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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
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GPCR & G Protein
Metabolism
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Bromides
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Chiral Compounds
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Fluorides
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Indoles and Oxindoles
Iodos
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Phenols
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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
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
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Other Azoles
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Name Index A
AMG-510 racemate
(Catalog# : 112194, Cas# :
2252403-56-6
)
AMG-510 is a potent KRAS G12C covalent inhibitor. AMG-510 selectively targets the KRA
Aprocitentan
(Catalog# : 112191, Cas# :
1103522-45-7
)
Aprocitentan is an orally active, dual endothelin (ET) receptor antagonist developed
Aramchol
(Catalog# : 6111903, Cas# :
246529-22-6
)
Galmed Pharmaceuticals Announces Successful Completion of End of Phase 2 Meeting With
Acibenzolar acid
(Catalog# : 513191, Cas# :
35272-27-6
)
benzo[d][1,2,3]thiadiazole-7-carboxylic acid,Acibenzolar acid,CGA 210 007
AR-C155858
(Catalog# : 193291, Cas# :
496791-37-8
)
AR-C155858 is a potent inhibitor of monocarboxylate transporters MCT1 and MCT2 that b
ACT-709478
(Catalog# : 193288, Cas# :
1838651-58-3
)
ACT-709478 is a Potent, Selective T-type Calcium Channel Blocker as a Drug Candidate
A1874
(Catalog# : 193287, Cas# :
2064292-12-0
)
A1874 is a nutlin-based and BRD4-degrading PROTAC which induces BRD4 degradation in c
AZD9567
(Catalog# : 193254, Cas# :
1893415-00-3
)
AZD9567 is an oral differentiated non-steroidal selective glucocorticoid receptor mod
AZ1495
(Catalog# : 193222, Cas# :
2196204-23-4
)
AZ1495 is a potent and selective IRAK4 inhibitor.
ATR-101 HCl
(Catalog# : 193208, Cas# :
133825-81-7
)
ATR-101, also known as PD-132301 (a free base) or PD-132301-2 (a HCl salt), is in cli
ARN-3236
(Catalog# : 193192, Cas# :
1613710-01-2
)
ARN-3236 is potent, orally active and selective SIK2 inhibitor. ARN-3236 inhibited th
ARN 077
(Catalog# : 193134, Cas# :
1373625-34-3
)
ARN 077 is a potent and selective N-acylethanolamine acid amidase (NAAA) inhibitor wi
Aleglitazar
(Catalog# : 193125, Cas# :
475479-34-6
)
Aleglitazar, also known as RG-1439 or RO-0728804, is a peroxisome proliferator-activa
Alvimopan
(Catalog# : 19382, Cas# :
156053-89-3
)
Alvimopan, also known as HSDB-7704 and LY246736, is a drug which behaves as a periphe
Abrocitinib
(Catalog# : 19381, Cas# :
1622902-68-4
)
Abrocitinib, Bulk in stock, contact us by email for the quotation. Kg scale intermedi
AA26-9
(Catalog# : 19372, Cas# :
1312782-34-5
)
AA26-9 is a potent and broad-spectrum serine hydrolase inhibitor. AA26-9-inhibited en
AZD-0284
(Catalog# : 19365, Cas# :
2101291-07-8
)
AZD-0284 is a potent, selective, inverse agonist of the nuclear receptor RORγ for th
AZ304
(Catalog# : 19363, Cas# :
942507-42-8
)
AZ304 is an ATP-competitive dual BRAF kinase inhibitor, potently inhibits wild type B
AZ876
(Catalog# : 19356, Cas# :
898800-26-5
)
AZ876, also known as AZ-876, is a liver X receptor agonist. AZ876 protects against pa
AGN-190299
(Catalog# : 19316, Cas# :
118292-41-4
)
Tazarotene is a retinoid prodrug which is converted to its active form, the cognate c
AM281
(Catalog# : 19315, Cas# :
202463-68-1
)
AM281 is a synthetic cannabinoid CB1 receptor antagonist.
ASP9521
(Catalog# : 19312, Cas# :
1126084-37-4
)
ASP9521 is a novel, selective, orally bioavailable inhibitor of 17β-hydroxysteroid d
AZD0364
(Catalog# : 192275, Cas# :
2097416-76-5
)
AZD0364 is an ERK1 and/or ERK2 kinase for the treatment of cancer. ERK1 and ERK2 kina
ATF6-activator-147
(Catalog# : 192212, Cas# :
393121-74-9
)
ATF6-activator-147 is an ATF6 simulator which acts as a prodrug that preferentially t
AZD1152
(Catalog# : 192156, Cas# :
722543-31-9
)
AZD1152 is a pro-drug of Barasertib-hQPA, which is a highly selective Aurora B inhibi
AZD3229
(Catalog# : 191287, Cas# :
2248003-60-1
)
AZD3229 is a potent pan-KIT mutant inhibitor for the treatment of gastrointestinal st
AM095 sodium
(Catalog# : 191251, Cas# :
1345614-59-6
)
AM095 is a potent LPA1 receptor antagonist because it inhibited GTPγS binding to Chi
AZD4573 free base
(Catalog# : 191212, Cas# :
2057509-72-3
)
AZD-4573 is a selective, short-acting inhibitor of the serine/threonine cyclin-depend
AR-9281
(Catalog# : 191146, Cas# :
913548-29-5
)
AR-9281 is a soluble epoxide hydrolase (s-EH) inhibitor potentially for the treatment
ARRY-797 (ARRY-371797)
(Catalog# : 191112, Cas# :
1036404-17-7
)
ARRY-797 is an oral, selective p38 mitogen-activated protein kinase inhibitor. ARRY-7
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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
-- 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
-- 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
-- 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
-- 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
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
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
PLX8394
(Catalog# : 20613, Cas# :
1393466-87-9
)
PLX8394 is an orally bioavailable inhibitor of serine/threonine-protein kinase B-raf
Zelasudil
(Catalog# : 24014, Cas# :
2365193-22-0
)
Zelasudil is a potent, highly selective and orally-active inhibitor that targets Rho-
Ziftomenib ( KO-539 )
(Catalog# : 24013, Cas# :
2134675-36-6
)
Ziftomenib is an oral, potent, and selective small molecule inhibitor that targets th
Zunsemetinib
(Catalog# : 24012, Cas# :
1640282-42-3
)
Zunsemetinib is an investigational oral mitogen-activated protein kinase-activated pr
Zongertinib
(Catalog# : 24011, Cas# :
2728667-27-2
)
Zongertinib [BI 1810631] is a human epidermal growth factor receptor 2 (HER2) inhibit
Zasocitinib
(Catalog# : 24010, Cas# :
2272904-53-5
)
Zasocitinib is under development for the treatment of moderate to severe plaque psori
RNK-05047
(Catalog# : 24008, Cas# :
2503036-46-0
)
RNK-05047 is a PROTAC degrader of BRD4 which displays significant tumor growth inhibi
Asengeprast (FT011)
(Catalog# : 24009, Cas# :
1001288-58-9
)
Asengeprast (FT011) is an anti-fibrotic agent thatreduces mRNA expression of collagen
ERAS-801 ( JGK-068S )
(Catalog# : 20635, Cas# :
2490431-16-6
)
ERAS-801 ( JGK-068S ) is a potent EGFR inhibitor.
T-1095
(Catalog# : 24004, Cas# :
209746-59-8
)
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs).