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+86-17702719238
sales@sun-shinechem.com
Home
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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
2095393-15-8 | ARQ-531
(Catalog# : 185176)
ARQ-531 is a potent and orally active BTK inhibitor with potential antineoplastic act
2089288-03-7 | AZD1390
(Catalog# : 18541)
AZD1390 is a potent and selective ATM inhibitor with the ability to cross the blood-b
252017-04-2 | AZD7545
(Catalog# : 179136)
AZD7545 is an inhibitor of pyruvate dehydrogenase kinase 2 (PDHK2) (IC50 value of 6.4
2091134-35-7 | AZD4205
(Catalog# : 20178710)
AZD4205 is a highly potent JAK1-selective kinase inhibitor with excellent preclinical
2002381-31-7 | APS-2-79
(Catalog# : 16122775)
APS-2-79 is a MAPK antagonist that modulating KSR-dependent MAPK signalling by antago
229961-45-9 | AGN 194310
(Catalog# : 6111516)
AGN 194310(VTP-194310) is a potent and selective pan-RARs agonist with Kd values of 3
2002381-25-9 | APS-2-79
(Catalog# : 6111501)
APS-2-79 is an antagonist of MEK phosphorylation by RAF through direct binding of the
21230-50-2 | 3-aMino-1-Methyl-1H-pyrazole-4-carbonitrile
(Catalog# : 6111001)
3-aMino-1-Methyl-1H-pyrazole-4-carbonitrile 21230-50-2
2070009-66-2 | A-674563 hydrochloride
(Catalog# : 611802)
A-674563 hydrochloride is a potent selective Akt1 inhibitor with an IC50 of 14 nM; al
297730-17-7 | AVN944
(Catalog# : 022201)
AVN944 is an orally available, synthetic small molecule with potential antineoplastic
252025-52-8 | Adjudin
(Catalog# : 122824)
Adjudin is a drug which is under development as a potential non-hormonal male contrac
249921-19-5 | Anamorelin
(Catalog# : 122407)
Anamorelin is a synthetic orally active ghrelin receptor agonist which is under devel
23828-92-4 | Ambroxol hydrochloride
(Catalog# : 120408)
Coming soon!
22059-21-8 | 1-aminocyclopropanecarboxylic acid
(Catalog# : 110211)
Coming soon!
256925-03-8 | AL 082D06
(Catalog# : 101921)
AL 082D06(D-06) is the first selective, nonsteroidal glucocorticoid receptor (GR) ant
219766-25-3 | ANA-12
(Catalog# : 101910)
ANA-12 is aTrkB receptor antagonist, which showed direct and selective binding to Trk
2756-85-6 | 1-aminocyclohexane-1-carboxylic acid
(Catalog# : 83110)
Coming soon!
2566-29-2 | 2-amino-2-ethylbutanoic acid
(Catalog# : 83109)
Coming soon!
20776-67-4 | 2-Amino-5-chloro-3-methylbenzoic acid
(Catalog# : 81720)
Coming soon!
2122-63-6 | 4-Amino-3-iodobenzoic acid
(Catalog# : 80311)
Coming soon!
219793-45-0 | AHAS inhibitor
(Catalog# : 52739)
AHAS inhibitor is a novel acetohydroxyacid synthase(AHAS) inhibitor, a promising drug
2627-69-2 | AICAR
(Catalog# : 52702)
AICAR (Acadesine), is an AMP-activated protein kinase activator, which is used for th
2649400-34-8 | Bexobrutideg ( NX-5948 )
(Catalog# : 25197)
Bexobrutideg (NX-5948) is a BTK degrader.
2242952-69-6 | BMS-986299
(Catalog# : 25169)
MS-986299 is a NLRP3 inflammasome agonist.
2644662-83-7 | BBC0403
(Catalog# : 25058)
BBC0403 is a selective BRD2 inhibitor. BBC0403 inhibits the progression of osteoarthr
2413020-56-9 | BAY-593 free base
(Catalog# : 25055)
BAY-593 is an orally active inhibitor of geranylgeranyltransferase-I (GGTase-I) that
2035818-24-5 | Bexicaserin
(Catalog# : 24117)
Bexicaserin is a serotonin 5-HT2C receptor agonist.
2770961-85-6 | BIIB-129
(Catalog# : 24086)
2770960-52-4 | BIIB-129
(Catalog# : 24025)
BIIB129 is a covalent, selective, small molecule inhibitor of Bruton's tyrosine k
2769954-39-2 | BLU-451
(Catalog# : 20668)
BLU-451, also known as LNG-451, orally bioavailable, central nervous system (CNS) pen
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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