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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
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
Vitamin D Related
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others
Building Blocks
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Amines
Amino Acids
Anilines
Boronic Acids
Bromides
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Catalysts
Chiral Compounds
Deuterated
Fluorides
Imidazoles
Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
Peg Linkers
Phenols
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Pyrimidines
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Ordering
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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
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Boronic Acids
Bromides
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Nitro Compounds
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Pyridines
Pyrimidines
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Cas Index 1
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Cas Index 1
1699717-32-2 | BAY-545
(Catalog# : 2071532)
BAY-545 is a potent and selective antagonist of the A2B adenosine receptor.
1549360-60-2 | 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine
(Catalog# : 2062328)
1628263-43-3 | 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine hydrochloride
(Catalog# : 202327)
1083325-87-4 | 7-bromo-2-(1-methyl-1H-pyrazol-4-yl)-quinoxaline
(Catalog# : 2062028)
101155-02-6 | BW-A 78U
(Catalog# : 2051512)
BW-A 78U is a PDE4 inhibitor with an IC50 of 3 μM.
1802637-39-3 | BB-Cl-Amidine
(Catalog# : 204505)
BB-Cl-Amidine is a Novel Therapeutic for Canine and Feline Mammary Cancer via Activat
195615-83-9 | Blarcamesine ( AVex-73 ; AE-37 )
(Catalog# : 6111902)
ANAVEX2-73 (blarcamesine) is a Sigma-1 receptor agonist and muscarinic receptor modul
1059630-11-3 | 6-bromo-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride
(Catalog# : ITI007_1)
Sun-shine Chemical is a supplier ofLumateperone, we may provideLumateperone and its i
1622180-31-7 | BMS-986104
(Catalog# : 193285)
BMS-986104 is a potent and selective S1P1 receptor modulator, which demonstrates liga
1613264-40-6 | BAY-1316957
(Catalog# : 193263)
BAY-1316957 is a highly potent, selective, orally available human prostaglandin E2 re
1800340-40-2 | BMS-986158
(Catalog# : 193255)
BMS-986158 is a potent and selective BET inhibitor. BMS-986158 binds to the acetyl-ly
1801151-09-6 | BMS-986163
(Catalog# : 193207)
BMS-986163 a Negative Allosteric Modulator of GluN2B with Potential Utility in Major
1009583-20-3 | BMS-816336
(Catalog# : 19351)
BMS-816336 is an orally active, potent and selective 11β-HSD1 inhibitor. BMS-816336
1446113-23-0 | Belvarafenib
(Catalog# : 19341)
Belvarafenib, also known as GDC-5573, HM95573, RG6185, is a selective inhibitor of th
1191450-19-7 | Burixafor HBr
(Catalog# : 192221)
Burixafor, also known as TG-0054, is an orally bioavailable inhibitor of CXC chemokin
1643368-58-4 | BMS-986142
(Catalog# : 191284)
BMS-986142 is a potent, selective, reversible BTK inhibitor.
1564268-08-1 | BAY1238097
(Catalog# : 191257)
BAY1238097 is a potent and selective BET inhibitor. BAY1238097 binds to the acetylate
166977-43-1 | BMS-189453
(Catalog# : 191253)
BMS-189453, also known as BMS453, is a potent and selective RARβ agonist and a poten
1093108-50-9 | BI-671800
(Catalog# : 191213)
BI-671800 is a CRTH2 antagonist that treats patients with asthma. BI 671800 is associ
1912445-55-6 | BMS-986195
(Catalog# : 1811264)
BMS-986195 is a potent, covalent, irreversible inhibitor of Bruton’s tyrosine kinas
1609392-27-9 | BMS-986165
(Catalog# : 1810163)
BMS-986165 potently binds to the Tyk2 pseudokinase domain (Ki = 0.02 nM). BMS-986165
1611493-60-7 | Bictegravir
(Catalog# : 187181)
Bictegravir, also known as GS-9883, is a potent, unboosted, once-Daily HIV-1 Integras
1034442-21-1 | Basimglurant
(Catalog# : 187121)
Basimglurant, also known as RO 4917523 and RG-7090, is a novel mGlu5 negative alloste
1923833-60-6 | BMS-986205
(Catalog# : 185314)
BMS-986205 is an anticancer drug candidate.
1260251-31-7 | Birinapant
(Catalog# : 185182)
Birinapant, also known as TL32711, is a synthetic small molecule and peptido mimetic
1286279-29-5 | BMS-813160
(Catalog# : 1842812)
BMS-813160 is a potent and selective CCR2/CCR5 antagonist with potential immunomodula
198480-56-7 | Bazedoxifene acetate
(Catalog# : 18496)
Bazedoxifene, also known as WAY-140424, is a third generation selective estrogen rece
1513879-21-4 | BQR695
(Catalog# : 184218)
BQR695,也被称为NVP-BQR695, 是一种有效且具有选择性的PI4K抑制剂。
1414943-88-6 | BAY1143572
(Catalog# : 181242)
Atuveciclib,也被称为BAY1143572,是一种具有高度选择性、有效和口服
1803274-65-8 | BAY-1436032
(Catalog# : 181181)
BAY-1436032 is a potent, selective and orally available inhibitor of mutant Isocitrat
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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).