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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
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NF-κB
Protein Tyrosine Kinase
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Cas Index 2
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Cas Index 2
256477-09-5 | UK-371804
(Catalog# : 1791114)
UK-371804 is a potent and selective uPA inhibitor with excellent enzyme potency (Ki 1
256476-36-5 | UK-371804 HCl
(Catalog# : 17031008)
UK-371804 is a potent and selective urokinase-type plasmogen activator (uPA) inhibi
2590556-80-0 | Velzatinib (IDRX-42, M-4205)
(Catalog# : 26A009)
Velzatinib is an orally bioavailable small molecule inhibitor of multiple mutated for
2506273-81-8 | VT-3989
(Catalog# : 25200)
VT3989, a first-in-class potent oral TEAD palmitoylation inhibitor, disrupts YAP tran
2129515-96-2 | Vepafestinib ( Synonyms: TAS0953 ; HM06)
(Catalog# : 25166)
Vepafestinib, also known as HM06 and TAS0953, is a RET-selective inhibitor with enhan
2647442-33-7 | VV116
(Catalog# : 20536)
VV116, also known as JT001, is an oral drug candidate of nucleoside analog against SA
2649467-58-1 | VX-548
(Catalog# : 20525)
2169916-18-9 | VTP-50469
(Catalog# : 20111202)
VTP-50469 is a novel, potent, selective, orally-available MeninMLL1 inhibitor, being
2173134-00-2 | VUN34002
(Catalog# : 2071534)
VUN34002, also known as Vanin-1-IN-1 is an inhibitor of vanin-1 enzyme which is a cel
23261-20-3 | VAL-083
(Catalog# : 112091)
VAL-083 is a bi-functional alkylating agent, with potential antineoplastic activity.
2097381-85-4 | VH298
(Catalog# : 18581)
VH-298 is a potent VHL inhibitor that stabilizes HIF-α and elicits a hypoxic respons
2095432-65-6 | Verubecestat TFA
(Catalog# : 18417)
Verubecestat, also known as MK-8931 or SCH 900931, is a potent and selective beta-sec
235106-62-4 | VP 14637
(Catalog# : 011112)
Coming soon!
212141-54-3 | Vatalanib
(Catalog# : 010434)
Vatalanib free base is an inhibitor of VEGFR2/KDR with IC50 of 37 nM, less potent aga
2630378-05-9 | Wu-5
(Catalog# : 24160)
Wu-5 is a USP10 inhibitor that can inhibit FLT3 and AMPK pathways, induce FLT3-ITD de
2229025-70-9 | WM 3835
(Catalog# : 20504)
WM 3835 is a lysine acetyltransferase HBO1 (KAT7) inhibitor. It reduces H3K14ac level
2253985-29-2 | WK500B
(Catalog# : 20491)
WK500B is a BCL6 inhibitor. WK500B engaged BCL6 inside cells, blocked BCL6 repression
2055397-28-7 | WM-1119
(Catalog# : 181181)
WM-1119 is a highly potent, selective inhibitor of lysine acetyltransferase KAT6A wit
211555-05-4 | WHI-P97
(Catalog# : 185710)
WHI-P97 is a JAK3 inhibitor.
214358-33-5 | 1400W
(Catalog# : 17021321)
1400W is a slow, tight binding, and highly selective inhibitor ofinducible nitric-oxi
2012607-27-9 | WNK463
(Catalog# : 6111509)
WNK463 is a pan-WNK-kinase inhibitor. It potently inhibits the in vitro kinase activi
211555-04-3 | WHI-P154
(Catalog# : 73107)
WHI-P 154 is a JAK3 inhibitor (IC50 = 1.8 M) that displays no activity at JAK1 or JAK
211555-08-7 | WHI-P180
(Catalog# : 52221)
WHI-P180 is a potent EGFR and Cdk2 inhibitors with IC50 of 4.0 and 1.0 uM, respective
2595308-10-2 | XRD-0394
(Catalog# : 25042)
XRD-0394 is a DNA-PKcs inhibitor. XRD-0394 selectively targets, binds to and inhibits
2700286-66-2 | XPW1
(Catalog# : 20659)
XPW1 is a potent and selective CDK9 inhibitor with excellent activity against clear c
2367004-54-2 | XL092
(Catalog# : 20506)
XL092 is an ATP-competitive inhibitor of multiple RTKs including MET, VEGFR2, AXL and
2061980-01-4 | XMU-MP-1
(Catalog# : 18579)
XMU-MP-1 is a potent and selective MST1/2 inhibitor.
284028-89-3 | XAV-939
(Catalog# : 52632)
XAV939 is a small molecule and selective Wnt pathway -catenin-mediated transcription
2225824-53-1 | YTX-465
(Catalog# : 24139)
YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
2863670-67-9 | YCT529
(Catalog# : 24120)
YCT529, an RAR-α inhibitor, is used as a contraceptive, with a 99% effectiveness. YC
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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)