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Chemical Structure| 1430844-80-6 Chemical Structure| 1430844-80-6

Structure of A-1331852
CAS No.: 1430844-80-6

Chemical Structure| 1430844-80-6

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A1331852 is a potent and selective BCL-XL inhibitor and may be useful in the treatment of cancer, immune and autoimmune diseases.

4.5 *For Research Use Only !

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Product Details of A-1331852

CAS No. :1430844-80-6
Formula : C38H38N6O3S
M.W : 658.81
SMILES Code : O=C(O)C1=NC(N2CC3=C(C=CC=C3C(NC4=NC5=CC=CC=C5S4)=O)CC2)=CC=C1C6=C(C)N(CC78CC9CC(C8)CC(C9)C7)N=C6
MDL No. :MFCD30532662
InChI Key :QCQQONWEDCOTBV-UHFFFAOYSA-N
Pubchem ID :71565985

Safety of A-1331852

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Isoform Comparison

Biological Activity

Target
  • Bcl-xL

    Bcl-xL, Ki:<0.01 nM

In Vitro:

Cell Line
Concentration Treated Time Description References
Meljuso cells 250 nM 2 weeks Evaluate the effect of A-1331852 on Meljuso cells, results showed MCL1 as a top sensitizer gene PMC7005275
OVCAR8 cells 250 nM 2 weeks Evaluate the effect of A-1331852 on OVCAR8 cells, results showed MCL1 as a top sensitizer gene PMC7005275
H2030 cells 1 μM 72 h To evaluate the effect of A-1331852 on H2030 cells, results showed that pre-treatment increased sensitivity to MEK + MCL-1 inhibition. PMC6279543
H1734 cells 1 μM 72 h To evaluate the effect of A-1331852 on H1734 cells, results showed that pre-treatment increased sensitivity to MEK + MCL-1 inhibition. PMC6279543
CAKI-2 10 nM 16 h To evaluate the apoptotic induction effect of A-1331852 on CAKI-2 cells, results showed a significant increase in apoptotic cell population PMC9633392
A-498 100 nM 36 h To evaluate the apoptotic induction effect of A-1331852 on A-498 cells, results showed a significant increase in apoptotic cell population PMC9633392

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice Tuberculosis model Oral 25 mg/kg Once daily for 2 weeks To evaluate the therapeutic effect of A-1331852 in a tuberculosis mouse model, results showed no significant difference in bacterial numbers in the lungs and spleens between A-1331852-treated and vehicle-treated mice PMC5985376
Athymic nude mice JH4.3 xenograft model Oral 25 mg/kg Once daily for 35 days To evaluate the antitumor efficacy of A-1331852 in the JH4.3 xenograft model. Results showed that A-1331852 significantly inhibited tumor growth, with a significant reduction in tumor volume compared to the control group. PMC6115427
Mice H2030 sub-cutaneous xenograft model Oral 25 mg/kg Pre-treatment for 4 days, followed by a 3-day drug holiday, then 5 days of MEK + MCL-1 inhibitor treatment To evaluate the effect of A-1331852 pre-treatment on H2030 xenograft tumors, results showed that pre-treatment increased sensitivity to MEK + MCL-1 inhibition and led to tumor regression. PMC6279543
Mice CCl4-induced liver fibrosis model Oral 20 mg/kg Every other day for 2 weeks To study the effects of A-1331852 on CCl4-induced liver fibrosis, results showed that A-1331852 exacerbated liver injury and fibrosis. PMC10416614
NCRnu/nu mice Subcutaneous tumor model Oral 25 mg/kg Twice daily for 4 weeks To evaluate the inhibitory effect of A-1331852 on subcutaneous tumor growth, results showed significant reduction in tumor volume and increased apoptotic cells PMC9633392

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.52mL

0.30mL

0.15mL

7.59mL

1.52mL

0.76mL

15.18mL

3.04mL

1.52mL

References

 

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