Classified by application
All Products
Signaling Pathways
- Angiogenesis/Protein Tyrosine Kinase
- Apoptosis Pathway
- Cell Cycle/DNA Damage
- Epigenetics
-
GPCR/G Protein
- Urotensin Receptor
- Melatonin Receptor
- Neurotensin Receptor
- Glucose Transporter
- Cholecystokinin Receptor
- TGR5
- Motilin Receptor
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- Imidazoline Receptor
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- Sigma Receptor
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- GHSR
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- OX Receptor
- Adenosine Receptor
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- NK Receptor
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- Leukotriene Receptor
- Glucocorticoid Receptor
- mAChR
- P2 Receptor
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- CXCR
- Histamine Receptor
- CaSR
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- Smoothened/Smo
- Opioid Receptor
- mGluR
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- Angiotensin Receptor
- Adrenergic Receptor
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- 5 HT Receptor/Serotonin Receptor
- Hormone Pathay
- Ion Channel/Membrane Transporter
- Jak/Stat Pathway
- MAPK Pathway
- Microbiology/Virology
-
Neuro Signaling Pathway
- Monoamine Oxidase
- Imidazoline Receptor
- COMT
- Amyloid β
- NK Receptor
- Beta secretase
- AChE
- SSRI
- CaMK
- P glycoprotein
- Opioid Receptor
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- Adrenergic Receptor
- Histamine Receptor
- mGluR
- Gamma secretase
- Dopamine Transporter
- 5 HT Receptor/Serotonin Receptor
- P2 Receptor
- FAAH
- CGRP Receptor
- nAChR
- COX
- GABA Receptor
- mAChR
- NFκB
- PI3K/Akt/mTOR
-
Protease/Metabolic Enzyme
- Xanthine Oxidase
- ACC
- Mitochondrial Metabolism
- Pyruvate Kinase
- ALDH
- SCD
- Serine Protease
- CETP
- Neprilysin
- FTase
- MLR
- MAGL
- E1 E2 E3 Enzyme
- Carbonic Anhydrase
- Elastase
- PAI1
- NOX
- ROR
- Glucokinase
- Aldose Reductase
- Tyrosinase
- FAS
- DGAT
- Lipoxygenase
- Nampt
- IDO
- IDH
- MMP
- Cathepsin
- Phosphatase
- Thrombin
- RAR/RXR
- FXR
- HMGCR
- FAAH
- RAAS/ACE
- Gamma secretase
- Caspase
- HIV Protease
- Aminopeptidase
- HCV Protease
- HSP
- Tryptophan Hydroxylase/TPH
- Factor Xa
- DPP
- Procollagen C Proteinase
- Integrase
- Phospholipase
- Phosphodiesterase/PDE
- LXR
- Proteasome
- Cytochrome P450
- Carboxypeptidase
- 11β HSD
- COMT
- TGF beta/Smad
- Wnt/Stem Cell
- Others Pathway
Research Areas
- Metabolic Disease
- Neurological Disease
- Diabetes
- Endocrinology
- Cardiovascular Disease
- Immunology
- Allergy
- Inflammation
- Infection
- Cancer
Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Pyrazole Series
- Quinazoline
- Nucleoside Series
- Azaindazole
- Ammonia Series
- Pyridazine 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
Wnt/Stem Cell
Chemical Structure | Cat. No. | Product Name | CAS No. |
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BCP25144 | Super-TDU New | 1599441-71-0 |
Super-TDU is an inhibitory peptide targeting YAP-TEADs interaction.
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BCP25257 | H-1152 Dihydrochloride New | 871543-07-6 |
H-1152 dihydrochloride is an isoquinolinesulfonamide derivative that is a membrane-permeable inhibitor of Rho-kinase but poor inhibitor of other serine/threonine kinases.
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BCP25428 | Ruxolitinib racemic New | 1160597-27-2 |
Ruxolitinib racemic is a Janus-associated kinase (JAK) inhibitor.
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BCP48402 | inS3-54-A18 New | 328998-53-4 |
inS3-54A18 is a potent STAT3 inhibitor, with anti-cancer properties.
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BCP48519 | GSK-3/CDK5/CDK2-IN-1 New | 395074-72-3 |
GSK-3/CDK5/CDK2-IN-1, an imidazole derivative, is an inhibitor of cdk5, cdk2, and GSK-3 extracted from patent WO2002010141A1, example 9a.
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BCP48537 | β-catenin-IN-2 New | 1458664-10-2 |
β-catenin-IN-2 is a potent β-catenin inhibitor, compound H1B1, extracted from patent US20150374662A1.
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BCP48533 | TED-347 New | 2378626-29-8 |
TED-347 is a covalent inhibitor of TEAD4-Yap1 protein-protein interaction in mammalian cells which blocks iTEAD transcriptional activity and inhibits glioblastoma cell viability.
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BCP45820 | TDI-011536 New | 2687970-96-1 |
TDI-011536 is a potent, ATP-competitive inhibitor of Lats kinases with IC50 of 0.76 nM (2 mM ATP) in vitro assays, prevents Yap phosphorylation in the cell-based assays with EC50 of 10 nM.
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BCP48249 | WAY316606 New | 915759-45-4 |
WAY-316606, a specific antagonist of SFRP1, functions as an activator of canonical Wnt/β-catenin signalling in the human hair bulb.
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BCP47996 | GDC-0214 New | 1831144-46-7 |
GDC0214 is a potent, selective inhalable and lung-restricted inhibitor of JAK1 with IC50 of 8.52 nM, displays 6.3/704/28 fold selectivity over JAK2/JAK3/TYK2.
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