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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Research Areas
- Metabolic Disease
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Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Quinoline Series
- Pyrazole Series
- Quinazoline
- Nucleoside Series
- Azaindazole
- Pyridazine Series
- Boric acid
- Pyrimidine Series
- 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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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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BCP13570 | GW-6604 New | 452342-37-9 |
GW6604 is a potent and selective ALK-5 inhibitor with potent anticancer activity.
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BCP29521 | Belizatinib | 1357920-84-3 |
Belizatinib is an oral, dual, potent inhibitor of ALK and TRKA, TRKB, and TRKC, with IC50 of 0.7 nM for wild-type recombinant ALK kinase.
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BCP29059 | Ensartinib dihydrochloride | 2137030-98-7 |
Ensartinib, also known as X-396, is a potent and dual ALK/MET inhibitor with IC50s of <0.4 nM and 0.74 nM, respectively.
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