DNA Damage/DNA Repair
DNA Damage/DNA Repair(DNA损伤/DNA修复)
- MTH1(4)
- PARP(124)
- ATM/ATR(29)
- DNA Alkylating(25)
- DNA Ligases(3)
- DNA Methyltransferase(32)
- DNA-PK(31)
- HDAC(182)
- Nucleoside Antimetabolite/Analogue(160)
- Telomerase(16)
- Topoisomerase(185)
- tankyrase(5)
- Antifolate(33)
- CDK(271)
- Checkpoint Kinase (Chk)(33)
- CRISPR/Cas9(9)
- Deubiquitinase(76)
- DNA Alkylator/Crosslinker(73)
- DNA/RNA Synthesis(473)
- Eukaryotic Initiation Factor (eIF)(27)
- IRE1(23)
- LIM Kinase (LIMK)(12)
- TOPK(6)
- Casein Kinase(48)
- DNA Intercalating Agents(8)
- DNA/RNA Oxidative Damage(13)
- Poly(ADP-ribose) Glycohydrolase (PARG)(1)
- Early 2 Factor (E2F)(1)
DNA Damage/DNA Repair 相关产品(1788)
- GC33389LMP744 (MJ-III65)CAS: 308246-52-8
LMP744 (MJ-III65) (MJ-III65) 是一种 DNA 嵌入剂和拓扑异构酶 I (Top1) 抑制剂,具有抗肿瘤活性。
- GC33426Rocaglamide (Rocaglamide A)CAS: 84573-16-0纯度: >98.50%
Rocaglamide (Rocaglamide A) 是从 Aglaia 属(楝科)中分离出来的。
- GC334962-(Methylamino)-1H-purin-6(7H)-one (N2-methylguanine)CAS: 10030-78-1纯度: >97.00%
2-(Methylamino)-1H-purin-6(7H)-one (N2-methylguanine) (N2-Methylguanine) 是一种修饰的核苷。
- GC335777-Aminoactinomycin D (7-AAD)CAS: 7240-37-1纯度: >95.00% / >97.00% / >98.00%
7-Aminoactinomycin D是放线菌素D的荧光衍生物,选择性地与DNA的GC区域结合。
- GC33944Pseudothymidine (5-Methyl-2'-Deoxypseudouridin)CAS: 65358-15-8纯度: >99.50%
Pseudothymidine (5-Methyl-2'-Deoxypseudouridin) 是胸苷的 C-核苷类似物。
- GC34059Atuveciclib Racemate (BAY-1143572 Racemate)CAS: 1414943-88-6纯度: >98.00%
Atuveciclib (BAY-1143572) is potent and highly selective PTEFb/CDK9 inhibitor with IC50 values of 13 nM for CDK9/CycT and the ratio of IC50 values for CDK2/CDK9 is about 100. Outside the CDK family, It inhibits GSK3 kinase with IC50 values of 45 nM and 87 nM for GSK3α and GSK3β respectively.
- GC34071Pamiparib (BGB-290)CAS: 1446261-44-4纯度: >99.50%
Pamiparib (BGB-290)是一种强效口服的聚腺苷二磷酸核糖聚合酶(PARP)抑制剂,对PARP-1和PARP-2的IC 50 值分别为1.3nM和0.9nM。
- GC34085Banoxantrone dihydrochloride (AQ4N dihydrochloride)CAS: 252979-56-9纯度: >99.00% / >98.00%
Banoxantrone dihydrochloride (AQ4N dihydrochloride) 是一种缺氧活化拓扑异构酶 II 抑制剂,AQ4N 以非共价方式与 DNA 结合,促进缺氧和缺氧肿瘤细胞的抗肿瘤活性。
- GC34086SJG-136 (NSC-694501)CAS: 232931-57-6纯度: >98.00%
SJG-136 (NSC-694501) 是一种 DNA 交联剂,对于 pBR322 DNA 的 XL50 为 45 nM。 SJG-136 (NSC-694501) 具有有效的抗肿瘤活性。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC33366 | CDK8-IN-4 | 1613638-82-6 | - | |
CDK8-IN-4是CDK8的抑制剂,来自专利WO2014090692A1,化合物实例16,IC50值为0.2nM。 | ||||
| GC33373 | LY309887 | 127228-54-0 | - | |
LY309887是一种有效的二氢叶酸还原酶(GARFT)抑制剂,Ki值为6.5nM,具有抗肿瘤活性。 | ||||
| GC33389 | LMP744 (MJ-III65) | 308246-52-8 | - | |
LMP744 (MJ-III65) (MJ-III65) 是一种 DNA 嵌入剂和拓扑异构酶 I (Top1) 抑制剂,具有抗肿瘤活性。 | ||||
| GC33392 | CHK-IN-1 | 1278405-51-8 | - | |
CHK-IN-1是一种CHK1和CHK2的抑制剂,具有抗增殖作用。 | ||||
| GC33395 | HDAC-IN-5 | 1314890-51-1 | - | |
HDAC-IN-5是组蛋白去乙酰化酶(HDAC)的一个抑制剂。 | ||||
| GC33404 | KU 59403 | 845932-30-1 | >98.50% | |
KU59403是ATM的一个有效抑制剂,其IC50值为3nM。 | ||||
| GC33406 | B I09 | 1607803-67-7 | >99.50% | |
BI09是IRE-1核糖核酸酶的一个抑制剂,其IC50值为1230nM。 | ||||
| GC33411 | MB-7133 | 685111-92-6 | - | |
MB-7133是一种DNAsynthesis抑制剂。 | ||||
| GC33420 | BAY-1895344 | 1876467-74-1 | >99.50% | |
An ATR inhibitor | ||||
| GC33426 | Rocaglamide (Rocaglamide A) | 84573-16-0 | >98.50% | |
Rocaglamide (Rocaglamide A) 是从 Aglaia 属(楝科)中分离出来的。 | ||||
| GC33430 | 2'-Deoxypseudoisocytidine | 65358-18-1 | - | |
2'-Deoxypseudoisocytidine是一个核苷类似物。 | ||||
| GC33494 | Deoxypseudouridine | 39967-60-7 | >98.00% | |
Deoxypseudouridine是一种核苷酸类似物。 | ||||
| GC33496 | 2-(Methylamino)-1H-purin-6(7H)-one (N2-methylguanine) | 10030-78-1 | >97.00% | |
2-(Methylamino)-1H-purin-6(7H)-one (N2-methylguanine) (N2-Methylguanine) 是一种修饰的核苷。 | ||||
| GC33577 | 7-Aminoactinomycin D (7-AAD) | 7240-37-1 | >95.00% / >97.00% / >98.00% | |
7-Aminoactinomycin D是放线菌素D的荧光衍生物,选择性地与DNA的GC区域结合。 | ||||
| GC33662 | Isoguanine | 3373-53-3 | >97.00% | |
An isomer of guanine | ||||
| GC33944 | Pseudothymidine (5-Methyl-2'-Deoxypseudouridin) | 65358-15-8 | >99.50% | |
Pseudothymidine (5-Methyl-2'-Deoxypseudouridin) 是胸苷的 C-核苷类似物。 | ||||
| GC33956 | Nucleoside-Analog-1 | 876707-99-2 | - | |
Nucleoside-Analog-1是抗病毒核苷R1479的类似物,用于HCV看病毒核苷类似物的合成。 | ||||
| GC33959 | Nucleoside-Analog-2 | 876708-01-9 | - | |
Nucleoside-Analog-2是针对丙型肝炎病毒(HCV)复制的4'-叠氮胞苷类似物。 | ||||
| GC34056 | NVP-2 | 1263373-43-8 | >99.00% | |
A Cdk9/cyclin T1 complex inhibitor | ||||
| GC34059 | Atuveciclib Racemate (BAY-1143572 Racemate) | 1414943-88-6 | >98.00% | |
Atuveciclib (BAY-1143572) is potent and highly selective PTEFb/CDK9 inhibitor with IC50 values of 13 nM for CDK9/CycT and the ratio of IC50 values for CDK2/CDK9 is about 100. Outside the CDK family, It inhibits GSK3 kinase with IC50 values of 45 nM and 87 nM for GSK3α and GSK3β respectively. | ||||
| GC34071 | Pamiparib (BGB-290) | 1446261-44-4 | >99.50% | |
Pamiparib (BGB-290)是一种强效口服的聚腺苷二磷酸核糖聚合酶(PARP)抑制剂,对PARP-1和PARP-2的IC 50 值分别为1.3nM和0.9nM。 | ||||
| GC34083 | EOAI3402143 | 1699750-95-2 | >99.00% | |
EOAI3402143是一种新型的、多靶点的去泛素化酶抑制剂。 | ||||
| GC34085 | Banoxantrone dihydrochloride (AQ4N dihydrochloride) | 252979-56-9 | >99.00% / >98.00% | |
Banoxantrone dihydrochloride (AQ4N dihydrochloride) 是一种缺氧活化拓扑异构酶 II 抑制剂,AQ4N 以非共价方式与 DNA 结合,促进缺氧和缺氧肿瘤细胞的抗肿瘤活性。 | ||||
| GC34086 | SJG-136 (NSC-694501) | 232931-57-6 | >98.00% | |
SJG-136 (NSC-694501) 是一种 DNA 交联剂,对于 pBR322 DNA 的 XL50 为 45 nM。 SJG-136 (NSC-694501) 具有有效的抗肿瘤活性。 | ||||
