DNA Damage/DNA Repair
Research Areas
- MTH1(4)
- PARP(103)
- ATM/ATR(31)
- DNA Alkylating(23)
- DNA Ligases(3)
- DNA Methyltransferase(27)
- DNA-PK(28)
- HDAC(143)
- Nucleoside Antimetabolite/Analogue(194)
- Telomerase(15)
- Topoisomerase(193)
- tankyrase(5)
- Antifolate(33)
- CDK(299)
- Checkpoint Kinase (Chk)(36)
- CRISPR/Cas9(9)
- Deubiquitinase(84)
- DNA Alkylator/Crosslinker(87)
- DNA/RNA Synthesis(575)
- Eukaryotic Initiation Factor (eIF)(33)
- IRE1(25)
- LIM Kinase (LIMK)(12)
- TOPK(6)
- Casein Kinase(59)
- DNA Intercalating Agents(8)
- DNA/RNA Oxidative Damage(13)
- Poly(ADP-ribose) Glycohydrolase (PARG)(5)
- Early 2 Factor (E2F)(2)
- Zinc Finger Protein(1)
Products Related to DNA Damage/DNA Repair(1968)
- GC73948UCHL1-IN-1Purity: >98.00%
UCHL1-IN-1 (Compound 46) is an inhibitor for Ubiquitin C-terminal drolase L1 (UCHL1), with an IC50 of 5.1 μM.
- GC73949METTL16-IN-1Purity: >99.00%
METTL16-IN-1 (Compound 45) is a potent METTL16 inhibitor with an IC50 value of 1.7 μM and a Kd value of 1.35 μM.
- GC73972METTL1-WDR4-IN-2CAS: 2919742-07-5Purity: >99.00%
METTL1-WDR4-IN-2(compound 6) is a selective metltransferase Like 1 (METTL1)-WDR4 inhibitor with an IC50 of 41 μM.
- GC73976CDK2-IN-23CAS: 2488073-20-5Purity: >99.00%
CDK2-IN-23 (Compound 17) is a kinase selective and highly potent CDK2 inhibitor (IC50 = 0.29 nM).
- GC74021P5(PEG24)-VC-PAB-exatecanCAS: 2928571-43-9Purity: >99.00%
P5(PEG24)-VC-PAB-exatecan is a camptothecin-based linker-payload platform based on the highly potent camptothecin derivative exatecan.
- GC74026DNA-PK-IN-12CAS: 2792146-91-7Purity: >99.00%
DNA-PK-IN-12 (compound 31t) is an oral active DNA-PK inhibitor with the IC50 of 0.1 nM.
- GC74050PROTAC CDK4/6 degrader 1CAS: 3025082-14-5Purity: >98.00%
PROTAC CDK4/6 degrader 1 (Compound 7f) is a dual degrader for CDK4 and CDK6 with DC50 of 10.5 and 2.5 nM.
- GC74062LSD1/HDAC6-IN-2CAS: 2982787-50-6Purity: >99.00%
LSD1/HDAC6-IN-2 (JBI-802) is an orally active LSD1/HDAC6/MAO-A inhibitor, with IC50 values of 5 nM, 11 nM, and 5 nM, respectively.
- GC74078PARP1-IN-29CAS: 1567375-93-2
PARP1-IN-29 is an orally active PARP-1 inhibitor with an IC50 value of 6.3 nM.
- GC74101Ditercalinium chlorideCAS: 74517-42-3Purity: >96.00%
Ditercalinium chloride is an anticancer agent.
- GC74107Tesirine intermediate-2CAS: 1430738-34-3Purity: >99.00%
Tesirine intermediate-2 is the intermediate of Tesirine.
- GC74127(R)-Exatecan Intermediate 1CAS: 110351-91-2Purity: >99.00%
(R)-Exatecan Intermediate 1 is an isomer of Exatecan Intermediate 1.
- GC74132Exatecan Intermediate 5CAS: 143655-70-3Purity: >99.00%
Exatecan Intermediate 5 is the intermediate of Exatecan And Exatecan (DX-8951) is a DNA topoisomerase I inhibitor with an IC50 value of 2.2 μM (0.975 μg/mL) that can be used in cancer research.
- GC74134Exatecan Intermediate 6CAS: 143655-58-7Purity: >98.00%
Exatecan Intermediate 6 is the intermediate of Exatecan And Exatecan (DX-8951) is a DNA topoisomerase I inhibitor with an IC50 value of 2.2 μM (0.975 μg/mL) that can be used in cancer research.
- GC74135Exatecan Intermediate 7CAS: 182182-32-7Purity: >99.00%
Exatecan Intermediate 7 is the intermediate of Exatecan And Exatecan (DX-8951) is a DNA topoisomerase I inhibitor with an IC50 value of 2.2 μM (0.975 μg/mL) that can be used in cancer research.
- GC74145Tesirine intermediate-1CAS: 1430738-05-8Purity: >99.00%
Tesirine intermediate-1 is the intermediate of Tesirine.
- GC74148L2H2-6OTD intermediate-2CAS: 890403-75-5Purity: >99.00%
L2H2-6OTD intermediate-2 is an intermediate of telomerase inhibitor, which can be used in the synthesis of ADC.
- GC74161Palbociclib hydrochlorideCAS: 571189-11-2Purity: >99.50%
Palbociclib (PD 0332991) drochloride is an orally active selective CDK4 and CDK6 inhibitor with IC50 values of 11 and 16 nM, respectively.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC73948 | UCHL1-IN-1 | - | >98.00% | |
UCHL1-IN-1 (Compound 46) is an inhibitor for Ubiquitin C-terminal drolase L1 (UCHL1), with an IC50 of 5.1 μM. | ||||
| GC73949 | METTL16-IN-1 | - | >99.00% | |
METTL16-IN-1 (Compound 45) is a potent METTL16 inhibitor with an IC50 value of 1.7 μM and a Kd value of 1.35 μM. | ||||
| GC73965 | INX-315 | 2745060-92-6 | >99.00% | |
INX-315 is an orally active and selective CDK2 inhibitor that induces cell cycle arrest in the G1 phase. | ||||
| GC73970 | CDDD11-8 | 2241659-94-7 | >99.00% | |
CDDD11-8 is an orally active, potent and selective inhibitor of CDK9 and FLT3-ITD, with Ki values of 8 and 13 nM, respectively. | ||||
| GC73972 | METTL1-WDR4-IN-2 | 2919742-07-5 | >99.00% | |
METTL1-WDR4-IN-2(compound 6) is a selective metltransferase Like 1 (METTL1)-WDR4 inhibitor with an IC50 of 41 μM. | ||||
| GC73976 | CDK2-IN-23 | 2488073-20-5 | >99.00% | |
CDK2-IN-23 (Compound 17) is a kinase selective and highly potent CDK2 inhibitor (IC50 = 0.29 nM). | ||||
| GC74007 | SelSA | 1225038-92-5 | >99.00% | |
SelSA is a selective, orally active inhibitor for histone deacetylase 6 (HDAC6) with IC50 of 56.9 nM. | ||||
| GC74021 | P5(PEG24)-VC-PAB-exatecan | 2928571-43-9 | >99.00% | |
P5(PEG24)-VC-PAB-exatecan is a camptothecin-based linker-payload platform based on the highly potent camptothecin derivative exatecan. | ||||
| GC74026 | DNA-PK-IN-12 | 2792146-91-7 | >99.00% | |
DNA-PK-IN-12 (compound 31t) is an oral active DNA-PK inhibitor with the IC50 of 0.1 nM. | ||||
| GC74050 | PROTAC CDK4/6 degrader 1 | 3025082-14-5 | >98.00% | |
PROTAC CDK4/6 degrader 1 (Compound 7f) is a dual degrader for CDK4 and CDK6 with DC50 of 10.5 and 2.5 nM. | ||||
| GC74062 | LSD1/HDAC6-IN-2 | 2982787-50-6 | >99.00% | |
LSD1/HDAC6-IN-2 (JBI-802) is an orally active LSD1/HDAC6/MAO-A inhibitor, with IC50 values of 5 nM, 11 nM, and 5 nM, respectively. | ||||
| GC74078 | PARP1-IN-29 | 1567375-93-2 | - | |
PARP1-IN-29 is an orally active PARP-1 inhibitor with an IC50 value of 6.3 nM. | ||||
| GC74101 | Ditercalinium chloride | 74517-42-3 | >96.00% | |
Ditercalinium chloride is an anticancer agent. | ||||
| GC74107 | Tesirine intermediate-2 | 1430738-34-3 | >99.00% | |
Tesirine intermediate-2 is the intermediate of Tesirine. | ||||
| GC74127 | (R)-Exatecan Intermediate 1 | 110351-91-2 | >99.00% | |
(R)-Exatecan Intermediate 1 is an isomer of Exatecan Intermediate 1. | ||||
| GC74132 | Exatecan Intermediate 5 | 143655-70-3 | >99.00% | |
Exatecan Intermediate 5 is the intermediate of Exatecan And Exatecan (DX-8951) is a DNA topoisomerase I inhibitor with an IC50 value of 2.2 μM (0.975 μg/mL) that can be used in cancer research. | ||||
| GC74134 | Exatecan Intermediate 6 | 143655-58-7 | >98.00% | |
Exatecan Intermediate 6 is the intermediate of Exatecan And Exatecan (DX-8951) is a DNA topoisomerase I inhibitor with an IC50 value of 2.2 μM (0.975 μg/mL) that can be used in cancer research. | ||||
| GC74135 | Exatecan Intermediate 7 | 182182-32-7 | >99.00% | |
Exatecan Intermediate 7 is the intermediate of Exatecan And Exatecan (DX-8951) is a DNA topoisomerase I inhibitor with an IC50 value of 2.2 μM (0.975 μg/mL) that can be used in cancer research. | ||||
| GC74145 | Tesirine intermediate-1 | 1430738-05-8 | >99.00% | |
Tesirine intermediate-1 is the intermediate of Tesirine. | ||||
| GC74148 | L2H2-6OTD intermediate-2 | 890403-75-5 | >99.00% | |
L2H2-6OTD intermediate-2 is an intermediate of telomerase inhibitor, which can be used in the synthesis of ADC. | ||||
| GC74150 | Exatecan analog 36 | - | >98.00% | |
Exatecan analog 36 is a analog of Exatecan. | ||||
| GC74161 | Palbociclib hydrochloride | 571189-11-2 | >99.50% | |
Palbociclib (PD 0332991) drochloride is an orally active selective CDK4 and CDK6 inhibitor with IC50 values of 11 and 16 nM, respectively. | ||||
| GC74178 | Ac-Exatecan | 2922852-48-8 | >98.00% | |
Ac-Exatecan is acetylated Exatecan. | ||||
| GC74194 | Uridine-15N2 | 92487-68-8 | >98.00% | |
Uridine-15N2 is the 15N labeled Uridine. | ||||
