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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
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
Trifluoroborates
Other Azoles
Other Heterocycles
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On Sale
Intermediates
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Custom Synthesis
Process Development
Ordering
Contact Us
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Contact Us
+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
Trifluoroborates
Other Azoles
Other Heterocycles
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Custom Synthesis
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Name Index C
CBL0137
(Catalog# : 184319, Cas# :
314761-14-3
)
CBL0137 activates p53 and inhibits NF-kB. It also inhibits the group protein molecula
CPI-444
(Catalog# : 18439, Cas# :
1202402-40-1
)
CPI-444, also known as V81444, is an orally administered antagonist of the adenosine
CCG-203971
(Catalog# : 18437, Cas# :
1443437-74-8
)
CCG-203971 is an inhibitor of SRE activation in the prostate cancer cell line PC-3 (I
CP-376395游离
(Catalog# : 184213, Cas# :
175140-00-8
)
CP-376395是一种CRF1的选择性拮抗剂。
Copanlisib HCI
(Catalog# : 18351, Cas# :
1402152-13-9
)
Copanlisib also known as BAY 80-6946, is a potent phosphoinositide 3-kinase (PI3K) in
CB-03-01
(Catalog# : 1712153, Cas# :
19608-29-8
)
CB-03-01,也被称为cortexolone 17alpha -丙酸,是一种局部和外围选择性
Cenicriviroc ( TAK-652 )
(Catalog# : S510902, Cas# :
497223-25-3
)
Cenicriviroc ( TAK-652, TBR-652) is an experimental drug candidate for the treatment
CHIR99021 HCl
(Catalog# : 179825, Cas# :
1797989-42-4
)
CHIR99021, also known as CT99021, is a glycogen synthase kinase 3β (GSK3β) inhibito
CDDO
(Catalog# : 92304, Cas# :
218600-44-3
)
CDDO is a synthetic oleanane triterpenoid that blocks the cellular synthesis of induc
CVT-10216
(Catalog# : 179818, Cas# :
1005334-57-5
)
CVT-10216 is a Potent and selective, reversible inhibitor of aldehyde dehydrogenase 2
Carubicin HCl
(Catalog# : 17914, Cas# :
52794-97-5
)
Carubicin HCl is an anthracycline antineoplastic antibiotic isolated from the bacteri
Cambinol
(Catalog# : 178313, Cas# :
14513-15-6
)
Cambinol is a SIRT inhibitor. It inhibits expression of pro-inflammatory cytokines, i
2-chloro-4-(methylamino) pyrimidine-5-carbaldehyde
(Catalog# : 1781601, Cas# :
839708-50-8
)
2-chloro-4-(methylamino) pyrimidine-5-carbaldehyde
2-Chloro-6-morpholinopyran-4-one
(Catalog# : 1781504, Cas# :
119671-47-5
)
2-Chloro-6-morpholinopyran-4-one
CCT196969
(Catalog# : 178913, Cas# :
1163719-56-9
)
CCT196969, a pan-RAF/SFK inhibitor is active against treatment-naive BRAF and NRAS mu
CCT365623
(Catalog# : 2017876)
CCT365623 is a Lysyl oxidase inhibitor.
CM-579
(Catalog# : 2017874, Cas# :
1846570-40-8
)
CM-579 is a bioactive chemical.
C188-9
(Catalog# : 2017873, Cas# :
432001-19-9
)
C188-9 is a bioactive chemical.
(5-Chloro-2-cyanophenyl)boronic acid
(Catalog# : 20178120, Cas# :
1072946-52-1
)
(5-Chloro-2-cyanophenyl)boronic acid
CY5.5-SE
(Catalog# : 20177314, Cas# :
442912-55-2
)
2-[5-[3-[6-[(2,5-Dioxo-1-pyrrolidinyl)oxy]-6-oxohexyl]-1,3-dihydro-1,1-dimethyl-6,8-d
Ceftriaxone
(Catalog# : 17032406, Cas# :
73384-59-5
)
Ceftriaxone is an antibiotic useful for the treatment of a number of bacterial infect
Ceftibuten
(Catalog# : 17032405, Cas# :
97519-39-6
)
Ceftibuten(Sch39720) is a third-generation cephalosporin antibiotic.
Ceftazidime
(Catalog# : 17032404, Cas# :
72558-82-8
)
Ceftazidime(GR20263) is an antibiotic useful for the treatment of a number of bacteri
Cefradine
(Catalog# : 17032403, Cas# :
38821-53-3
)
Cefradine is a first generation cephalosporin antibiotic.
Cefozopran
(Catalog# : 17032402, Cas# :
113359-04-9
)
Cefozopran(SCE 2787) is a fourth-generation cephalosporin.
Cefoselis
(Catalog# : 17032401, Cas# :
122841-10-5
)
Cefoselis is a widely used beta-lactam antibiotic.
CC-122
(Catalog# : 17030313, Cas# :
1015474-32-4
)
CC-122 is an orally available pleiotropic pathway modulator with potential antineopla
CP21R7
(Catalog# : 17022715, Cas# :
125314-13-8
)
CP21R7, also known CP21, is a potent and selective GSK-3 inhibitor.
Citarinostat
(Catalog# : 17022701, Cas# :
1316215-12-9
)
Citarinostat is a HDAC6 specific inhibitor, with IC50 of 4 nM and 76 nM for HDAC6 and
(+)-Camphor
(Catalog# : 17021401, Cas# :
464-49-3
)
(+)-Camphor is an ingredient in cooking, and as an embalming fluid for medicinal purp
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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).