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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
Proteases
Immunology & Inflammation
Vitamin D Related
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others
PROTAC
Building Blocks
Aldehydes
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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
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Ordering
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+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
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Services
Custom Synthesis
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Name Index S
SAR-020106
(Catalog# : 17031004, Cas# :
1184843-57-9
)
SAR-020106 is an ATP-competitive, potent, and selective CHK1 inhibitor with an IC50
SH5-07
(Catalog# : 17031002, Cas# :
1456632-41-9
)
SH5-07 is a robust hydroxamic acid-based STAT3 inhibitor, which induce antitumor ce
SUN11602
(Catalog# : 17030603, Cas# :
704869-38-5
)
SUN11602 is a novel aniline compound, which mimics the neuroprotective mechanisms of
Sardomozide HCl
(Catalog# : 17030306, Cas# :
138794-73-7
)
Sardomozide , also known as SAM486A or CGP48664, is a second-generation polyamine syn
Sacubitril sodium
(Catalog# : 17030108, Cas# :
149690-05-1
)
Sacubitril, also known as AHU377, is angiotensin receptor neprilysin inhibitor being
SHP099 free base
(Catalog# : 17030107, Cas# :
1801747-42-1
)
SHP099 is a potent, selective, orally bioavailable, and efficacious SHP2 inhibitor wi
Semagacestat
(Catalog# : 17022802, Cas# :
425386-60-3
)
Semagacestat (LY450139) is a -secretase blocker for A42, A40 and A38 with IC50 of 10.
(S)-Tedizolid
(Catalog# : 17021402, Cas# :
1431699-67-0
)
Tedizolid is the active moiety of the prodrug tedizolid phosphate, with high potency
STO-609
(Catalog# : 17021319, Cas# :
52029-86-4
)
STO-609 is a specific inhibitor of the Ca2+/Calmodulin-dependent protein kinase kina
S49076
(Catalog# : 17021309, Cas# :
1265965-22-7
)
S49076 is a novel, potent inhibitor of MET, AXL/MER, and FGFR1/2/3 with IC50 valu
SRT2183
(Catalog# : 17021306, Cas# :
1001908-89-9
)
SRT2183 is a small-molecule activator of the sirtuin subtype SIRT1, currently being
SW044248
(Catalog# : 17011714, Cas# :
522650-83-5
)
SW044248 is a potent and selective Topoisomerase I inhibitor. SW044248 killed approxi
Sugammadex sodium
(Catalog# : 17011713, Cas# :
343306-79-6
)
Sugammadex soidum is an agent for reversal of neuromuscular blockade by the agent roc
Streptozocin
(Catalog# : 17011712, Cas# :
18883-66-4
)
Streptozocin is a methylnitrosourea antineoplastic antibiotic isolated from the bacte
Sotagliflozin
(Catalog# : 17011711, Cas# :
1018899-04-1
)
Sotagliflozin, also known as LX4211, is an orally active and a dual SGLT1/SGLT2 inhib
Solithromycin
(Catalog# : 17011710, Cas# :
760981-83-7
)
Solithromycin, also known as CEM-101 and OP-1068, is a ketolide antibiotic undergoing
SMER28
(Catalog# : 17011709, Cas# :
307538-42-7
)
SMER28 is a small molecule modulator of autophagy, inducing autophagy independently o
SKF-38393 hydrochloride
(Catalog# : 17011707, Cas# :
62717-42-4
)
SKF-38393, aslo known as (+/-)-SKF-38393, is a synthetic compound of the benzazepine
Sitafloxacin anhydrous
(Catalog# : 17011706, Cas# :
127254-12-0
)
Sitafloxacin is a new-generation, broad-spectrum oral fluoroquinolone that is very ac
SHP099 HCl
(Catalog# : 17011704, Cas# :
1801747-11-4
)
SHP099 is a potent, selective, orally bioavailable, and efficacious SHP2 inhibitor wi
Shogaol (6-Shogaol)
(Catalog# : 17011703, Cas# :
555-66-8
)
Shogaol, also known as (6)-shogaol, is a pungent constituent of ginger similar in che
SGC707
(Catalog# : 17011702, Cas# :
1687736-54-4
)
SGC707 is a potent, selective and cell-active allosteric inhibitor of protein arginin
SC66
(Catalog# : 17011701, Cas# :
871361-88-5
)
SC66 is a novel and potent AKT inhibitor, which reduced cell viability in a dose- and
SBI0206965
(Catalog# : 71161, Cas# :
1884220-36-3
)
SBI0206965 is a potent and selective autophagy Kinase ULK1 Inhibitor. Many tumors bec
SB-743921 HCl
(Catalog# : 17011609, Cas# :
940929-33-9
)
SB-743921 is a synthetic small molecule with potential antineoplastic properties. SB-
Sardomozide
(Catalog# : 17011607, Cas# :
149400-88-4
)
Sardomozide , also known as SAM486A or CGP48664, is a second-generation polyamine syn
SAR407899 HCl
(Catalog# : 17011606, Cas# :
923262-96-8
)
SAR407899 is a potent and selective Rho kinase inhibitor with promising antihypertens
SAR131675
(Catalog# : 17011605, Cas# :
1092539-44-0
)
SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine
4SC-202
(Catalog# : 161227110, Cas# :
910462-43-0
)
4SC-202 is an orally bioavailable benzamide and inhibitor of human class I histone de
SKL2001
(Catalog# : 16122784, Cas# :
909089-13-0
)
SKL2001 is a novel agonist of the Wnt/-catenin pathway that disrupts the Axin/-cateni
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Products Catalog
Signaling Pathway
-- PI3K/Akt/mTOR
----
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
Inhibitors & Agonists
Intermediates
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
New Products
Natural Compounds
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