2832047-80-8
2832047-80-8 structure
- Name: RP-6685
- Chemical Name: RP-6685
- CAS Number: 2832047-80-8
- Molecular Formula: C22H14F7N5O
- Molecular Weight: 497.37
- Catalog: Signaling Pathways Cell Cycle/DNA Damage DNA/RNA Synthesis
- Create Date: 2022-11-21 18:40:58
- Modify Date: 2024-04-03 23:58:21
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RP-6685 is a potent, selective and orally active DNA polymerase theta (Polθ) inhibitor with an IC50 value of 5.8 nM (PicoGreen assay). RP-6685 shows antitumor efficacy in mouse tumor xenograft model[1].
| Name | RP-6685 |
|---|
| Description | RP-6685 is a potent, selective and orally active DNA polymerase theta (Polθ) inhibitor with an IC50 value of 5.8 nM (PicoGreen assay). RP-6685 shows antitumor efficacy in mouse tumor xenograft model[1]. |
|---|---|
| Related Catalog | |
| Target |
IC50: 5.8 nM (Polθ)[1] |
| In Vitro | RP-6685 is extremely potent with an IC50 of 550 pM against the pol activity of full-length Polθ and inactive on the ATPase activity[1]. RP-6685 inhibits Polθ in HEK293 LIG4-/- cellswith an IC50 of 0.94 μM[1]. |
| In Vivo | RP-6685 (80 mg/kg; p.o.; BID for 21 days) exhibits potent antitumor efficacy in BRCA2-deficient HCT116 mice[1]. Animal Model: Female CD1 nude mice (HCT116 BRCA2+/+ and BRCA2-/- xenograft tumor models)[1] Dosage: 80 mg/kg Administration: p.o.; BID for 21 days Result: Showed tumor regression during the first 8 days of treatment in BRCA2-/- HCT116 model, while did not inhibit tumor growth in BRCA2+/+ HCT116 tumors mice. Animal Model: CD1 mice (20-30 g)[1] Dosage: 2.5 mg/kg Administration: i.v. or p.o.; single dosage Result: CL (mL/min/kg) Vdss (L/kg) t1/2 (h) F (%) 36.8 1.1 0.4 66 |
| Molecular Formula | C22H14F7N5O |
|---|---|
| Molecular Weight | 497.37 |