Welcome to Sun-shine chemical
+86-17702719238
sales@sun-shinechem.com
- Home
- Inhibitors&Agonists
- PI3K/Akt/mTOR
- Epigenetics
- Protein Tyrosine Kinase
- Angiogenesis
- Apoptosis
- Autophagy
- JAK/STAT
- MAPK
- Cytoskeletal Signaling
- Cell Cycle
- TGF-beta/Smad
- DNA Damage
- Stem Cells & Wnt
- Ubiquitin
- Neuronal Signaling
- NF-κB
- GPCR & G Protein
- Metabolism
- Anti-infection
- Proteases
- Immunology & Inflammation
- Vitamin D Related
- Membrane Transporter/Ion Channel
- others
- PROTAC
- Antibody-drug Conjugate/ADC Related
- Building Blocks
- Aldehydes
- Amines
- Amino Acids
- Anilines
- Boronic Acids
- Bromides
- Carboxes
- Catalysts
- Chiral Compounds
- Deuterated
- Fluorides
- Imidazoles
- Indoles and Oxindoles
- Iodos
- Nitro Compounds
- Oxazoles
- Peg Linkers
- Phenols
- Piperidines
- Pyridines
- Pyrimidines
- Quinolines
- Sulfonamides
- Thiazoles
- Trifluoroborates
- Other Azoles
- Other Heterocycles
- Other Building Blocks
- On Sale
- Intermediates
- Services
- Ordering
- Contact Us
Name Index B
- BIIB068 (Catalog# : 20453, Cas# : 1798787-27-5)
- Baxdrostat (Catalog# : 20451, Cas# : 1428652-17-8)Baxdrostat is an aldosterone synthase inhibitor.
- BMS-986251 (Catalog# : 20445, Cas# : 2114324-48-8)
- BMS-986195 (Catalog# : 20444, Cas# : 1912445 -55-6)
- Branebrutinib (Catalog# : 20428, Cas# : 1912445-55-6)Branebrutinib, also known as BMS-986195, is a potent, covalent, irreversible inhibito
- Bexotegrast ( PLN-74809 ) (Catalog# : 171680, Cas# : 2376257-44-0)Bexotegrast (Synonyms: PLN-74809) is a small-molecule, dual selective inhibitor of α
- 4-Bromo-6-methylpyridine-2-carbonitrile (Catalog# : 171653, Cas# : 886372-53-8)4-Bromo-6-methylpyridine-2-carbonitrile, CAS 886372-53-8
- 1-(4-Bromo-6- methylpyridin-2- yl)ethan-1-one (Catalog# : 171454, Cas# : 1060810-24-3)1-(4-Bromo-6- methylpyridin-2- yl)ethan-1-one, CAS 1060810-24-3.
- BGB-15025 (Catalog# : 171452, Cas# : 2766481-17-6)BGB-15025 is a potent and selective HPK1 inhibitor that is efficacious as a single ag
- Benzeneacetamide, N-ethyl-4-formyl- (Catalog# : 20419, Cas# : 2477812-42-1)
- 8-[4-(2-butoxyethoxy)phenyl]-1,2,3,4-tetrahydro-1-(2-methylpropyl)-1-Benzazocine-5-carboxylic acid (Catalog# : 20403, Cas# : 497223-19-5)
- Benzeneacetic acid, 4-[[(2,4-dimethylbenzoyl)oxy]methyl]-, methyl ester (Catalog# : 20391, Cas# : 2097334-15-9)
- 8-[4-(2-butoxyethoxy)phenyl]-1,2,3,4-tetrahydro-1-(2-methylpropyl)-1-Benzazocine-5-carboxylic acid (Catalog# : 20386, Cas# : 497223-19-5)
- 1,10-BIS[4-AZA-1-AZONIABICYCLO[2.2.2]OCTAN-1-YL]DECANE DIBROMIDE (Catalog# : G20381, Cas# : 94630-53-2)
- 6-BENZYLOXY-3,4-DIHYDRO-1H-NAPHTHALEN-2-ONE (Catalog# : 20372, Cas# : 885280-42-2)
- BIBF0775 (Catalog# : L20357, Cas# : 334951-90-5)BIBF0775 is an inhibitor of the transforming growth factor β receptor I (TGFβRI). X
- Blarcamesine HCl (Catalog# : 6111905, Cas# : 195615-84-0)Anavex2-73 is a muscarinic/σ1 ligand. ANAVEX2-73 (0.01-3.0 mg/kg i.p.) alleviated th
- Bunamidine hydrochloride (Catalog# : 20271, Cas# : 1055-55-6)Bunamidine is a anti-parasitic drug, which was approved by FDA for the treatment of t
- BIT225 (Catalog# : 20270, Cas# : 917909-71-8)BIT-225 is a NCp7 zinc finger inhibitor potentially for the treatment of HCV infectio
- BI-3406 (Catalog# : 21234, Cas# : 2230836-55-0)BI-3406 is Potent & Selective SOS1::KRAS Inhibitor (IC50=5 nM), which Opens a New
- BI-187004 (Catalog# : 21224, Cas# : 1303515-32-3)BI-187004, also known as VTP-34072, is an 11β-hydroxysteroid dehydrogenase 1 inhibit
- Bafetinib (Catalog# : 2021221, Cas# : 887650-05-7)Bafetinib, also known as INNO-406 and NS187, is an orally bioavailable 2-phenylaminop
- BRD0705 (Catalog# : 202112701, Cas# : 2056261-41-5)BRD0705 is a potent, paralog selective and orally active GSK3α inhibitor. BRD0705 ca
- BLU-782 (Catalog# : 20121701, Cas# : 2141955-96-4)
- Benzyl(2S,5R)-5-amino-2-methylpiperidine-1-carboxylatehydrochloride (Catalog# : 20103006, Cas# : 1207853-23-3)
- Benpyrine racemate (Catalog# : 2091907, Cas# : 1333714-43-4)(Rac)-Benpyrine is a racemate of Benpyrine. (Rac)-Benpyrine is a potent and orally ac
- BAY-2416964 (Catalog# : 2091906, Cas# : 2242464-44-2)BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist
- BI-894999 (Catalog# : 2091902, Cas# : 1660117-38-3)BI-894999 is a potent and selective BET inhibitor potentially useful for the Treatmen
- 1-Bromo-4-(2-butoxyethoxy)benzene (Catalog# : 2091206, Cas# : 39255-24-8)
- 4-(2-Butoxyethoxy)phenylboronic acid (Catalog# : 2091203, Cas# : 279262-28-1)
Products Catalog
- ---- PI3K
- ---- Akt
- ---- GSK-3
- ---- S6 Kinase
- ---- AMPK
- ---- DNA-PK
- ---- MELK
- ---- PIKfyve
- ---- PI4K
- ---- PTEN
- ---- mTOR
- ---- ATM
- ---- PDK-1
- ---- ATR
- -- Epigenetics
- ---- PARP
- ---- JAK
- ---- Pim
- ---- PKC
- ---- PKD
- ---- Sirtuin
- ---- Histone Demethylase
- ---- Histone Acetyltransferase
- ---- HDAC
- ---- HIF-PH
- ---- Aurora Kinase
- ---- Histone Methyltransferase
- ---- METTL3
- ---- Epigenetic Reader Domain
- -- Protein Tyrosine Kinase
- ---- VEGFR
- ---- EGFR
- ---- PDGFR
- ---- IGF-1R
- ---- FLT3
- ---- FGFR
- ---- c-Kit
- ---- Src
- ---- ALK
- ---- Ephrin receptor
- ---- BTK
- ---- Trk receptor
- ---- c-Met/HGFR
- ---- Syk (Spleen tyrosine kinase)
- ---- TAM Receptor
- ---- ULK1
- ---- CSF-1R
- ---- TYK2
- ---- ROS Kinase
- -- Angiogenesis
- ---- VEGFR
- ---- JAK
- ---- EGFR
- ---- PDGFR
- ---- FLT3
- ---- FGFR
- ---- Bcr-Abl
- ---- Src
- ---- ALK
- ---- Syk
- ---- FAK
- ---- BTK
- ---- HIF
- -- Apoptosis
- ---- PD-1
- ---- PD-L1
- ---- Bcl-2
- ---- Caspase
- ---- TNF-alpha
- ---- Survivin
- ---- IAP
- ---- PERK
- ---- p53
- ---- Mdm2
- ---- E1/E2/E3 Enzyme
- -- Autophagy
- ---- LRRK2
- ---- CXCR
- ---- Autophagy
- -- JAK/STAT
- ---- JAK
- ---- STAT
- ---- Pim
- ---- EGFR
- -- MAPK
- ---- MEK
- ---- Raf
- ---- p38 MAPK
- ---- ERK
- ---- MNK
- ---- Mixed Lineage Kinase
- ---- JNK
- ---- MAP4K
- -- Cytoskeletal Signaling
- ---- Akt
- ---- Bcr-Abl
- ---- PKC
- ---- FAK
- ---- HSP
- ---- Kinesin
- ---- Integrin
- ---- Dynamin
- ---- Wnt
- ---- β-catenin
- -- Cell Cycle
- ---- CDK
- ---- PD-1
- ---- PD-L1
- ---- Chk
- ---- ROCK
- ---- PLK
- ---- APC
- ---- Wee1
- ---- DYRK
- ---- c-Myc
- ---- Aurora Kinase
- ---- ROCK inhibitor
- -- TGF-beta/Smad
- ---- Bcr-Abl
- ---- PKC
- ---- ROCK
- ---- TGF-beta/Smad
- -- DNA Damage
- ---- PARP
- ---- DNA/RNA Synthesis
- ---- Sirtuin
- ---- Topoisomerase
- ---- DNA-PK
- ---- Telomerase
- ---- RAD51
- ---- HDAC
- ---- ATM
- ---- DNA alkylator
- ---- Mps1
- -- Stem Cells & Wnt
- ---- GSK-3
- ---- JAK
- ---- STAT
- ---- ROCK
- ---- TGF-beta/Smad
- ---- Wnt
- ---- γ-secretase
- ---- β-catenin
- ---- smo
- -- Ubiquitin
- ---- Proteasome
- ---- p97
- ---- Deubiquitinase
- -- Neuronal Signaling
- ---- COX
- ---- Histamine Receptor
- ---- Dopamine Receptor
- ---- Opioid Receptor
- ---- GABA Receptor
- ---- OX Receptor
- ---- Amyloid-β
- ---- 5-HT Receptor
- ---- γ-secretase
- ---- Adrenergic Receptor
- ---- NMDA Receptor
- ---- GlyT1
- ---- Beta-secretase
- ---- α-Synuclein
- ---- Tau Protein
- ---- Cannabinoid Receptor
- ---- Transthyretin (TTR)
- -- NF-κB
- ---- NF-κB
- ---- HDAC
- ---- IKK
- -- GPCR & G Protein
- ---- Histamine Receptor
- ---- Dopamine Receptor
- ---- Opioid Receptor
- ---- Endothelin Receptor
- ---- SGLT
- ---- OX Receptor
- ---- CaSR
- ---- CXCR
- ---- Vasopressin Receptor
- ---- Glucagon Receptor
- ---- Prostaglandin Receptor
- ---- 5-HT Receptor
- ---- Adrenergic Receptor
- ---- Cannabinoid Receptor
- ---- Sphingosine 1 Phosphate Receptor
- ---- PKA
- ---- Adenosine Receptor
- ---- GnRH
- ---- LPL Receptor
- ---- Sigma Receptor
- ---- Ras
- ---- mAChR
- ---- Cholecystokinin Receptor
- ---- Melanocortin Receptor
- ---- RXFP Receptor
- -- Metabolism
- ---- PPAR
- ---- P450
- ---- HSP
- ---- PDE
- ---- Factor Xa
- ---- Phospholipase
- ---- FAAH
- ---- CETP
- ---- Lipoxygenase
- ---- HMG-CoA Reductase
- ---- Fatty Acid Synthase
- ---- FXR
- ---- NAMPT
- ---- TDO
- ---- Carbonic Anhydrase
- ---- Monoamine Oxidase
- ---- IDO
- ---- MAGL
- ---- Epoxide Hydrolase
- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- RAR/RXR
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- -- Anti-infection
- ---- CMV
- ---- Filovirus
- ---- HBV
- ---- HCV
- ---- HIV
- ---- HSV
- ---- Influenza Virus
- ---- RSV
- ---- SARS-CoV
- ---- Antibacterial
- ---- Antifungal
- ---- Parasite
- -- Proteases
- ---- Proteasome
- ---- Caspase
- ---- HIV Protease
- ---- MMP
- ---- γ-secretase
- ---- DPP4
- ---- Mitochondrial Metabolism
- ---- Isocitrate Dehydrogenase (IDH)
- ---- FPTase
- ---- Acetyl-CoA Carboxylase
- ---- Glutaminase
- -- Immunology & Inflammation
- ---- PD-1
- ---- PD-L1
- ---- COX
- ---- CCR
- ---- Histamine Receptor
- ---- TLR
- ---- CXCR
- ---- MALT
- ---- TDO
- ---- NOS
- ---- NADPH-oxidase
- ---- IDO
- ---- Thrombopoietin Receptor(TPO)
- ---- NLR inhibitor
- ---- Interleukin Related
- ---- CD73
- ---- Complement System
- ---- Aryl Hydrocarbon Receptor
- -- Vitamin D Related
- ---- VD/VDR
- -- Membrane Transporter/Ion Channel
- ---- BCRP
- ---- CFTR
- ---- EAAT2
- ---- GABA Receptor
- ---- HCN Channel
- ---- Monoamine Transporter
- ---- Na+/Ca2+ Exchanger
- ---- Na+/K+ ATPase
- ---- nAChR
- ---- Calcium Channel
- ---- Chloride Channel
- ---- CRAC Channel
- ---- GlyT1
- ---- iGluR
- ---- P2X Receptor
- ---- P-glycoprotein
- ---- Amino acid transporter
- ---- Monocarboxylate Transporter
- ---- Potassium Channel
- -- others
- ---- PKK
- ---- Others modulator
- ---- Estrogen Receptor/ERR
- ---- ChoKα
- -- PROTAC
- ---- Molecular Glues
- -- Antibody-drug Conjugate/ADC Related
- -- Aldehydes
- -- Amines
- -- Amino Acids
- -- Anilines
- -- Boronic Acids
- -- Bromides
- -- Carboxes
- -- Catalysts
- -- Chiral Compounds
- -- Deuterated
- -- Fluorides
- -- Imidazoles
- -- Indoles and Oxindoles
- -- Iodos
- -- Nitro Compounds
- -- Oxazoles
- -- Peg Linkers
- -- Phenols
- -- Piperidines
- -- Pyridines
- -- Pyrimidines
- -- Quinolines
- -- Sulfonamides
- -- Thiazoles
- -- Trifluoroborates
- -- Other Azoles
- -- Other Heterocycles
- -- Other Building Blocks
- -- On Sale
Latest Products
- Reparixin (Catalog# : 25050, Cas# : 266359-83-5)Reparixin is an inhibitor of CXCR2 function, which attenuates inflammatory responses
- TAK-779 (Catalog# : 25049, Cas# : 229005-80-5)TAK-779 is a C-C chemokine receptor type 5 (CCR5) receptor antagonist potentially for
- BAY-1125976 (Catalog# : 25048, Cas# : 1402608-02-9)BAY-1125976 is a potent and selective allosteric AKT1/2 inhibitor. BAY-1125976 exhibi
- Vimseltinib free base (Catalog# : 25047, Cas# : 1628606-05-2)Vimseltinib, also known as DCC-3014, is a potent and orally active inhibitor of the t
- 2-Propynamide, 3-[(3Z)-3-[[[4-[(dimethylamino)methyl]phenyl]amino]phenylmethylene]-2,3-dihydro-2-oxo-1H-indol-6-yl]-N-ethyl- (Catalog# : 25046, Cas# : 2128698-24-6)
- Cavosonstat (Catalog# : 25045, Cas# : 1371587-51-7)Cavosonstat, alos known as N91115) an orally bioavailable inhibitor of S-nitrosogluta
- Ivospemin Hydrochloride (Catalog# : 25044, Cas# : 259657-09-5)Ivospemin is an antineoplastic spermine analogue.
- Survodutide (Catalog# : 25043, Cas# : 2805997-46-8)
- XRD-0394 (Catalog# : 25042, Cas# : 2595308-10-2)XRD-0394 is a DNA-PKcs inhibitor. XRD-0394 selectively targets, binds to and inhibits
- CC-90003 (Catalog# : 25041, Cas# : 1621999-82-3)CC-90003 is an orally available inhibitor of extracellular signal-regulated kinase (E