1. Cell Cycle/DNA Damage Epigenetics
  2. PARP
  3. PARP1-IN-20

PARP1-IN-20 (compound 19A10) is a potent inhibitor of PARP1, with the IC50 of 4.62 nM and has similar low PARP-Trapping effect compared with Veliparib (HY-10129), IC50 (MDA-MB-436) >100 μM.

For research use only. We do not sell to patients.

PARP1-IN-20 Chemical Structure

PARP1-IN-20 Chemical Structure

CAS No. : 2659357-95-4

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Description

PARP1-IN-20 (compound 19A10) is a potent inhibitor of PARP1, with the IC50 of 4.62 nM and has similar low PARP-Trapping effect compared with Veliparib (HY-10129), IC50 (MDA-MB-436) >100 μM[1].

IC50 & Target

PARP1

4.62 nM (IC50)

Molecular Weight

539.40

Formula

C23H19BrN6O3S

CAS No.
SMILES

O=C(N)C1=C2C(NC(C3=CC=C(C(N4CCN(C(C5=CSC(Br)=N5)=O)CC4)=O)C=C3)=N2)=CC=C1

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
PARP1-IN-20
Cat. No.:
HY-161517
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