11 Results for "

PARP15

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "PARP15" in MCE Product Catalog:

  • Isoforms Recommended:
  • Targets Recommended:
2
2 Cited Publications
Cat. No.: HY-148566
CAS No.: 943119-42-4
Purity:  99.86%
Target:  

PARP

Research Areas:  

Cancer

OUL232 is a potent inhibitor of mono-ARTs PARP7, PARP10, PARP11, PARP12, PARP14, and PARP15. OUL232 is the most potent PARP10 inhibitor described to date (IC50=7.8 nM), as well as the first PARP12 inhibitor ever reported .
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Cat. No.: HY-148753
CAS No.: 1042780-52-8
Purity:  98.02%
Target:  

PARP

Research Areas:  

Cancer

PARP10-IN-2 is a potent mono‐ADP‐ribosyltransferase PARP10 inhibitor with an IC50 of 3.64 μM for human PARP10. PARP10-IN-2 reveals potent inhibition on PARP2 and PARP15 with IC50s of 27 μM and 11 μM for human PARP2 and human PARP15, respectively .
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Cat. No.: HY-148754
CAS No.: 2225800-19-9
Purity:  98.89%
Target:  

PARP

Research Areas:  

Cancer

PARP10-IN-3 is a selective mono‐ADP‐ribosyltransferase PARP10 inhibitor with an IC50 of 480 nM for human PARP10. PARP10-IN-3 reveals potent inhibition on PARP2 and PARP15 with IC50s of 1.7 μM for human PARP2 and human PARP15, respectively .
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Cat. No.: HY-143398
CAS No.: 2892065-01-7
Purity:  95.00%
Target:  

PARP

Research Areas:  

Cancer

PARP10/15-IN-1 (compound 8l) is a potent inhibitor of dual inhibitor of PARP10 and PARP15, with IC50s of 160 nM and 370 nM, respectively. PARP10/15-IN-1 can be used for cancer .
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Cat. No.: HY-178317
Target:  

PARP Apoptosis

OUL312 is a potent PARP10 inhibitor (IC50 = 20 nM), showing more than 75-fold greater selectivity for PARP15 (IC50 = 1500 nM). OUL312 is also at least 18-fold higher than all other human enzymes in the family. OUL312 has a good ADME profile, is able to enter cells, is not toxic, and effectively rescues human cells from PARP10-induced apoptosis at sub-micromolar concentrations. OUL312 can be used for the study of cervical cancer .
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Cat. No.: HY-146502
CAS No.: 2892064-88-7
Purity:  99.98%
Target:  

PARP Apoptosis

Research Areas:  

Cancer

PARP10/15-IN-3 (Compound 8a) is a potent PARP10 and PARP15 dual inhibitor with IC50 values of 0.14 µM and 0.40 µM against PARP10 and PARP15, respectively. PARP10/15-IN-3 is able to enter cells and rescue cells from apoptosis .
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Cat. No.: HY-146501
CAS No.: 2892064-99-0
Purity:  99.00%
Target:  

PARP Apoptosis

Research Areas:  

Cancer

PARP10/15-IN-2 (Compound 8h) is a potent PARP10 and PARP15 dual inhibitor with IC50 values of 0.15 µM and 0.37 µM against PARP10 and PARP15, respectively. PARP10/15-IN-2 is able to enter cells and rescue cells from apoptosis .
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Cat. No.: HY-RS10058
Research Areas:  

Others

PARP15 Human Pre-designed siRNA Set A contains three designed siRNAs for PARP15 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-143338
CAS No.: 2418014-98-7
Purity:  98.91%
Target:  

PARP

Research Areas:  

Cancer

ART-IN-1 (compound 7) is a selective PARP inhibitor with IC50s of 19, 22, 2.4, >100, 1.1 µM for PARP2, TNKS2, PARP10, PARP14, PARP15, respectively .
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Cat. No.: HY-148709
CAS No.: 1708103-76-7
Target:  

PARP

Research Areas:  

Inflammation/Immunology

ARTD10/PARP10-IN-1 (compound 23) is a potent and non-selective PARP inhibitor, targeting to mono-ADP-ribosyltransferases ARTD7/PARP15, ARTD8/PARP14, ARTD10/PARP10 and poly(ADP-ribose) polymerase-1 (ARTD1/PARP1) with IC50s of 1.7 μM, 1.6 μM, 0.8 μM, and 4.4 μM, respectively .
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Cat. No.: HY-P701953
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PARP15; Protein mono-ADP-ribosyltransferase PARP15; ADP-ribosyltransferase diphtheria toxin-like 7; ARTD7; B-aggressive lymphoma protein 3; Poly [ADP-ribose] polymerase 15; PARP-15
Species:  
Source:  
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