Date published: 2025-10-20

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ABT-199 (CAS 1257044-40-8)

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Alternate Names:
ABT-199 is also known as GDC-0199.
Application:
ABT-199 is a BH3 mimetic and a Bcl-2-selective inhibitor with a subnanomolar affinity Ki of <0.01 nM.
CAS Number:
1257044-40-8
Purity:
≥98%
Molecular Weight:
868.44
Molecular Formula:
C45H50ClN7O7S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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ABT-199 is extensively used in research focusing on its role in targeting B-cell lymphoma 2 (BCL-2) proteins. This compound is for studies investigating the mechanisms of apoptosis in cancer cells, where it acts by selectively inhibiting BCL-2, promoting cell death in tumor cells while sparing healthy cells. Research involving ABT-199 often aims to understand its effects on cellular pathways that lead to cancer cell survival and proliferation. Additionally, ABT-199 is used in studies examining its potential to enhance the efficacy of other cancer research strategies. Furthermore, investigations into the specificity and binding affinity of ABT-199 provide insights into the design of more effective cancer research tools.


ABT-199 (CAS 1257044-40-8) References

  1. ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets.  |  Souers, AJ., et al. 2013. Nat Med. 19: 202-8. PMID: 23291630
  2. ABT-199: taking dead aim at BCL-2.  |  Davids, MS. and Letai, A. 2013. Cancer Cell. 23: 139-41. PMID: 23410971
  3. Bcl-2 family inhibition sensitizes human prostate cancer cells to docetaxel and promotes unexpected apoptosis under caspase-9 inhibition.  |  Tamaki, H., et al. 2014. Oncotarget. 5: 11399-412. PMID: 25333266
  4. BCL2 inhibitor ABT-199 and BCL2L1 inhibitor WEHI-539 coordinately promote NOXA-mediated degradation of MCL1 in human leukemia cells.  |  Chiou, JT., et al. 2022. Chem Biol Interact. 361: 109978. PMID: 35561756
  5. Erythroid/megakaryocytic differentiation confers BCL-XL dependency and venetoclax resistance in acute myeloid leukemia.  |  Kuusanmäki, H., et al. 2023. Blood. 141: 1610-1625. PMID: 36508699
  6. Predictors of response to venetoclax plus hypomethylating agent therapy and survival in blast-phase myeloproliferative neoplasm.  |  Gangat, N., et al. 2022. Haematologica.. PMID: 36519330
  7. Anti-tumor effect of antibody drug conjugate ASP1235 targeting Fms-like tyrosine kinase 3 with venetoclax plus azacitidine in an acute myeloid leukemia xenograft mouse model.  |  Tsuzuki, H., et al. 2022. Oncotarget. 13: 1359-1368. PMID: 36537913
  8. Persistent splenomegaly due to littoral cell angiomatosis in venetoclax-induced undetectable minimal residual disease of chronic lymphocytic leukemia.  |  Cellini, A., et al. 2023. Ann Hematol. 102: 681-682. PMID: 36542103
  9. JAK-STAT signalling shapes the NF-κB response in CLL towards venetoclax sensitivity or resistance via Bcl-XL.  |  Haselager, MV., et al. 2022. Mol Oncol.. PMID: 36550750
  10. DNA hypermethylation-induced miR-182 silence targets BCL2 and HOXA9 to facilitate the self-renewal of leukemia stem cell, accelerate acute myeloid leukemia progression, and determine the sensitivity of BCL2 inhibitor venetoclax.  |  Ye, S., et al. 2023. Theranostics. 13: 77-94. PMID: 36593968

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

ABT-199, 1 mg

sc-472284
1 mg
$116.00

ABT-199, 5 mg

sc-472284A
5 mg
$330.00

ABT-199, 10 mg

sc-472284B
10 mg
$510.00

ABT-199, 100 mg

sc-472284C
100 mg
$816.00

ABT-199, 3 g

sc-472284D
3 g
$1632.00