Classified by application
All Products
Signaling Pathways
- Angiogenesis/Protein Tyrosine Kinase
- Apoptosis Pathway
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- Epigenetics
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GPCR/G Protein
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Neuro Signaling Pathway
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Protease/Metabolic Enzyme
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- 11β HSD
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Research Areas
- Metabolic Disease
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Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Pyridazine Series
- Quinazoline
- Nucleoside Series
- Azaindazole
- Pyrazole Series
- Quinoline Series
- Pyrimidine Series
- Boric acid
- Pyrrole Series
- Thiophene Series
- Saccharide
- Azaindole
- Indole Series
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Pyridine Series
- Benzene Series
Raw Materials
ALK
Chemical Structure | Cat. No. | Product Name | CAS No. |
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BCP25191 | R-268712 New | 879487-87-3 |
R-268712 is a specific inhibitor of activin receptor-like kinase 5 (ALK5). It is also an orally active transforming growth factor-β type I receptor inhibitor.
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BCP45485 | ZX-29 New | 2254805-62-2 |
ZX-29 is a potent and selective ALK inhibitor for ALK, ALK L1196M and ALK G1202R mutations, respectively.
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BCP42131 | TPX-0131 New | 2648641-36-3 |
TPX-0131 is a CNS-penetrant, next-generation ALK inhibitor that has potency against wild-type ALK and a spectrum of acquired resistance mutations, especially the G1202R solvent front mutation and compound mutations, for which there are currently no effective therapies.
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BCP36914 | TL13-12 New | 2229037-04-9 |
TL13-12 is a novel selective anaplastic lymphoma kinase (ALK) degrader.
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BCP36884 | TL13-112 New | 2229037-19-6 |
TL13-112 shows chemically induced degradation of anaplastic lymphoma kinase (ALK).
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BCP32539 | MS4078 New | 2229036-62-6 |
MS4078 is an anaplastic lymphoma kinase (ALK) PROTAC (degrader) with a Kd of 19 nM for binding affinity to ALK.
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BCP31069 | SAR348830 New | 1462949-64-9 |
SAR348830 is novel potent and selective inhibitor of anaplastic lymphoma kinase (ALK).
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BCP30371 | BIBF0775 New | 334951-90-5 |
BIBF0775 is a potent and selective transforming growth factor β (TGFβ) type I receptor (Alk5) inhibitor with an IC50 of 34 nM.
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BCP30149 | SM16 New | 614749-78-9 |
SM16 is a ALK5/ALK4 kinase inhibitor with Kis of 10 and 1.5 nM, respectively.
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BCP30129 | BIO-013077-01 New | 746667-48-1 |
BIO-013077-01 is a novel potent antagonist of the TGFbeta family type I receptors, Alk5 and/or Alk4.
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