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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
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
PI3K/Akt/mTOR
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Cas Index 2
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Cas Index 2
23110-15-8 | Fumagillin
(Catalog# : 122910)
Fumagillin is a complex biomolecule and used as an antimicrobial agent.
2369-11-1 | 5-Fluoro-2-nitroaniline
(Catalog# : 110216)
Coming soon!
25451-15-4 | Felbamate
(Catalog# : 52752)
Felbamate (FBM) is a potent nonsedative anticonvulsant whose clinical effect may be r
2446929-86-6 | Gridegalutamide
(Catalog# : 26A044)
gridegalutamide is an orally bioavailable androgen receptor (AR) degrader, with poten
2314467-61-1 | GLO1 inhibitor-Compound 60
(Catalog# : 26A012)
GLO1 inhibitor-Compound 60 is a novel potent Glyoxalase 1 (GLO1) inhibitor.
2658538-04-4 | Glecirasib
(Catalog# : 25105)
2375779-31-8 | GP130 modulator-1
(Catalog# : 25062)
GP130 modulator-1 (compound A33) is agp130signaling pathway modulator. GP130 modulato
2413455-99-7 | G-5758
(Catalog# : 24076)
2091134-68-6 | Golidocitinib ( AZD-4205 )
(Catalog# : 24028)
Golidocitinib (AZD-4205) is an oral JAK1 selective kinase inhibitor.
2657613-87-9 | Glecirasib
(Catalog# : 20672)
2648450-42-2 | GNE-7883
(Catalog# : 20589)
GNE-7883 is a pan-TEAD inhibitor.
2060571-02-8 | GDC-0077
(Catalog# : L20335)
Inavolisib, also known as GDC-0077, is a potent and selective PI3K inhibitor. GDC-007
2507-91-7 | Gloxazone
(Catalog# : 20304)
Gloxazone is an effective but toxic anaplasmacide.
2407529-33-1 | Giredestrant tartrate
(Catalog# : 20263)
Giredestrant tartrate (GDC-9545 tartrate), a non-steroidal ER ligand, is an orally ac
2183470-12-2 | GCN2iB
(Catalog# : 2071802)
GCN2iB is an ATP-competitive GCN2 inhibitory compound with a better pharmacokinetic p
2101626-26-8 | GSK2894631A
(Catalog# : 2071528)
GSK2894631A is a hematopoietic PGD synthase (HPGDS) inhibitor.
2361659-62-1 | GSK8612
(Catalog# : 2071527)
GSK8612 is a potent and highly selective TBK1 inhibitor. GSK8612 inhibited recombinan
2049868-46-2 | GSK-963
(Catalog# : 193185)
GSK-963, also known as GSK'963 or GSK963, is a potent and selective inhibitor of
2138814-32-9 | GSK3004774
(Catalog# : 192281)
GSK3004774 is a potent, nonabsorbable agonist of CaSR, with an pEC50 of 7.3, 6.6 and
2095432-71-4 | GSK269962 HCl
(Catalog# : 192201)
GSK269962 is a selective ROCK inhibitor with IC50 values of 1.6 and 6 nM for ROCK-I a
2245255-65-4 | GSK-2807
(Catalog# : 19185)
GSK-2807 is a potent and selective, SAM-competitive inhibitor of SMYD3.
2009273-67-8 | GNE-6640
(Catalog# : 1812291)
GNE-6640 is a novel selective USP7 inhibitor, inducing tumor cell death. GNE-6640 enh
2070864-35-4 | GENZ-882706
(Catalog# : 1810176)
GENZ-882706 is a potent colony stimulating factor-1 receptor (CSF-1R) Inhibitor.
2077980-83-5 | GLL398
(Catalog# : 185313)
GLL398 is an Oral Selective Estrogen Receptor Downregulator.
278779-30-9 | GW4064
(Catalog# : 16071018)
GW-4064 is a selective agonist of FXR (EC50 = 15 nM).2 It displays no activity at oth
263890-70-6 | GR148672X
(Catalog# : 032404)
Coming soon!
22978-25-2 | GW9662
(Catalog# : 52304)
GW9662 is a selective PPAR antagonist forPPARwithIC50of 3.3 nM, with at least 100 to
2803470-63-3 | HC-7366
(Catalog# : 25076)
HC-7366 is a potent and selective activator of the general control nonderepressible 2
2247396-91-2 | HC-5404
(Catalog# : 25001)
HC-5404 is a novel, highly selective and potent PERK inhibitor.
2922069-42-7 | HH-0043
(Catalog# : 24077)
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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)
----
NEKs
-- 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
----
Methionine Adenosyltransferase (MAT)
-- 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
----
GLP Receptor
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- 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
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
-- 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)
----
CGRP-Receptor
----
TRP-Channel
-- 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)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- 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
-- Nuclear Receptor
----
Androgen Receptor(AR)
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
3118994-80-9 | DPTX-3186
(Catalog# : 26A010)
DPTX3186, an orally administered small molecule condensate modulator (c-mod) inhibiti
435327-40-5 | Avasopasem manganese (GC-4419; M-40419)
(Catalog# : 25108)
Avasopasem manganese, also known as GC-4419; M 40419 and SC-72325A, is amimetic of th
1421936-85-7 | Iclepertin (BI-425809)
(Catalog# : 24084)
Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
4727-31-5 | Kartogenin ( KGN )
(Catalog# : 52215)
Kartogenin (KGN) is a synthetic small molecule that stimulates chondrogenic cellular
218791-21-0 | Imisopasem manganese ( M40403; GC4403 )
(Catalog# : 72602)
Imisopasem manganese ( M40403; GC4403 ) is a stable non-peptidyl mimetic of MnSOD tha
2311863-36-0 | Apecotrep (BI 764198)
(Catalog# : 26A048)
Apecotrep (BI 764198) is a potential first-in-class, oral, selective TRPC6 inhibitor.
902614-04-4 | Pantothenate kinase-IN-2
(Catalog# : 26A038)
Pantothenate kinase-IN-2 is a pantothenate kinase inhibitor with IC50 values of 92 nM
3062177-59-4 | BH-30643
(Catalog# : 26A047)
BH-30643 is a novel, orally available, non-covalent, macrocyclic, mutant selective OM
2446929-86-6 | Gridegalutamide
(Catalog# : 26A044)
gridegalutamide is an orally bioavailable androgen receptor (AR) degrader, with poten
2446928-30-7 | BMS-986365 (Synonyms: CC-94676 )
(Catalog# : 25138)
BMS-986365, also known as CC-94676, is an orally bioavailable androgen receptor (AR)