For research use only. Not for therapeutic Use.
NU6102（Cat No.:R039904）is a potent and selective inhibitor of the protein kinase ATR (ataxia telangiectasia and Rad3-related protein), which plays a critical role in the DNA damage response and cell cycle regulation. By inhibiting ATR, NU6102 sensitizes cancer cells to DNA-damaging agents, enhancing their therapeutic efficacy. This compound has shown promise in preclinical studies for various cancers, particularly those with deficiencies in DNA repair mechanisms. Ongoing research aims to evaluate its safety and effectiveness in clinical trials, focusing on its potential use in combination therapies to improve outcomes in cancer treatment.
| Catalog Number | R039904 |
| CAS Number | 444722-95-6 |
| Synonyms | 4-[[6-(cyclohexylmethoxy)-9H-purin-2-yl]amino]benzenesulfonamide; 4-[[6-(Cyclohexylmethoxy)-1H-purin-2-yl]amino]benzenesulfonamide; |
| Molecular Formula | C18H22N6O3S |
| Purity | ≥95% |
| Target | CDK inhibitor |
| Storage | -20°C |
| IUPAC Name | 4-[[6-(cyclohexylmethoxy)-7H-purin-2-yl]amino]benzenesulfonamide |
| InChI | InChI=1S/C18H22N6O3S/c19-28(25,26)14-8-6-13(7-9-14)22-18-23-16-15(20-11-21-16)17(24-18)27-10-12-4-2-1-3-5-12/h6-9,11-12H,1-5,10H2,(H2,19,25,26)(H2,20,21,22,23,24) |
| InChIKey | OWXORKPNCHJYOF-UHFFFAOYSA-N |
| SMILES | C1CCC(CC1)COC2=NC(=NC3=C2NC=N3)NC4=CC=C(C=C4)S(=O)(=O)N |
| Reference | 1:Eur J Cancer. 2011 Sep;47(13):2052-9. doi: 10.1016/j.ejca.2011.04.008. Epub 2011 May 12. Preclinical in vitro and in vivo evaluation of the potent and specific cyclin-dependent kinase 2 inhibitor NU6102 and a water soluble prodrug NU6301.Thomas HD,Wang LZ,Roche C,Bentley J,Cheng Y,Hardcastle IR,Golding BT,Griffin RJ,Curtin NJ,Newell DR, PMID: 21570822 DOI: 10.1016/j.ejca.2011.04.008 </br><span>Abstract:</span> To facilitate the evaluation of CDK2 (cyclin-dependent kinase 2) as a cancer target, the in vitro and in vivo properties of NU6102 (O⁶-cyclohexylmethyl-2-(4/’-sulphamoylanilino)purine) and a water soluble prodrug (NU6301) were investigated. NU6102 selectively inhibited the growth of CDK2 WT (wild type) versus KO MEFs (knockout mouse embryo fibroblasts) (GI₅₀ (concentration required to inhibit cell growth by 50%) 14 μM versus >30 μM), and was more growth-inhibitory in p53 mutant or null versus p53 WT cells (p=0.02), and in Rb (retinoblastoma protein) WT SKUT-1B versus SKUT 1 Rb deficient cells (p=0.01). In SKUT-1B cells NU6102 induced a G2 arrest, inhibition of Rb phosphorylation and cytotoxicity (LC₅₀ 2.6 μM for a 24h exposure). The prodrug NU6301 rapidly generated NU6102 in vitro in mouse plasma, and tumour NU6102 levels in vivo consistent with activity in vitro. Eight or 12 hourly dosing of 120 mg/kg NU6301 for 10 days was well tolerated in SKUT-1B tumour-bearing mice and inhibited Rb phosphorylation in tumour tissue. Two (8 hourly dosing) and 3 (12 hourly dosing) day tumour growth delay was observed (p=0.04 and p=0.007, respectively) following NU6301 administration. NU6102 and its prodrug NU6301 have pharmacological properties consistent with CDK2 inhibition, and represent useful tool molecules for the evaluation of CDK2 as a target in cancer.Copyright © 2011 Elsevier Ltd. All rights reserved. |
