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
- Motilin Receptor
- TGR5
- Cholecystokinin Receptor
- Adenylate Cyclase
- Somatostatin Receptor
- Oxytocin Receptor
- Bradykinin Receptor
- Guanylate Cyclase
- Melanocortin Receptor
- Imidazoline Receptor
- PAR
- Neuropeptide Receptor
- CRFR
- Sigma Receptor
- S1P Receptor
- GHSR
- PKA
- Prostaglandin Receptor
- OX Receptor
- Adenosine Receptor
- Glucagon Receptor
- NK Receptor
- GnRH Receptor
- Leukotriene Receptor
- Glucocorticoid Receptor
- mAChR
- P2 Receptor
- GPR
- CGRP Receptor
- CXCR
- Histamine Receptor
- CaSR
- Ras/Rho
- Smoothened/Smo
- Vasopressin Receptor
- Opioid Receptor
- mGluR
- Cannabinoid Receptor
- Dopamine Receptor
- Angiotensin Receptor
- Adrenergic Receptor
- SGLT
- Endothelin Receptor
- CCR
- 5 HT Receptor/Serotonin Receptor
- Hormone Pathay
- Ion Channel/Membrane Transporter
- Jak/Stat Pathway
- MAPK Pathway
- Microbiology/Virology
-
Neuro Signaling Pathway
- Imidazoline Receptor
- Monoamine Oxidase
- COMT
- Amyloid β
- NK Receptor
- Beta secretase
- AChE
- SSRI
- CaMK
- P glycoprotein
- Opioid Receptor
- Dopamine Receptor
- Adrenergic Receptor
- Histamine Receptor
- mGluR
- Gamma secretase
- Dopamine Transporter
- 5 HT Receptor/Serotonin Receptor
- P2 Receptor
- nAChR
- FAAH
- CGRP Receptor
- COX
- GABA Receptor
- mAChR
- NFκB
- PI3K/Akt/mTOR
-
Protease/Metabolic Enzyme
- COMT
- Xanthine Oxidase
- Carboxypeptidase
- 11β HSD
- ACC
- Mitochondrial Metabolism
- Pyruvate Kinase
- ALDH
- Serine Protease
- SCD
- Neprilysin
- FTase
- CETP
- MLR
- Carbonic Anhydrase
- MAGL
- E1 E2 E3 Enzyme
- PAI1
- Elastase
- NOX
- ROR
- Glucokinase
- 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
- HSP
- HCV Protease
- Tryptophan Hydroxylase/TPH
- Factor Xa
- DPP
- Procollagen C Proteinase
- Integrase
- Phospholipase
- Phosphodiesterase/PDE
- LXR
- Proteasome
- Cytochrome P450
- TGF beta/Smad
- Wnt/Stem Cell
- Others Pathway
Research Areas
- Metabolic Disease
- Neurological Disease
- Endocrinology
- Diabetes
- Cardiovascular Disease
- Immunology
- Allergy
- Infection
- Inflammation
- Cancer
Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Pyridazine Series
- Ammonia Series
- Amino acid
- Nucleoside Series
- Azaindazole
- Quinazoline
- Pyrazole Series
- Quinoline Series
- Pyrrole Series
- Boric acid
- Pyrimidine Series
- Thiophene Series
- Saccharide
- Azaindole
- Indole Series
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Pyridine Series
- Benzene Series
Raw Materials
MAP4K
Chemical Structure | Cat. No. | Product Name | CAS No. |
---|
![]() |
BCP46896 | MAP4K4-IN-3 New | 1811510-58-3 |
MAP4K4-IN-3 may be a viable target for antidiabetic agents, a serine/threonine protein kinase.
|
![]() |
BCP43399 | HPK1-IN-7 New | 2320462-65-3 |
HPK1-IN-7 is a potent, orally active HPK1 inhibitor.
|
![]() |
BCP36075 | GNE-495 New | 1449277-10-4 |
GNE-495 is a potent and selective MAP4K4 inhibitor with an IC50 of 3.7 nM.
|
![]() |
BCP21395 | TAK1/MAP4K2 inhibitor 1 New | 1315330-11-0 |
TAK1/MAP4K2 inhibitor 1 is a B-Raf inhibitor, pyrazine and pyrrolo[2,3-b]pyridine derivatives, useful in the treatment of cancer and proliferative diseases.
|
![]() |
BCP30841 | DMX-5084 New | 2306178-56-1 |
DMX-5804 is a potent, orally active and selective MAP4K4 inhibitor.
|
![]() |
BCP11080 | HG6-64-1 | 1315329-43-1 |
HG6-64-1 is a potent and selective B-Raf and mutant B-Raf inhibitor.HG6-64-1 is a potent dual TAK1 and MAP4K2 ((germinal center kinase, GCK)) inhibitor with IC50 of 41 nM and 98 nM, respectively.
|
![]() |
BCP28968 | PF-06260933 | 1811510-56-1 |
PF-06260933 is a potent and highly selective inhibitor of MAP4K4.
|
![]() |
BCP28969 | PF-06260933 dihydrochloride New | 1883548-86-4 |
PF 6260933 is a potent, selective and orally bioavailable MAP4K4 inhibitor with kinase IC50 of 3.7 nM, cell IC50 of 160 nM.
|
![]() |
BCP28970 | PF-06260933 HCl New | 2118243-34-6 |
PF-06260933 dihydrochloride is a MAP4K4 (HGK) inhibitor (IC50 = 140 nM).
|
![]() |
BCP20048 | NCB-0846 | 1792999-26-8 |
NCB-0846 is a novel, orally small-molecule Wnt inhibitor that inhibits TNIK (TRAF2 and NCK-Interacting Kinase) with an IC50 value of 21 nM.
|
