Welcome to Sun-shine chemical
+86-17702719238
sales@sun-shinechem.com
- Home
- Inhibitors & Agonists
- Angiogenesis
- Anti-infection
- Apoptosis
- Autophagy
- Cell Cycle
- Cytoskeleton
- DNA Damage
- Epigenetics
- GPCR & G Protein
- Immunology & Inflammation
- JAK/STAT
- MAPK
- Membrane Transporter/Ion Channel
- Metabolism
- Neuronal Signaling
- NF-κB
- Protein Tyrosine Kinase
- Proteases
- PI3K/Akt/mTOR
- Stem Cells & Wnt
- TGF-beta/Smad
- Ubiquitin
- Vitamin D Related
- PROTAC
- Antibody-drug Conjugate/ADC Related
- Microbiology
- Others
- 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
- 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)
- 6-bromo-2-ethyl-N,8-dimethylimidazo[1,2-a]pyridin-3-amine (Catalog# : 2091201, Cas# : 1628264-07-2)
- BCH001 (Catalog# : 208192, Cas# : 384859-58-9)BCH001,a specific PAPD5 inhibitor, restored telomerase activity and telomere length i
- BMS-1166 (Catalog# : 2073102, Cas# : 1818314-88-3)BMS-1166is a potent PD-1/PD-L1 interaction inhibitor with an IC50 of 1.4 nM, antagoni
- BAY-1816032 (Catalog# : 2071615, Cas# : 1891087-61-8)BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazole
- BAY-2402234 (Catalog# : 2071553, Cas# : 2225819-06-5)BAY-2402234 is a potent and selective dihydroorotate dehydrogenase (DHODH) inhibitor
- BMVC-8C3O (Catalog# : 2071550, Cas# : 1301708-12-2)BMVC-8C3O is a DNA G-quadruplexe (G4) ligand which can induce topological conversion
- BAY-545 (Catalog# : 2071532, Cas# : 1699717-32-2)BAY-545 is a potent and selective antagonist of the A2B adenosine receptor.
- Belnacasan (Catalog# : 52004, Cas# : 273404-37-8)Belnacasan is a prodrug ofVRT-043198, a caspase-1 inhibitor that was developed by Ver
- BMS-1001 (Catalog# : 2062901, Cas# : 2113650-03-4)
- 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine (Catalog# : 2062328, Cas# : 1549360-60-2)
- 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine hydrochloride (Catalog# : 202327, Cas# : 1628263-43-3)
- 4-bromo-2-fluoro-1-propan-2-yloxybenzene (Catalog# : 2062316, Cas# : 202865-80-3)
- 1-bromo-4-propan-2-ylsulfonylbenzene (Catalog# : 2062315, Cas# : 70399-02-9)
- 5-(2,4-bis(benzyloxy)-5-isopropylphenyl)-N-ethyl-4-iodoisoxazole-3-carboxamide (Catalog# : 2062305, Cas# : 741414-22-8)
- 7-bromo-2-(1-methyl-1H-pyrazol-4-yl)-quinoxaline (Catalog# : 2062028, Cas# : 1083325-87-4)
- (3-bromoprop-1-en-2-yl)benzene (Catalog# : 2062001, Cas# : 3360-54-1)
- BW-A 78U (Catalog# : 2051512, Cas# : 101155-02-6)BW-A 78U is a PDE4 inhibitor with an IC50 of 3 μM.
- 9-bromo-2-hydroxy-7-methyl-4H-pyrido[1,2-a]pyrimidin-4-one (Catalog# : S-204156, Cas# : 663619-90-7)
- BB-Cl-Amidine (Catalog# : 204505, Cas# : 1802637-39-3)BB-Cl-Amidine is a Novel Therapeutic for Canine and Feline Mammary Cancer via Activat
- BAY-218 (Catalog# : 204301, Cas# : 2162982-11-6)BAY-218, also known as BAY-2335218, is a potent and selective small-molecule AhR inhi
- Blarcamesine ( AVex-73 ; AE-37 ) (Catalog# : 6111902, Cas# : 195615-83-9)ANAVEX2-73 (blarcamesine) is a Sigma-1 receptor agonist and muscarinic receptor modul
- (6bR,10aS)-2-oxo-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline-8-carboxylic acid ethyl ester (Catalog# : ITI007_2, Cas# : 313369-16-3)Sun-shine Chemical is a supplier Lumateperone and its intermediate from 100g scale to
Products Catalog
- ---- VEGFR
- ---- JAK
- ---- EGFR
- ---- PDGFR
- ---- FLT3
- ---- FGFR
- ---- Src
- ---- ALK
- ---- Syk
- ---- HIF
- -- Anti-infection
- ---- CMV
- ---- Filovirus
- ---- HBV
- ---- HCV
- ---- HIV
- ---- HSV
- ---- Influenza Virus
- ---- RSV
- ---- SARS-CoV
- ---- Antibacterial
- ---- Antifungal
- ---- Parasite
- -- Apoptosis
- ---- PD-1
- ---- PD-L1
- ---- Bcl-2
- ---- Caspase
- ---- TNF-alpha
- ---- Survivin
- ---- IAP
- ---- PERK
- ---- p53
- ---- Mdm2
- ---- E1/E2/E3 Enzyme
- -- Autophagy
- ---- LRRK2
- ---- CXCR
- ---- Autophagy
- -- Cell Cycle
- ---- CDK
- ---- PD-1
- ---- PD-L1
- ---- Chk
- ---- ROCK
- ---- PLK
- ---- APC
- ---- Wee1
- ---- DYRK
- ---- c-Myc
- ---- Aurora Kinase
- ---- ROCK inhibitor
- ---- Eukaryotic Initiation Factor (eIF)
- -- Cytoskeleton
- ---- HSP
- ---- Kinesin
- ---- Integrin
- ---- Dynamin
- ---- Wnt
- ---- β-catenin
- ---- Gap Junction Protein
- -- DNA Damage
- ---- PARP
- ---- DNA/RNA Synthesis
- ---- Sirtuin
- ---- Topoisomerase
- ---- DNA-PK
- ---- Telomerase
- ---- RAD51
- ---- HDAC
- ---- ATM
- ---- DNA alkylator
- ---- Mps1
- -- Epigenetics
- ---- PARP
- ---- JAK
- ---- Pim
- ---- PKC
- ---- PKD
- ---- Sirtuin
- ---- Histone Demethylase
- ---- Histone Acetyltransferase
- ---- HDAC
- ---- HIF-PH
- ---- Aurora Kinase
- ---- Histone Methyltransferase
- ---- METTL3
- ---- Epigenetic Reader Domain
- -- 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
- ---- Ras
- ---- Cholecystokinin Receptor
- ---- Melanocortin Receptor
- ---- RXFP Receptor
- ---- Bradykinin Receptor
- -- 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
- ---- Kallikrein
- ---- IRAK
- -- JAK/STAT
- ---- JAK
- ---- STAT
- ---- Pim
- ---- EGFR
- -- MAPK
- ---- MEK
- ---- Raf
- ---- p38 MAPK
- ---- ERK
- ---- MNK
- ---- Mixed Lineage Kinase
- ---- JNK
- ---- MAP4K
- -- 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
- ---- Proton Pump
- ---- Potassium Channel
- -- 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
- ---- Mitochondrial Metabolism
- ---- MAGL
- ---- Epoxide Hydrolase
- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- RAR/RXR
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- ---- Ketohexokinase(KHK)
- -- 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
- ---- Sigma Receptor
- ---- mAChR
- ---- α-Synuclein
- ---- Tau Protein
- ---- Cannabinoid Receptor
- ---- Transthyretin (TTR)
- ---- Melanocortin Receptor
- ---- Glucosylceramide Synthase (GCS)
- -- NF-κB
- ---- NF-κB
- ---- HDAC
- ---- IKK
- ---- Keap1-Nrf2
- -- 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
- ---- Bcr-Abl
- ---- FAK
- ---- RET
- ---- Phosphoglycerate Kinase (PGK)
- -- Proteases
- ---- Proteasome
- ---- Caspase
- ---- HIV Protease
- ---- MMP
- ---- γ-secretase
- ---- DPP4
- ---- Isocitrate Dehydrogenase (IDH)
- ---- FPTase
- ---- Acetyl-CoA Carboxylase
- ---- Glutaminase
- ---- Methionine Adenosyltransferase (MAT)
- ---- Lipase
- -- PI3K/Akt/mTOR
- ---- PI3K
- ---- Akt
- ---- GSK-3
- ---- S6 Kinase
- ---- AMPK
- ---- DNA-PK
- ---- MELK
- ---- PIKfyve
- ---- PI4K
- ---- PTEN
- ---- mTOR
- ---- ATM
- ---- PDK-1
- ---- ATR
- -- Stem Cells & Wnt
- ---- GSK-3
- ---- JAK
- ---- STAT
- ---- ROCK
- ---- TGF-beta/Smad
- ---- Wnt
- ---- γ-secretase
- ---- β-catenin
- ---- smo
- -- TGF-beta/Smad
- ---- PKC
- ---- ROCK
- ---- TGF-beta/Smad
- -- Ubiquitin
- ---- Proteasome
- ---- p97
- ---- Deubiquitinase
- ---- DUB
- -- Vitamin D Related
- ---- VD/VDR
- -- PROTAC
- ---- Molecular Glues
- ---- PROTACs
- -- Antibody-drug Conjugate/ADC Related
- -- Microbiology
- -- Others
- ---- PKK
- ---- Others modulator
- ---- Estrogen Receptor/ERR
- ---- ChoKα
- ---- Newest added products
- -- 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
- Dabogratinib ( TYRA-300 ) (Catalog# : 24073, Cas# : 2800223-30-5)Dabogratinib ( TYRA-300 ) is an Oral Selective FGFR3 Inhibitor (IC50 = 11 nM) for the
- AF710B (Catalog# : 25205, Cas# : N/A)AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1
- MAT2A inhibitor 5 (Catalog# : 25204, Cas# : 2957874-18-7)MAT2A inhibitor 5 has a high potency for inhibiting MAT2A and a remarkable selectivit
- (Rac)-AF710B (Catalog# : 24083, Cas# : 1235733-73-9)AF-710B is an agonist of sigma and M1 muscarinic receptors; AF710B is an enantiomer o
- Flurpiridaz-nonradiolabeled (Catalog# : 25203, Cas# : 863888-33-9)Flurpiridazis a promising novel cardiac PET imaging tracer formed by the radiolabelin
- Flurpiridaz-Precursor (Catalog# : 25202, Cas# : 863888-32-8)Flurpiridaz-Precursor in stock.
- KL1333 (Catalog# : 25201, Cas# : 1800405-30-4)KL1333 is an orally available, small organic molecule that reacts with NAD(P)H:quinon
- Palupiprant ( E7046 ) (Catalog# : 24055, Cas# : 1369489-71-3)E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece
- Oveporexton ( TAK-861 ) (Catalog# : 25194, Cas# : 2460722-04-5)Oveporexton isan oral small molecule selective orexin type-2 receptor (OX2R) agonist.
- VT-3989 (Catalog# : 25200, Cas# : 2506273-81-8)VT3989, a first-in-class potent oral TEAD palmitoylation inhibitor, disrupts YAP tran