM Receptor | Angiogenesis; Metabolism; Tyrosine Kinase/Adaptors |
NCT-503 是一种磷酸甘油酸脱氢酶 (PHGDH) 抑制剂,其IC50=2.5 µM。 | |||
T38605 |
NCT-504
|
Others | Others |
NCT-504,作为一种选择性的PIP4Kγ的变构抑制剂,展现出15.8 μM的IC50值。该化合物对于亨廷顿病的研究具有潜力。 | |||
T16277 |
NCT-502
N-(4,6-dimethylpyridin-2-yl)-4-[5-(trifluoromethyl)pyridin-2-yl]piperazine-1-carbothioamide |
Dehydrogenase | Metabolism |
NCT-502 (N-(4,6-dimethylpyridin-2-yl)-4-[5-(trifluoromethyl)pyridin-2-yl]piperazine-1-carbothioamide) 是磷酸甘油酸脱氢酶 (PHGDH) 抑制剂(IC50:3.7 μM),对 PHGDH 依赖性癌细胞具有细胞毒性,能够减少葡萄糖衍生的丝氨酸的产生,。 | |||
T9996 |
NCT-58
NCT58 |
HSP | Cytoskeletal Signaling; Metabolism |
NCT-58是一种有效的C 端HSP90抑制剂。NCT-58不会引起热休克反应(HSR)。NCT-58通过同时下调HER 家族成员以及抑制Akt 磷酸化来激发抗肿瘤活性。NCT-58杀死对曲妥珠单抗耐药的乳腺癌干细胞样细胞。NCT-58诱导HER2阳性乳腺癌细胞凋亡。 | |||
T12196 |
NCT-505
|
Dehydrogenase | Metabolism |
NCT-505是乙醛脱氢酶的选择性抑制剂,IC50为 7 nM。对 hALDH1A2,hALDH1A3,hALDH2,hALDH3A1的抑制作用较弱,IC50分别为 >57,22.8,20.1,>57 μM。 | |||
T6903 |
NCT-501
NCT501 |
Dehydrogenase | Metabolism |
NCT-501 是一种茶碱类化合物,有效抑制醛脱氢酶 1A1(ALDH1A1), 抑制 hALDH1A1 IC50为 40 nM, 选择性超过其它 ALDH 同工酶和其它脱氢酶 (作用于 hALDH1B1, hALDH3A1, 和 hALDH2 时,IC50值 >57 UM)。 | |||
T25858 |
NCT-10b
NCT 10b |
||
NCT-10b is a selective inhibitor of HDAC6. | |||
T39485 |
NCT-501 hydrochloride
|
||
NCT-501 hydrochloride is a highly potent and selective inhibitor of aldehyde dehydrogenase 1A1 (ALDH1A1), which is based on theophylline. It effectively inhibits hALDH1A1 with an IC50 value of 40 nM, exhibiting superior selectivity towards hALDH1A1 compared to other ALDH isozymes and dehydrogenases such as hALDH1B1, hALDH3A1, and hALDH2 (with IC50 values exceeding 57 μM). | |||
T41159 | NCT 501 hydrochloride | ||
NCT 501 hydrochloride is a potent and selective ALDH1A1 inhibitor (IC50 = 40 nM). Exhibits >1000-fold selectivity for ALDH1A1 over ALDH3A1, ALDH1B1, ALDH2, HPGD and HSD17β4. Also selective over a panel of 168 GPCRs. Blood-brain barrier permeable. | |||
T12197 | NCT-506 | Others | Others |
NCT-506 is an orally bioavailable inhibitors of aldehyde dehydrogenase 1A1 (ALDH1A1) (IC50 of 7 nM). | |||
T75344 | NCT-TFP | ||
NCT-TFP 是 PARP 探针,用于鉴定聚 (ADP-核糖) 聚合酶 (PARP) 抑制剂。 | |||
T60030 | NCT02 | ||
NCT02 是一种细胞周期蛋白 K 降解剂,可诱导细胞周期蛋白 K (CCNK) 的泛素化和 CCNK 及其复合物 CDK12 的蛋白酶体降解。NCT02具有研究转移性结直肠癌 (CRC) 的潜力。 | |||
T23150 |
PHGDH-inactive
|
Others | Others |
PHGDH-inactive 对 PHGDH 无活性,IC50大于57 μM,可用作 NCT-502 和 NCT-503 的阴性对照。 | |||
T34193 |
Punctaporonin D
M 167906,M167906 |
||
Punctaporonin D is an isomeric allylic alcohol from the fungus Poronia punctata. | |||
T80371 |
Distinctin
|
||
Distinctin是一种源自青蛙皮肤的抗菌肽,具有针对E. faecalis, P. aeruginosa, S. aureus和E. coli的抗菌活性,其最小抑菌浓度(MIC)分别为14.5 μM,28.0 μM,28.0 μM和14.5 μM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN3290 | 8-O-Demethyl-7-O-methyl-3,9-dihydropunctatin | Others | Others |
8-O-Demethyl-7-O-methyl-3,9-dihydropunctatin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3290,CAS号为 93078-83-2。 | |||
T26167 |
Rubropunctatin
Rubropunctamine |
||
Rubropunctatin is a monascus pigment with very potent cancer cell proliferation inhibitory effects. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-02910 |
Nicastrin Protein, Mouse, Recombinant (His)
AA727311,NCSTN,Aph2,9430068N19Rik,Kiaa0253,Nct,D1Da... |
Mouse | HEK293 Cells |
Nicastrin Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 73 kDa and the accession number is P57716. | |||
TMPY-03074 |
Nicastrin Protein, Mouse, Recombinant (hFc)
Aph2,AA727311,Nct,NCSTN,nicastrin,mKIAA0253,D1Dau13... |
Mouse | HEK293 Cells |
Nicastrin Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 98.5 kDa and the accession number is P57716. | |||
TMPH-03528 |
Chemotaxis inhibitory Protein, S. aureus (strain NCTC 8325/PS47), Recombinant (His & Myc)
chp,Chemotaxis inhibitory protein,CHIPS |
Staphylococcus aureus | E. coli |
Involved in countering the first line of host defense mechanisms. Specifically inhibits the response of human neutrophils and monocytes to complement anaphylatoxin C5a and formylated peptides, like N-formyl-methionyl-leucyl-phenylalanine (fMLP). Acts by binding directly to the C5a receptor (C5aR) and formylated peptide receptor (FPR), thereby blocking the C5a- and fMLP-induced calcium responses. Prevents phagocytosis of the bacterium. Chemotaxis inhibitory Protein, S. aureus (strain NCTC 8325/PS... |