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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8880 |
PFM01
|
Others | Others |
PFM01 是 MRE11核酸内切酶抑制剂,是 N-烷基化的 Mirin 衍生物。它可以通过非同源末端连接 (NHEJ) 和同源重组 (HR) 调节双链断裂修复 (DSBR)。 | |||
T9168 |
NSC 617145
NSC617145,NSC-617145 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
NSC 617145 (NSC617145) 是一种 WRN 解旋酶抑制剂,IC50值为 230 nM。它以浓度依赖性方式抑制 WRN 解旋酶的 ATP 酶,并诱导双链断裂和染色体异常。 | |||
T4470 |
Pyridostatin TFA
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Pyridostatin TFA 是一种 G-四链体稳定剂,靶向原癌基因 Src,降低人乳腺癌细胞 SRC 蛋白水平和 SRC 依赖的细胞运动。它通过诱导复制和转录依赖的 DNA 损伤促进人类癌细胞生长停滞。 | |||
T9760 |
IC 86621
|
DNA-PK | DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
IC 86621 是一种选择性和可逆的 ATP 竞争性 DNA-PK 抑制剂,IC50 为 120 nM。 IC 86621 增加 DNA 双链断裂 (DSB) 诱导的抗肿瘤活性,其 EC50 为 68 µM,用于 DNA-PK 介导的细胞 DSB 修复。 | |||
T1899 |
Pyridostatin
RR82,Pyridostatin Trifluoroacetate Salt |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Pyridostatin (RR82) 是一种 G-四链体稳定剂,靶向原癌基因 Src,降低人乳腺癌细胞 SRC 蛋白水平和 SRC 依赖的细胞运动。它通过诱导复制和转录依赖的 DNA 损伤促进人类癌细胞生长停滞。 | |||
T8587 |
EcDsbB-IN-12
4,5-dichloro-2-[(2-chlorophenyl)methyl]pyridazin-3-one |
Others | Others |
EcDsbB-IN-12 (4,5-dichloro-2-[(2-chlorophenyl)methyl]pyridazin-3-one) 靶向二硫键形成酶,是一种新型强效特异性EcDsbB 抑制剂。 | |||
T19925 |
EcDsbB-IN-9
|
Others | Others |
EcDsbB-IN-9 是一种特异性 EcDsbB 抑制剂,靶向革兰氏阴性菌的二硫键形成酶 DsbB。 | |||
T66152 |
NDSB-211
|
Others | Others |
NDSB-211 是一种具有较小的疏水端并能温和地溶解蛋白质的表面活性剂,可用于蛋白提取和分析。 | |||
TF0120 |
NDSB-201
|
Others | Others |
NDSB-201 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 TF0120,CAS号为 15471-17-7。 | |||
TF0032 |
NDSB-256
|
Others | Others |
NDSB-256 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 TF0032,CAS号为 81239-45-4。 | |||
TF0078 |
NDSB-195
|
Others | Others |
NDSB-195 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 TF0078,CAS号为 160255-06-1。 | |||
TF0121 |
NDSB-221
|
Others | Others |
NDSB-221 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 TF0121,CAS号为 160788-56-7。 | |||
T8637 |
DMNB
6-Nitroveratraldehyde,6-硝基藜芦醛 |
DNA-PK | DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
DMNB (6-Nitroveratraldehyde) 可用于合成no-carrier-added 6-[18F]fluoro-L-DOPA (6-FDOPA)。它可用于研究多巴胺能系统的PET。 | |||
T0987 |
Gimeracil
吉美嘧啶,吉莫斯特,Gimestat |
Autophagy | Autophagy |
Gimeracil (Gimestat) 是一种竞争性可逆的 DPYD(二氢嘧啶脱氢酶,DPD) 有效抑制剂,是口服氟嘧啶衍生物 S-1 的成分,能够抑制 DNA DSB 的修复。 | |||
T63228 |
Simmiparib
SMOCL-9112 |
Apoptosis; PARP | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Simmiparib (SMOCL-9112) 是一种新型有效的 PARP1 和 PARP2 抑制剂,是一种Olaparib 衍生物。Simmiparib 在同源重组修复 (HR) 缺陷细胞中诱导 DNA 双链断裂 (DSB) 和 细胞周期阻滞,从而促使细胞凋亡 (apoptosis)。Simmiparib 可用于研究帕金森病、阿尔茨海默病、乳腺癌和黑色素瘤。 | |||
T68895 |
CBP-93872
|
Others | Others |
CBP-93872 is a G2 checkpoint inhibitor. CBP-93872 specifically abrogates the DNA double-stranded break (DSB)-induced G2 checkpoint through inhibiting maintenance. CBP-93872 is an inhibitor of maintenance of the DSB-specific G2 checkpoint and thus might be a strong candidate as the basis for a drug that specifically sensitizes p53-mutated cancer cells to DSB-inducing DNA damage therapy. | |||
T68985 |
Amonafide L-malate
|
Others | Others |
Amonafide L-malate is the malate salt of amonafide, an imide derivative of naphthalic acid, with potential antineoplastic activity. Amonafide intercalates into DNA and inhibits topoisomerase II, resulting in DNA double-strand breaks (DSB) and inhibition of DNA replication and RNA synthesis. | |||
T74501 |
NHEJ inhibitor-1
|
Others | Others |
NHEJ inhibitor-1 (Compound C2) 是一种三功能 Pt(II) 复合物,可缓解非同源末端连接 (NHEJ)/同源重组 (HR) 相关的双链断裂 (DSB) 修复,从而避免非小细胞肺对顺铂的耐药性。NHEJ inhibitor-1 抑制损伤修复蛋白 Ku70 和 Rad51,从而使肿瘤对活性分子重新敏感。NHEJ inhibitor-1 还诱导 ROS 产生和MMP 降低。 | |||
T61017 |
Topoisomerase II inhibitor 6
|
Others | Others |
Topoisomerase II inhibitor 6 (Compound 5) 是色胺酮的衍生物。它是一种有效的拓扑异构酶的选择性抑制剂。Topoisomerase II inhibitor 6 在 G2 期阻断 CCRF-CEM 的细胞周期并诱导 DNA 双链断裂。Topoisomerase II inhibitor 6 对不同的肿瘤细胞系具有抗增殖活性,在癌症疾病研究中具有潜力。 | |||
T78747 |
DiPT-4
|
Topoisomerase | DNA Damage/DNA Repair |
DiPT-4为一种TOP1/PARP1双重抑制剂,可引发癌细胞大量DNA双链断裂(DSB)、细胞周期阻滞及凋亡。DiPT-4具有研究癌症耐药性克服潜力。 | |||
T80899 |
UNC3474
|
Others | Others |
UNC3474为小分子配体,与53BP1相结合。该化合物针对53BP1TT的芳香族甲基赖氨酸结合笼展现出1.0 ± 0.3μM的解离常数(Kd)。UNC3474抑制53BP1募集至DSB,其机制为稳定细胞内预存的53BP1自抑制状态。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-03341 |
ASF1B Protein, Human, Recombinant (His)
anti-silencing function 1B histone chaperone,CIA-II |
Human | Baculovirus Insect Cells |
The histone chaperone anti-silencing factor 1a (ASF1a) interacts with MDC1 and is recruited to sites of DSBs to facilitate the interaction of phospho-ATM with MDC1 and phosphorylation of MDC1, which are required for the recruitment of RNF8/RNF168 histone ubiquitin ligases. Thus, ASF1a deficiency reduces histone ubiquitination at DSBs, decreasing the recruitment of 53BP1, and decreases NHEJ, rendering cells more sensitive to DSBs. This role of ASF1a in DSB repair cannot be provided by the closely... | |||
TMPH-03440 |
RAD52 Protein, S. cerevisiae, Recombinant (His & SUMO)
RAD52,DNA repair and recombination protein RAD52 |
Saccharomyces cerevisiae | E. coli |
Involved in DNA double-strand break (DSB) repair and recombination. Promotes the annealing of complementary single-stranded DNA and by stimulation of the RAD51 recombinase. RAD52 Protein, S. cerevisiae, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 41.1 kDa and the accession number is P06778. | |||
TMPH-01431 |
HELQ Protein, Human, Recombinant (His & Myc)
Mus308-like helicase,POLQ-like helicase,HELQ,Helicase POLQ-l... |
Human | E. coli |
Single-stranded DNA-dependent ATPase and 5' to 3' DNA helicase. Involved in the repair of DNA cross-links and double-strand break (DSB) resistance. Participates in FANCD2-mediated repair. Forms a complex with POLN polymerase that participates in homologous recombination (HR) repair and is essential for cellular protection against DNA cross-links. HELQ Protein, Human, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 4... |