Linrodostat mesylate
Based on 7 publication(s) in Google Scholar
Linrodostat (BMS-986205) mesylate is a selective irreversible inhibitor of indoleamine 2,3-dioxygenase 1 (IDO1), which effectively inhibits IDO1-HEK293 mesylate cells with an IC50 value of 1.1 nM. Linrodostat mesylate demonstrates good pharmacological activity in advanced cancer.
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- CAS No.: 2221034-29-1
- Formule: C25H28ClFN2O4S
- Masse moléculaire:507.02
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications Citing Use of MedChemExpress (MCE) Linrodostat mesylate
More- Immunity. 2021 Oct 12;54(10):2354-2371.e8. [Abstract]
- MedComm (2020). 2026 Mar 30;7(4):e70709. [Abstract]
- Cell Death Differ. 2021 Feb;28(2):715-729. [Abstract]
- J Neuroinflammation. 2024 Nov 28;21(1):307. [Abstract]
- Cell Rep. 2024 Sep 13;43(9):114741. [Abstract]
- Heidelberg University. 2025.
- SSRN. 2023 Dec 1.
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IF
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RT-PCR
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In Vivo Efficacy Study
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Flow Cytometry
Activité biologique
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IDO1 1.1 nM (IC50) |
Chemical Information
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CAS No. 2221034-29-1
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Masse moléculaire 507.02
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Formule C25H28ClFN2O4S
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SMILES
O=C(NC1=CC=C(Cl)C=C1)[C@H](C)[C@@](CC2)([H])CC[C@H]2C3=CC=NC4=C3C=C(F)C=C4.OS(C)(=O)=O
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Synonyms
BMS-986205 mesylate; ONO-7701 mesylate
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications (7)
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Journal Impact Factor
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Most Recent
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Immunity
Inhibition of the BTK-IDO-mTOR axis promotes differentiation of monocyte-lineage dendritic cells and enhances anti-tumor T cell immunity. [Abstract]2021 Oct 12;54(10):2354-2371.e8. PMID: 34614413
Linrodostat mesylate purchased from MedChemExpress. Usage Cited in: Immunity. 2021 Oct 12;54(10):2354-2371.e8. [Abstract]
Linear regression analysis of Ly6c+CD103+ DCs versus tumor response across graded doses of the IDO-inhibitor Linrodostat (10-5-2-0 mg/kg/day) plus CTX (given day 10) and ibrutinib (16 mg/kg/day), on a schedule similar to panel A. Regression analysis shows pooled data from all groups, measured on day 15.
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MedComm (2020)
Metabolic Alterations in Macrophage Subtypes Propel Immune and Stromal Remodeling in Neurofibroma's Malignant Progression. [Abstract]2026 Mar 30;7(4):e70709. PMID: 41930352 -
Cell Death Differ
Exosome-derived miR-142-5p remodels lymphatic vessels and induces IDO to promote immune privilege in the tumour microenvironment. [Abstract]2021 Feb;28(2):715-729. PMID: 32929219
Linrodostat mesylate purchased from MedChemExpress. Usage Cited in: Cell Death Differ. 2021 Feb;28(2):715-729. [Abstract]
HDLECs pre-treated with indicated exosomes were cocultured with in vitro-activated CD8+ T cells at a ratio of 1:1 with or without 100 nM of an IDO inhibitor (BMS-986205). The expression of CD69.
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J Neuroinflammation
Taprenepag restores maternal-fetal interface homeostasis for the treatment of neurodevelopmental disorders. [Abstract]2024 Nov 28;21(1):307. PMID: 39609821
Linrodostat mesylate purchased from MedChemExpress. Usage Cited in: J Neuroinflammation. 2024 Nov 28;21(1):307. [Abstract]
linrodostat (Lin: 5 mg/kg).Immunofluorescence staining of TPH-2+ neurons and 5-HT in newborn MRN pups at P10.
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Cell Rep
Integrated metabolic-transcriptomic network identifies immunometabolic modulations in human macrophages. [Abstract]2024 Sep 13;43(9):114741. PMID: 39276347
Linrodostat mesylate purchased from MedChemExpress. Usage Cited in: Cell Rep. 2024 Sep 13;43(9):114741. [Abstract]
qPCR and ELISA of pro-/anti-inflammatory marker genes in macrophages treated with IDO1 inhibitor (LRDS: 50 nM) and IL4I1 inhibitor (CB668) followed by pro-/anti-inflammatory stimuli (n = 4). Anti-inflammatory CCL22 gene and protein levels in IL-4-activated macrophages.
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Pureté et documentation
Références
[1]. Richards T, et al. Cell based functional assays for IDO1 inhibitor screening and characterization. Oncotarget. 2018 Jul 20;9(56):30814-30820. [Content Brief]
[2]. Lillian L. Siu, et al. Abstract CT116: BMS-986205, an optimized indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor, is well tolerated with potent pharmacodynamic (PD) activity, alone and in combination with nivolumab (nivo) in advanced cancers in a phase 1/2a trial. AACR; Cancer Res. 2017; 77 (13 Suppl): Abstract nr CT116. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)