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)
- GC34087Trilaciclib hydrochloride (G1T28 hydrochloride)CAS: 1977495-97-8纯度: >98.00%
Trilaciclib hydrochloride (G1T28 hydrochloride) (G1T28 hydrochloride) 是一种 CDK4/6 抑制剂,对 CDK4 和 CDK6 的 IC50 分别为 1 nM 和 4 nM。
- GC34100Lerociclib dihydrochloride (G1T38 dihydrochloride)CAS: 2097938-59-3纯度: >99.50%
Lerociclib dihydrochloride (G1T38 dihydrochloride) (G1T38 dihydrochloride) 是一种有效的选择性 CDK4/CDK6 抑制剂,对 CDK4/CyclinD1 和 CDK6/CyclinD3 的 IC50 分别为 1 nM 和 2 nM。
- GC34111NSC95682 (6-Bromo-2-hydroxy-3-methoxybenzaldehyde)CAS: 20035-41-0纯度: >99.50%
6-Bromo-2-hydroxy-3-methoxybenzaldehyde is a bromobenzaldehyde derivative that participates in the synthesis of (±)-norannuradhapurine. 6-Bromo-2-hydroxy-3-methoxybenzaldehyde is an IRE-1α inhibitor with an IC50 of 0.08 μM.
- GC34112Ethynylcytidine (ECyD)CAS: 180300-43-0纯度: >99.50%
A nucleoside analog with anticancer activity
- GC34118Trilaciclib (G1T28)CAS: 1374743-00-6
Trilaciclib (G1T28, G1T28-1) is a highly potent, selective and reversible cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitor. Trilaciclib inhibits CDK4/cyclin D1 and CDK6/cyclin D3 with IC50 of 1 nM and 4 nM, respectively.
- GC34120Niraparib R-enantiomer (MK 4827 (R-enantiomer))CAS: 1038915-58-0纯度: >99.50%
Niraparib R-enantiomer (MK-4827 R-enantiomer) 是一种出色的 PARP1 抑制剂,IC50 为 2.4 nM。
- GC34124(rel)-MC180295CAS: 2237942-08-2纯度: >98.00%
MC180295 ((rel)-MC180295) is a novel potent and selective CDK9 inhibitor with an IC50 of 5 nM and is at least 22-fold more selective for CDK9 over other CDKs.
- GC34127GDC-0575 dihydrochloride (ARRY-575 dihydrochloride)CAS: 1657014-42-0纯度: >99.50%
A Chk1 inhibitor
- GC34144Karenitecin (Cositecan)CAS: 203923-89-1纯度: >98.00%
Karenitecin (Cositecan) (Cositecan) 是一种拓扑异构酶 I 抑制剂,具有有效的抗癌活性。
- GC34163Lerociclib (G1T38)CAS: 1628256-23-4
G1T38 (Lerociclib) is a novel, potent, selective, and orally bioavailable CDK4/6 inhibitor with IC50 values of 0.001 μM, 0.002 μM and 0.028 μM for CDK4, CDK6 and CDK9 respectively.
- GC34169Banoxantrone D12 dihydrochloride (AQ4N D12 dihydrochloride)CAS: 1562066-98-1纯度: >98.00%
Banoxantrone-d12 (AQ4N-d12) dihydrochloride 是氘标记的 Banoxantrone dihydrochloride。 Banoxantrone 是一种新型生物还原剂,可以还原为稳定的 DNA 亲和化合物 AQ4,它是一种有效的拓扑异构酶 II 抑制剂。
- GC34205GSK2850163 hydrochlorideCAS: 2319838-09-8
GSK2850163hydrochloride是一个新型的肌醇需要酶-1α(IRE1α)抑制剂,它可抑制IRE1α的激酶活性和RNA酶活性,其IC50值分别为20和200nM。
- GC34305Bendamustine D4 (SDX-105 D4)
BendamustineD4是Bendamustine的氘代化合物标准品。Bendamustine是一种DNA交联剂(DNAcrosslinker),能够导致DNA断裂,具有烷基化和抗代谢物的作用。
- GC34354GSK2643943ACAS: 2449301-27-1纯度: >98.00%
GSK2643943A是一种靶向USP20的去泛素化酶(DUB)抑制剂,GSK2643943A通过抑制USP20/Ub-Rho(IC 50 =160nM)的活性来阻断蛋白质-泛素键的裂解。
- GC34356Casein Kinase II Inhibitor IV HydrochlorideCAS: 2320347-54-2
CaseinKinaseIIInhibitorIVHydrochloride是表皮角质形成细胞分化的小分子诱导剂。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC34087 | Trilaciclib hydrochloride (G1T28 hydrochloride) | 1977495-97-8 | >98.00% | |
Trilaciclib hydrochloride (G1T28 hydrochloride) (G1T28 hydrochloride) 是一种 CDK4/6 抑制剂,对 CDK4 和 CDK6 的 IC50 分别为 1 nM 和 4 nM。 | ||||
| GC34090 | Acelarin (NUC-1031) | 840506-29-8 | >99.50% | |
A prodrug form of gemcitabine | ||||
| GC34100 | Lerociclib dihydrochloride (G1T38 dihydrochloride) | 2097938-59-3 | >99.50% | |
Lerociclib dihydrochloride (G1T38 dihydrochloride) (G1T38 dihydrochloride) 是一种有效的选择性 CDK4/CDK6 抑制剂,对 CDK4/CyclinD1 和 CDK6/CyclinD3 的 IC50 分别为 1 nM 和 2 nM。 | ||||
| GC34111 | NSC95682 (6-Bromo-2-hydroxy-3-methoxybenzaldehyde) | 20035-41-0 | >99.50% | |
6-Bromo-2-hydroxy-3-methoxybenzaldehyde is a bromobenzaldehyde derivative that participates in the synthesis of (±)-norannuradhapurine. 6-Bromo-2-hydroxy-3-methoxybenzaldehyde is an IRE-1α inhibitor with an IC50 of 0.08 μM. | ||||
| GC34112 | Ethynylcytidine (ECyD) | 180300-43-0 | >99.50% | |
A nucleoside analog with anticancer activity | ||||
| GC34118 | Trilaciclib (G1T28) | 1374743-00-6 | - | |
Trilaciclib (G1T28, G1T28-1) is a highly potent, selective and reversible cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitor. Trilaciclib inhibits CDK4/cyclin D1 and CDK6/cyclin D3 with IC50 of 1 nM and 4 nM, respectively. | ||||
| GC34120 | Niraparib R-enantiomer (MK 4827 (R-enantiomer)) | 1038915-58-0 | >99.50% | |
Niraparib R-enantiomer (MK-4827 R-enantiomer) 是一种出色的 PARP1 抑制剂,IC50 为 2.4 nM。 | ||||
| GC34121 | CC-115 hydrochloride | 1300118-55-1 | >98.00% | |
A dual inhibitor of mTOR and DNA-PK | ||||
| GC34123 | Deoxycytidine triphosphate (dCTP) | 2056-98-6 | - | |
脱氧胞苷三磷酸 (dCTP) (dCTP) 是一种核苷三磷酸,可用于 DNA 合成。 | ||||
| GC34124 | (rel)-MC180295 | 2237942-08-2 | >98.00% | |
MC180295 ((rel)-MC180295) is a novel potent and selective CDK9 inhibitor with an IC50 of 5 nM and is at least 22-fold more selective for CDK9 over other CDKs. | ||||
| GC34127 | GDC-0575 dihydrochloride (ARRY-575 dihydrochloride) | 1657014-42-0 | >99.50% | |
A Chk1 inhibitor | ||||
| GC34144 | Karenitecin (Cositecan) | 203923-89-1 | >98.00% | |
Karenitecin (Cositecan) (Cositecan) 是一种拓扑异构酶 I 抑制剂,具有有效的抗癌活性。 | ||||
| GC34156 | Namitecan (ST-1968) | 372105-27-6 | >98.00% | |
Namitecan (ST-1968) 是一种有效的拓扑异构酶 I 抑制剂,具有抗肿瘤特性。 | ||||
| GC34163 | Lerociclib (G1T38) | 1628256-23-4 | - | |
G1T38 (Lerociclib) is a novel, potent, selective, and orally bioavailable CDK4/6 inhibitor with IC50 values of 0.001 μM, 0.002 μM and 0.028 μM for CDK4, CDK6 and CDK9 respectively. | ||||
| GC34165 | Corin | 1808113-09-8 | >98.00% | |
Corin是组氨酸赖氨酸特异性去甲基化酶(LSD1)和组氨酸脱乙酰化酶(HDAC)的双重抑制剂,其对LSD1的Ki(inact)值为110nM,对HDAC1的IC50值为147nM。 | ||||
| GC34169 | Banoxantrone D12 dihydrochloride (AQ4N D12 dihydrochloride) | 1562066-98-1 | >98.00% | |
Banoxantrone-d12 (AQ4N-d12) dihydrochloride 是氘标记的 Banoxantrone dihydrochloride。 Banoxantrone 是一种新型生物还原剂,可以还原为稳定的 DNA 亲和化合物 AQ4,它是一种有效的拓扑异构酶 II 抑制剂。 | ||||
| GC34195 | K-756 | 130017-40-2 | >99.00% | |
K-756是一种直接的选择性tankyrase(TNKS)抑制剂,抑制TNKS1和TNKS2的ADP-核糖基化活性,IC50分别为31和36nM。 | ||||
| GC34204 | JSH-150 | 2247481-21-4 | >98.00% | |
JSH-150 is a highly selective and potent inhibitor of CDK9 with IC50 of 1 nM. | ||||
| GC34205 | GSK2850163 hydrochloride | 2319838-09-8 | - | |
GSK2850163hydrochloride是一个新型的肌醇需要酶-1α(IRE1α)抑制剂,它可抑制IRE1α的激酶活性和RNA酶活性,其IC50值分别为20和200nM。 | ||||
| GC34305 | Bendamustine D4 (SDX-105 D4) | - | - | |
BendamustineD4是Bendamustine的氘代化合物标准品。Bendamustine是一种DNA交联剂(DNAcrosslinker),能够导致DNA断裂,具有烷基化和抗代谢物的作用。 | ||||
| GC34309 | Cycloguanil D6 (Chlorguanide triazine D6) | - | - | |
CycloguanilD6是Cycloguanil的氘代化合物标准品。 | ||||
| GC34354 | GSK2643943A | 2449301-27-1 | >98.00% | |
GSK2643943A是一种靶向USP20的去泛素化酶(DUB)抑制剂,GSK2643943A通过抑制USP20/Ub-Rho(IC 50 =160nM)的活性来阻断蛋白质-泛素键的裂解。 | ||||
| GC34355 | SEL120-34A monohydrochloride | - | >99.50% | |
A dual inhibitor of Cdk8 and Cdk19 | ||||
| GC34356 | Casein Kinase II Inhibitor IV Hydrochloride | 2320347-54-2 | - | |
CaseinKinaseIIInhibitorIVHydrochloride是表皮角质形成细胞分化的小分子诱导剂。 | ||||
