5 Results for "

BRCA1/2 mutations

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "BRCA1/2 mutations" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-139156
CAS No.: 2523016-96-6
Purity:  99.86%
Target:  

PROTACs PARP

Research Areas:  

Cancer

SK-575 is a highly potent and specific proteolysis-targeting chimera (PROTAC) degrader of PARP1, with an IC50 of 2.30 nM. SK-575 potently inhibits the growth of cancer cells bearing BRCA1/2 mutations .
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1
1 Cited Publications
Cat. No.: HY-162859
CAS No.: 2565637-94-5
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

AB25583 is a Polθ helicase (Polθ-hel) small molecule inhibitor, with an IC50 value of 6 nM. AB25583 selectively kills BRCA1/2 deficient cells and works in synergy with Olaparib (HY-10162) in cancer cells carrying pathogenic BRCA1/2 mutations. AB25583 can be used for tumor research .
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Cat. No.: HY-160700
CAS No.: 2839740-79-1
Target:  

Deubiquitinase JNK

Research Areas:  

Cancer

TNG348 is an orally available allosteric inhibitor of the ubiquitin-specific protease USP1. TNG348 specifically and efficiently inhibits the activity of USP1, inhibiting its deubiquitination of proliferative PCNA and FANCD2, thereby disrupting the DNA repair process. TNG348 has inhibitory activity against breast and ovarian cancers carrying BRCA1/2 mutations and other homologous recombination defects (HRD) .
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Cat. No.: HY-122583
CAS No.: 1225141-73-0
Target:  

RAD51

Research Areas:  

Cancer

D-G23 is a selective RAD52 inhibitor. D-G23 disrupts RAD52-mediated DNA repair pathways and suppresses the growth of BRCA1- and BRCA2-deficient cancer cells. D-G23 is promising for research of homologous recombination-related cancers, such as hereditary breast cancer and ovarian cancer caused by BRCA1/2 mutations .
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Cat. No.: HY-174446
CAS No.: 3054988-47-2
Target:  

PARP

Research Areas:  

Cancer

PARP1-IN-39 is an inhibitor of PARP1 with an IC50 of 0.22 nM. PARP1-IN-39 has an IC50 of 1.57 nM in human breast cancer cells. PARP1-IN-39 can be studied in breast, ovarian, pancreatic, and prostate cancers associated with DNA repair deficiencies, such as BRCA1/2 mutations .
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