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+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
Metabolism
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NF-κB
Protein Tyrosine Kinase
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Cas Index 3
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Cas Index 3
382180-17-8 | Pyroxamide
(Catalog# : 121802)
Pyroxamide is a synthetic derivative of hydroxamic acid with antineoplastic propertie
3022-15-9 | Piperazine-2-carboxylic acid dihydrochloride
(Catalog# : 81814)
Coming soon!
30195-30-3 | Ro5-3335
(Catalog# : 20460)
Ro5-3335 is a lipophilic small molecule RUNX1 inhibitor.
361185-42-4 | RBC8
(Catalog# : 19313)
RBC8 is a RalA and RalB GTPase inhibitor (EC50 ~3.5 μM). RBC8 suppresses growth of x
313348-27-5 | Regadenoson
(Catalog# : 1810224)
Regadenoson is an A2A adenosine receptor agonist that is a coronary vasodilator that
359625-79-9 | Roluperidone ( CYR-101 )
(Catalog# : 2017889)
Roluperidone, also known as MIN-101, CYR-101, and MT-210, is a 5-HT2A and sigma 2 rec
334969-03-8 | Recilisib sodium
(Catalog# : 17022712)
Recilisib, also known as ON 01210.Na, is a radioprotectant, which modifys cell cycle
37854-59-4 | Ro 08-2750
(Catalog# : 17011602)
Ro 08-2750 is a potent and selective Nerve growth factor (NGF) inhibitor that binds t
328023-11-6 | Rbin-1
(Catalog# : 1710902)
Rbin-1(ribozinoindole-1) is a potent chemical inhibitor of eukaryotic ribosome assemb
390362-78-4 | RHPS4
(Catalog# : 6111024)
RHPS4 is a potent inhibitor of Telomerase at submicromolar.
312756-74-4 | RS-1
(Catalog# : 16061501)
4-BroMo-N-(4-broMophenyl)-3-[[(phenylMethyl)aMino]sulfonyl]benzaMide;RAD51-stimulator
321429-49-6 | (R)-1-(3-Fluorophenyl)ethylamine Hydrochloride
(Catalog# : 90725)
Coming soon!
334618-23-4 | (3R)-piperidin-3-amine,dihydrochloride
(Catalog# : 83126)
Coming soon!
33375-06-3 | (R)-(+)-1-Phenylethyl isocyanate
(Catalog# : 82717)
Coming soon!
3026272-26-1 | Seladelpar sodium salt
(Catalog# : 25063)
Seladelpar is a PPAR-delta agonist.
3036109-10-8 | SDU-071
(Catalog# : 25059)
SDU-071 is a potent and orally active inhibitor of BRD4-p53 inhibitor. SDU-071 suppre
3029695-07-3 | SMU-L11
(Catalog# : 24090)
303126-97-8 | SR-0987
(Catalog# : 1810263)
SR-0987 is a T cell-specific RORγ (RORγt) agonist. SR-0987 induces IL-17 expression
307543-71-1 | STF-083010
(Catalog# : 185151)
STF-083010, also known as IRE1 Inhibitor I, is an inhibitor of the IRE1/XBP1 pathway.
343306-79-6 | Sugammadex sodium
(Catalog# : 17011713)
Sugammadex soidum is an agent for reversal of neuromuscular blockade by the agent roc
307538-42-7 | SMER28
(Catalog# : 17011709)
SMER28 is a small molecule modulator of autophagy, inducing autophagy independently o
312636-16-1 | SKI II
(Catalog# : 6111526)
SKI-II is a synthetic inhibitor of sphingosine kinase (SK) activity with IC50 of 78 M
305834-79-1 | SC79
(Catalog# : 161009025)
Akt Activator II, SC79, CAS 305834-79-1, is a cell-permeable compound that interacts
380899-24-1 | SB-649868
(Catalog# : 011815)
Coming soon!
379231-04-6 | Saracatinib
(Catalog# : 122913)
Saracatinib is an orally available 5-, 7-substituted anilinoquinazoline with anti-inv
356559-20-1 | SB 525334
(Catalog# : 102205)
SB 525334 is a potent and selective inhibitor of TGF_beta_ receptor I (ALK5) with IC5
321429-48-5 | (1S)-1-(3-fluorophenyl)ethanamine,hydrochloride
(Catalog# : 90726)
Coming soon!
325145-35-5 | (S)-1-Boc-2-Ethylpiperazine
(Catalog# : 81901)
Coming soon!
314741-40-7 | (S)-1-Boc-3-(Hydroxymethyl)piperazine
(Catalog# : 81825)
Coming soon!
330161-87-0 | SU6656
(Catalog# : 52754)
SU 6656 is a selective inhibitor of Src kinases, Including Src, Yes, Lyn, and Fyn (IC
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Products Catalog
Signaling Pathway
-- Angiogenesis
----
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)
-- 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
-- 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
-- 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
----
Kallikrein
----
IRAK
-- 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
----
Potassium Channel
-- 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
----
Mitochondrial Metabolism
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Ketohexokinase(KHK)
-- 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)
-- 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)
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
----
Lipase
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- 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
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
1820812-16-5 | TAK-071
(Catalog# : 186269)
TAK-071 is a muscarinic M1 receptor positive allosteric modulator.
2750895-97-5 | MTX115325
(Catalog# : 186264)
MTX115325 is a potent, selective, brain-penetrant USP30 inhibitor with good drug-like
2166616-75-5 | LY-3381916
(Catalog# : 193123)
LY-3381916 is a potent, selective and brain penetrated inhibitor of IDO1 activity, bi
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim (BHV-7000) is an oral, small-molecule activator of Kv7.2/7.3 potassium chann
2488609-21-6 | DS68591889
(Catalog# : 25158)
DS68591889 (PTDSS1i) specifically inhibits PTDSS1, which catalyzes serine incorporati
944808-88-2 | CAY 10566
(Catalog# : 10403)
CAY 10566 is a potent selective SCD-1 inhibitor.
2308520-97-8 | Cadefrecitinib (GLPG-3667)
(Catalog# : 20509)
Cadefrecitinib (GLPG-3667) is an oral, small molecule inhibitor of the TYK2 kinase in
1802735-28-9 | QBS10072S
(Catalog# : 25190)
QBS10072S isa blood-brain-barrier (BBB) penetrative agent composed of a cytotoxic che
2377000-84-3 | Dencatistat
(Catalog# : 25177)
Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
1898207-64-1 | DS-1001b
(Catalog# : 25178)
DS-1001 is an oral brain-penetrant mutant IDH1 selective inhibitor.