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- 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
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Name Index S
- (S)-Benzyl 2-(aminomethyl)pyrrolidine-1-carboxylate (Catalog# : 90108, Cas# : 141774-68-7)Coming soon!
- (S)-N-Boc-Pyrrolidine-3-Carboxylic Acid (Catalog# : 83127, Cas# : 140148-70-5)Coming soon!
- (S)-1-Boc-3-Aminomethylpyrrolidine hydrochloride (Catalog# : 83120, Cas# : 916214-30-7)Coming soon!
- (S)-3-Amino-1-N-Boc-piperidine (Catalog# : 83119, Cas# : 625471-18-3)Coming soon!
- Solcitinib (Catalog# : 82803, Cas# : 1206163-45-2)Solcitinib is a Janus kinase 1 (JAK1) inhibitor, which may be potential useful for tr
- (2S,4S)-1-(2-chloroacetyl)-4-fluoropyrrolidine-2-carbonitrile (Catalog# : 82714, Cas# : 596817-06-0)Coming soon!
- Sitagliptin phosphate (Catalog# : 82607, Cas# : 654671-78-0)Sitagliptin phosphate(MK 0431 phosphate) is a potent inhibitor of DPP4 with IC50 of 1
- SW033291 (Catalog# : 81945, Cas# : 459147-39-8)SW033291 is a small-molecule inhibitor of 15-PGDH (Ki=0.1 nM) that increases prostagl
- (S)-1-Boc-2-Isopropylpiperazine (Catalog# : 81902, Cas# : 674792-05-3)Coming soon!
- (S)-1-Boc-2-Ethylpiperazine (Catalog# : 81901, Cas# : 325145-35-5)Coming soon!
- (S)-tert-Butyl 2-isobutylpiperazine-1-carboxylate (Catalog# : 81830, Cas# : 674792-06-4)Coming soon!
- (S)-1-Boc-2-Propylpiperazine (Catalog# : 81829, Cas# : 888972-67-6)Coming soon!
- (S)-1-Boc-(2-Hydroxymethyl)piperazine (Catalog# : 81828, Cas# : 1030377-21-9)Coming soon!
- (S)-1-Boc-3-(Hydroxymethyl)piperazine (Catalog# : 81825, Cas# : 314741-40-7)Coming soon!
- (S)-Piperazin-2-ylmethanol dihydrochloride (Catalog# : 81823, Cas# : 149629-73-2)Coming soon!
- (2S)-4-[(2-methylpropan-2-yl)oxycarbonyl]piperazine-2-carboxylic acid (Catalog# : 81816, Cas# : 848482-93-9)Coming soon!
- (S)-Benzyl 2-methylpiperazine-1-carboxylate hydrochloride (Catalog# : 81813, Cas# : 1217720-49-4)Coming soon!
- (S)-4-N-Boc-2-methylpiperazine (Catalog# : 81731, Cas# : 147081-29-6)Coming soon!
- (S)-Piperazine-2-carboxylic acid dihydrochloride (Catalog# : 81718, Cas# : 158663-69-5)Coming soon!
- (1S)-1-(4-chloro-3-methylphenyl)ethanamine (Catalog# : 81017, Cas# : 943760-74-5)Coming soon!
- (1S)-1-(4-fluoro-3-methoxyphenyl)ethanamine (Catalog# : 81015, Cas# : 870849-59-5)Coming soon!
- SR9243 (Catalog# : 80701, Cas# : 1613028-81-1)SR9243 is a LXR inverse agonist that induces LXR-corepressor interaction, which shows
- Sapitinib(AZD8931) (Catalog# : 60301, Cas# : 848942-61-0)AZD8931(Sapitinib)is a novel potent reversible small molecule epidermal growth factor
- SU6656 (Catalog# : 52754, Cas# : 330161-87-0)SU 6656 is a selective inhibitor of Src kinases, Including Src, Yes, Lyn, and Fyn (IC
- SBE13 Hydrochloride (Catalog# : 52751, Cas# : 1052532-15-6)SBE13 Hcl is a potent and selective PLK1 with IC50 of 0.2 nM; no inhibition om Aurora
- SGI-1027 (Catalog# : 52737, Cas# : 1020149-73-8)SGI-1027 is a potent and selective inhibitor of DNA methyltransferase (DNMT) with IC5
- SB225002 (Catalog# : 52714, Cas# : 182498-32-4)SB225002 is a potent and selective non-peptide inhibitor of CXCR2 with IC50 of 22 nM;
- SU9516 (Catalog# : 52579, Cas# : 377090-84-1)SU-9516 is a selective CDK2 inhibtor with IC50 of 22 nM; less potent for CDK1/CDK4(IC
- SCH900776 (Catalog# : 52575, Cas# : 891494-63-6)SCH900776 is a potent, selective and orally bioavailable inhibitor of checkpoint kina
- Selumetinib (Catalog# : 52571, Cas# : 606143-52-6)Selumetinib (AZD6244; ARRY-142886) is a potent, highly selective MEK1 inhibitor with
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