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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
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Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
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Immunology & Inflammation
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MAPK
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Cas Index 1
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Cas Index 1
1627902-21-9 | JNJ-54175446
(Catalog# : 20534)
JNJ-54175446 is a potent and selective P2X7 Receptor Antagonist. JNJ-54175446 is pote
1638611-48-9 | JC124
(Catalog# : 20495)
JC124 is a NLRP3 Inflammasome Inhibitor.
188791-09-5 | JTE-607 HCl
(Catalog# : 20479)
JTE-607, also known as TO-207, is a cytokine production inhibitor potentially for the
1309784-09-5 | JTE-051
(Catalog# : 20458)
JTE-051 is a novel inhibitor of interleukin-2-inducible T cell kinase (ITK), suppress
1380392-05-1 | JMS-17-2
(Catalog# : 2071624)
JMS-17-2 is a potent and selective antagonist of CX3CR1.
1443235-95-7 | JAK3-IN-2
(Catalog# : 2071551)
JAK3-IN-2 is a potent and highly selective JAK3 inhibitor.
1572510-42-9 | JNJ-632
(Catalog# : 2071507)
JNJ-632 is a potent HVV capsid assembly modulator and HBV replication inhibitor with
1408064-71-0 | JNK-IN-7
(Catalog# : 2061305)
JNK-IN-7 is a relatively selective JNKs inhibitor(IC50= 1.54/1.99/0.75 for JNK1/2/3);
1408064-71-0 | JNK-IN-7
(Catalog# : 2061305)
1597402-27-1 | JPH203 HCl ( Nanvuranlat )
(Catalog# : 18381)
JPH203, also known as KYT-0353, is a potent and selective LAT1 selective ( L-type ami
1142363-52-7 | JNJ-40346527
(Catalog# : 1711221)
JNJ-40346527 is a small molecule and orally available inhibitor of colony-stimulating
1254977-87-1 | JNJ-42153605
(Catalog# : 1791311)
JNJ-42153605 is a potent and selective mGlu2 receptor PAM with an acceptable pharmaco
1346528-51-5 | JNJ-42165279(2HCl salt)
(Catalog# : 1783012)
JNJ-42165279 exhibited excellent ADME and pharmacodynamic properties as evidenced by
1346528-52-6 | JNJ-42165279(mono HCl salt)
(Catalog# : 1783011)
JNJ-42165279 is a potent and selective fatty acid amide hydrolase (FAAH) inhibitor. J
1913252-04-6 | JQ-EZ-05
(Catalog# : 2017871)
JQ-EZ-05, also known as JQEZ5, is a bio active chemical.
1410880-22-6 | JNK-IN-8
(Catalog# : 16123027)
JNK-IN-8, also known as JNK Inhibitor XVI, is a selective JNK inhibitor that inhibits
1802326-66-4 | JNJ 63533054
(Catalog# : 16123026)
JNJ 63533054 is a potent and selective GPR139 agonist (EC50 = 16 nM) that is brain an
1346528-50-4 | JNJ-42165279
(Catalog# : 16123025)
JNJ-42165279 is a potent and selective fatty acid amide hydrolase (FAAH) inhibitor. J
1037592-40-7 | JPH203 ( KYT-0353 )
(Catalog# : 6112701)
JPH203(also known as KYT-0353) is a potent and selective LAT1 selective ( L-type amin
1805787-93-2 | JAK3-IN-1
(Catalog# : 6111506)
JAK3-IN-1 is a potent JAK3 inhibitor with IC50 of 4.8 nM, also inhibits JAK1 (IC50 =
1268524-70-4 | (+)-JQ1
(Catalog# : 16070105)
(+)-JQ1 is a BET potent BET bromodomain Inhibitor. Bromodomain and extra terminal dom
1193383-09-3 | JNJ-42041935
(Catalog# : 031401)
JNJ-42041935 is a potent (pKi = 7.3-7.9), 2-oxoglutarate competitive, reversible, and
1639422-97-1 | JH-VIII-157-02
(Catalog# : 62103)
JH-VIII-157-02, a structural analogue of alectinib, is potent against the G1202R muta
1700693-08-8 | JH-II-127
(Catalog# : 012010)
JH-II-127 is a potent and selective inhibitor of both wild-type and G2019S mutant LRR
1127498-03-6 | JNJ 40411813
(Catalog# : 122939)
JNJ-40411813 is a novel positive allosteric modulator of the metabotropic Glutamate 2
1210004-12-8 | JZL195
(Catalog# : 111007)
JZL195 is a selective and efficacious dual FAAH/MAGL inhibitor with IC50 of 13 nM and
1094873-14-9 | JNJ-31020028
(Catalog# : 100903)
JNJ-31020028 is a selective brain penetrant small molecule antagonist of the neuropep
1146963-51-0 | J-147
(Catalog# : 52505)
J-147 is a broad spectrum neuroprotective phenyl hydrazide compound(EC50=60-115 nM) w
199596-05-9 | JIB-04
(Catalog# : 52225)
JIB-04 is a pan-selective Jumonji histone demethylase inihibitor with IC50 of 230, 34
1215115-03-9 | KH-3
(Catalog# : 24143)
KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
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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
----
Bradykinin 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
----
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
-- 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
2377000-84-3 | Dencatistat
(Catalog# : 25177)
Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
1898207-64-1 | DS-1001b
(Catalog# : 25178)
DS-1001 is an oral brain-penetrant mutant IDH1 selective inhibitor.
1016340-64-9 | Z57346765
(Catalog# : 25191)
Z57346765 is a PGK1-specific inhibitor that reduces the activity of metabolic enzymes
2416095-06-0 | CBR-470-1
(Catalog# : 25192)
CBR-470-1 is an Inhibitor of the glycolytic enzyme PGK1that induces Nrf2 activity.
1898206-17-1 | Safusidenib
(Catalog# : 25149)
Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl
2803470-63-3 | HC-7366
(Catalog# : 25076)
HC-7366 is a potent and selective activator of the general control nonderepressible 2
146426-40-6 | Flavopiridol ( Alvocidib )
(Catalog# : 237071)
Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
2201056-66-6 | AG-270
(Catalog# : 25176)
MAT2A Inhibitor AG-270 is an orally available small molecule inhibitor of methionine
618913-30-7 | AZD-5904
(Catalog# : 181121)
AZD5904 is a potent orally bioavailable MPO inhibitor. In preclinical studies, AZD590
2035010-37-6 | ALT-007
(Catalog# : 25157)
ALT-007 is an orally bioavailable SPT inhibitor that is more potent than myriocin, sa