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
Name Index N
- N,N-DIETHYL-2,6-CIS-DIMETHYLPIPERIDINIUM IODIDE (Catalog# : G20383, Cas# : 1335241-44-5)
- Navoximod free base (Catalog# : 20290, Cas# : 1402837-78-8 (free base))
- NE 52-QQ57 (Catalog# : 21233, Cas# : 1401728-56-0)NE52-QQ57 is an orally available GPR4 antagonist with an IC50 of 70 nM. NE 52-QQ57 si
- NVS-PAK1-1 (Catalog# : 21231, Cas# : 1783816-74-9)NVS-PAK1-1 is a a specific allosteric PAK1 inhibitor.
- Niraparib tosylate hydrate (Catalog# : 2021115, Cas# : 1613220-15-7)Niraparib, also know as MK-4827, is an inhibitor of poly (ADP-ribose) polymerase (PAR
- N-(8-Benzyl-8-azabicyclo[3.2.1]oct-3-yl-exo)-2-methylpropanamide (Catalog# : 2071632, Cas# : 376348-67-3)
- NCC007 (Catalog# : 2071529)NCC007 is a novel CKIα and CKIδ dual inhibitor. NCC007 that showed stronger period
- N-tert-butyl-3-[(2-chloro-5-methylpyrimidin-4-yl)amino]benzenesulfonamide (Catalog# : 2062304, Cas# : 936092-53-4)
- N,N-dibenzyl-6-chloro-5-nitropyrimidine-4-amine (Catalog# : 2062033, Cas# : 882272-97-1)
- N-(3,5-dimethoxyphenyl)-3-(1-methyl-1H-pyrazol-4-yl)quinoxalin-6-amine (Catalog# : 2062032, Cas# : 1346133-39-8)
- N-(2-methylbenzyl)-4,5-dihydro-1H-imidazol-2-amine (Catalog# : 2062031, Cas# : 38941-29-6)
- 5-(N-PHTHALIMIDO)-2-PENTANONE (Catalog# : 2062010, Cas# : 3197-25-9)
- N-Fmoc-O-[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-α-D-galactopyranosyl]-L-serine (Catalog# : 2061601, Cas# : 120173-57-1)
- NTP42 (Catalog# : 2051509, Cas# : 2055599-51-2)NTP42 is a novel antagonist of the thromboxane prostanoid receptor (TP), currently in
- N-tert-butyloxycarbonyl-pyrrole (Catalog# : S-204153, Cas# : 5176-27-2)
- N-(4-PENTYNYL)PHTHALIMIDE 97 (Catalog# : S-204150, Cas# : 6097-07-0)
- N-benzyl-2,4-dichloropyrimidine-5-carboxamide (Catalog# : 197101, Cas# : 1019115-13-9)
- NVS-ZP7-4 (Catalog# : 204506, Cas# : 2349367-89-9 (free base))NVS-ZP7-4 is a potent ZIP7 Inhibitor, which inhibits Notch signaling with IC50 of 0.1
- NVP-2 (Catalog# : 193205, Cas# : 1263373-43-8)NVP-2 is an inhibitor of the cyclin-dependent kinase, CDK9.
- NS-1652 (Catalog# : 19361, Cas# : 1566-81-0)NS-1652 is an anion conductance inhibitor.
- NCT-506 (Catalog# : 19354, Cas# : 2231098-99-8)NCT-506 is an orally bioavailable aldehyde dehydrogenase 1A1 (ALDH1A1) inhibitors wit
- Nelotanserin (Catalog# : 191121, Cas# : 839713-36-9)Nelotanserin(APD125) is a potent and selective human 5-hydroxytryptamine2A inverse ag
- ND-646 (Catalog# : 191102, Cas# : 1434639-57-2)ND-646 is-an allosteric inhibitor of the ACC enzymes ACC1 and ACC2 that prevents ACC
- ND-630 (Catalog# : 19133, Cas# : 1434635-54-7)ND-630, also known as GS-0976, NDI-010976, and firsocostat, is a potent ACC inhibitor.
- Naquotinib free base (Catalog# : 1812297, Cas# : 1448232-80-1)Naquotinib, also known as ASP8273, is an orally available, irreversible, third-genera
- N6022 (Catalog# : 1811304, Cas# : 1208315-24-5)N6022 is a potent, selective, reversible, and efficacious S-nitrosoglutathione reduct
- Nexinhib20 (Catalog# : 1811152, Cas# : 331949-35-0)Nexinhib20 is a Rab27 inhibitor that inhibits neutrophil exocytosis and is active in
- NGI-1 (Catalog# : 181171, Cas# : 790702-57-7)NGI-1, also knowns ML414, is a a cell-permeable inhibitor of oligosaccharyltransferas
- NMS-E973 (Catalog# : 1810293, Cas# : 1253584-84-7)NMS-E973 is a novel, selective and potent inhibitor of heat shock protein 90 (Hsp90).
- NCT-505 (Catalog# : 1810261, Cas# : 2231079-74-4)NCT-505 is an Orally Bioavailable aldehyde Dehydrogenase 1A1 (ALDH1A1) Inhibitor with
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
- -- 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)
- -- 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
- DPTX-3186 (Catalog# : 26A010, Cas# : 3118994-80-9)DPTX3186, an orally administered small molecule condensate modulator (c-mod) inhibiti
- Avasopasem manganese (GC-4419; M-40419) (Catalog# : 25108, Cas# : 435327-40-5)Avasopasem manganese, also known as GC-4419; M 40419 and SC-72325A, is amimetic of th
- Iclepertin (BI-425809) (Catalog# : 24084, Cas# : 1421936-85-7)Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
- Kartogenin ( KGN ) (Catalog# : 52215, Cas# : 4727-31-5)Kartogenin (KGN) is a synthetic small molecule that stimulates chondrogenic cellular
- Imisopasem manganese ( M40403; GC4403 ) (Catalog# : 72602, Cas# : 218791-21-0)Imisopasem manganese ( M40403; GC4403 ) is a stable non-peptidyl mimetic of MnSOD tha
- Apecotrep (BI 764198) (Catalog# : 26A048, Cas# : 2311863-36-0)Apecotrep (BI 764198) is a potential first-in-class, oral, selective TRPC6 inhibitor.
- Pantothenate kinase-IN-2 (Catalog# : 26A038, Cas# : 902614-04-4)Pantothenate kinase-IN-2 is a pantothenate kinase inhibitor with IC50 values of 92 nM
- BH-30643 (Catalog# : 26A047, Cas# : 3062177-59-4)BH-30643 is a novel, orally available, non-covalent, macrocyclic, mutant selective OM
- Gridegalutamide (Catalog# : 26A044, Cas# : 2446929-86-6)gridegalutamide is an orally bioavailable androgen receptor (AR) degrader, with poten
- BMS-986365 (Synonyms: CC-94676 ) (Catalog# : 25138, Cas# : 2446928-30-7)BMS-986365, also known as CC-94676, is an orally bioavailable androgen receptor (AR)