Classified by application
All Products
Signaling Pathways
- Angiogenesis/Protein Tyrosine Kinase
- Apoptosis Pathway
- Cell Cycle/DNA Damage
- Epigenetics
-
GPCR/G Protein
- Melatonin Receptor
- Urotensin Receptor
- Neurotensin Receptor
- Motilin Receptor
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- Adenylate Cyclase
- Cholecystokinin Receptor
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- Smoothened/Smo
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- Hormone Pathay
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- Microbiology/Virology
-
Neuro Signaling Pathway
- Imidazoline Receptor
- Monoamine Oxidase
- COMT
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- NK Receptor
- Beta secretase
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- SSRI
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- P glycoprotein
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- mGluR
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- FAAH
- P2 Receptor
- nAChR
- CGRP Receptor
- COX
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- mAChR
- NFκB
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-
Protease/Metabolic Enzyme
- 11β HSD
- COMT
- Carboxypeptidase
- ACC
- Xanthine Oxidase
- Mitochondrial Metabolism
- Pyruvate Kinase
- SCD
- ALDH
- Serine Protease
- Neprilysin
- CETP
- FTase
- MLR
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- Carbonic Anhydrase
- E1 E2 E3 Enzyme
- Elastase
- Glucokinase
- ROR
- NOX
- PAI1
- Aldose Reductase
- Tyrosinase
- FAS
- DGAT
- Lipoxygenase
- Nampt
- IDO
- IDH
- MMP
- Cathepsin
- Phosphatase
- Thrombin
- FXR
- RAR/RXR
- HMGCR
- FAAH
- Gamma secretase
- RAAS/ACE
- Caspase
- HIV Protease
- Aminopeptidase
- HCV Protease
- HSP
- Tryptophan Hydroxylase/TPH
- Factor Xa
- DPP
- Procollagen C Proteinase
- Integrase
- Phosphodiesterase/PDE
- Phospholipase
- LXR
- Proteasome
- Cytochrome P450
- TGF beta/Smad
- Wnt/Stem Cell
- Others Pathway
Research Areas
- Metabolic Disease
- Neurological Disease
- Endocrinology
- Diabetes
- Cardiovascular Disease
- Immunology
- Allergy
- Inflammation
- Infection
- Cancer
Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Nucleoside Series
- Azaindazole
- Pyridazine Series
- Quinazoline
- Pyrimidine Series
- Pyrazole Series
- Quinoline Series
- Boric acid
- Pyrrole Series
- Thiophene Series
- Saccharide
- Azaindole
- Indole Series
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Pyridine Series
- Benzene Series
Raw Materials
Angiogenesis/Protein Tyrosine Kinase
Chemical Structure | Cat. No. | Product Name | CAS No. |
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BCP38668 | HIF-2a Translation Inhibitor 76 New | 882268-69-1 |
HIF-2a Translation Inhibitor 76 is a cell-permeable HIF-2a translation inhibitor (IC50 value 5 µM).
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BCP38649 | JND3229 New | 2260886-64-2 |
JND3229 is a New EGFRC797S Mutant Inhibitor with In Vivo Monodrug Efficacy (IC50 = 5.8 nM).
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BCP38312 | Almonertinib New | 1899921-05-1 |
Almonertinib is an EGFR tyrosine kinase inhibitor. Upon administration, HS-10296 binds to and inhibits EGFR T790M, a secondarily acquired resistance mutation, inhibits the tyrosine kinase activity of EGFR T790M, prevents EGFR T790M-mediated signaling and leads to cell death in EGFR T790M-expressing tumor cells.
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BCP38296 | Olmutinib dihydrochloride New | 1842366-97-5 |
Olmutinib is an orally available, mutant-selective third-generation epidermal growth factor receptor tyrosine kinase inhibitor (EGFR TKI) that is being developed for treatment of advanced and metastatic EGFR mutation-positive non-small cell lung cancer (NSCLC).
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BCP33271 | CA-4948 New | 1801344-14-8 |
CA-4948 is a potent IRAK4/FLT3 inhibtor with anti-tumor activity.
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BCP38229 | TP0463518 New | 1558021-37-0 |
TP0463518 is a novel prolyl hydroxylase (PHD) 1/2/3 pan inhibitor, inducing erythropoietin (EPO) production in both the kidney and liver, increasing the HIF-2α and EPO mRNA expression levels in the kidney cortex.
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BCP38228 | TL02-59 New | 1315330-17-6 |
TL02-59 is a novel potent and selective inhibitor of the myeloid Src-family kinase Fgr, suppressing AML cell growth in vitro and in vivo.
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BCP37982 | Epertinib hydrochloride New | 2071195-74-7 |
Epertinib hydrochloride is a potent, orally active, reversible, and selective tyrosine kinase inhibitor of EGFR, HER2 and HER4. It shows potent antitumor activity.
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BCP37917 | LDN-192960 dihydrochloride New | 2309172-48-1 |
LDN-192960 is a potent and selective inhibitor of haspin.
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BCP37896 | TX1-85-1 New | 1603845-32-4 |
TX1-85-1 is an inhibitor of the epidermal growth factor receptor tyrosine kinase ErbB3 (IC50 = 23 nM).
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