61
8
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9810 |
TNIK-IN-5
|
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
TNIK-IN-5 是高效的 TNIK 抑制剂 (IC50= 0.05 μM)。TNIK-IN-5 可以有效抑制细胞中的 Wnt 信号通路。TNIK-IN-5 在体外显示出良好的抗结直肠癌活性。 | |||
T60037 |
SR15006
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
SR15006 是 Krüppel 样因子 5 (KLF5) 抑制剂 (IC50 = 41.6 nM)。 | |||
T6255 |
Bromosporine
|
Epigenetic Reader Domain; CDK | Cell Cycle/Checkpoint; Chromatin/Epigenetic |
Bromosporine 是广谱 BRD2/4/9 和 CECR2 溴结构域抑制剂,IC50为0.41、0.29、0.122和0.017 μM。 | |||
T8545 |
FEN1-IN-4
FEN1 Inhibitor C2 |
Others | Others |
FEN1-IN-4 (FEN1 Inhibitor C2) 是人类皮瓣内切核酸酶-1 (hFEN1) 抑制剂。 | |||
T14953 |
Chloroquinoxaline sulfonamide
NSC-339004,Chloroquinoxaline |
Topoisomerase | DNA Damage/DNA Repair |
Chloroquinoxaline sulfonamide (Chloroquinoxaline) 是拓扑异构酶 II alpha/beta 毒物,具有抗肿瘤活性和免疫抑制特性,可抑制小鼠 B16 黑色素瘤细胞的增殖,可用于研究转移性结直肠癌。 | |||
T83641 |
HNPMI
|
Apoptosis; EGFR | Angiogenesis; Apoptosis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
HNPMI 是一种 EGFR 抑制剂,诱导 CRC 细胞的G0/G1 期停滞结直肠癌,可调节与细胞凋亡相关的酶,可促进细胞凋亡,可用于研究结直肠癌。 | |||
T28740 |
SDZ-62-434
SDZ 62 434,SDZ62434 |
Platelet aggregation | Others |
SDZ-62-434 是一种血小板活化因子抑制剂,具有抗肿瘤活性,抑制静止的瑞士 3T3 细胞中 bombesin 和血小板衍生生长因子诱导的 DNA 合成,可用于研究白血病、人异种移植结直肠癌和肺癌。 | |||
T64066 |
CSF1R-IN-3
|
c-Fms; CSF-1R | Tyrosine Kinase/Adaptors |
CSF1R-IN-3是一种口服有效的 CSF-1R 抑制剂,IC50值为2.1nM。CSF1R-IN-3对结直肠癌细胞具有抗增殖活性。CSF1R-IN-3 通过抑制巨噬细胞的迁移,诱导 M2 型巨噬细胞重新编程为 M1 型巨噬细胞,从而表现出抗肿瘤作用和提高免疫力的作用,展现对结直肠癌细胞的活性。 | |||
T24855 |
TASIN-1 Hydrochloride
塔辛-1盐酸盐,TASIN-1 HCl,TASIN 1 HCl,TASIN1 HCl |
APC | Cell Cycle/Checkpoint |
TASIN-1 Hydrochloride (TASIN-1 HCl) 是一种截短型 APC 的选择性抑制剂,通过降低细胞胆固醇水平和通过结肠癌细胞中的 ER 应激/ROS/JNK 信号传导诱导凋亡细胞死亡来选择性杀死表达截短型 APC 的结肠直肠癌细胞。 | |||
T21567L |
Cyclosomatostatin Acetate
Cyclosomatostatin Acetate (84211-54-1 Free base) |
Somatostatin | GPCR/G Protein |
Cyclosomatostatin Acetate 是有效的生长抑素受体拮抗剂。Cyclosomatostatin Acetate 在直肠癌 (CRC) 细胞中可以抑制 SSTR1的信号传导,并降低结细胞增殖、ALDH+ 细胞群体大小和球形成。 | |||
T76674 |
Cibisatamab
|
Others | Others |
Cibisatamab 是一种 T 细胞双特异性抗体,可被当作 T 细胞接合器。Cibisatamab 靶向癌细胞上的癌胚抗原 (CEA) 和 T 细胞上的 CD3,当癌细胞表面的 CEA从中等水平到高水平会触发 T 细胞杀伤。Cibisatamab 可用于研究结直肠癌类的实体癌。 | |||
T2618 |
LGK974
LGK 974,LGK-974,NVP-LGK974,WNT974 |
Porcupine | Stem Cells |
LGK974 (NVP-LGK974) 是一种有效的、特异性的、具有口服活性的Porcupine(PORCN) 抑制剂(IC50:0.1 nM)。 | |||
T77519 |
FC-116
FC116 |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
FC-116 是一种有效的 Tubulin 抑制剂,具有抗肿瘤活性,抑制小鼠体内肿瘤的生长。FC-116 诱导大肠癌 (CRC) 细胞凋亡,可促进蛋白降解。 | |||
T72068 |
SFI003
|
Apoptosis; ROS | Apoptosis; Immunology/Inflammation |
SFI003是一种新型SRSF3抑制剂,通过调节SRSF3 / DHCR24 / ROS 轴对结直肠癌发挥抗癌活性,通过SRSF3 / DHCR24 /活性氧(ROS)轴驱动CRC 细胞凋亡。 | |||
T39664 |
Ethaselen
BBSKE |
Others | Others |
Ethaselen (BBSKE) 是具有口服活性和选择性的硫氧还蛋白还原酶1 (TrxR) 抑制剂,具有抗癌活性,直接抑制 TrxR1 活性,常用奥沙利铂联合使用来抑制肿瘤生长。Ethaselen 可诱导癌细胞凋亡,抑制结直肠癌细胞增殖。 | |||
T77719 |
TNIK-IN-7
|
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
TNIK-IN-7 是一种具有高效性和选择性的 Traf2 和 Nck 相互作用激酶 (TNIK) 抑制剂(IC50:11 nM),具有抗肿瘤活性,可用于研究结直肠癌细胞中信号传导和增殖。 | |||
T76890 |
Petosemtamab
MCLA 158 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Petosemtamab (MCLA 158) 是一种高效的抗 EGFR (Kd: 0.22 nM) 和抗 LGR5 (Kd: 0.86 nM) 单克隆抗体。Petosemtamab 促使 LGR5+ 癌细胞中的 EGFR 信号传导中断和受体分解。Petosemtamab 可用于头颈部鳞状细胞癌 (HNSCC)、转移性结直肠癌 (CRC) 等实体瘤的研究。 | |||
T80644 |
DNA polymerase-IN-1
|
Antiviral; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation |
DNA polymerase-IN-1 作为DNA聚合酶抑制剂,展现出对肿瘤细胞的抗增殖活性,其半抑制浓度(IC50)为20.7 μM。DNA polymerase-IN-1 抑制 Taq DNA 聚合酶,IC 值低于 250μM。DNA polymerase-IN-1 通过RT-PCR检测在体外显示出抗逆转录病毒活性,可用于研究氧化损伤和结直肠癌。 | |||
T4013 |
SGC2085 HCl
|
Histone Methyltransferase | Chromatin/Epigenetic |
SGC2085 HCl 是一种有效的选择性辅激活剂相关的精氨酸甲基转移酶 1 (CARM1) 抑制剂,IC50 为 50 nM,选择性比其他 PRMT 高出数倍。 CARM1 是结直肠癌中 Wnt/β-catenin 转录和肿瘤转化的重要正调节因子,也是雌激素刺激的乳腺癌生长的关键因素,其耗竭导致体内髓性白血病细胞增殖减少。 | |||
T34120 |
PQ1
PQ-1,PQ 1 |
Others | Others |
PQ1, as an enhancer of gap junction in SW480 human colorectal cancer cells can act by restoring GJIC and increasing connexin expression in breast cancer cell lines while not affecting normal mammary cells. | |||
T32419 |
KRAS4b-PDEδ stabilizer C19
|
Others | Others |
KRAS4b-PDEδ stabilizer C19 is a stabilizer of the KRAS4b-PDEδ complex which decreases the proliferation of colorectal cancer cells, and increases apoptosis via decreased activation of oncogenic KRAS4b signaling. | |||
T38519 |
YB-0158
Wnt pathway inhibitor 2,YB-0158 |
Others | Others |
YB-0158 (Wnt pathway inhibitor 2) is a powerful peptidomimetic compound that effectively targets colorectal cancer stem cells (CSCs) by disrupting the interaction between Sam68 and Src proteins. This compound acts as a reverse-turn agent, inducing apoptosis in CRC cells and displaying strong anti-cancer activities. | |||
T36275 |
xStAx-VHLL
|
||
Selective peptide-based β-catenin Degrader. Comprises a β-catenin-targeted stapled peptide, xStAx, linked to a VHL-binding peptide. Reduces β-catenin levels in HEK293T cells and colorectal cancer cell lines. Selectively degrades β-catenin over other Wnt signaling pathway components. Inhibits tumor growth in APCmin/+ mice, with constitutively active Wnt signaling, and reduces survival of patient-derived colorectal cancer cell organoids. | |||
TP1979 |
NLS-StAx-h
|
||
Wnt inhibitor (IC50 = 1.4 μM). Stapled peptide inhibitor of oncogenic Wnt signaling. Inhibits β-catenin-transcription factor interactions. Inhibits proliferation and migration of colorectal cancer cells. Cell permeable. | |||
T81922 |
LM2I
|
Others | Others |
LM2I是一种多杀菌素(SPA)衍生物,兼具精氨酸琥珀酸合成酶(ASS1)激活剂和针对ASS1的直接作用的肿瘤抑制剂功能。在7种结直肠癌细胞系和结直肠癌异种移植肿瘤中,LM2I展现出明显的抗增殖活性,并且通过EGFR途径阻断结直肠癌细胞增长。 | |||
T73377 |
IGUANA-1
|
Others | Others |
IGUANA-1 是一种高效的 ALDH1B1抑制剂,ALDH1B1则是一种促进结直肠癌和胰腺癌的线粒体酶。IGUANA-1 对癌细胞具有显著的抑制作用。 | |||
T71624 |
GB1874
|
Others | Others |
GB1874 inhibitor of the Wnt pathway that targets the β-cat-TCF4 PPI. GB1874 also affected the proliferation and stemness of Wnt-addicted colorectal cancer (CRC) cells in vitro. Encouragingly, GB1874 inhibited the growth of CRC tumor xenografts in vivo, thus demonstrating its potential for further development into therapeutics against Wnt-associated cancer indications. | |||
T68721 |
Cantharidin imide
|
Others | Others |
Cantharidin imide is a PP1/2A inhibitor found in Canarthis vesicatoria. It inhibits proliferation of colorectal cancer cells, increases MCP-1, IL-6, and IL-β levels, and inhibits differentiation and resorptive activity of osteoclasts. This compound can produce severe skin inflammation, and is extremely toxic if ingested orally. | |||
T25611 |
Lanatoside
Lantoside,ABC lanatoside complex |
Others | Others |
Lanatoside 是一种 FDA 批准的强心苷,已被确定为候选的抗登革热化合物。它也被发现可以促进脉粥样硬化,还具有抗肿瘤活性,可抑制结直肠癌细胞、肝癌细胞的生长。 | |||
T36458 |
CAY10701
CAY10701 |
Others | Others |
CAY10701 is a 7-deazahypoxanthine analog that prevents microtubule formation, blocking the proliferation of HeLa and MCF-7 cells (GI50s = 22 and 38 nM, respectively). It also inhibits the growth of several different colorectal cancer cell lines (GI50 values range from 9 to 17 nM), while being at least 1,500-fold less effective against normal human fibroblast WI38 cells. CAY10701 is effective in vivo, reducing tumor volume in colorectal cell xenografts in mice without significantly altering body ... | |||
T35774 |
HC Toxin
|
Others | Others |
HC Toxin is a cell-permeable, reversible inhibitor of histone deacetylases (HDACs) (IC50 = 30 nM). Through its effects on HDACs, HC toxin has been shown to up-regulate the expression of 15-lipoxygenase-1 in colorectal cancer cells and induce fetal hemoglobin in human primary erythroid cells. HC Toxin is a cyclic tetrapeptide first isolated from H. carbonum (now C. carbonum), a pathogen of maize. | |||
T39200 |
β-catenin-IN-37
|
Others | Others |
β-Catenin-IN-37 is a selective inhibitor of the protein-protein interaction between β-Catenin and T-cell factor (Tcf), known as β-catenin/Tcf PPI. It effectively inhibits canonical Wnt signaling and impedes the growth of colorectal cancer cells SW480 and HCT116, with IC50 values of 20 μM and 31 μM, respectively. | |||
T69898 |
NG25 trihydrochloride
|
Others | Others |
NG25 trihydrochloride is a type II kinase inhibitor that inhibits MAP4K2 and TAK1. It also inhibits the Src family kinases Src and LYN and Abl family kinases as well as CSK, FER, and p38α. NG 25 prevents TNF-α-induced IKKα/β phosphorylation and IκB-α degradation in L929 cells. It inhibits secretion of IFN-α and IFN-β induced by CpG type B and CL097, respectively. NG 25 decreases cell viability of HCT116KRASWT, and to a greater degree of HCT116KRASG13D, colorectal cancer cells in a concentration... | |||
T36702 |
CAY10753
|
Others | Others |
CAY10753 is an inhibitor of tankyrase 2 (TNKS2; IC50= 0.3 nM).1It is selective for TNKS2 over TNKS1 (IC50= 6.1 nM), as well as poly(ADP-ribose) polymerase 1 (PARP1) and PARP2 (IC50s = 89.6 and 37.8 nM, respectively). CAY10753 inhibits proliferation of DLD-1 colorectal cancer cells when used at a concentration of 1 μM. 1.Tomassi, S., Pfahler, J., Mautone, N., et al.From PARP1 to TNKS2 inhibition: A structure-based approachMed. Chem. Lett.(2020) | |||
T81749 |
MRV03-068
|
Others | Others |
MRV03-068(化合物2)作为一种选择性的ClbP抑制剂,有效抑制Colibactin对真核细胞的基因毒性。该化合物在结直肠癌研究中具有潜在应用价值。 | |||
T81748 |
MRV03-069
|
Others | Others |
MRV03-069(化合物3)为一种选择性ClbP抑制剂,具备阻止Colibactin对真核细胞基因毒性的能力,适用于结直肠癌的研究。 | |||
T36779 |
NG 25 (hydrochloride hydrate)
|
Others | Others |
NG 25 is a type II kinase inhibitor that inhibits MAP4K2 and TAK1 (IC50s = 21.7 and 149 nM, respectively).1It also inhibits the Src family kinases Src and LYN (IC50s = 113 and 12.9 nM, respectively) and Abl family kinases (IC50s = 75.2 nM), as well as CSK, FER, and p38α (IC50s = 56.4, 82.3, and 102 nM, respectively). NG 25 (100 nM) prevents TNF-α-induced IKKα/β phosphorylation and IκB-α degradation in L929 cells. It inhibits secretion of IFN-α and IFN-β induced by CpG type B and CL097, respectiv... | |||
T37541 |
Amycolatopsin C
|
Others | Others |
Amycolatopsin C is a polyketide macrolide originally isolated fromAmycolatopsisthat has antimycobacterial and anticancer activities.1It is active againstM. bovisandM. tuberculosis(IC50s = 2.7 and 5.7 μM, respectively) but notB. subtilis,S. aureus,E. coli, orP. aeruginosa(IC50s = >30 μM for all). Amycolatopsin C is cytotoxic to SW620 colorectal and NCI H460 lung cancer cells (IC50s = 10 and 5.9 μM, respectively). 1.Khalil, Z.G., Salim, A.A., Vuong, D., et al.Amycolatopsins A-C: Antimycobacterial ... | |||
T73478 |
ME-143
NV-143 |
Others | Others |
ME-143为第二代特异性NADH氧化酶抑制剂,针对结直肠癌细胞中WNT/β-catenin通路展现抑制作用。该化合物在体外及体内显示出广泛的抗癌活性。 | |||
T61942 |
SKLB0565
|
Others | Others |
SKLB0565 是有效的微管蛋白 (tubulin) 抑制剂。SKLB0565 明显抑制结直肠癌细胞的增殖,IC50为 0.012 - 0.081 μM。SKLB0565 诱导 G2/M 期阻滞和线粒体介导的内源性凋亡 (apoptosis)。SKLB0565 破坏 HUVECs 细胞的微管形成,抑制细胞迁移。 | |||
T78120 |
β-catenin-IN-6
|
Others | Others |
β-catenin-IN-6是一种针对Wnt/β-catenin(典型的wingless相关整合位点)通路的抑制剂,能够抑制人类结直肠癌细胞的增殖,并在β-catenin/RK3E小鼠模型上展现出效果。 | |||
T37539 |
Amycolatopsin A
|
Others | Others |
Amycolatopsin A is a macrolide polyketide originally isolated fromAmycolatopsisthat has antimycobacterial and anticancer activities.1It is active againstM. bovisandM. tuberculosis(IC50s = 0.4 and 4.4 μM, respectively) but notB. subtilis,S. aureus,E. coli, orP. aeruginosa(IC50s = >30 μM for all). Amycolatopsin A is cytotoxic to SW620 colorectal and NCI H460 lung cancer cells (IC50s = 0.08 and 1.2 μM, respectively). 1.Khalil, Z.G., Salim, A.A., Vuong, D., et al.Amycolatopsins A-C: Antimycobacteria... | |||
T73391 |
BLM-IN-2
|
Others | Others |
BLM-IN-2是一种针对布鲁姆氏综合征蛋白(BLM)的抑制剂,IC50为0.8 μM。该化合物能够有效抑制结直肠癌(CRC)细胞的增殖、侵袭、诱导细胞周期阻滞及凋亡,因此适用于结直肠癌的研究。 | |||
T61905 |
RKI-1447 dihydrochloride
|
Others | Others |
RKI 1447 dihydrochloride 是一种有效的,选择性的 ROCK 抑制剂(ROCK1 IC50=14.5 nM,ROCK2 IC50 = 6.2 nM)。RKI 1447 dihydrochloride 对结直肠癌细胞的生长具有抑制作用,并促进其凋亡。 | |||
T75842 |
Cyclosomatostatin TFA
|
||
Cyclosomatostatin TFA 作为一种有效的生长抑素(SST)受体拮抗剂,在直肠癌(CRC)细胞中通过抑制1型生长抑素受体(SSTR1)的信号传导,有效降低结细胞增殖、ALDH+细胞群体的大小以及球形成。 | |||
T79654 |
CRM1-IN-1
|
CRM1 | Membrane transporter/Ion channel |
CRM1-IN-1 (Compound KL1) 为非共价CRM1抑制剂,能诱导核CRM1降解(IC50: 0.27 μM),抑制CRM1介导的核输出与细胞增殖,同时触发结直肠癌细胞凋亡 (apoptosis)。 | |||
T79655 |
CRM1-IN-2
|
CRM1 | Membrane transporter/Ion channel |
CRM1-IN-2(Compound KL2)为非共价CRM1抑制剂,能够定位CRM1于核外围,耗尽核内CRM1,从而抑制CRM1介导的核输出。该化合物能抑制结直肠癌细胞的生长并诱导细胞凋亡(apoptosis)。 | |||
T81374 |
PROTAC TTK degrader-2
|
PROTACs | PROTAC |
PROTACTTK degrader-2是一种TTK(苏氨酸酪氨酸激酶)的高效PROTAC降解剂,其在COLO-205和HCT-116细胞中分别展现出3.1和12.4 nM的DC50值。在COLO-205人结直肠癌细胞异种移植小鼠模型中,此化合物证实了其针对性降解与抗癌活性。 | |||
T63464 |
ERCC1-XPF-IN-1
|
Others | Others |
ERCC1-XPF-IN-1 是有效的、高亲和力的 ERCC1-XPF 抑制剂 (IC50: 0.49 μM)。ERCC1-XPF-IN-1 能够抑制 CPDs 的去除,降低环磷酰胺对结直肠癌细胞的毒性,提高了 UV 辐射的细胞毒性作用,阻碍 DNA 修复。 | |||
T62784 |
KRAS inhibitor-18
|
Others | Others |
KRAS inhibitor-18 (compound 3-10) 是一种 KRAS G12C 的有效抑制剂 (IC50: 4.74 μM)。KRAS inhibitor-18 在 MIA PaCA-2,A549 细胞中表现出 p-ERK 抑制作用,IC50s 分别为 66.4,11.1 μM。KRAS inhibitor-18 具有潜力进行胰腺癌、结直肠癌和肺癌的研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1305 |
Ethoxysanguinarine
乙氧基血根碱,6-Ethoxydihydrosanguinarine |
Apoptosis; AChR | Apoptosis; Neuroscience |
Ethoxysanguinarine (6-Ethoxydihydrosanguinarine) 是存在于龙葵中的一种苯并菲啶生物碱天然产物,通过抑制蛋白磷酸酶 2A,可抑制结直肠癌细胞活力,诱导细胞凋亡。 | |||
T2988 |
(-)-Epigallocatechin Gallate
Epigallocatechol Gallate,(-)-表没食子儿茶素没食子酸酯,EGCG |
Ferroptosis; Reactive Oxygen Species; HIV Protease; Mitochondrial Metabolism; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome |
(-)-Epigallocatechin Gallate (EGCG) 属于茶类黄酮天然产物,可抑制 EGFR 信号传导,抑制 GLUD 1/2。(-)-Epigallocatechin Gallate 具有抗氧化、抗炎和抗肿瘤活性。(-)-Epigallocatechin Gallate 可以通过激活细胞色素 c 氧化酶来诱导氧化磷酸化。 | |||
TN1237 |
3-O-Methylgallic acid
3,4-Dihydroxy-5-methoxybenzoic acid,3-O-甲基没食子酸 |
Apoptosis; NF-κB; OCT; DNA/RNA Synthesis; STAT | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; JAK/STAT signaling; Membrane transporter/Ion channel; NF-κB; Stem Cells |
3-O-Methylgallic acid (3,4-Dihydroxy-5-methoxybenzoic acid) 是一种花青素代谢产物,具有强大的抗氧化能力。它还诱导细胞凋亡并具有抗癌作用,可抑制 Caco-2 细胞增殖,IC50值为 24.1 μM。 | |||
T2938 |
(E/Z)-Polydatin
云杉新甙,(E/Z)-虎杖苷,Polydatin,(E/Z)-Piceid |
Phospholipase | Metabolism |
(E/Z)-Polydatin (Polydatin) 是从虎杖的根和根茎中分离得到的一种单晶化合物。它具有抗血小板聚集、心脏保护作用、抗低密度脂蛋白 (LDL) 氧化作用、抗炎和免疫调节功能。 | |||
TN3812 |
Dehydrovomifoliol
|
AChR | Neuroscience |
Dehydrovomifoliol could be a marker of Polish heather honey. Dehydrovomifoliol exhibits moderate acetylcholinesterase (AChE) inhibitory activities. Dehydrovomifoliol shows significant cytotoxic activities against three human cancer cell lines, namely, HONE-1 nasopharyngeal, KB oral epidermoid carcinoma, and HT29 colorectal carcinoma cells, and the IC(50) values in the range 3.7-8.1 microM. | |||
TMA0291 |
Dehydroglyasperin D
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GSK-3; p38 MAPK; ROS; Akt; COX; PI3K; DNA/RNA Synthesis; Prostaglandin Receptor; JNK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; MAPK; Neuroscience; PI3K/Akt/mTOR signaling; Stem Cells |
Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 human colorectal cancer cells through direct interaction with phosphatidylinositol 3-kinase; it also mediates suppression of both COX-2 expression and the MLK3 signalling pathway through direct binding and inhibition of MLK3. Dehydroglyasperin D shows strong ferric reducing activities and effectively scavenged DPPH, ABTS(+), and singlet o... | |||
TN7345 |
(±)-Enterodiol
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Others | Others |
(±)-Enterodiol,Enterodiol的外消旋体,由人体肠道细菌从全麦谷物、坚果、豆类、亚麻籽及蔬菜中的木脂素转化而来。此化合物对结直肠癌(CRC)细胞显示出凋亡作用,表现出抗癌活性。 | |||
T36815 |
Chevalone C
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Others | Others |
Chevalone C is a meroterpenoid fungal metabolite originally isolated from E. chevalieri. It is active against M. tuberculosis H37Ra (MIC = 6.3 μg/ml) and is cytotoxic to BC1 human breast cancer cells (IC50 = 8.7 μg/ml). Chevalone C inhibits the growth of multidrug-resistant isolates of E. coli, S. aureus, and E. faecium in a disc diffusion assay when used at a concentration of 15 μg/disc. It also induces cell death in HCT116 colorectal carcinoma cells. |
Cat. No. | Product Name | Target | Signaling Pathways |
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T71401 |
Oxaliplatin-d10
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Oxaliplatin-d10 is intended for use as an internal standard for the quantification of oxaliplatin by GC- or LC-MS. Oxaliplatin is a platinum-containing DNA-crosslinking agent. It induces the formation of DNA inter- and intrastrand crosslinks and DNA-protein adducts, inhibits DNA and RNA synthesis, and induces apoptosis in cancer cells. Oxaliplatin is cytotoxic to cisplatin-sensitive A2780(1A9) and KB-3-1 cells and cisplatin-resistant A2780-E(80) and KB-CP20 cells (IC50s = 0.12, 0.39, 4.7, and 2.... | |||
T71055 |
Albendazole-d7
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Albendazole-d7 is intended for use as an internal standard for the quantification of albendazole by GC- or LC-MS. Albendazole is an orally bioavailable benzimidazole anthelmintic that is active against a variety of helminths, including liver flukes, tapeworms, and roundworms. It eliminates Trichostrongylus in the fourth stomach of cattle and sheep when orally administered at doses ranging from 2.5 to 10 mg/kg as well as other species in the fourth stomach and the small and large intestine. Alben... |