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MAPK
Cytoskeletal Signaling
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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
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others
PROTAC
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Cas Index 1
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Cas Index 1
1443530-05-9 | Rogaratinib
(Catalog# : 192277)
Rogaratinib, also known as BAY-1163877, is an aberrant fibroblast growth factor recep
1342276-76-9 | RKI-1313
(Catalog# : 19183)
RKI-1313 Negative control for RKI-1447 (GLXC-05200) which is a potent inhibitor of th
1187075-34-8 | Resminostat HCl
(Catalog# : 185317)
Resminostat HCl is a potent inhibitor of HDAC1/3/6.
1454288-88-0 | Rovazolac
(Catalog# : 185234)
Rovazolac is an anti-inflammatory drug candidate.
189744-46-5 | RO10-5824
(Catalog# : 185141)
RO10-5824 is a D4-selective partial agonist. RO10-5824 is a potent candidate for the
117086-68-7 | Ricasetron
(Catalog# : 184281)
Ricasetron, also known as Brl 46470, is antiemetic and axiolytic.
1289023-67-1 | Rimegepant
(Catalog# : 18441)
Rimegepant, aslo known as BMS-927711, is a potent, selective, competitive and orally
1792180-81-4 | Ritlecitinib ( PF-06651600 )
(Catalog# : 18435)
Ritlecitinib ( PF-06651600 ) is a potent and selective JAK3 inhibitor. PF-06651600, a
1174018-99-5 | Relebactam
(Catalog# : 1712156)
Relebactam,也称为MK- 7655,一个强有力的、具有选择性的β-lactamase抑制
158681-13-1 | Rimonabant HCl
(Catalog# : 179137)
Rimonabant, also known as SR141716, is an anorectic anti-obesity drug. It is an inver
147254-64-6 | Ranirestat
(Catalog# : 178118)
Ranirestat, also known as AS-3201; SX-3201, is an aldose reductase inhibitor being de
1449598-06-4 | RG7800 ( RO6885247 )
(Catalog# : 174192)
RG7800(RO6885247) is a small molecule modifier of survival motor neuron 2 splicing.
1628838-42-5 | RAF709
(Catalog# : 17030605)
RAF709 is a Raf kinase inhibitor.
1211443-80-9 | Ribociclib HCl
(Catalog# : 17011305)
Ribociclib hydrochloride is an potent and orally available cyclin-dependent kinase (C
112887-68-0 | Raltitrexed
(Catalog# : 17011303)
Raltitrexed, also known as ZD 1694, is an antimetabolite drug used in treatment of co
150812-13-8 | Retigabine 2HCl
(Catalog# : 17011108)
Retigabine is a novel anticonvulsant with activity in a broad range of seizure models
1446790-62-0 | RO9021
(Catalog# : 17109007)
RO9021 potently inhibits SYK kinase activity with an average IC50 of 5.6 nM and suppr
1043797-53-0 | RU-SKI 43
(Catalog# : 6111503)
RU-SKI 43 is a small molecule inhibitor of Hhat(Hedgehog acyltransferase), the enzyme
1070773-09-9 | RK-33
(Catalog# : 611909)
RK-33 is an RNA helicase inhibitor against DDX3, and inhibit its helicase activity.RK
1309684-94-3 | RO8994
(Catalog# : 1673101)
RO8994 is a potent and selective spiroindolinone MDM2 inhibitor for cancer therapy.
1219810-16-8 | RSL 3
(Catalog# : 16070103)
RSL 3
127500-84-9 | Ro41-1049(HCl)
(Catalog# : 166154)
Ro 41-1049 is an inhibitor of the enzyme monoamine oxidase type A(MAO-A).
138489-18-6 | RO31-8220 mesylate
(Catalog# : 16060303)
Ro 31-8220 is a PKC-inhibitor, which inhibits stimulated fluid pinocytosis of human P
150725-87-4 | Ro 46-2005
(Catalog# : 031001)
Ro 46-2005 is a novel synthetic non-peptide endothelin receptor antagonist, inhibits
1182367-47-0 | RAD140
(Catalog# : 030909)
Coming soon!
169758-66-1 | Robalzotan tartrate hydrate
(Catalog# : 011907)
Coming soon!
1037624-75-1 | R428
(Catalog# : 123010)
R428 is a potent and selective small-molecule inhibitor(IC50=14 nM), blocks the activ
1303533-81-4 | Ravidasvir hydrochloride
(Catalog# : 122904)
Ravidasvir is a second-generation, orally active, potent and selective HCV NS5A prote
162011-90-7 | Rofecoxib
(Catalog# : 122837)
Rofecoxib is a synthetic, nonsteroidal derivative of phenyl-furanone with antiinflamm
1622921-15-6 | Remodelin hydrobromide
(Catalog# : 122823)
Remodelin HBr salt is a novel potent and selective inhibitor of the acetyl-transferas
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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
2891709-58-1 | INDEX NAME NOT YET ASSIGNED
(Catalog# : 25002)
2247396-91-2 | HC-5404
(Catalog# : 25001)
HC-5404 is a novel, highly selective and potent PERK inhibitor.
3034479-99-4 | HC-5404-FU
(Catalog# : 24112)
HC-5404-FU is a novel, highly selective and potent PERK inhibitor.
2309409-79-6 | CMP-5 2HCl
(Catalog# : 24161)
CMP-5 is a potent, specific, and selective PRMT5 inhibitor, while displays no activit
2630378-05-9 | Wu-5
(Catalog# : 24160)
Wu-5 is a USP10 inhibitor that can inhibit FLT3 and AMPK pathways, induce FLT3-ITD de
890764-36-0 | VU-29
(Catalog# : 24159)
VU 29 is a potent allosteric potentiator at the rat mGlu5 receptor (EC50 = 9 nM); bin
1221186-52-2 | ML-202
(Catalog# : 24158)
ML-202 is an activator of pyruvate kinase M2 (PKM2).
921193-28-4 | BTA-EG4 hydrate
(Catalog# : 24157)
BTA-EG4 is a catalase-amyloid interaction inhibitor, which can significantly enhance
2415281-52-4 | CYD19
(Catalog# : 24156)
CYD19 is a potent Snail/HDAC dual target inhibitor.
98570-83-3 | Phylloflavan
(Catalog# : 24155)
Phylloflavan is an antileishmanial agent with an intracellular EC50 of 3.2 nM in RAW