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Search Results for " rad51 "

Targets Recommended: DNA/RNA Synthesis

29

抑制剂 & 化合物

5

重组蛋白

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Cat. No.	Product Name	Target	Signaling Pathways
T9271	RAD51-IN-1	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	RAD51-IN-1 是 B02 的衍生物，是一种RAD51的有效抑制剂，可研究癌症。
T4656	RAD51 Inhibitor B02 B02	Apoptosis; DNA/RNA Synthesis	Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	RAD51 Inhibitor B02 (B02) 是一种人 RAD51的抑制剂，IC50值为27.4 μM。
T39824	RAD51-IN-3 RAD51-IN-3	Others	Others
	RAD51-IN-3 is a Rad51 inhibitor.
T12682	Emzadirib CYT-0851,RAD51-IN-2	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Emzadirib (RAD51-IN-2) 是一种有效的 RAD51 抑制剂，具有潜在的抗癌活性，可用于研究 DNA 损伤修复。
T2276	RI-1 RI-1; 3-氯-1-(3,4-二氯苯基)-4-(4-吗啉基)-1H-吡咯-2,5-二酮,RI1,RAD51 inhibitor 1	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	RI-1 (RAD51 inhibitor 1) 是一种选择性 RAD51的抑制剂，IC50值为 5-30 μM，可以破坏人类细胞中的同源重组。它在半胱氨酸 319 处与 RAD51 蛋白表面共价结合，并通过直接结合到 RAD51 细丝中蛋白质亚基之间的界面的蛋白质表面来灭活 RAD51。
T61469	RAD51-IN-8	Others	Others
	RAD51-IN-8，一种新型 RAD51 结合剂，是一种RAD51-BRCA2抑制剂，可在微摩尔范围内抑制 RAD51-BRCA2 蛋白的相互作用。RAD51-IN-8 也是一种蛋白质-蛋白质相互作用 (PPI) 抑制剂。RAD51-IN-8 对 H4A4 具有抑制活性，EC50值为19 μM。
T63728	RAD51-IN-7	Others	Others
	RAD51-IN-7 是 RAD51 的有效抑制剂。其中 RAD51 是一种真核生物基因。RAD51-IN-7 对线粒体缺陷病症表现出研究潜力。
T63892	RAD51-IN-5	Others	Others
	RAD51-IN-5 是 RAD51 有效的抑制剂。其中 RAD51 是一种真核生物基因。RAD51-IN-5 对线粒体缺陷病症表现出研究潜力。
T2628	RI-2	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	RI-2 是一种可逆的RAD51抑制剂，IC50值为 44.17 μM，可抑制人体细胞中的同源重组修复。
T63883	RAD51-IN-6	Others	Others
	RAD51-IN-6 是 RAD51 的有效抑制剂。其中 RAD51 是一种真核生物基因。RAD51-IN-6 对线粒体缺陷病症表现出研究潜力。
T73107	RAD51-IN-4	Others	Others
	RAD51-IN-4 是一种有效的RAD51抑制剂。RAD51是一种真核生物基因。RAD51-IN-4 具有研究线粒体缺陷病症的潜力。
T6972	RS-1	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	RS-1 是一种 RAD51 的激活剂，同时可增强 CRISPR/Cas9 的活性。
T11600	IBR2 Isoquinoline	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	IBR2（Isoquinoline）是一种针对RAD51的强效特异性抑制剂，通过干预RAD51多聚体形成，加速蛋白酶体介导的RAD51蛋白降解，抑制癌细胞生长并诱导凋亡。实验证明在抑制RAD51介导的DNA双链断裂修复方面有效。
T8873	Bractoppin	Others; DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Others
	Bractoppin 是一种BRCA1 (t)BRCT domain 识别磷酸肽的选择性抑制剂，IC50为 74 nM。它优先抑制 BRCA1 -tBRCT 依赖的 DNA 损伤。它减少 BRCA1 对 DNA 断裂片段的招募，进而抑制损伤诱导的 G2 期阻滞和重组酶 RAD51 的组装。
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。
T2516	Amuvatinib MP470,HPK 56	Apoptosis; FLT; c-Met/HGFR; c-RET; DNA/RNA Synthesis; PDGFR; c-Kit	Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Tyrosine Kinase/Adaptors
	Amuvatinib (MP470) 是一种多靶点酪氨酸激酶抑制剂，对突变 c-Kit，PDGFRα，Flt3，c-Met 和 c-Ret 具有活性。它还是一种 DNA 修复抑制剂，靶向蛋白 DNA 修复 RAD51，从而破坏 DNA 损伤修复，具有抗肿瘤活性。
T60006	Aromatase inhibitor 23	Others	Others
	Aromatase inhibitor 23 是一种针对 RAD51 重组酶家族中蛋白质-蛋白质相互作用的抑制剂。
T6960L	PU-H71 HCl PU-H71 HCl(873436-91-0 Free base),Zelavespib HCl	HSP; DNA/RNA Synthesis	Cell Cycle/Checkpoint; Cytoskeletal Signaling; DNA Damage/DNA Repair; Metabolism
	PU-H71 HCl (Zelavespib HCl) 是一种新型Hsp90抑制剂，是一种新型嘌呤基类似物，也是一种可能是CIRT的一种有前途的放射增敏剂。PU-H71 HCL 在许多恶性肿瘤临床前模型中显示出抗肿瘤活性。PU-H71 HCL 对 Rad51 和Ku70 的蛋白表达水平有抑制作用，这可能与双链断裂修复的同源重组途径和非同源末端连接途径有关。
T10936	D-I03 DI03	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	D-I03 是一种选择性的RAD52 抑制剂，Kd 为 25.8 µM。D-I03 抑制 RAD52 依赖性单链退火 (SSA) 和 D 环形成，IC50 分别为 5 µM 和 8 µM。D-I03 抑制 BRCA1 和 BRCA2 缺陷细胞的生长，并抑制顺铂诱导的 RAD52 病灶形成，但对 RAD51 无影响。
T41211	CAM 833	Others	Others
	CAM 833 是一种有效的正位抑制剂，对 BRCA2 和 RAD51 之间相互作用具有抑制作用，对 ChimRAD51 蛋白的 Kd 为 366 nM。 CAM833 抑制 RAD51 的寡聚，促进 G2/M 阻滞细胞的凋亡 (apoptosis) 进程。
T27526	Halenaquinone	Others	Others
	Halenaquinone is a phosphatidylinositol 3-kinase inhibitor. Halenaquinone specifically inhibits the secondary DNA binding of RAD51. Halenaquinone inhibits RANKL-induced osteoclastogenesis. Halenaquinone induces apoptosis in PC12 cells.
T28536	RI(dl)-2 TFA RI(dl)-2	Others	Others
	RI(dl)-2 TFA 是一种有效的选择性 RAD51 介导的 D 环形成 (RAD51-mediated D-loop formation) 抑制剂，IC50为 11.1 μM，并抑制人细胞中的同源重组 (HR) 活性，IC50为 3.0 μM。
T63717	CAM833	Others	Others
	CAM833 是有效的抑制 BRCA2 和 RAD51 之间相互作用的正位抑制剂，也能够抑制 RAD51 的寡聚，能够作用于 ChimRAD51 蛋白 (Kd: 366 nM)。
T14282	Amuvatinib hydrochloride HPK 56 hydrochloride,MP470 hydrochloride	Others	Others
	Amuvatinib hydrochloride (MP470 hydrochloride) is an orally bioavailable multi-targeted tyrosine kinase inhibitor with potent activity against mutant c-Kit, PDGFRα, Flt3, c-Met and c-Ret and is also a DNA repair suppressor through suppression of DNA repai
T20694	DIDS	Others	Others
	DIDS, an anion exchange inhibitor, acts by blocking reversibly and later irreversibly, exchangers such as chloride-bicarbonate exchanger. It is also a RAD51 inhibitor.
T36703	CAY10760	Others	Others
	CAY10760 is an inhibitor of the protein-protein interaction between RAD51 recombinase and BRCA2 (EC50= 19 μM in a cell-free competitive ELISA).1It decreases homologous recombination by 54% in wild-typeBRCA2-expressing BxPC-3 pancreatic cancer cells when used at a concentration of 20 μM. CAY10760 (20 μM) decreases proliferation of BxPC-3, as well as mutantBRCA2-expressing Capan-1, cancer cells when used alone or in combination with the poly(ADP-ribose) polymerase (PARP) inhibitor olaparib . 1.Bag...
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。
T83854	BRC4wt TFA
	BRC4wt是一种从人类BRCA2的BRC4重复区(1521-1536)衍生而来的乙酰化肽，并且是BRCA2与RAD51之间的蛋白质-蛋白质相互作用的抑制剂。当与阳离子穿膜肽(Arg)9结合时，BRC4wt缩短了体外DNA复制轨迹长度，并降低了由DNA拓扑异构酶I抑制剂坎普特西汀引起的DNA损伤的同源修复频率，同时也增强了聚(ADP-核糖)聚合酶(PARP)抑制剂奥拉帕尼在HeLa人类宫颈癌细胞和U2OS人类骨肉瘤细胞中诱导的细胞死亡，但在非癌症细胞hTERT RPE-1、MRC-5或MCF-10A中则不然。
T36701	Phosphoramide mustard (cyclohexanamine)	Others	Others
	Phosphoramide mustard cyclohexanamine is the major metabolite for Cyclophosphamide , with anticancer activitiy. Phosphoramide mustard cyclohexanamine induces DNA adduct formation in ovarian granulosa cells, induces DNA damage and elicits the ovarian DNA repair response[1][2]. Phosphoramide mustard cyclohexanamine causes cytotoxicity through forming cross-linked DNA adducts which inhibit DNA strand separation during replication[1].Phosphoramide mustard cyclohexanamine destroys rapidly dividing ce...

化合物

Cat.No: T9271

Target: DNA/RNA Synthesis

RAD51 Inhibitor B02

Cat.No: T4656

Synonym: B02

Target: Apoptosis, DNA/RNA Synthesis

Cat.No: T39824

Synonym: RAD51-IN-3

Target: Others

Cat.No: T12682

Synonym: CYT-0851,RAD51-IN-2

Target: DNA/RNA Synthesis

Cat.No: T2276

Synonym: RI-1; 3-氯-1-(3,4-二氯苯基)-4-(4-吗啉基)-1H-吡咯-2,5-二酮,RI1,RAD51 inhibitor 1

Target: DNA/RNA Synthesis

Cat.No: T61469

Target: Others

Cat.No: T63728

Target: Others

Cat.No: T63892

Target: Others

Cat.No: T2628

Target: DNA/RNA Synthesis

Cat.No: T63883

Target: Others

Cat.No: T73107

Target: Others

Cat.No: T6972

Target: DNA/RNA Synthesis

Cat.No: T11600

Synonym: Isoquinoline

Target: DNA/RNA Synthesis

Cat.No: T8873

Target: Others, DNA/RNA Synthesis

Cat.No: T9168

Synonym: NSC617145,NSC-617145

Target: DNA/RNA Synthesis

Cat.No: T2516

Synonym: MP470,HPK 56

Target: Apoptosis, FLT, c-Met/HGFR, c-RET, DNA/RNA Synthesis, PDGFR, c-Kit

Aromatase inhibitor 23

Cat.No: T60006

Target: Others

Cat.No: T6960L

Synonym: PU-H71 HCl(873436-91-0 Free base),Zelavespib HCl

Target: HSP, DNA/RNA Synthesis

Cat.No: T10936

Synonym: DI03

Target: DNA/RNA Synthesis

Cat.No: T41211

Target: Others

Cat.No: T27526

Target: Others

Cat.No: T28536

Synonym: RI(dl)-2

Target: Others

Cat.No: T63717

Target: Others

Amuvatinib hydrochloride

Cat.No: T14282

Synonym: HPK 56 hydrochloride,MP470 hydrochloride

Target: Others

Cat.No: T20694

Target: Others

Cat.No: T36703

Target: Others

NHEJ inhibitor-1

Cat.No: T74501

Target: Others

Cat.No: T83854

Phosphoramide mustard (cyclohexanamine)

Cat.No: T36701

Target: Others

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPJ-01179	SWSAP1 Protein, Human, Recombinant (His) SWS1-associated protein 1,SWIM-type zinc finger 7-associated...	Human	E. coli
	SWSAP1 is a nucleus ATPase protein, interacts with ZSWIM7 and forms a functional complex. The complexs involved in homologous recombination repair and stabilizes each other. SWS1AP1 also interacts with RAD51, RAD51B, RAD51C, RAD51D and XRCC3. It involves in homologous recombination repair. ATPase is preferentially stimulated by single-stranded DNA and is involved in homologous recombination repair (HRR). SWSAP1 has a DNA-binding activity which is independent of its ATPase activity.
TMPH-03440	RAD52 Protein, S. cerevisiae, Recombinant (His & SUMO) RAD52,DNA repair and recombination protein RAD<...	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-01237	POLQ Protein, Human, Recombinant (E. coli, His) DNA polymerase eta,POLQ,DNA polymerase theta	Human	E. coli
	DNA polymerase that promotes microhomology-mediated end-joining (MMEJ), an alternative non-homologous end-joining (NHEJ) machinery triggered in response to double-strand breaks in DNA. MMEJ is an error-prone repair pathway that produces deletions of sequences from the strand being repaired and promotes genomic rearrangements, such as telomere fusions, some of them leading to cellular transformation. POLQ acts as an inhibitor of homology-recombination repair (HR) pathway by limiting RAD51 accumul...
TMPH-01238	POLQ Protein, Human, Recombinant (His) DNA polymerase eta,POLQ,DNA polymerase theta	Human	Baculovirus Insect Cells
	DNA polymerase that promotes microhomology-mediated end-joining (MMEJ), an alternative non-homologous end-joining (NHEJ) machinery triggered in response to double-strand breaks in DNA. MMEJ is an error-prone repair pathway that produces deletions of sequences from the strand being repaired and promotes genomic rearrangements, such as telomere fusions, some of them leading to cellular transformation. POLQ acts as an inhibitor of homology-recombination repair (HR) pathway by limiting RAD51 accumul...
TMPH-01267	RNF13 Protein, Human, Recombinant (His & Myc) RING finger protein 8,RNF8,E3 ubiquitin-protein ligase RNF8,...	Human	E. coli
	E3 ubiquitin-protein ligase that plays a key role in DNA damage signaling via 2 distinct roles: by mediating the 'Lys-63'-linked ubiquitination of histones H2A and H2AX and promoting the recruitment of DNA repair proteins at double-strand breaks (DSBs) sites, and by catalyzing 'Lys-48'-linked ubiquitination to remove target proteins from DNA damage sites. Following DNA DSBs, it is recruited to the sites of damage by ATM-phosphorylated MDC1 and catalyzes the 'Lys-63'-linked ubiquitination of hist...

重组蛋白

SWSAP1 Protein, Human, Recombinant (His)

Cat.No: TMPJ-01179

Species: Human

Expression System: E. coli

RAD52 Protein, S. cerevisiae, Recombinant (His & SUMO)

Cat.No: TMPH-03440

Species: Saccharomyces cerevisiae

Expression System: E. coli

POLQ Protein, Human, Recombinant (E. coli, His)

Cat.No: TMPH-01237

Species: Human

Expression System: E. coli

POLQ Protein, Human, Recombinant (His)

Cat.No: TMPH-01238

Species: Human

Expression System: Baculovirus Insect Cells

RNF13 Protein, Human, Recombinant (His & Myc)

Cat.No: TMPH-01267

Species: Human

Expression System: E. coli

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