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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
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Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
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Cas Index 2
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Cas Index 2
2064269-82-3 | YK-029A
(Catalog# : 20670)
2131223-85-1 | YW2065
(Catalog# : 20494)
YW2065 has excellent anti-colorectal cancer effects in vitro and in vivo. YW2065 achi
2226534-49-0 | Y06137
(Catalog# : 193193)
Y06137 is a potent and selective BET inhibitor, which binds to the BRD4(1) bromodomai
223499-30-7 | YM-58483 (BTP2)
(Catalog# : 17109009)
YM-58483/BTP2 is a blocker of store-operated Ca2+ entry (SOCE), which regulates the a
288250-47-5 | Y-320
(Catalog# : 52516)
Y-320 is a new phenylpyrazoleanilide immunomodulator; inhibits IL-17 production by CD
2243882-74-6 | Zedoresertib
(Catalog# : 26A023)
Zedoresertib (Debio 0123) is a brain-penetrant, highly selective WEE1 kinase inhibito
2306303-35-3 | ZINC20451377
(Catalog# : 24132)
ZINC20451377 is a small molecule that binds to hepatitis B surface antigen (HBsAg) wi
210345-04-3 | Z-LEHD-FMK
(Catalog# : 24127)
Z-LEHD-FMK is a potent, cell-permeable, and irreversible inhibitor of caspase-9. Z-LE
210344-98-2 | Z-IETD-FMK
(Catalog# : 24126)
MDK4982, also known as Z-IETD-FMK, is a potent, cell-permeable, irreversible inhibito
210344-95-9 | Z-DEVD-fmk
(Catalog# : 24125)
Z-DEVD-fmk is a cell-permeable, irreversible inhibitor of caspase-3. Caspase-3 is a c
2133852-18-1 | Zastaprazan ( JP-1366 )
(Catalog# : 24123)
Zastaprazan, also known as JP-1366, is a proton pump inhibitor. JP-1366 mediates stro
2403703-30-8 | Zurletrectinib
(Catalog# : 24104)
Zurletrectinib is a tyrosine kinase inhibitor with potential as an antineoplastic age
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
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
2173389-57-4 | Zilurgisertib
(Catalog# : 20657)
Zilurgisertib (earlier known as INCB 00928) is an activin receptor-like kinase-2 (ALK
2201048-82-8 | Zagociguat
(Catalog# : 20628)
Zagociguat is a guanylate cyclase activator.
2739829-00-4 | Zidesamtinib ( NVL-520 )
(Catalog# : 20524)
Zidesamtinib ( NVL-520 ) is a novel brain-penetrant ROS1-selective tyrosine kinase in
2648641-36-3 | Zotizalkib ( TPX-0131 )
(Catalog# : 20318)
TPX-0131 is a next-generation ALK inhibitor drug candidate currently being evaluated
2254001-81-3 | ZK824859
(Catalog# : 2071513)
ZK824859 is a potent uPA inhibitor as a potential treatment for multiple sclerosis. Z
2229042-77-5 | ZL0454
(Catalog# : 193281)
ZL0454 is a potent and selective BRD4 inhibitor. ZL0454 reduces airway inflammation a
2031177-48-5 | ZM223
(Catalog# : 19352)
ZM223 is a novel non-sulfamide NEDD8 activating enzyme inhibitor that inhibits HCT116
210344-98-2 | Z-IETD-FMK
(Catalog# : 16122771)
Z-IETD-FMK is a specific Caspase-8 inhibitor.Z-IETD-FMK, which inhibits the cleavage
221877-54-9 | Zotarolimus
(Catalog# : 161009018)
It is a semi-synthetic derivative of rapamycin. It was designed for use in stents wit
210344-95-9 | Z-DEVD-FMK
(Catalog# : 16062112)
Z-DEVD-FMK(Caspase-3 Inhibitor) is a specific, irreversible Caspase-3 inhibitor, and
25775-90-0 | Zucapsaicin
(Catalog# : 121415)
Comig soon!
208260-29-1 | ZM 336372
(Catalog# : 52239)
ZM 336372 is a potent and selective c-Raf inhibitor with IC50 of 70 nM, 10-fold selec
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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)
----
NEKs
-- 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
----
Bradykinin Receptor
----
GLP 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
----
Potassium Channel
-- 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)
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
-- 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
----
Glucosylceramide Synthase (GCS)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
----
Keap1-Nrf2
-- 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
----
RET
----
Phosphoglycerate Kinase (PGK)
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
----
Lipase
-- 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
----
DUB
-- 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
2243882-74-6 | Zedoresertib
(Catalog# : 26A023)
Zedoresertib (Debio 0123) is a brain-penetrant, highly selective WEE1 kinase inhibito
3033961-38-2 | BEN-28010
(Catalog# : 26A022)
BEN-28010 is a freely brain-penetrant, potent, and selective CHK1 inhibitor.
3107291-07-3 | Tert-butyl 4-((2-(methylamino)-6-(2,2,2-trifluoroethyl)thieno[2,3-d]pyrimidin-4-yl)amino)piperidine-1-carboxylate
(Catalog# : 26B007)
2565656-70-2 | Muvalaplin
(Catalog# : 20528)
Muvalaplin is a small molecule that inhibits formation of Lp(a) by interfering with t
2925330-18-1 | MAT2A-IN-22
(Catalog# : 26A021)
MAT2A-IN-22 (Compound 29-1) is a blood-brain barrier-penetrant and orally active MAT2
1497439-74-3 | AD-8007
(Catalog# : 26A018)
AD-8007 is a selective and brain-penetrant inhibitor of acetyl CoA synthase 2 (ACSS2).
1802650-31-2 | ZY-444
(Catalog# : 26A020)
ZY-444 is an anti-cancer agent by inhibiting PC ( pyruvate carboxylase ) activity.
2306525-79-9 | AD-5584
(Catalog# : 26A019)
AD-5584 is a novel brain-permeable ACSS2 inhibitors.
3079716-11-0 | IDB-003
(Catalog# : 26A017)
IDB-003 inhibits MDA-MB-231 tumor growth in vivo.
1357362-02-7 | Vafidemstat
(Catalog# : 18891)
Vafidemstat, also known as ORY 2001, is a lysine-specific histone demethylase (LSD1)