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MAPK
Membrane Transporter/Ion Channel
Metabolism
Neuronal Signaling
NF-κB
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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
Vitamin D Related
PROTAC
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Name Index A
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Name Index A
ALC-0315
(Catalog# : 20264, Cas# :
2036272-55-4
)
ALC-0315 is a synthetic cationic lipid (or ionizable lipid). It is a colorless oily m
AP1189 acetate
(Catalog# : 2105071, Cas# :
959850-74-9
)
AP1189 is a melanocortin receptor agonist on MC1 and MC3 receptors.
AMG-221
(Catalog# : 21223, Cas# :
1095565-81-3
)
AMG-221, BVT-83370, is a potent and selective 11β-HSD1 inhibitor. AMG-221 decreased
ACT-389949 (ACT389949)
(Catalog# : 20211801, Cas# :
1258417-54-7
)
ACT-389949 is a potent and selective agonist of formyl peptide receptor type 2 (FPR2)
AT-56
(Catalog# : 20111201, Cas# :
162640-98-4
)
AT-56 is a selective, competitive, and highly bioavailable inhibitor of lipocalin-typ
ASN007
(Catalog# : 20103001, Cas# :
2055597-12-9
)
ASN007 , a novel oral ERK inhibitor , has shown anti-tumor activity in both solid tum
AB-680
(Catalog# : 2091501, Cas# :
2105904-82-1
)
AB-680 is highly potent, reversible and selective CD73 inhibitor. AB680 to be a rever
Apilimod mesylate ( STA-5326 )
(Catalog# : 23948, Cas# :
870087-36-8
)
Apilimod, also known as STA-5326, is a potent IL-12/IL-23 inhibitor. Apilimod inhibit
AVN-101 HCl
(Catalog# : 2071801, Cas# :
1061354-48-0
)
AVN-101 is a very potent 5-HT7 receptor antagonist (Ki = 153 pM), with slightly
APX-115 freebase
(Catalog# : 2071628, Cas# :
1270084-92-8
)
Apcin
(Catalog# : 2071626, Cas# :
300815-04-7
)
Apcin is an inhibitor of the anaphase-promoting complex/cyclosome (APC/C). It acts by
Astemizole
(Catalog# : 2071552, Cas# :
68844-77-9
)
Astemizole is a histamine H1-receptor antagonist. Astemizole competitively binds to h
ARV-771
(Catalog# : 2071539, Cas# :
1949837-12-0
)
ARV-771 is a small-molecule pan-BET degrader. ARV-771 demonstrates dramatically impro
AZD-7648
(Catalog# : 2071531, Cas# :
2230820-11-6
)
AZD-7648 is a potent and selective DNA-PK inhibitor.
AWZ1066S
(Catalog# : 2071530, Cas# :
239272-16-1
)
AWZ1066S is a highly specific anti-Wolbachia drug candidate for a short-course treatm
AER-271
(Catalog# : 2071523, Cas# :
634913-39-6
)
AER-271 is a potent aquaporin-4 (AQP4) inhibitor. AER-271 blocks acute cerebral edema
ABX-1431
(Catalog# : 2071517, Cas# :
1446817-84-0
)
ABX-1431 is a covalent, irreversible MGLL inhibitor. ABX-1431 is currently entering c
AZ31
(Catalog# : 2071508, Cas# :
2088113-98-6
)
AZ31 is a potent and highly selective ATM inhibitor.
AB-423
(Catalog# : 2071503, Cas# :
1572510-80-5
)
AB-423 is a novel inhibitor of hepatitis b virus pregenomic rna encapsidation
2-aminopyrazolo[1,5-a]pyridine-3-carboxylic acid
(Catalog# : 202323, Cas# :
1542020-25-6
)
1-acetyl-5-nitro-3H-indol-2-one
(Catalog# : 2062319, Cas# :
114985-63-6
)
1-acetyl-5-amino-2-indolinone
(Catalog# : 2061313, Cas# :
422518-10-3
)
(4aS,9bR)-Ethyl 6-bromo-5-(2-(methylamino)-2-oxoethyl)-3,4,4a,5-tetrahydro-1H-pyrido[4,3-b]indole-2(9bH)-carboxylate
(Catalog# : 2062312, Cas# :
2098497-32-4
)
8-Acetyl-5-(benzyloxy)-2H-benzo[b][1,4]oxazin-3(4H)-one
(Catalog# : 2062311, Cas# :
1035299-32-3
)
2-Amino-5-cyanopyrazine
(Catalog# : 2062307, Cas# :
113305-94-5
)
5-amino-3,4-dimethylthieno[2,3-c]pyridazine-6-carboxylic acid
(Catalog# : 2062025, Cas# :
1452226-14-0
)
AT13148 intermediate(N1)
(Catalog# : 2062009, Cas# :
1056901-64-4
)
Anacetrapib
(Catalog# : 2061701, Cas# :
875446-37-0
)
Anacetrapib, also known as MK-0859, is a CETP inhibitor being developed to treat hype
Ambrisentan
(Catalog# : 2061308, Cas# :
177036-94-1
)
Ambrisentan, also known as BSF-208075 and LU-208075, is a drug indicated for use in t
AZD0364
(Catalog# : 206101, Cas# :
2097416-76-5
)
AZD-0364 is a potent and selectiveERK2inhibitor extracted from patent WO2017080979A1,
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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
TAK-071
(Catalog# : 186269, Cas# :
1820812-16-5
)
TAK-071 is a muscarinic M1 receptor positive allosteric modulator.
MTX115325
(Catalog# : 186264, Cas# :
2750895-97-5
)
MTX115325 is a potent, selective, brain-penetrant USP30 inhibitor with good drug-like
LY-3381916
(Catalog# : 193123, Cas# :
2166616-75-5
)
LY-3381916 is a potent, selective and brain penetrated inhibitor of IDO1 activity, bi
Opakalim
(Catalog# : 25193, Cas# :
2376397-93-0
)
Opakalim (BHV-7000) is an oral, small-molecule activator of Kv7.2/7.3 potassium chann
DS68591889
(Catalog# : 25158, Cas# :
2488609-21-6
)
DS68591889 (PTDSS1i) specifically inhibits PTDSS1, which catalyzes serine incorporati
CAY 10566
(Catalog# : 10403, Cas# :
944808-88-2
)
CAY 10566 is a potent selective SCD-1 inhibitor.
Cadefrecitinib (GLPG-3667)
(Catalog# : 20509, Cas# :
2308520-97-8
)
Cadefrecitinib (GLPG-3667) is an oral, small molecule inhibitor of the TYK2 kinase in
QBS10072S
(Catalog# : 25190, Cas# :
1802735-28-9
)
QBS10072S isa blood-brain-barrier (BBB) penetrative agent composed of a cytotoxic che
Dencatistat
(Catalog# : 25177, Cas# :
2377000-84-3
)
Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
DS-1001b
(Catalog# : 25178, Cas# :
1898207-64-1
)
DS-1001 is an oral brain-penetrant mutant IDH1 selective inhibitor.