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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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Indoles and Oxindoles
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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
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Immunology & Inflammation
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Cas Index 1
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Cas Index 1
1434141-67-9 | 2-azaspiro[3.5]nonan-7-ol hydrochloride
(Catalog# : 1781602)
2-azaspiro[3.5]nonan-7-ol hydrochloride
1231929-97-7 | Abemaciclib ( LY2835219)
(Catalog# : 178141)
Abemaciclib, also known as LY2835219, is orally available cyclin-dependent kinase (CD
1609281-86-8 | AZD3264
(Catalog# : 178910)
AZD3264 is a novel and small molecule IKK2 inhibitor.IKK2 serves as a protein subunit
1240308-45-5 | A-971432
(Catalog# : 178816)
A‑971432 is highly selective for S1P5 and has excellent plasma and CNS exposure aft
1221443-94-2 | A-1165442
(Catalog# : 20178812)
A-1165442 is a temperature-neutral transient receptor potential vanilloid-1 (TRPV1) a
1375466-18-4 | ACY-775
(Catalog# : 77821)
ACY-775 is a potent and selective HDAC6 inhbiitor. ACY-775 inhibits HDAC6 with low na
1001404-83-6 | AAI-101
(Catalog# : 1773101)
AAI101(AAI-101) is a novel extended-spectrum -lactamase inhibitor.The combination of
1196509-60-0 | AZD-7594
(Catalog# : 17022812)
AZD-7594, also known as AZ13189620, is an inhaled selective glucocorticoid receptor (
1227163-56-5 | AZD3839
(Catalog# : 17022710)
AZD3839 is a potent and selective BACE1 inhibitor. AZD3839 is clinical candidate for
1668553-26-1 | A-1210477
(Catalog# : 17022404)
A-1210477 is a potent and selective MCL-1 inhibitor. A-1210477 induces the hallmarks
1383982-64-6 | AZD3293 (LY3314814)
(Catalog# : 17021318)
AZD3293, also known as LY3314814 is an oral beta-secretase 1 cleaving enzyme (BACE)
1620576-64-8 | AZD-8835
(Catalog# : 102703)
AZD8835 is a potent and selective inhibitor of PI3Kalpha and PI3Kdelata with excellen
1173900-37-2 | AZD6482 (S-isomer)
(Catalog# : 17011901)
AZD6482 is a potent, selective and ATP competitive PI3K inhibitor (IC(50) 0.01 μm).
1472624-85-3 | 7ACC2
(Catalog# : 17011302)
7ACC2 is a potent MCT inhibitor. Monocarboxylate transporters (MCTs) catalyze the pro
1174043-16-3 | AZD-2461
(Catalog# : 16122863)
AZD2461 is a novel and potent PARP inhibitor with lower affinity to P-glycoprotein. A
1557268-88-8 | Avitinib maleate
(Catalog# : 16122862)
Avitinib is an orally available, irreversible, epidermal growth factor receptor (EGFR
1192491-61-4 | Avibactam sodium
(Catalog# : 16122861)
Avibactam is a non--lactam -lactamase inhibitor antibiotic, which is a new drug appli
141396-28-3 | Argatroban
(Catalog# : 16122858)
Argatroban is an anticoagulant that is a direct thrombin inhibitor. Argatroban was ap
1442684-77-6 | AM-2394
(Catalog# : 16122855)
AM-2394 is a potent and selective Glucokinase agonist (GKA), which catalyzes the phos
1047645-82-8 | Afuresertib HCl
(Catalog# : 161227116)
Afuresertib, also known as GSK2110183, is an orally bioavailable inhibitor of the ser
1375465-91-0 | ACY-738
(Catalog# : 161227114)
ACY-738 is a potent and selective HDAC6 inhibitor with improved brain bioavailability
182167-02-8 | Acolbifene
(Catalog# : 161227113)
Acolbifene, also known as EM-652, or SCH-57068, is a selective estrogen receptor modu
1762-34-1 | Abametapir
(Catalog# : 161227111)
Abametapir is the active ingredient of Xeglyze Lotion. Abametapir inhibits metallopro
106566-58-9 | AS101
(Catalog# : 161227106)
AS101, a potent in vitro and in vivo immunomodulator, is a novel inhibitor of IL-1bet
1420477-60-6 | ACP-196
(Catalog# : 16122783)
Acalabrutinib is a selective second-generation Brutons tyrosine kinase (BTK) inhibito
1527503-11-2 | A-366
(Catalog# : 16122743)
A-366 is a potent and selective G9a/GLP histone lysine methyltransferase inhibitor wi
1821428-35-6 | AZD0156
(Catalog# : 16122713)
AZD0156 is a potent and selective inhibitors of ATM kinase, with potential chemo-/rad
1189904-01-5 | Acetazolamide D3
(Catalog# : 6111513)
Acetazolamide D3 is deuterium labeled Acetazolamide, which is a potent carbonic anhyd
152918-26-8 | AB-MECA
(Catalog# : 6111105)
AB-MECA is a high affinity A3 adenosine receptor agonist, has high affinity for recom
1337878-62-2 | ATI-2341
(Catalog# : 6111101)
ATI-2341, pepducin targeting the C-X-C chemokine receptor type 4 (CXCR4), is an allos
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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
1393466-87-9 | PLX8394
(Catalog# : 20613)
PLX8394 is an orally bioavailable inhibitor of serine/threonine-protein kinase B-raf
2365193-22-0 | Zelasudil
(Catalog# : 24014)
Zelasudil is a potent, highly selective and orally-active inhibitor that targets Rho-
2134675-36-6 | Ziftomenib ( KO-539 )
(Catalog# : 24013)
Ziftomenib is an oral, potent, and selective small molecule inhibitor that targets th
1640282-42-3 | Zunsemetinib
(Catalog# : 24012)
Zunsemetinib is an investigational oral mitogen-activated protein kinase-activated pr
2728667-27-2 | Zongertinib
(Catalog# : 24011)
Zongertinib [BI 1810631] is a human epidermal growth factor receptor 2 (HER2) inhibit
2272904-53-5 | Zasocitinib
(Catalog# : 24010)
Zasocitinib is under development for the treatment of moderate to severe plaque psori
2503036-46-0 | RNK-05047
(Catalog# : 24008)
RNK-05047 is a PROTAC degrader of BRD4 which displays significant tumor growth inhibi
1001288-58-9 | Asengeprast (FT011)
(Catalog# : 24009)
Asengeprast (FT011) is an anti-fibrotic agent thatreduces mRNA expression of collagen
2490431-16-6 | ERAS-801 ( JGK-068S )
(Catalog# : 20635)
ERAS-801 ( JGK-068S ) is a potent EGFR inhibitor.
209746-59-8 | T-1095
(Catalog# : 24004)
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs).