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Chemical Structure| 1633350-06-7 Chemical Structure| 1633350-06-7

Structure of (±)-Zanubrutinib
CAS No.: 1633350-06-7

Chemical Structure| 1633350-06-7

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(±)-Zanubrutinib, also known as (±)-BGB-3111, is an efficacious, selective, oral Btk inhibitor that exhibits nanomolar-level Btk inhibitory activity.

Synonyms: (±)-BGB-3111

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Product Details of (±)-Zanubrutinib

CAS No. :1633350-06-7
Formula : C27H29N5O3
M.W : 471.55
SMILES Code : O=C(C1=C2NCCC(C3CCN(C(C=C)=O)CC3)N2N=C1C4=CC=C(OC5=CC=CC=C5)C=C4)N
Synonyms :
(±)-BGB-3111
MDL No. :MFCD30738015

Safety of (±)-Zanubrutinib

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Related Pathways of (±)-Zanubrutinib

RTK

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
697 cells 193 nM 3 days Evaluate the antiproliferative effect of zanubrutinib on 697 cells, IC50 = 193 nM PMC11176965
RCH-ACV cells 220 nM 3 days Evaluate the antiproliferative effect of zanubrutinib on RCH-ACV cells, IC50 = 220 nM PMC11176965
HEK293 cells 0.1, 0.3, 5 μM 10 minutes Evaluate whether zanubrutinib is a substrate of OATP1B1, OATP1B3, OAT1, OAT3, or OCT2, finding uptake ratios <2 at all concentrations, indicating zanubrutinib is unlikely to be a substrate of these transporters PMC8524670
BCRP vesicles 0.1, 5 μM 5 minutes Assess whether zanubrutinib is a BCRP substrate, finding uptake ratios of 0.970 ± 0.101-fold at 0.1 µM and 0.720 ± 0.209-fold at 5 µM, suggesting zanubrutinib is unlikely to be a BCRP substrate PMC8524670
MDCK-MDR1 cells 1, 10 μM 90 minutes Evaluate whether zanubrutinib is a P-gp substrate, finding efflux ratios of 3.46 at 1 µM and 2.19 at 10 µM, indicating zanubrutinib is a potential P-gp substrate PMC8524670
Human hepatocytes 0.3, 3, 30 μM 2 days Assess the induction potential of zanubrutinib on CYP1A2, CYP2B6, and CYP3A4 mRNA expression and enzymatic activity, finding significant induction of CYP3A4 mRNA (15.0-fold) and CYP2C8 mRNA (9.8-fold) at 30 μM PMC8524670
Recombinant CYP enzymes 1 μM 15 minutes Identify the major CYP isoform responsible for zanubrutinib metabolism, finding that only rCYP3A4 led to a remarkable disappearance of zanubrutinib PMC8524670
Human liver microsomes 10 μM 60 minutes Evaluate the in vitro metabolic pathways of zanubrutinib, identifying 11 metabolites with major pathways including hydroxylation of the phenoxy phenyl (M5) and oxidation and ring opening of the piperidine (M3, M7/M8, M9, M10, M11) PMC8524670
TMD8 cells 0.7 nM 6 days To evaluate the anti-proliferative effects of BGB-10188 and zanubrutinib in TMD8 cells. Results showed that the combination of BGB-10188 and zanubrutinib had synergistic anti-proliferative effects. PMC11415975
Human platelets 0.5-2.0 μM 10 minutes To study the effect of BTK inhibitors on α- and dense granule release. Both ibrutinib and zanubrutinib significantly inhibited rhodocytin- and CRP-XL-induced P-selectin expression and dense granule release. PMC6929381
Human platelets 0.5 μM 30 minutes To study platelet adhesion and thrombus formation on collagen, VWF, or fibrinogen. Ibrutinib significantly reduced platelet adhesion and thrombus formation, while zanubrutinib was similar to the control. PMC6929381
Maver-1 5 μM 3 hours To evaluate the effect of BGB-3111 on Akt phosphorylation, results showed that BGB-3111 significantly inhibited Akt phosphorylation at 5 μM concentration. PMC6363842
Mino 5 μM 1 hour To evaluate the inhibitory effect of BGB-3111 on BTK phosphorylation, results showed that BGB-3111 significantly inhibited BTK phosphorylation at 5 μM concentration. PMC6363842
Jeko-1 5 μM and 15 μM 72 hours To evaluate the inhibitory effect of BGB-3111 on MCL cell proliferation, results showed that BGB-3111 significantly inhibited cell proliferation at 5 μM and 15 μM concentrations. PMC6363842
OCI-Ly-10 (ABC DLBCL cell line) 1.5 nM 72 hours Evaluate single-agent antitumor activity, showing activity in the nanomolar range PMC6601092
TMD8 (ABC DLBCL cell line) 0.4 nM 72 hours Evaluate single-agent antitumor activity, showing activity in the nanomolar range PMC6601092
REC1 (MCL cell line) 0.9 nM 72 hours Evaluate single-agent antitumor activity, showing activity in the nanomolar range PMC6601092
RAW264.7, mouse leukemia cells of monocyte macrophage 1 μmol L−1 24 hours ZB reduced β-AR-induced macrophage pro-inflammatory cytokine production. PMC10458081
Primary neonatal rat cardiac fibroblasts (NRCFs) 1 μmol L−1 24 hours ZB alleviated β-AR-induced cardiac fibroblast activation, including proliferation, trans-differentiation, and ECM synthesis. PMC10458081

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice E2A-PBX1+/preBCR+ leukemia model Intraperitoneal injection 10 mg/kg Once daily for 20 days Evaluate the effect of zanubrutinib monotherapy and combination with dasatinib on survival in leukemia mice, combination significantly prolonged disease-free survival PMC11176965
Mice Farage subcutaneous xenograft model Oral 7.5 mg/kg Twice daily for 22 days To evaluate the anti-tumor effects of BGB-10188 and zanubrutinib in the Farage subcutaneous xenograft model. Results showed that the combination of BGB-10188 and zanubrutinib significantly enhanced anti-tumor activity. PMC11415975
C57BL/6 mice Thrombosis model Oral gavage 10 mg/kg Single dose, tested after 2 hours To study the effect of ibrutinib and zanubrutinib on thrombus formation. Ibrutinib significantly inhibited thrombus growth, while zanubrutinib was similar to the control. PMC6929381
NSG mice MCL PDX model Oral gavage 30 mg/kg Twice daily for 25 days To evaluate the antitumor activity of BGB-3111 in the MCL PDX model, results showed that BGB-3111 significantly inhibited tumor growth. PMC6363842
Male C57BL/6J mice ISO-induced cardiac fibrosis model Oral gavage 20 mg/kg Once daily for 7 days ZB ameliorates β-AR-induced cardiac fibrosis and inflammation by the BTK, STAT3, NF-κB, and PI3K/Akt signal pathways both in vivo and in vitro. PMC10458081

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.12mL

0.42mL

0.21mL

10.60mL

2.12mL

1.06mL

21.21mL

4.24mL

2.12mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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