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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
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Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
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Cas Index 1
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Cas Index 1
1123-09-7 | 3,5-Dimethyl-2-cyclohexen-1-one
(Catalog# : 110210)
Coming soon!
1421252-90-5 | 3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-indazole
(Catalog# : 91814)
Coming soon!
1449685-96-4 | DDR1-IN-1
(Catalog# : 90801)
DDR1-IN-1 is a potent and selective DDR1 receptor tyrosine kinase inhibitor with IC50
130408-16-1 | 4,7-Difluoroindan-1-one
(Catalog# : 83107)
Coming soon!
161712-77-2 | 5,6-difluoro-2,3-dihydroinden-1-one
(Catalog# : 83106)
Coming soon!
162548-73-4 | 4,6-difluoro-2,3-dihydroinden-1-one
(Catalog# : 81938)
Coming soon!
1700-02-3 | 2,4-Dichloro-6-phenyl-1,3,5-triazine
(Catalog# : 81719)
Coming soon!
1195765-45-7 | Dabrafenib
(Catalog# : 52731)
Dabrafenib (GSK2118436) is a mutant BRAFV600 specific inhibitor with IC50 of 0.8 nM,
1206711-16-1 | DMH-1
(Catalog# : 52730)
DMH-1 is a potent and selective BMP inhibitor with IC50s of 27/107.9/<5 nM for ALK
1219168-18-9 | Dorsomorphin dihydrochloride
(Catalog# : 52704)
Dorsomorphin 2Hcl (Compound C; BML-275) has been shown to act as a potent and selecti
1020172-07-9 | DCC-2036(Rebastinib)
(Catalog# : 52023)
Rebastinib(DCC-2036;DCC2036) is an inhibitor of tyrosine kinases TIE2 and ABL1.Rebast
1995067-59-8 | Emlenoflast ( Synonyms: MCC7840 ; IZD174)
(Catalog# : 25168)
Emlenoflast (MCC7840, formerly IZD174) is a small molecule inhibitor of the NLRP3 inf
1353567-32-4 | EP6
(Catalog# : 25161)
EP6 is a 5-lipoxygenase (5-LO) inhibitor. 5-LO is a crucial enzyme of the arachidonic
1593673-23-4 | Etripamil
(Catalog# : 25123)
Etripamil is a calcium channel blocker. Calcium channel blockers (CCB), calcium chann
1799824-08-0 | E-7386
(Catalog# : 25086)
E-7386 is an orally active CBP/beta-catenin modulator.
1801344-14-8 | Emavusertib
(Catalog# : 25069)
Emavusertib, also known as CA-4948 is a potent IRAK4/FLT3 inhibitor with anti-tumor a
112108-01-7 | Ecopipam ( SCH 39166 )
(Catalog# : 25065)
Ecopipam ( SCH 39166 ) is a Selective Dopamine Receptor D1/D5 Antagonist used in the
1369489-71-3 | E7046
(Catalog# : 24055)
E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece
1914148-73-4 | Ezurpimtrostat HCl
(Catalog# : 20607)
Ezurpimtrostat is a palmitoyl protein thioesterase 1 (PPT-1) inhibitor.
1419865-05-6 | (E)-4-Morpholinobut-2-enoic acid hydrochloride
(Catalog# : 20546)
1354745-52-0 | ELQ300
(Catalog# : 20447)
ELQ300 is a novel inhibitor of the mitochondrial cytochrome bc1 complex (complex III
1219925-73-1 | E6446
(Catalog# : 20436)
E6446 is a TLR inhibitor. E6446 inhibits Toll-like receptor (TLR)7 and 9 signaling. E
1352925-63-3 | ethyl 4,6-dihydroxypyridazine-3-carboxylate
(Catalog# : 20390)
1443978-76-4 | ethyl 4-hydroxy-6-methylpyrazolo[1,5-a]pyrazine-2-carboxylate
(Catalog# : 20360)
1449598-75-7 | ethyl 4-chloro-6-methylpyrazolo[1,5-a]pyrazine-2-carboxylate
(Catalog# : 20359)
1449598-76-8 | ethyl 4,6-dimethylpyrazolo[1,5-a]pyrazine-2-carboxylate
(Catalog# : 20358)
1174046-84-4 | Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate
(Catalog# : 20327)
190133-94-9 | Ecopipam hydrochloride ( SCH-39166 )
(Catalog# : 20296)
Ecopipam HCl is a Selective Dopamine Receptor D1/D5 Antagonist used in the treatment
1219925-73-1 | E6446
(Catalog# : 21240)
1884461-72-6 | Ensifentrine ( RPL554 )
(Catalog# : 61726)
Ensifentrine (RPL554) is an investigational, first-in-class, inhaled dual inhibitor o
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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
-- 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
-- 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
1016340-64-9 | Z57346765
(Catalog# : 25191)
Z57346765 is a PGK1-specific inhibitor that reduces the activity of metabolic enzymes
2416095-06-0 | CBR-470-1
(Catalog# : 25192)
CBR-470-1 is an Inhibitor of the glycolytic enzyme PGK1that induces Nrf2 activity.
1898206-17-1 | Safusidenib
(Catalog# : 25149)
Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl
2803470-63-3 | HC-7366
(Catalog# : 25076)
HC-7366 is a potent and selective activator of the general control nonderepressible 2
2377000-84-3 | Dencatistat
(Catalog# : 25177)
Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
146426-40-6 | Flavopiridol ( Alvocidib )
(Catalog# : 237071)
Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
2201056-66-6 | AG-270
(Catalog# : 25176)
MAT2A Inhibitor AG-270 is an orally available small molecule inhibitor of methionine
618913-30-7 | AZD-5904
(Catalog# : 181121)
AZD5904 is a potent orally bioavailable MPO inhibitor. In preclinical studies, AZD590
2035010-37-6 | ALT-007
(Catalog# : 25157)
ALT-007 is an orally bioavailable SPT inhibitor that is more potent than myriocin, sa
1633666-49-5 | Nizubaglustat ( Synonyms: AZ-3102 )
(Catalog# : 25175)
Nizubaglustat (AZ-3102) is an oral small molecule which inhibits glucosylceramide syn