Structure of (±)-Zanubrutinib
CAS No.: 1633350-06-7
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
(±)-Zanubrutinib, also known as (±)-BGB-3111, is an efficacious, selective, oral Btk inhibitor that exhibits nanomolar-level Btk inhibitory activity.
Synonyms: (±)-BGB-3111
4.5
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Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
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Batch number can be found on the product's label following the word 'Batch'.
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 |
GHS Pictogram: |
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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 |
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 |
Tags: (±)-Zanubrutinib | (±)-BGB-3111 | Btk | Bruton tyrosine kinase | Btk inhibitor | Bruton's tyrosine kinase |chronic lymphocytic leukemia | B-cell receptor | Btk pathway | 1633350-06-7
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