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
- Metabolic Enzyme/Protease
- Neuronal Signaling
- NF-κB
- Protein Tyrosine Kinase
- PI3K/Akt/mTOR
- Stem Cells & Wnt
- TGF-beta/Smad
- Ubiquitin
- Vitamin D Related
- PROTAC
- Antibody-drug Conjugate/ADC Related
- Microbiology
- Others
- Nuclear Receptor
- 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
Cas Index 1
- 1075705-01-9 | 4-fluoro-2-Methoxy-5-nitroaniline (Catalog# : 521191)AZD9291 drug intermediate-1
- 125802-18-8 | 1-(3-Fluorophenyl)-cyclohexanamine HCl (Catalog# : 178221)1-(3-Fluorophenyl)-cyclohexanamine HCl
- 13311-84-7 | Flutamide (Catalog# : 16123001)Flutamide, also known as SCH13521, is a toluidine derivative and nonsteroidal antiand
- 1637735-84-2 | FIIN-3 (Catalog# : 16122945)FIIN-3 is a potent, selective, irreversible and the next-generation covalent FGFR inh
- 1708971-72-5 | FGFR4-IN-1 (Catalog# : 16122813)FGFR4-IN-1 is a potent and selective FGFR4 inhibitor. FGFR4 may be a novel therapeuti
- 108409-83-2 | FH535 (Catalog# : 16122788)FH535 is a Wnt/-catenin signaling inhibitor and also a dual PPAR and PPAR antagonist.
- 1226895-15-3 | FLLL32 (Catalog# : 16122709)FLLL32 is a potent JAK2/STAT3 inhibitor with IC50 of <5 M.In MDA-MB-231 breast and
- 1633044-56-0 | FIIN-2 (Catalog# : 16062117)FIIN-2 is a potent, selective, irreversible and the next-generation covalent FGFR inh
- 196612-93-8 | Falnidamol (Catalog# : 122807)Falnidamol is a pyrimido-pyrimidine with antitumor activity.
- 154540-49-5 | Fluoroclebopride (Catalog# : 120811)Coming soon!
- 167933-07-5 | Flibanserin (Catalog# : 101906)Flibanserin is a full agonist of the 5-HT1A receptor (Ki = 1 nM) and, with lower affi
- 146137-76-0 | 2-Fluoro-5-iodobenzaldehyde (Catalog# : 91818)Coming soon!
- 1250921-20-0 | 3-Fluoro-2-(methylamino)benzoic acid (Catalog# : 91805)Coming soon!
- 1643-26-1 | 3-(2-Fluorophenyl)propionic acid (Catalog# : 90609)Coming soon!
- 138423-98-0 | 3-Formylindol-1-yl-Acetic Acid (Catalog# : 81944)Coming soon!
- 1481-32-9 | 6-Fluoro-1-indanone (Catalog# : 81933)Coming soon!
- 1286739-19-2 | FRAX597 (Catalog# : 72803)FRAX597 inhibits the proliferation of NF2-deficient schwannoma cells in culture and d
- 116686-15-8 | FK 3311 (Catalog# : 60203)FK 3311 is a selective inhibitor of COX-2; antiinflammatory agent.
- 131740-09-5 | Flavopiridol(Alvocidib) (Catalog# : 52310)Flavopiridol HCl competes with ATP to inhibit CDKs includingCDK1,CDK2,CDK4andCDK6with
- 1206161-97-8 | Filgotinib (Catalog# : 51612)Filgotinib (GLPG0634) is a selective JAK1 inhibitor with IC50 of 10 nM, 28 nM, 810 nM
- 1345982-69-5 | GSK-2330672 (Catalog# : 25082)GSK-2330672, also known as linerixibat, is highly potent, nonabsorbable apical sodium
- 1191044-58-2 | GSK1059865 (Catalog# : 24131)GSK1059865 is a potent orexin 1 receptor antagonist.
- 1637394-01-4 | GDC-0134 (Catalog# : 20432)GDC-0134 is a MAP3K12 (DLK) Inhibitor.
- 1260907-17-2 | GSK 525762A (Catalog# : 171459)
- 133052-90-1 | GF-109203X (Catalog# : L20356)GF-109203X is a potent and highly selective PCK inhibitor, which inhibits PKC isozyme
- 1258292-64-6 | GDC-046 (Catalog# : L20342)GDC-046 is a potent, selective, and orally bioavailable TYK2 inhibitor for TYK2, JAK1
- 1831144-46-7 | GDC-0214 (Catalog# : c20341)iJak-381 is a highly potent, selective, and inhalable Janus kinase-1 (JAK-1) inhibito
- 106740-09-4 | GYY4137 (Catalog# : L20339)GYY4137 is a novel water-soluble and slow releasing H2S donor. Hydrogen sulfide (H2S)
- 1139889-93-2 | Golgicide A (Catalog# : 20292)Golgicide A is a Potent, selective and reversible inhibitor of GBF1 ArfGEF. Golgicide
- 113852-41-8 | GS 0573 ( PMEDAP ) (Catalog# : 20275)GS 0573 is an antiviral compound that has been studied for potential treatment of Fel
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)
- ---- NEKs
- -- 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
- ---- Methionine Adenosyltransferase (MAT)
- -- 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
- ---- GLP Receptor
- ---- SSTR
- -- Immunology & Inflammation
- ---- PD-1
- ---- PD-L1
- ---- COX
- ---- CCR
- ---- Histamine Receptor
- ---- TLR
- ---- CXCR
- ---- MALT
- ---- TDO
- ---- NOS
- ---- IDO
- ---- Thrombopoietin Receptor(TPO)
- ---- NLR inhibitor
- ---- Interleukin Related
- ---- CD73
- ---- Complement System
- ---- Aryl Hydrocarbon Receptor
- ---- Kallikrein
- ---- IRAK
- ---- Reactive Oxygen Species(ROS)
- ---- SOD
- -- 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
- -- Metabolic Enzyme/Protease
- ---- PPAR
- ---- Proteasome
- ---- P450
- ---- Caspase
- ---- HSP
- ---- HIV Protease
- ---- PDE
- ---- MMP
- ---- Factor Xa
- ---- γ-secretase
- ---- Phospholipase
- ---- DPP4
- ---- FAAH
- ---- CETP
- ---- Lipoxygenase
- ---- HMG-CoA Reductase
- ---- Fatty Acid Synthase
- ---- NADPH-oxidase
- ---- FXR
- ---- NAMPT
- ---- TDO
- ---- Carbonic Anhydrase
- ---- Monoamine Oxidase
- ---- IDO
- ---- Mitochondrial Metabolism
- ---- Isocitrate Dehydrogenase (IDH)
- ---- MAGL
- ---- Epoxide Hydrolase
- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- FPTase
- ---- RAR/RXR
- ---- Acetyl-CoA Carboxylase
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- ---- Glutaminase
- ---- Ketohexokinase(KHK)
- ---- Lipase
- ---- Lactate dehydrogenase
- ---- Glyoxalase (GLO)
- ---- E1/E2/E3 Enzyme
- ---- PANK(pantothenate kinase)
- ---- Phosphoglycerate Dehydrogenase (PHGDH)
- ---- Hemoglobin
- -- 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)
- ---- CGRP-Receptor
- ---- TRP-Channel
- -- 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)
- -- PI3K/Akt/mTOR
- ---- PI3K
- ---- Akt
- ---- GSK-3
- ---- S6 Kinase
- ---- AMPK
- ---- DNA-PK
- ---- MELK
- ---- PIKfyve
- ---- PI4K
- ---- PTEN
- ---- mTOR
- ---- ATM
- ---- PDK-1
- ---- ATR
- ---- Vps34
- -- Stem Cells & Wnt
- ---- GSK-3
- ---- JAK
- ---- STAT
- ---- ROCK
- ---- TGF-beta/Smad
- ---- Wnt
- ---- γ-secretase
- ---- β-catenin
- ---- smo
- ---- Notch
- -- 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
- -- Nuclear Receptor
- ---- Androgen Receptor(AR)
- -- 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
- 1429882-07-4 | MRX-2843 (Catalog# : 26A087)MRX-2843 is an orally bioavailable inhibitor of two receptor tyrosine kinases (RTKs),
- 1637394-01-4 | GDC-0134 (Catalog# : 20432)GDC-0134 is a MAP3K12 (DLK) Inhibitor.
- 2128698-24-6 | BI-847325 (Catalog# : 25046)BI-847325 is a novel, ATP-competitive, orally available inhibitor of Aurora kinases a
- 3137699-54-5 | GDD-261 (Catalog# : 26A084)GDD-261 is an orally active, allosteric inhibitor of phosphoglycerate dehydrogenase (
- 2669009-92-9 | Atebimetinib (Catalog# : 25148)Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1
- 3062177-59-4 | BH-30643 (Catalog# : 26A047)BH-30643 is a novel, orally available, non-covalent, macrocyclic, mutant selective OM
- 2490431-16-6 | ERAS-801 ( JGK-068S ) (Catalog# : 20635)ERAS-801 ( JGK-068S ) is a potent EGFR inhibitor.
- 877176-23-3 | Aderamastat ( Synonyms: FP-025 ) (Catalog# : 26A086)Aderamastat (FP-025) is an oral, selective, non-hydroxamate-based, non-competitive in
- 1857296-22-0 | 5-Formyl-4-methyl-1H-indole-2-carbonitrile (Catalog# : 25095)
- 2923986-48-3 | MAT2A inhibitor-[Compound 1] (Catalog# : 26A083)Compound 1 is a new MAT2A inhibitor.