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poseltinib , Tyrosine-protein kinase BTK inhibitor, CAS No.1353552-97-2, Tyrosine-protein kinase BTK inhibitor

  • Moligand™
  • ≥98%
Item Number
P612898
Grouped product items
SKUSizeAvailabilityPrice Qty
P612898-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$39.90
P612898-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$169.90
P612898-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$299.90
P612898-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$499.90

Basic Description

SynonymsPoseltinib|1353552-97-2|Poseltinib [INN]|HM71224|LY3337641|Poseltinib (HM-71224; LY-3337641)|D01E4B1U35|HM-71224|N-[3-[2-[4-(4-methylpiperazin-1-yl)anilino]furo[3,2-d]pyrimidin-4-yl]oxyphenyl]prop-2-enamide|2-Propenamide, N-(3-((2-((4-(4-methyl-1-piperazi
Specifications & PurityMoligand™, ≥98%
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionTyrosine-protein kinase BTK inhibitor
Product Description

Poseltinib (HM71224) is an orally active, selective, irreversible small molecule Bruton tyrosine kinase (BTK) inhibitor. With an IC50 of 1.95 nM. Poseltinib effectively inhibits the signaling mediated by B cell receptors (BCR), Fc receptors (FcR), and Toll-like receptors (TLR). Poseltinib has anti-inflammatory activity and can be used in the research of rheumatoid arthritis

Product Properties

ALogP4.1

Associated Targets

CD69 Tchem Early activation antigen CD69 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

JAK3 Tclin Tyrosine-protein kinase JAK3 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

BTK Tclin Tyrosine-protein kinase BTK 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name N-[3-[2-[4-(4-methylpiperazin-1-yl)anilino]furo[3,2-d]pyrimidin-4-yl]oxyphenyl]prop-2-enamide
INCHI InChI=1S/C26H26N6O3/c1-3-23(33)27-19-5-4-6-21(17-19)35-25-24-22(11-16-34-24)29-26(30-25)28-18-7-9-20(10-8-18)32-14-12-31(2)13-15-32/h3-11,16-17H,1,12-15H2,2H3,(H,27,33)(H,28,29,30)
InChi Key LZMJNVRJMFMYQS-UHFFFAOYSA-N
Canonical SMILES CN1CCN(CC1)C2=CC=C(C=C2)NC3=NC4=C(C(=N3)OC5=CC=CC(=C5)NC(=O)C=C)OC=C4
Isomeric SMILES CN1CCN(CC1)C2=CC=C(C=C2)NC3=NC4=C(C(=N3)OC5=CC=CC(=C5)NC(=O)C=C)OC=C4
Alternate CAS 1353552-97-2
PubChem CID 56644522
MeSH Entry Terms N-(3-(2-(4-(4-methylpiperazin-1-yl)anilino)furo(3,2-d)pyrimidin-4-yl)oxyphenyl)prop-2-enamide;poseltinib
Molecular Weight 470.52

Certificates

Certificate of Analysis(COA)

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Related Documents

References

1. Park JK, Byun JY, Park JA, Kim YY, Lee YJ, Oh JI, Jang SY, Kim YH, Song YW, Son J et al..  (2015)  HM71224, a novel Bruton's tyrosine kinase inhibitor, suppresses B cell and monocyte activation and ameliorates arthritis in a mouse model: a potential drug for rheumatoid arthritis..  Arthritis Res Ther,  18  (3): (91).  [PMID:27090981]
2. Kim YY, Park KT, Jang SY, Lee KH, Byun JY, Suh KH, Lee YM, Kim YH, Hwang KW.  (2017)  HM71224, a selective Bruton's tyrosine kinase inhibitor, attenuates the development of murine lupus..  Arthritis Res Ther,  19  (1): (211).  [PMID:28950886]

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