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
- 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 S
- Siramesine hydrochloride (Catalog# : 52549, Cas# : 224177-60-0)Siramesine(Lu 28-179) Hcl is a selective sigma-2 receptor agonist, which has been sho
- Siramesine (Catalog# : 52548, Cas# : 147817-50-3)Siramesine(Lu 28-179) is a selective sigma-2 receptor agonist, which has been shown t
- S1RA (Catalog# : 52546, Cas# : 878141-96-9)S1RA(E-52862) is a potent and selective sigma-1 receptor(1R, Ki=17 nM) antagonist, sh
- SMI-4a (Catalog# : 52537, Cas# : 438190-29-5)SMI-4a is a selective ATP-competitive Pim-1 kinase inhibitor with an IC50 of 21 nM fo
- SKLB610 (Catalog# : 52536, Cas# : 1125780-41-7)SKLB610, a novel multi-targeted inhibitor, inhibits angiogenesis-related tyrosine kin
- StemRegenin 1 (Catalog# : 52531, Cas# : 1227633-49-9)StemRegenin 1(SR1) is an antagonist of the aryl hydrocarbon receptor.SR1 is the first
- S0859 (Catalog# : 52507, Cas# : 1019331-10-2)S0859, an N-cyanosulphonamide compound, reversibly inhibit NBC-mediated pH(i) recover
- SRPIN340 (Catalog# : 52210, Cas# : 218156-96-8)SRPIN340 is a serine/arginine-rich protein kinase (SRPK)-specific inhibitor with an I
- 5S rRNA modificator (Catalog# : 52243, Cas# : 1415238-77-5)5S rRNA modificator is a suitable electrophile for 2-hydroxyl acylation on structured
- SB431542 (Catalog# : 52312, Cas# : 301836-41-9)SB431542 is a potent and selective inhibitor ofALK5withIC50of 94 nM, 100-fold more se
- Salirasib (Catalog# : 52106, Cas# : 162520-00-5)Salirasib(S-Farnesylthiosalicylic aci) is an S-farnesyl cysteine analog that interfer
- SNS-032 ( BMS-387032 ) (Catalog# : 52105, Cas# : 345627-80-7)SNS-032 has firstly been described as a selective inhibitor ofCDK2withIC50of 48 nM an
- SNS-314 Mesylate (Catalog# : 52102, Cas# : 1057249-41-8)SNS-314 Mesylate is a potent and selective inhibitor ofAurora A,Aurora BandAurora Cwi
- Semaxanib (SU5416) (Catalog# : 51803, Cas# : 204005-46-9)Semaxanib (SU5416) is a potent and selectiveVEGFR(Flk-1/KDR) inhibitor withIC50of 1.2
- SSR128129E (Catalog# : 51608, Cas# : 848318-25-2)SSR128129E is an orally-active and allostericFGFR1inhibitor withIC50of 1.9 M, while n
- SRT1720 (Catalog# : 52007, Cas# : 1001645-58-4)SRT1720 is a selectiveSIRT1activator withEC50of 0.16 M, but is >230-fold less pote
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
- -- 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
- STX-478 (Catalog# : 20633, Cas# : 2883540-92-7)STX-478 is a second generation, mutant-selective, oral PI3Ka small molecule allosteri
- Iclepertin (BI-425809) (Catalog# : 24084, Cas# : 1421936-85-7)Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
- Bomedemstat (Catalog# : 24001, Cas# : 1990504-34-1)Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl
- PLX-4545 (Catalog# : 24111, Cas# : 2892065-45-9)PLX-4545 is an orally bioavailable molecular glue degrader of IKZF2 designed to desta
- VVD-130037 ( BAY-3605349 ) (Catalog# : 24110, Cas# : 3034880-93-5)VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
- CBR-5884 (Catalog# : 24109, Cas# : 681159-27-3)CBR 5884 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor which was able to inhi
- JHU-083 (Catalog# : 24108, Cas# : 1998725-11-3)JHU-083 selectively blocks glutaminase activity in brain CD11b+ cells and prevents de
- LXH-3-71 (Catalog# : 24107, Cas# : 2251753-65-6)LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH
- CC-92480 ( Mezigdomide ) (Catalog# : 20510, Cas# : 2259648-80-9)CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno
- Adrixetinib ( Q-702 ) (Catalog# : 20617, Cas# : 2394874-66-7)Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag