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+86-17702719238
sales@sun-shinechem.com
Home
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Anti-infection
Apoptosis
Autophagy
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Cytoskeleton
DNA Damage
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MAPK
Membrane Transporter/Ion Channel
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Cas Index 2
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Cas Index 2
2114324-48-8 | BMS-986251
(Catalog# : 20445)
2376257-44-0 | Bexotegrast ( PLN-74809 )
(Catalog# : 171680)
Bexotegrast (Synonyms: PLN-74809) is a small-molecule, dual selective inhibitor of α
2766481-17-6 | BGB-15025
(Catalog# : 171452)
BGB-15025 is a potent and selective HPK1 inhibitor that is efficacious as a single ag
2477812-42-1 | Benzeneacetamide, N-ethyl-4-formyl-
(Catalog# : 20419)
2097334-15-9 | Benzeneacetic acid, 4-[[(2,4-dimethylbenzoyl)oxy]methyl]-, methyl ester
(Catalog# : 20391)
2230836-55-0 | BI-3406
(Catalog# : 21234)
BI-3406 is Potent & Selective SOS1::KRAS Inhibitor (IC50=5 nM), which Opens a New
2056261-41-5 | BRD0705
(Catalog# : 202112701)
BRD0705 is a potent, paralog selective and orally active GSK3α inhibitor. BRD0705 ca
2141955-96-4 | BLU-782
(Catalog# : 20121701)
2242464-44-2 | BAY-2416964
(Catalog# : 2091906)
BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist
279262-28-1 | 4-(2-Butoxyethoxy)phenylboronic acid
(Catalog# : 2091203)
2225819-06-5 | BAY-2402234
(Catalog# : 2071553)
BAY-2402234 is a potent and selective dihydroorotate dehydrogenase (DHODH) inhibitor
273404-37-8 | Belnacasan
(Catalog# : 52004)
Belnacasan is a prodrug ofVRT-043198, a caspase-1 inhibitor that was developed by Ver
2113650-03-4 | BMS-1001
(Catalog# : 2062901)
202865-80-3 | 4-bromo-2-fluoro-1-propan-2-yloxybenzene
(Catalog# : 2062316)
2162982-11-6 | BAY-218
(Catalog# : 204301)
BAY-218, also known as BAY-2335218, is a potent and selective small-molecule AhR inhi
2091135-02-1 | 3-bromo-7-nitro-1-tosyl-1H-indole
(Catalog# : 511191)
2244904-70-7 | BAY-293
(Catalog# : 193121)
BAY-293 is a potent SOS1 inhibitors that block RAS activation via disruption of the R
2097132-94-8 | Blu667
(Catalog# : 191282)
Blu667 is a highly potent and selective RET inhibitor with an IC50 of 0.4 nM for wild
2166387-64-8 | BI-3812
(Catalog# : 19124)
BI-3812 is a potent inhibitor of the interaction of the BTB/POZ domain of BCL6 with s
2080306-23-4 | BAY-299
(Catalog# : 1811262)
BAY-299 is a potent and selective BRD1 and TAF1 inhibitor (IC50 values are 6 and 13 n
298708-79-9 | BAY41-4109 racemic
(Catalog# : 1791117)
BAY41-4109 racemic is a mixture of R-isomer of BAY41-4109 and S-isomer of BAY41-4109.
214066-78-1 | B-1613
(Catalog# : 20178216)
(2S,4S)-1-tert-butyl 2-Methyl 4-(aMinoMethyl)pyrrolidine-1,2-dicarboxylate
222638-67-7 | BEC HCl
(Catalog# : 17030110)
BEC, also known as S-(2-boronoethyl)-L-cysteine, is an a slow-binding and competitive
209799-67-7 | BCX-1777
(Catalog# : 16071105)
BCX-1777
2116-36-1 | 1-benzyl-4-bromobenzene
(Catalog# : 032510)
Coming soon!
2655-19-8 | Butacarb
(Catalog# : 020301)
Coming soon!
251111-30-5 | Beloranib
(Catalog# : 122918)
Beloranib is a fumagillin analogue and inhibitor of methionine aminopeptidase 2 (META
202189-78-4 | Bilastine
(Catalog# : 121807)
Bilastine is a selective histamine H1 receptor antagonist used for treatment of aller
213819-48-8 | Belotecan hydrochloride
(Catalog# : 121401)
Belotecan Hydrochloride is the hydrochloride salt of the semi-synthetic camptothecin
217645-70-0 | BX471
(Catalog# : 120108)
BX471 is a potent, selective non-peptide CCR1 antagonist (Ki = 1 nM for human CCR1);
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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
-- 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
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
-- 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
2669009-92-9 | Atebimetinib
(Catalog# : 25148)
Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1
2242751-53-5 | Acoramidis hydrochloride
(Catalog# : 24068)
Acoramidis is an oral, potent, and highly selective small molecule transthyretin (TTR
2230263-60-0 | Crelosidenib
(Catalog# : 24101)
Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor.
2833703-74-3 | LOXO-435
(Catalog# : 25080)
LOXO-435 is a selective small molecule inhibitor of FGFR3. It is active against both
2439277-80-0 | MAT2A-IN-9
(Catalog# : 25147)
MAT2A-IN-9 (compound 167), a 2-oxoquinazoline derivative, is a potent MAT2A (methioni
2446928-30-7 | Gridegalutamide
(Catalog# : 25138)
Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
1256349-48-0 | Chiauranib
(Catalog# : 25146)
Chiauranib also known as orally available, small molecule inhibitor of select serine-
1581714-49-9 | Atuzabrutinib
(Catalog# : 25145)
Atuzabrutinib, also known as PRN 473, is a Bruton's tyrosine kinase inhibitor.
2254145-43-0 | Andamertinib
(Catalog# : 25144)
Andamertinib is an epidermal growth factor receptor tyrosine kinase inhibitor. It is
2769008-22-0 | MEN-1703
(Catalog# : 25143)