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+86-17702719238
sales@sun-shinechem.com
Home
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Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
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Immunology & Inflammation
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MAPK
Membrane Transporter/Ion Channel
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Cas Index 2
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Cas Index 2
2416875-06-2 | Pyrazolo[1,5-a]pyrimidine, 7-chloro-5-(1-ethylpropyl)-
(Catalog# : 24081)
2893778-31-7 | PHGDH-IN-3
(Catalog# : 25077)
PHGDH-IN-3 is an orally active phosphoglycerate dehydrogenase (PHGDH) inhibitor.
2101700-15-4 | Pirtobrutinib
(Catalog# : 20618)
2904682-19-3 | PDS-0330
(Catalog# : 231106)
PDS0330 is a new claudin-1 inhibitor in Colorectal Cancer.
2253123-16-7 | Pimicotinib ( ABSK02 )
(Catalog# : 20548)
Pimicotinib is a novel small molecule inhibitor of CSF-1R, which is orally available,
260415-63-2 | PD-173955
(Catalog# : 20499)
PD-173955 is a src tyrosine kinase inhibitor. PD173955 inhibited Bcr-Abl-dependent ce
217171-01-2 | PD-173212
(Catalog# : 20468)
PD-173212 is a small molecule N-type calcium channel blocker. PD173212 fully reduced
2172870-89-0 | Paltusotine ( CRN-00808 )
(Catalog# : 20294)
Paltusotine is a new class of oral, selective, nonpeptide, somatostatin receptor type
26305-03-3 | Pepstatin
(Catalog# : 2071607)
Pepstatin inhibits the aspartic protease endothiapepsin.
2227425-05-8 | PF-06869206
(Catalog# : 2071506)
PF-06869206 is an Orally Bioavailable Selective Inhibitors of the Sodium-Phosphate Co
26033-20-5 | 3-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE
(Catalog# : 2062020)
248282-01-1 | Paquinimod
(Catalog# : 2061706)
Paquinimod, also known as ABR‑215757, is a S100A9 inhibitor preventing S100A9 bindi
2170608-82-7 | PZ-2891
(Catalog# : 193282)
PZ-2891 is a potent and selective, orally active Pantothenate kinase (PANK) modulator
2102501-84-6 | PF-06835919 ( MDK-1846 )
(Catalog# : 193264)
MDK1846 is a potent ketohexokinase (KHK) inhibitor.
2185857-97-8 | PF-06873600
(Catalog# : 191145)
PF-06873600 is an orally bioavailable, cyclin-dependent kinase (CDK) inhibitor, with
2070014-93-4 | PF-CBP1 HCl
(Catalog# : 179112)
PF-CBP1, also known as PF-06670910, is potent and highly-selective inhibitor of the b
25606-41-1 | Propamocarb hydrochloride
(Catalog# : 2017080115)
Propamocarb hydrochloride is an efficient, broad-spectrum, carbamate fungicide safe.
257933-82-7 | Pelitinib
(Catalog# : 17022702)
Pelitinib (EKB-569; WAY-EKB 569) is a potent irreversible EGFR inhibitor with IC50 of
202350-68-3 | PNU-159682
(Catalog# : 16071409)
PNU-159682 is a major active metabolite of nemorubicin (MMDX) in human liver microsom
269718-84-5 | Pardoprunox
(Catalog# : 122523)
Pardoprunox is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT
219580-11-7 | PD173074
(Catalog# : 122212)
PD173074 is a small-molecule FGFR3-selective tyrosine kinase inhibitor (TKI), as a th
269718-83-4 | Pardoprunox hydrochloride
(Catalog# : 111010)
Pardoprunox hydrochloride is a novel partial dopamine D2 and D3 receptor agonist and
20062-91-3 | 3-(4-phenoxyphenyl)propanoic acid
(Catalog# : 90709)
Coming soon!
212844-53-6 | Purvalanol A
(Catalog# : 52564)
Purvalanol A(NG-60) is a potent, cell-permeable, and selective inhibitor of cyclin-de
212844-54-7 | Purvalanol B
(Catalog# : 52559)
Purvalanol B(NG-95) is a cyclin-dependent kinase inhibitor with IC50 values of 6, 6,
2645-32-1 | PR-619
(Catalog# : 52227)
PR-619 is a broad-range DUB inhibitor with potential for further development as a che
2416858-84-7 | Quecitinib
(Catalog# : 26A002)
Quecitinib is a dual inhibitor of JAK1 and TYK2.
2301974-60-5 | Ranosidenib
(Catalog# : 25150)
Ranosidenib, also known as HMPL-306, is an isocitrate dehydrogenase (IDH) inhibitor.
2169919-21-3 | Revumenib
(Catalog# : 25140)
Revumenib, also known as SNDX-5613, is a potent and specific Menin-MLL inhibitor. It
206885-38-3 | Ronopterin
(Catalog# : 25084)
Ronopterin is a potent Nitric oxide synthase inhibitor and Neuroprotectant.
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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)