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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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Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
Fluorides
Imidazoles
Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
Peg Linkers
Phenols
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Pyrimidines
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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
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
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
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Name Index B
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Name Index B
BAY41-4109 racemic
(Catalog# : 1791117, Cas# :
298708-79-9
)
BAY41-4109 racemic is a mixture of R-isomer of BAY41-4109 and S-isomer of BAY41-4109.
BAR-501
(Catalog# : 179821, Cas# :
1632118-69-4
)
BAR-501 is a selective GPBAR1 agonist devoid of any FXR agonistic activity. BAR501 ef
Batefenterol(free base)
(Catalog# : 179820, Cas# :
743461-65-6
)
Batefenterol, also known as GSK961081 and TD-5959, is a Muscarinic Antagonist and β2
BI-847325
(Catalog# : 83101, Cas# :
1207293-36-4
)
BI-847325 is an orally bioavailable, and selective dual MEK/Aurora kinase inhibitor w
BAY-598
(Catalog# : 17982, Cas# :
1906919-67-2
)
BAY-598 is a potent, peptide-competitive chemical probe for SMYD2. BAY-598 has a uniq
BAY-598 R-isomer
(Catalog# : 17981, Cas# :
1906920-28-2
)
BAY-598 R-isomer is the R-isomer of BAY589. BAY-598 R-isomer may be used as a referen
Brasofensine
(Catalog# : 17916, Cas# :
171655-91-7
)
Brasofensine is a monoamine reuptake blocker is a phenyltropane that had been under d
B02
(Catalog# : 1783013, Cas# :
1290541-46-6
)
B02, also known as RAD51-IN-02, is a RAD51 inhibitor. B02 can enhance DOX sensitivity
BLU-285
(Catalog# : 1781003, Cas# :
1703793-34-3
)
BLU-285 is a potent and selective inhibitor of PDGFR D842V and KIT Exon 17 mutants an
BAY-1895344
(Catalog# : 1781002, Cas# :
1876467-74-1
)
BAY-1895344 is developed for the treatment of patients with advanced solid tumors and
BIBR1532
(Catalog# : 178813, Cas# :
321674-73-1
)
BIBR1132 is highly selective for inhibition of telomerase, resulting in delayed growt
BMS-932481
(Catalog# : 2017877, Cas# :
1263871-36-8
)
BMS-932481 modulates A Peptides in the Plasma and Cerebrospinal Fluid of Healthy Volu
B-1613
(Catalog# : 20178216, Cas# :
214066-78-1
)
(2S,4S)-1-tert-butyl 2-Methyl 4-(aMinoMethyl)pyrrolidine-1,2-dicarboxylate
Balamapimod
(Catalog# : 2017822, Cas# :
863029-99-6
)
Balamapimod, also known as MKI-822, is a Ras/Raf/MEK inhibitor. Balamapimod, may be p
BP-1-102
(Catalog# : 17030606, Cas# :
1334493-07-0
)
BP-1-102 is a potent, orally bioavailable and selective STAT3 inhibitor. BP-1-102 bin
BAY-876
(Catalog# : 17030604, Cas# :
1799753-84-6
)
BAY-876 is a potent and Selective GLUT1 Inhibitor. BAY-876 showed good metabolic stab
BRD-7552
(Catalog# : 17030312, Cas# :
1137359-47-7
)
BRD-7552 is a PDX1 transcription factor inducer. It up regulates PDX1 expression in b
BDA-366
(Catalog# : 17030305, Cas# :
1821496-27-8
)
BDA-366 is a BCL2-BH4 antagonist. BDA-366 suppresses human myeloma growth. BDA-366 in
Bimiralisib
(Catalog# : 17030116, Cas# :
1225037-39-7
)
Bimiralisib, also known as PQR309, is an orally bioavailable pan inhibitor of phospho
BEC HCl
(Catalog# : 17030110, Cas# :
222638-67-7
)
BEC, also known as S-(2-boronoethyl)-L-cysteine, is an a slow-binding and competitive
BGP-15
(Catalog# : 17109003, Cas# :
66611-37-8
)
BGP-15, is a nicotinic amidoxime derivative with PARP inhibitory activity. It has bee
Butylphthalide
(Catalog# : 16122908, Cas# :
6066-49-5
)
Butylphthalide, also known as 3-n-butylphthalide or NBP, is an antioxidant and one of
Buthionine Sulphoximine
(Catalog# : 16122907, Cas# :
5072-26-4
)
Buthionine Sulphoximine, also known as NSC-326231, is a gamma-glutamylcysteine synthe
Brivaracetam
(Catalog# : 16122906, Cas# :
357336-20-0
)
Brivaracetam, also known as UCB 34714, is a chemical analog of levetiracetam, is a ra
Brigatinib (AP-26113)
(Catalog# : 16122905, Cas# :
1197953-54-0
)
Brigatinib, also known as AP-26113, is an orally active, potent and selective Dual AL
Brevianamide F
(Catalog# : 16122904, Cas# :
38136-70-8
)
Brevianamide F , also known as cyclo-(L-Trp-L-Pro), belongs to a class of naturally o
Bohemine
(Catalog# : 16122903, Cas# :
189232-42-6
)
Bohemine is a potent and selective, cell-permeable, cyclin-dependent kinase (CDK) inh
BMS-687453
(Catalog# : 16122902, Cas# :
1000998-59-3
)
BMS-687453 is a potent and selective peroxisome proliferator activated receptor (PPAR
BML-210
(Catalog# : 16122901, Cas# :
537034-17-6
)
BML-210, also known as CAY10433, is HDAC inhibitor. BML-210 induces growth inhibition
BIIB021
(Catalog# : 16122868, Cas# :
848695-25-0
)
BIIB021, also known as CNF2024, is an orally active, purine-scaffold, small-molecule
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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
STX-478
(Catalog# : 20633, Cas# :
2883540-92-7
)
STX-478 is a second generation, mutant-selective, oral PI3Ka small molecule allosteri
Iclepertin (BI-425809)
(Catalog# : 24084, Cas# :
1421936-85-7
)
Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
Bomedemstat
(Catalog# : 24001, Cas# :
1990504-34-1
)
Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl
PLX-4545
(Catalog# : 24111, Cas# :
2892065-45-9
)
PLX-4545 is an orally bioavailable molecular glue degrader of IKZF2 designed to desta
VVD-130037 ( BAY-3605349 )
(Catalog# : 24110, Cas# :
3034880-93-5
)
VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
CBR-5884
(Catalog# : 24109, Cas# :
681159-27-3
)
CBR 5884 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor which was able to inhi
JHU-083
(Catalog# : 24108, Cas# :
1998725-11-3
)
JHU-083 selectively blocks glutaminase activity in brain CD11b+ cells and prevents de
LXH-3-71
(Catalog# : 24107, Cas# :
2251753-65-6
)
LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH
CC-92480 ( Mezigdomide )
(Catalog# : 20510, Cas# :
2259648-80-9
)
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno
Adrixetinib ( Q-702 )
(Catalog# : 20617, Cas# :
2394874-66-7
)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag