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Angiogenesis
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Immunology & Inflammation
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MAPK
Membrane Transporter/Ion Channel
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Neuronal Signaling
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Proteases
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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
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
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Name Index B
BMS-986104
(Catalog# : 193285, Cas# :
1622180-31-7
)
BMS-986104 is a potent and selective S1P1 receptor modulator, which demonstrates liga
BAY-1316957
(Catalog# : 193263, Cas# :
1613264-40-6
)
BAY-1316957 is a highly potent, selective, orally available human prostaglandin E2 re
BMS-986158
(Catalog# : 193255, Cas# :
1800340-40-2
)
BMS-986158 is a potent and selective BET inhibitor. BMS-986158 binds to the acetyl-ly
BMS-986163
(Catalog# : 193207, Cas# :
1801151-09-6
)
BMS-986163 a Negative Allosteric Modulator of GluN2B with Potential Utility in Major
BAY-293
(Catalog# : 193121, Cas# :
2244904-70-7
)
BAY-293 is a potent SOS1 inhibitors that block RAS activation via disruption of the R
BMS-816336
(Catalog# : 19351, Cas# :
1009583-20-3
)
BMS-816336 is an orally active, potent and selective 11β-HSD1 inhibitor. BMS-816336
Belvarafenib
(Catalog# : 19341, Cas# :
1446113-23-0
)
Belvarafenib, also known as GDC-5573, HM95573, RG6185, is a selective inhibitor of th
Burixafor HBr
(Catalog# : 192221, Cas# :
1191450-19-7
)
Burixafor, also known as TG-0054, is an orally bioavailable inhibitor of CXC chemokin
BMS-986142
(Catalog# : 191284, Cas# :
1643368-58-4
)
BMS-986142 is a potent, selective, reversible BTK inhibitor.
Blu667
(Catalog# : 191282, Cas# :
2097132-94-8
)
Blu667 is a highly potent and selective RET inhibitor with an IC50 of 0.4 nM for wild
BAY1238097
(Catalog# : 191257, Cas# :
1564268-08-1
)
BAY1238097 is a potent and selective BET inhibitor. BAY1238097 binds to the acetylate
BMS-189453
(Catalog# : 191253, Cas# :
166977-43-1
)
BMS-189453, also known as BMS453, is a potent and selective RARβ agonist and a poten
BI-671800
(Catalog# : 191213, Cas# :
1093108-50-9
)
BI-671800 is a CRTH2 antagonist that treats patients with asthma. BI 671800 is associ
BI-3812
(Catalog# : 19124, Cas# :
2166387-64-8
)
BI-3812 is a potent inhibitor of the interaction of the BTB/POZ domain of BCL6 with s
BAY 678
(Catalog# : 1812286, Cas# :
675103-36-3
)
BAY 678 is a potent and selective cell-permeable human neutrophil elastase (HNE) inhi
BN-82002
(Catalog# : 1812261, Cas# :
396073-89-5
)
BN-82002, also known as CDC25 Phosphatase Inhibitor I, is a cell-permeable ortho-hydr
BMS-509744
(Catalog# : 1811291, Cas# :
439575-02-7
)
BMS-509744 is a potent interleukin-2 inducible T cell kinase (ITK) inhibitor (IC50 =
BMS-688521
(Catalog# : 1811281, Cas# :
893397-44-9
)
BMS-688521 is a small molecule antagonist of leukocyte function associated antigen-1
BMS-986195
(Catalog# : 1811264, Cas# :
1912445-55-6
)
BMS-986195 is a potent, covalent, irreversible inhibitor of Bruton’s tyrosine kinas
BAY-299
(Catalog# : 1811262, Cas# :
2080306-23-4
)
BAY-299 is a potent and selective BRD1 and TAF1 inhibitor (IC50 values are 6 and 13 n
BMS-986165
(Catalog# : 1810163, Cas# :
1609392-27-9
)
BMS-986165 potently binds to the Tyk2 pseudokinase domain (Ki = 0.02 nM). BMS-986165
Bictegravir
(Catalog# : 187181, Cas# :
1611493-60-7
)
Bictegravir, also known as GS-9883, is a potent, unboosted, once-Daily HIV-1 Integras
Basimglurant
(Catalog# : 187121, Cas# :
1034442-21-1
)
Basimglurant, also known as RO 4917523 and RG-7090, is a novel mGlu5 negative alloste
3BDO
(Catalog# : 186232, Cas# :
890405-51-3
)
3BDO, a butyrolactone derivative, could target FKBP1A and activate the mTOR signaling
BMS-986205
(Catalog# : 185314, Cas# :
1923833-60-6
)
BMS-986205 is an anticancer drug candidate.
Birinapant
(Catalog# : 185182, Cas# :
1260251-31-7
)
Birinapant, also known as TL32711, is a synthetic small molecule and peptido mimetic
Bryostatin 1
(Catalog# : 18573, Cas# :
83314-01-6
)
Bryostatin 1 is a potent Protein Kinase C modulator isolated from the bryozoan Bugula
BMS-813160
(Catalog# : 1842812, Cas# :
1286279-29-5
)
BMS-813160 is a potent and selective CCR2/CCR5 antagonist with potential immunomodula
BRD7116
(Catalog# : 184282, Cas# :
329059-55-4
)
BRD7116 is a potent and selective Inhibitor of leukemia stem cell (LSC) activity (EC5
Bazedoxifene acetate
(Catalog# : 18496, Cas# :
198480-56-7
)
Bazedoxifene, also known as WAY-140424, is a third generation selective estrogen rece
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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
Atebimetinib
(Catalog# : 25148, Cas# :
2669009-92-9
)
Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1
Acoramidis hydrochloride
(Catalog# : 24068, Cas# :
2242751-53-5
)
Acoramidis is an oral, potent, and highly selective small molecule transthyretin (TTR
Crelosidenib
(Catalog# : 24101, Cas# :
2230263-60-0
)
Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor.
LOXO-435
(Catalog# : 25080, Cas# :
2833703-74-3
)
LOXO-435 is a selective small molecule inhibitor of FGFR3. It is active against both
MAT2A-IN-9
(Catalog# : 25147, Cas# :
2439277-80-0
)
MAT2A-IN-9 (compound 167), a 2-oxoquinazoline derivative, is a potent MAT2A (methioni
Gridegalutamide
(Catalog# : 25138, Cas# :
2446928-30-7
)
Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
Chiauranib
(Catalog# : 25146, Cas# :
1256349-48-0
)
Chiauranib also known as orally available, small molecule inhibitor of select serine-
Atuzabrutinib
(Catalog# : 25145, Cas# :
1581714-49-9
)
Atuzabrutinib, also known as PRN 473, is a Bruton's tyrosine kinase inhibitor.
Andamertinib
(Catalog# : 25144, Cas# :
2254145-43-0
)
Andamertinib is an epidermal growth factor receptor tyrosine kinase inhibitor. It is
MEN-1703
(Catalog# : 25143, Cas# :
2769008-22-0
)