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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
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Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
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Immunology & Inflammation
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MAPK
Membrane Transporter/Ion Channel
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Cas Index 2
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Cas Index 2
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);
223463-13-6 | 5-Bromo-2-iodopyridine
(Catalog# : 110204)
Coming soon!
218600-53-4 | Bardoxolone methyl
(Catalog# : 92303)
Bardoxolone methyl (also known as “RTA 402” and “CDDO-methyl ester”) is an or
206274-42-2 | benzyl 4-(benzylamino)piperidine-1-carboxylate
(Catalog# : 81809)
Coming soon!
207296-89-7 | benzyl N-piperidin-4-ylcarbamate,hydrochloride
(Catalog# : 81806)
Coming soon!
264905-39-7 | 1-Boc-4-Ethylaminopiperidine
(Catalog# : 81728)
Coming soon!
220844-83-7 | 3-bromo-4-(dimethylamino)benzoic acid
(Catalog# : 81008)
Coming soon!
2416095-06-0 | CBR-470-1
(Catalog# : 25192)
CBR-470-1 is an Inhibitor of the glycolytic enzyme PGK1that induces Nrf2 activity.
2736508-60-2 | Catadegbrutinib (Synonyms: BGB-16673; BTK-IN-29)
(Catalog# : 25174)
2882165-79-7 | CFT1946
(Catalog# : 25078)
CFT1946 is an investigational, orally bioavailable small molecule degrader of BRAF V6
2309409-79-6 | CMP-5 2HCl
(Catalog# : 24161)
CMP-5 is a potent, specific, and selective PRMT5 inhibitor, while displays no activit
2415281-52-4 | CYD19
(Catalog# : 24156)
CYD19 is a potent Snail/HDAC dual target inhibitor.
2095432-28-1 | CPI-455 HCl
(Catalog# : 24144)
CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
2230263-60-0 | Crelosidenib
(Catalog# : 24101)
Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor.
2143917-62-6 | Cirtuvivint
(Catalog# : 24064)
Cirtuvivint is a CDC-like kinase (CLK) and dual-specificity tyrosine-phosphorylation-
2417489-10-0 | Camonsertib
(Catalog# : 24052)
Camonsertib, also known as RP 3500, is aA Novel, Potent, and Selective ATR Inhibitor
2815296-08-1 | CVN-293
(Catalog# : 24024)
CVN-293 is an oral, brain-penetrant, small-molecule inhibitor of KCNK13.
2227304-19-8 | CP-506 ( Synonyms: SN-36506 )
(Catalog# : 20645)
CP-506 (SN-36506) is an hypoxia-activated prodrug of a DNA-alkylating nitrogen mustar
209986-17-4 | Compound E
(Catalog# : 20575)
Compound E is a cell-permeable, potent, selective inhibitor of ɣ-secretase and Notch
20217-22-5 | COH1 inhibitor
(Catalog# : 20555)
COH1 is a ribonucleotide reductase (RR) inhibitor.
2259648-80-9 | CC-92480 ( Mezigdomide )
(Catalog# : 20510)
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno
2308520-97-8 | Cadefrecitinib (GLPG-3667)
(Catalog# : 20509)
Cadefrecitinib (GLPG-3667) is an oral, small molecule inhibitor of the TYK2 kinase in
218457-67-1 | CB-103
(Catalog# : 20322)
CB-103 is a γ-secretase inhibitor. CB-103 inhibits Notch signaling in primary human
2316817-88-4 | CB-6644
(Catalog# : 41788)
CB-6644 acts as a noncompetitive ATPase inhibitor. Additionally, it can inhibit RUVBL
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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
----
Potassium Channel
-- 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
----
DUB
-- 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
2800223-30-5 | Dabogratinib ( TYRA-300 )
(Catalog# : 24073)
Dabogratinib ( TYRA-300 ) is an Oral Selective FGFR3 Inhibitor (IC50 = 11 nM) for the
N/A | AF710B
(Catalog# : 25205)
AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1
2957874-18-7 | MAT2A inhibitor 5
(Catalog# : 25204)
MAT2A inhibitor 5 has a high potency for inhibiting MAT2A and a remarkable selectivit
1235733-73-9 | (Rac)-AF710B
(Catalog# : 24083)
AF-710B is an agonist of sigma and M1 muscarinic receptors; AF710B is an enantiomer o
863888-33-9 | Flurpiridaz-nonradiolabeled
(Catalog# : 25203)
Flurpiridazis a promising novel cardiac PET imaging tracer formed by the radiolabelin
863888-32-8 | Flurpiridaz-Precursor
(Catalog# : 25202)
Flurpiridaz-Precursor in stock.
1800405-30-4 | KL1333
(Catalog# : 25201)
KL1333 is an orally available, small organic molecule that reacts with NAD(P)H:quinon
1369489-71-3 | Palupiprant ( E7046 )
(Catalog# : 24055)
E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece
2460722-04-5 | Oveporexton ( TAK-861 )
(Catalog# : 25194)
Oveporexton isan oral small molecule selective orexin type-2 receptor (OX2R) agonist.
2506273-81-8 | VT-3989
(Catalog# : 25200)
VT3989, a first-in-class potent oral TEAD palmitoylation inhibitor, disrupts YAP tran