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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
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Immunology & Inflammation
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Bromides
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Chiral Compounds
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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
Antibody-drug Conjugate/ADC Related
Building Blocks
Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
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Chiral Compounds
Deuterated
Fluorides
Imidazoles
Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
Peg Linkers
Phenols
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Pyridines
Pyrimidines
Quinolines
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Name Index A
AZ32
(Catalog# : 1810223, Cas# :
no
)
AZ32 is an orally bioavailable and blood-brain barrier-penetrating ATM inhibitor with
ARS-1620
(Catalog# : 1810222, Cas# :
1698055-85-4
)
ARS-1620 is an atropisomeric selective KRAS-G12C inhibitor with desirable pharmacokin
AGL-2263
(Catalog# : 1810175, Cas# :
638213-98-6
)
AGL-2263 is a novel insulin receptor inhibitor.
AM211
(Catalog# : 1810173, Cas# :
1175526-27-8
)
AM-211 is a novel and potent antagonist of the prostaglandin D2 receptor type 2.
Arimoclomol maleate
(Catalog# : 188281, Cas# :
289893-26-1
)
Arimoclomol, also known as BRX-220, is potentially useful for the treatment of Nieman
ASP7663
(Catalog# : 187123, Cas# :
1190217-35-6
)
ASP7663 is an orally bioavailable selective TRPA1 activator.
Aldoxorubicin HCl
(Catalog# : 187111, Cas# :
480998-12-7
)
Aldoxorubicin, also known as INNO-206 and Doxo-EMCH, is the 6-maleimidocaproyl hydraz
ABT 702 Dihydrochloride
(Catalog# : 18791, Cas# :
1188890-28-9
)
ABT 702 Dihydrochloride is a potent non-nucleoside adenosine kinase inhibitor, select
Avacopan
(Catalog# : 18761, Cas# :
1346623-17-3
)
Avacopan, also known as CCX168, is an orally active, selective and potent C5aR inhibi
AEW-541
(Catalog# : 18753, Cas# :
475489-16-8
)
AEW541, also known as NVP-AEW541, is a novel, potent IGF-IR kinase inhibitor.
AMD-070 HCl
(Catalog# : 18741, Cas# :
880549-30-4
)
AMD11070, also known as AMD070, X4P-001 and mavorixafor, is an orally bioavailable an
AG-494
(Catalog# : 186273, Cas# :
133550-35-3
)
AG-494, also known as Tyrphostin AG-494, is an inhibitor of epidermal growth factor r
AZD5153
(Catalog# : 186254, Cas# :
1869912-39-9
)
AZD5153 is a potent bivalent triazolopyridazine based Bromodomain and Extraterminal (
Amenamevir
(Catalog# : 186252, Cas# :
841301-32-4
)
Amenamevir, also known as ASP2151, is a herpes virus helicase-primase inhibitor.
A22 hydrochloride
(Catalog# : 186211, Cas# :
22816-60-0
)
A22 is an inhibitor of MreB, an actin-like bacterial protein, and has been shown to a
AST487
(Catalog# : 186158, Cas# :
630124-46-8
)
AST487, also known as NVP- AST487, is a RET kinase inhibitor/FLT3 inhibitor.
ARV-825
(Catalog# : 185253, Cas# :
1818885-28-7
)
ARV-825 is a PROTAC (proteolysis-targeting chimera). ARV-825 exerts superior lethal a
Alobresib
(Catalog# : 185222, Cas# :
1637771-14-2
)
Alobresib is an antineoplastic drug candidate.
Adavivint
(Catalog# : 185221, Cas# :
1467013-03-3
)
Adavivint is a Wnt pathway inhibitor and immunomodulator drug candidate.
ALX 1393
(Catalog# : 185213, Cas# :
949164-09-4
)
ALX 1393 is a glycine transporter-2 inhibitor.
A-485
(Catalog# : 185211, Cas# :
1889279-16-6
)
A-485 is a potent and selective HAT inhibitor of p300/CBP in vitro with an IC50 of 10
AS-1517499
(Catalog# : 185187, Cas# :
919486-40-1
)
AS-1517499 is a potent and selective STAT6 inhibitor.
AMG-176
(Catalog# : 185185, Cas# :
1883727-34-1
)
AMG-176 is an inhibitor of induced myeloid leukemia cell differentiation protein MCL-
A-350619 HCI
(Catalog# : 185183, Cas# :
1217201-17-6
)
A-350619 hydrochloride is an activator of soluble guanylyl cyclase (sGC).
ARQ-531
(Catalog# : 185176, Cas# :
2095393-15-8
)
ARQ-531 is a potent and orally active BTK inhibitor with potential antineoplastic act
ADX-47273
(Catalog# : 185173, Cas# :
851881-60-2
)
ADX-47273 is a potent and selective mGluR5 receptor PAM (positive allosteric modulato
AMG-511
(Catalog# : 18542, Cas# :
1253573-53-3
)
AMG-511 is a potent and selective pan class I PI3K inhibitor.
AZD1390
(Catalog# : 18541, Cas# :
2089288-03-7
)
AZD1390 is a potent and selective ATM inhibitor with the ability to cross the blood-b
ALW-II-41-27
(Catalog# : 1842813, Cas# :
1186206-79-0
)
ALW-II-41-27 is a Eph receptor tyrosine kinase inhibitor.
AZD4635
(Catalog# : 184289, Cas# :
1321514-06-0
)
AZD-4635, also known as HTL-1071, is an orally available, small molecule adenosine A2
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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
--
Antibody-drug Conjugate/ADC Related
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
Reparixin
(Catalog# : 25050, Cas# :
266359-83-5
)
Reparixin is an inhibitor of CXCR2 function, which attenuates inflammatory responses
TAK-779
(Catalog# : 25049, Cas# :
229005-80-5
)
TAK-779 is a C-C chemokine receptor type 5 (CCR5) receptor antagonist potentially for
BAY-1125976
(Catalog# : 25048, Cas# :
1402608-02-9
)
BAY-1125976 is a potent and selective allosteric AKT1/2 inhibitor. BAY-1125976 exhibi
Vimseltinib free base
(Catalog# : 25047, Cas# :
1628606-05-2
)
Vimseltinib, also known as DCC-3014, is a potent and orally active inhibitor of the t
2-Propynamide, 3-[(3Z)-3-[[[4-[(dimethylamino)methyl]phenyl]amino]phenylmethylene]-2,3-dihydro-2-oxo-1H-indol-6-yl]-N-ethyl-
(Catalog# : 25046, Cas# :
2128698-24-6
)
Cavosonstat
(Catalog# : 25045, Cas# :
1371587-51-7
)
Cavosonstat, alos known as N91115) an orally bioavailable inhibitor of S-nitrosogluta
Ivospemin Hydrochloride
(Catalog# : 25044, Cas# :
259657-09-5
)
Ivospemin is an antineoplastic spermine analogue.
Survodutide
(Catalog# : 25043, Cas# :
2805997-46-8
)
XRD-0394
(Catalog# : 25042, Cas# :
2595308-10-2
)
XRD-0394 is a DNA-PKcs inhibitor. XRD-0394 selectively targets, binds to and inhibits
CC-90003
(Catalog# : 25041, Cas# :
1621999-82-3
)
CC-90003 is an orally available inhibitor of extracellular signal-regulated kinase (E