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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
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Name Index F
Fezolinetant
(Catalog# : 18722, Cas# :
1629229-37-3
)
Fezolinetant, also known as ESN-364, is Neurokinin-3 (NK-3) receptor antagonist which
FRAX486
(Catalog# : 18721, Cas# :
1232030-35-1
)
FRAX486 is a potent p21-activated kinase (PAK) inhibitor (IC50 values are 14, 33, 39
Fialuridine
(Catalog# : 184283, Cas# :
69123-98-4
)
Fialuridine, also known as FIAU, DRG-0098, is a DNA-directed DNA polymerase inhibitor
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
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Products Catalog
Signaling Pathway
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
----
Eukaryotic Initiation Factor (eIF)
-- Cytoskeleton
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
----
Gap Junction Protein
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- 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
----
Ras
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
-- 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
----
Kallikrein
----
IRAK
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- 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
----
Proton Pump
-- 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
----
Mitochondrial Metabolism
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Ketohexokinase(KHK)
-- 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
----
Sigma Receptor
----
mAChR
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
----
Melanocortin Receptor
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
----
Bcr-Abl
----
FAK
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- TGF-beta/Smad
----
PKC
----
ROCK
----
TGF-beta/Smad
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
-- Vitamin D Related
----
VD/VDR
-- PROTAC
----
Molecular Glues
----
PROTACs
--
Antibody-drug Conjugate/ADC Related
--
Microbiology
-- Others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
----
Newest added products
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
Atebimetinib
(Catalog# : 25148, Cas# :
2669009-92-9
)
Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1
Acoramidis hydrochloride
(Catalog# : 24068, Cas# :
2242751-53-5
)
Acoramidis is an oral, potent, and highly selective small molecule transthyretin (TTR
Crelosidenib
(Catalog# : 24101, Cas# :
2230263-60-0
)
Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor.
LOXO-435
(Catalog# : 25080, Cas# :
2833703-74-3
)
LOXO-435 is a selective small molecule inhibitor of FGFR3. It is active against both
MAT2A-IN-9
(Catalog# : 25147, Cas# :
2439277-80-0
)
MAT2A-IN-9 (compound 167), a 2-oxoquinazoline derivative, is a potent MAT2A (methioni
Gridegalutamide
(Catalog# : 25138, Cas# :
2446928-30-7
)
Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
Chiauranib
(Catalog# : 25146, Cas# :
1256349-48-0
)
Chiauranib also known as orally available, small molecule inhibitor of select serine-
Atuzabrutinib
(Catalog# : 25145, Cas# :
1581714-49-9
)
Atuzabrutinib, also known as PRN 473, is a Bruton's tyrosine kinase inhibitor.
Andamertinib
(Catalog# : 25144, Cas# :
2254145-43-0
)
Andamertinib is an epidermal growth factor receptor tyrosine kinase inhibitor. It is
MEN-1703
(Catalog# : 25143, Cas# :
2769008-22-0
)