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Inhibitors&Agonists
PI3K/Akt/mTOR
Epigenetics
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Angiogenesis
Apoptosis
Autophagy
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MAPK
Cytoskeletal Signaling
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DNA Damage
Stem Cells & Wnt
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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
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Amino Acids
Anilines
Boronic Acids
Bromides
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Deuterated
Fluorides
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Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
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Pyridines
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Cas Index 1
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Cas Index 1
1561178-17-3 | SGC0946
(Catalog# : 122504)
SGC0946 is a highly potent and selective DOT1L methyltransferase inhibitor with IC50
128427-05-4 | (S)-2-Ethylpiperazine dihydrochloride
(Catalog# : 122503)
Coming soon!
1221411-72-8 | SP-420
(Catalog# : 122304)
SP-420 is an orally active small molecule that selectively binds iron and removes it
1123837-84-2 | Sitravatinib (MGCD516)
(Catalog# : 178906)
Sitravatinib, also known as MGCD516 or MG516, is a novel small molecule inhibitor tar
1262888-28-7 | Spautin-1
(Catalog# : 102622)
Spautin-1 is a novel autophagy inhibitor, IM inhibited the growth of K562 cells with
1234708-04-3 | SAR191801
(Catalog# : 101917)
Coming soon!
1516895-53-6 | SEP-0372814
(Catalog# : 101913)
Coming soon!
1423715-09-6 | SP-2509
(Catalog# : 101909)
SP-2509 is a novel histone demethylase LSD1 inhibitor, which showed high actitivity o
193551-21-2 | SB239063
(Catalog# : 101908)
SB 239063 is a potent p38MAPK inhibitor, which had an IC(50) of 44 nM for inhibition
1174161-69-3 | SCR-1481B1
(Catalog# : 101901)
SCR-1481B1 is a potent and selective MET inhibitor. SCR-1481B1 inhibited MET kinase w
1448428-04-3 | Selonsertib(GS-4997)
(Catalog# : 100503)
Selonsertib is a apoptosis signal-regulating kinase inhibitor (ASK1). Selonsertib may
1421249-72-0 | (1S,3r,5R)-8-(5,6,7,8-tetrahydro-6-(5-isopropyl-2-methylphenyl)-2-(3,5-dimethyl-1H-indazol-4-yl)
(Catalog# : 91813)
Coming soon!
135383-60-7 | (S)-2-phenyl-1-(thiazol-2-yl)ethanaMine hydrochloride
(Catalog# : 91811)
Coming soon!
165377-44-6 | SA-4503.HCl (Cutamesine.HCl)
(Catalog# : 91414)
SA4503 (1-(3,4-dimethoxyphenethyl)-4-(3-phenylpropyl)piperazine dihydrochloride) is a
1145786-74-8 | (S)-1-(4-Fluorophenyl)propan-1-amine hydrochloride
(Catalog# : 91122)
Coming soon!
1114333-11-7 | (S)-5-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride
(Catalog# : 91112)
Coming soon!
1213479-78-7 | (1S)-1-(2,6-dimethylphenyl)ethanamine,hydrochloride
(Catalog# : 91109)
Coming soon!
173952-44-8 | SYM2206
(Catalog# : 91004)
SYM 2206 is a potent, novel, non-competitive AMPA receptor antagonist (IC50 = 2.8 M ).
127852-22-6 | (S)-3-(1-Aminoethyl)benzonitrile
(Catalog# : 90728)
Coming soon!
138457-18-8 | (1S)-1-(3-methylphenyl)ethanamine,hydrochloride
(Catalog# : 90718)
Coming soon!
122536-94-1 | (S)-3-Hydroxypyrrolidine hydrochloride
(Catalog# : 90603)
Coming soon!
132622-66-3 | (2S,4S)-1-Boc-4-Aminopyrrolidine-2-carboxylic acid
(Catalog# : 90118)
Coming soon!
1217779-15-1 | (2S,4S)-Methyl 4-((tert-butoxycarbonyl)amino)pyrrolidine-2-carboxylate hydrochloride
(Catalog# : 90117)
Coming soon!
1217803-39-8 | (2S,4S)-tert-Butyl 4-amino-2-(hydroxymethyl)pyrrolidine-1-carboxylate hydrochloride
(Catalog# : 90116)
Coming soon!
122536-74-7 | S-1-Cbz-3-Boc-aminopyrrolidine
(Catalog# : 90114)
Coming soon!
1070968-08-9 | (S)-tert-Butyl (pyrrolidin-2-ylmethyl)carbamate hydrochloride
(Catalog# : 90113)
Coming soon!
141774-68-7 | (S)-Benzyl 2-(aminomethyl)pyrrolidine-1-carboxylate
(Catalog# : 90108)
Coming soon!
140148-70-5 | (S)-N-Boc-Pyrrolidine-3-Carboxylic Acid
(Catalog# : 83127)
Coming soon!
1206163-45-2 | Solcitinib
(Catalog# : 82803)
Solcitinib is a Janus kinase 1 (JAK1) inhibitor, which may be potential useful for tr
1030377-21-9 | (S)-1-Boc-(2-Hydroxymethyl)piperazine
(Catalog# : 81828)
Coming soon!
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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
2891709-58-1 | INDEX NAME NOT YET ASSIGNED
(Catalog# : 25002)
2247396-91-2 | HC-5404
(Catalog# : 25001)
HC-5404 is a novel, highly selective and potent PERK inhibitor.
3034479-99-4 | HC-5404-FU
(Catalog# : 24112)
HC-5404-FU is a novel, highly selective and potent PERK inhibitor.
2309409-79-6 | CMP-5 2HCl
(Catalog# : 24161)
CMP-5 is a potent, specific, and selective PRMT5 inhibitor, while displays no activit
2630378-05-9 | Wu-5
(Catalog# : 24160)
Wu-5 is a USP10 inhibitor that can inhibit FLT3 and AMPK pathways, induce FLT3-ITD de
890764-36-0 | VU-29
(Catalog# : 24159)
VU 29 is a potent allosteric potentiator at the rat mGlu5 receptor (EC50 = 9 nM); bin
1221186-52-2 | ML-202
(Catalog# : 24158)
ML-202 is an activator of pyruvate kinase M2 (PKM2).
921193-28-4 | BTA-EG4 hydrate
(Catalog# : 24157)
BTA-EG4 is a catalase-amyloid interaction inhibitor, which can significantly enhance
2415281-52-4 | CYD19
(Catalog# : 24156)
CYD19 is a potent Snail/HDAC dual target inhibitor.
98570-83-3 | Phylloflavan
(Catalog# : 24155)
Phylloflavan is an antileishmanial agent with an intracellular EC50 of 3.2 nM in RAW