Welcome to Sun-shine chemical
+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
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
Intermediates
Services
Custom Synthesis
Process Development
Ordering
Contact Us
About Us
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
PROTAC
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
Intermediates
Services
Custom Synthesis
Process Development
Ordering
Contact Us
About Us
Contact Us
Search
Home
Sitemaps
Name Index F
Search By Initial
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
1
2
3
4
5
6
7
8
9
«
1
2
3
»
Name Index F
Fonadelpar
(Catalog# : 18445, Cas# :
515138-06-4
)
Fonadelpar is a potent and selective peroxisome proliferator activated receptor δ (P
FM-381
(Catalog# : 18436, Cas# :
unknown
)
FM-381 is a Chemical Probe For JAK3 and JAK3 specific reversible covalent inhibitor.
Fmoc-Val-Ala-PAB
(Catalog# : 18431, Cas# :
1394238-91-5
)
Fmoc-Val-Ala-PAB,也称为Fmoc-Val-Ala-PAB-OH,是一种有效的药物结合剂,
Ferrostatin-1
(Catalog# : 184210, Cas# :
347174-05-4
)
Ferrostatin-1 (fe -1)是一种亲脂的抗氧化剂,有效地阻断了铁蛋白的形
Fostemsavir
(Catalog# : 1712155, Cas# :
864953-29-7
)
Fostemsavir, also known as BMS-663068, is a oral, safe and effective HIV-1 attachment
Farampator
(Catalog# : 179156, Cas# :
211735-76-1
)
Farampator, also known as Org-24448; CX-691, is an AMPA receptor positive allosteric
FRAX1036
(Catalog# : 1791315, Cas# :
1432908-05-8
)
FRAX1036 is a potent and selective PAK1 inhibitor.
FITM
(Catalog# : 17989, Cas# :
932737-65-0
)
FITM is a potent mGlu1 inhibitor.
Fluralaner
(Catalog# : 178309, Cas# :
864731-61-3
)
Fluralaner, also known as AH252723, is a systemic insecticide and acaricide that is a
4-fluoro-2-Methoxy-5-nitroaniline
(Catalog# : 521191, Cas# :
1075705-01-9
)
AZD9291 drug intermediate-1
4-FORMYL-2-METHOXY-3-NITROPHENYL ACETATE
(Catalog# : 178225, Cas# :
2698-69-3
)
4-FORMYL-2-METHOXY-3-NITROPHENYL ACETATE
1-(3-Fluorophenyl)-cyclohexanamine HCl
(Catalog# : 178221, Cas# :
125802-18-8
)
1-(3-Fluorophenyl)-cyclohexanamine HCl
FPS-ZM1
(Catalog# : 16123002, Cas# :
945714-67-0
)
FPS-ZM1 is a high-affinity RAGE-specific blocker that inhibits amyloid- binding to RA
Flutamide
(Catalog# : 16123001, Cas# :
13311-84-7
)
Flutamide, also known as SCH13521, is a toluidine derivative and nonsteroidal antiand
Fluoxymesterone
(Catalog# : 16122947, Cas# :
76-43-7
)
Fluoxymesterone is an anabolic steroid with strong androgenic properties that has bee
Firategrast
(Catalog# : 16122946, Cas# :
402567-16-2
)
Firategrast, also known as SB-683699 or T-0047, is an orally bioavailable alpha4 beta
FIIN-3
(Catalog# : 16122945, Cas# :
1637735-84-2
)
FIIN-3 is a potent, selective, irreversible and the next-generation covalent FGFR inh
FGFR4-IN-1
(Catalog# : 16122813, Cas# :
1708971-72-5
)
FGFR4-IN-1 is a potent and selective FGFR4 inhibitor. FGFR4 may be a novel therapeuti
FG-2216
(Catalog# : 16122812, Cas# :
223387-75-5
)
FG-2216, also known as YM311, is orally bioavailable HIF-prolyl hydroxylase inhibitor
FH535
(Catalog# : 16122788, Cas# :
108409-83-2
)
FH535 is a Wnt/-catenin signaling inhibitor and also a dual PPAR and PPAR antagonist.
FLLL32
(Catalog# : 16122709, Cas# :
1226895-15-3
)
FLLL32 is a potent JAK2/STAT3 inhibitor with IC50 of <5 M.In MDA-MB-231 breast and
Fevipiprant ( NVP-QAW039 )
(Catalog# : 90102, Cas# :
872365-14-5
)
Fevipiprant (QAW039; NVP-QAW039) is a selective, potent, reversible competitive CRTh2
Filanesib
(Catalog# : 16071102, Cas# :
885060-09-3
)
Filanesib, also known as ARRY-520, is a synthetic, small molecule targeting the kines
FK866(APO866,Daporinad)
(Catalog# : 1662306, Cas# :
658084-64-1
)
FK866 is a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltra
FIIN-2
(Catalog# : 16062117, Cas# :
1633044-56-0
)
FIIN-2 is a potent, selective, irreversible and the next-generation covalent FGFR inh
FPH2
(Catalog# : 032513, Cas# :
957485-64-2
)
Coming soon!
Fludarabine
(Catalog# : 021901, Cas# :
21679-14-1
)
Fludarabine, a DNA synthesis inhibitor, is a chemotherapy drug used in the treatment
Fumagillin
(Catalog# : 122910, Cas# :
23110-15-8
)
Fumagillin is a complex biomolecule and used as an antimicrobial agent.
Falnidamol
(Catalog# : 122807, Cas# :
196612-93-8
)
Falnidamol is a pyrimido-pyrimidine with antitumor activity.
Fedratinib ( TG-101348 )
(Catalog# : 122306, Cas# :
936091-26-8
)
Fedratinib ( TG-101348 ) is a selective inhibitor of JAK2 with IC50 of 3 nM, 35- and
«
1
2
3
»
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
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
STX-478
(Catalog# : 20633, Cas# :
2883540-92-7
)
STX-478 is a second generation, mutant-selective, oral PI3Ka small molecule allosteri
Iclepertin (BI-425809)
(Catalog# : 24084, Cas# :
1421936-85-7
)
Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
Bomedemstat
(Catalog# : 24001, Cas# :
1990504-34-1
)
Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl
PLX-4545
(Catalog# : 24111, Cas# :
2892065-45-9
)
PLX-4545 is an orally bioavailable molecular glue degrader of IKZF2 designed to desta
VVD-130037 ( BAY-3605349 )
(Catalog# : 24110, Cas# :
3034880-93-5
)
VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
CBR-5884
(Catalog# : 24109, Cas# :
681159-27-3
)
CBR 5884 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor which was able to inhi
JHU-083
(Catalog# : 24108, Cas# :
1998725-11-3
)
JHU-083 selectively blocks glutaminase activity in brain CD11b+ cells and prevents de
LXH-3-71
(Catalog# : 24107, Cas# :
2251753-65-6
)
LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH
CC-92480 ( Mezigdomide )
(Catalog# : 20510, Cas# :
2259648-80-9
)
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno
Adrixetinib ( Q-702 )
(Catalog# : 20617, Cas# :
2394874-66-7
)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag