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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
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Cas Index 1
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Cas Index 1
1020634-41-6 | Soclenicant (BNC-210 ; IW-2143)
(Catalog# : 25195)
Soclenicant (BNC-210 ; IW-2143) is a novel α7 nicotinic acetylcholine receptor-negat
1898207-64-1 | Safusidenib Erbumine
(Catalog# : 25178)
DS-1001 is an oral brain-penetrant mutant IDH1 selective inhibitor.
1898206-17-1 | Safusidenib
(Catalog# : 25149)
Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl
17094-01-8 | Sepiapterin
(Catalog# : 25117)
Sepiapterin is a tetrahydrobiopterin (BH4) precursor.
1415792-84-5 | Sovleplenib
(Catalog# : 25107)
Sovleplenib is a tyrosine kinase inhibitor. It is also an antineoplastic agent.
1394808-20-8 | SUVN-G3031 HCl
(Catalog# : 25087)
SUVN-G3031 is a Histamine H3 receptor antagonist, which is potentially useful for tre
160162-42-5 | SR-11302
(Catalog# : 24153)
SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor.
1150153-86-8 | SR 16584
(Catalog# : 24137)
SR 16584 is an antagonist of the α3β4 nAChR subtype (IC50 = 10.2 μM).
1262873-06-2 | Sepetaprost
(Catalog# : 24119)
Sepetaprost is a prodrug of ONO-AG-367. It has been used in trials studying the treat
152121-30-7 | SB-202190
(Catalog# : 24106)
SB-202190 is a highly selective, potent and cell-permeable inhibitor of p38 MAP kinas
1648843-04-2 | SX-682
(Catalog# : 24082)
SX-682 is a potent and selective Cxcr1/2 inhibitor potentially useful for castration-
1933514-13-6 | Sebetralstat free base
(Catalog# : 24048)
Sebetralstat (KVD-900), an oral plasma kallikrein inhibitor.
1246960-09-7 | SPG-601 ( VSN-16R )
(Catalog# : 24042)
SPG-601 (formerly VSN-16R) is an oral, first-in-class, small-molecule, positive modul
1878218-66-6 | SY-008 Acetate
(Catalog# : 24016)
SY-008 is a sodium glucose transporter 1 (SGLT1) inhibitor.
1480443-32-0 | SY-008
(Catalog# : 24021)
SY-008 is a sodium glucose transporter 1 (SGLT1) inhibitor.
194032-32-1 | (S)-1-BOC-2-METHYL-[1,4]DIAZEPANE
(Catalog# : 20541)
131690-60-3 | (S)-3-AMINO-3-(4-CHLORO-PHENYL)-PROPIONIC ACID
(Catalog# : 20516)
1980023-96-8 | (S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethanamine
(Catalog# : 20396)
100874-08-6 | SB-4 agonist
(Catalog# : G20378)
SB 4 is a potent BMP4 agonist.
1310422-41-3 (HCl) | SEP-363856 HCl ( SEP-856 )
(Catalog# : 822222)
SEP-363856 is a novel trace amine receptor 1 (TAAR1) agonist with serotonin 5-HT1A ac
1629138-41-5 | SRI-011381
(Catalog# : L20355)
SRI-011381 is an agonist of the TGF-beta signaling pathway for treatment of Alzheimer
1449597-34-5 | SMN-C3
(Catalog# : 20344)
SMN-C3is an orally active SMN2 splicing modulator and has the potential to treat spin
1619931-27-9 | Seralutinib
(Catalog# : 21238)
Seralutinib, also known as PK-10571 and GB002, is a Novel Inhaled Pdgfr Kinase Inhibi
1446712-19-1 | SNG-1153
(Catalog# : 21228)
SNG-1153 is a modulator of estrogen receptor ER-alpha36.
1293281-49-8 | Seltorexant
(Catalog# : 81498)
Seltorexant, also known as JNJ-42847922 and MIN-202, is a selective orexin-2 receptor
1415792-84-5 | Samelisant
(Catalog# : 20123101)
Samelisant is a novel, highly selective and potent small molecule oral inhibitor targ
1401682-78-7 | Senaparib
(Catalog# : 20103002)
Senaparib (IMP4297) is a novel agent targeting PARP (poly-ADP ribose polymerase) with
1433953-83-3 | SAR 131675
(Catalog# : 2091901)
SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine
18298-32-4 | SB 225002
(Catalog# : 2071510)
1369767-20-3 | ((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2-diyl)dimethanol
(Catalog# : 202331)
The bulk may be provided by custom synthesis.
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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
----
Methionine Adenosyltransferase (MAT)
-- 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
----
SSTR
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- 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
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
----
Hemoglobin
-- 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)
----
CGRP-Receptor
----
TRP-Channel
-- 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)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- 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
-- Nuclear Receptor
----
Androgen Receptor(AR)
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
1429882-07-4 | MRX-2843
(Catalog# : 26A087)
MRX-2843 is an orally bioavailable inhibitor of two receptor tyrosine kinases (RTKs),
1637394-01-4 | GDC-0134
(Catalog# : 20432)
GDC-0134 is a MAP3K12 (DLK) Inhibitor.
2128698-24-6 | BI-847325
(Catalog# : 25046)
BI-847325 is a novel, ATP-competitive, orally available inhibitor of Aurora kinases a
3137699-54-5 | GDD-261
(Catalog# : 26A084)
GDD-261 is an orally active, allosteric inhibitor of phosphoglycerate dehydrogenase (
2669009-92-9 | Atebimetinib
(Catalog# : 25148)
Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1
3062177-59-4 | BH-30643
(Catalog# : 26A047)
BH-30643 is a novel, orally available, non-covalent, macrocyclic, mutant selective OM
2490431-16-6 | ERAS-801 ( JGK-068S )
(Catalog# : 20635)
ERAS-801 ( JGK-068S ) is a potent EGFR inhibitor.
877176-23-3 | Aderamastat ( Synonyms: FP-025 )
(Catalog# : 26A086)
Aderamastat (FP-025) is an oral, selective, non-hydroxamate-based, non-competitive in
1857296-22-0 | 5-Formyl-4-methyl-1H-indole-2-carbonitrile
(Catalog# : 25095)
2923986-48-3 | MAT2A inhibitor-[Compound 1]
(Catalog# : 26A083)
Compound 1 is a new MAT2A inhibitor.