General Information of Drug (ID: DM97I5L)

Drug Name
Branebrutinib Drug Info
Synonyms
Branebrutinib; BMS-986195; 1912445-55-6; (S)-4-(3-(but-2-ynamido)piperidin-1-yl)-5-fluoro-2,3-dimethyl-1H-indole-7-carboxamide; 7LBRZUYSHU; Branebrutinib [USAN]; BMS986195; 4-[(3S)-3-(but-2-ynoylamino)piperidin-1-yl]-5-fluoro-2,3-dimethyl-1H-indole-7-carboxamide; Branebrutinib (USAN); 1H-Indole-7-carboxamide, 5-fluoro-2,3-dimethyl-4-((3S)-3-((1-oxo-2-butyn-1-yl)amino)-1-piperidinyl)-; 4-((3S)-3-(But-2-ynamido)piperidin-1-yl)-5-fluoro-2,3-dimethyl-1H-indole-7-carboxamide; 4-[(3S)-3-(but-2-ynamido)piperidin-1-yl]-5-fluoro-2,3-dimethyl-1H-indole-7-carboxamide; UNII-7LBRZUYSHU; BRANEBRUTINIB [INN]; BRANEBRUTINIB [WHO-DD]; GTPL9869; CHEMBL4297674; SCHEMBL17699728; Branebrutinib (BMS-986195); C20H23FN4O2; VJPPLCNBDLZIFG-ZDUSSCGKSA-N; BDBM164638; BDBM166759; BCP29496; EX-A2720; MFCD31631584; NSC807627; s8832; WHO 11026; AKOS037649047; DB15347; NSC-807627; AC-31535; BS-16393; BMS986195; BMS986195; HY-112161; CS-0043577; Example 223 [US20160115126A1]; D11478; EN300-2007801; US9688629, 123; US9688629, 223; Q50825082; 4-((3S)-3-(2-Butynoylamino)-1-piperidinyl)-5-fluoro-2,3-dimethyl-1H-indole-7-carboxamide; (S)-4-(3-(2-BUTYNOYLAMINO)PIPERIDIN-1-YL)-5-FLUORO-2,3-DIMETHYL-1H-INDOLE-7-CARBOXAMIDE; 4-((3S)-3-(2-BUTYNOYLAMINO)-1-PIPERIDINYL)-5-FLUORO-2,3-DIMETHYL-1HINDOLE-7-CARBOXAMIDE
Indication
Disease Entry ICD 11 Status REF
Rheumatoid arthritis FA20 Phase 2 [1]
Cross-matching ID
PubChem CID
121293929
TTD Drug ID
DM97I5L

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Ibrutinib DMHZCPO Mantle cell lymphoma 2A85.5 Approved [3]
Acalabrutinib DM7GCVW leukaemia 2A60-2B33 Approved [4]
Zanubrutinib DMJWRQP Mantle cell lymphoma 2A85.5 Approved [5]
Pirtobrutinib DMRG1X3 Non-hodgkin lymphoma 2B33.5 Approved [6]
GDC-0853 DMBEL3Q Multiple sclerosis 8A40 Phase 3 [7]
ICP-022 DMU72KL Chronic lymphocytic leukaemia 2A82.0 Phase 3 [8]
Tolebrutinib DML19V6 Multiple sclerosis 8A40 Phase 3 [9]
CC-292 DMJR9H0 Chronic lymphocytic leukaemia 2A82.0 Phase 2 [10]
BMS-986142 DMZB8AJ Rheumatoid arthritis FA20 Phase 2 [7]
LOU064 DME8O5K Chronic idiopathic urticaria EB00.1 Phase 2 [11]
⏷ Show the Full List of 10 Drug(s)

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Tyrosine-protein kinase BTK (ATK) TTGM6VW BTK_HUMAN Inhibitor [2]

References

1 ClinicalTrials.gov (NCT04186871) A Randomized, Placebo-Controlled, Double-Blind, Multicenter Study to Assess the Efficacy and Safety of Branebrutinib Treatment in Subjects With Active Systemic Lupus Erythematosus or Primary Sj?gren's Syndrome, or Branebrutinib Treatment Followed by Open-label Abatacept Treatment in Subjects With Active Rheumatoid Arthritis. U.S.National Institutes of Health.
2 Safety, pharmacokinetics and pharmacodynamics of branebrutinib (BMS-986195), a covalent, irreversible inhibitor of Bruton's tyrosine kinase: Randomised phase I, placebo-controlled trial in healthy participants. Br J Clin Pharmacol. 2020 Sep;86(9):1849-1859.
3 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 1948).
4 2017 FDA drug approvals.Nat Rev Drug Discov. 2018 Feb;17(2):81-85.
5 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
6 Targeting BTK in CLL: Beyond Ibrutinib. Curr Hematol Malig Rep. 2019 Jun;14(3):197-205.
7 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
8 Clinical pipeline report, company report or official report of InnoCare Pharma.
9 Safety and efficacy of tolebrutinib, an oral brain-penetrant BTK inhibitor, in relapsing multiple sclerosis: a phase 2b, randomised, double-blind, placebo-controlled trial. Lancet Neurol. 2021 Sep;20(9):729-738.
10 Inhibition of Btk with CC-292 provides early pharmacodynamic assessment of activity in mice and humans. J Pharmacol Exp Ther. 2013 Aug;346(2):219-28.
11 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)