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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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MAPK
Membrane Transporter/Ion Channel
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Cas Index 3
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Cas Index 3
3002056-30-3 | NST-628
(Catalog# : 24058)
NST-628 is a potent pan-RAF-MEK molecular glue that prevents the phosphorylation and
3032452-90-4 | NPD-3519
(Catalog# : 24089)
357400-13-6 | NNC-55-0396
(Catalog# : 24038)
NNC-55-0396 is a highly selective T-type calcium channel blocker which can be used fo
376348-67-3 | N-(8-Benzyl-8-azabicyclo[3.2.1]oct-3-yl-exo)-2-methylpropanamide
(Catalog# : 2071632)
38941-29-6 | N-(2-methylbenzyl)-4,5-dihydro-1H-imidazol-2-amine
(Catalog# : 2062031)
3197-25-9 | 5-(N-PHTHALIMIDO)-2-PENTANONE
(Catalog# : 2062010)
331949-35-0 | Nexinhib20
(Catalog# : 1811152)
Nexinhib20 is a Rab27 inhibitor that inhibits neutrophil exocytosis and is active in
341001-38-5 | Nucleozin
(Catalog# : 185164)
Nucleozin is an antivirus agent. Nucleozin targets influenza A nucleoprotein (NP), a
357-08-4 | Naloxone HCl
(Catalog# : 178305)
Naloxone is a μ-opioid receptor (MOR) inverse agonist. Naloxone has an extremely hig
343351-67-7 | NSC697923
(Catalog# : 16122791)
NSC697923 is a cell-permeable and selective inhibitor of the Ub-conjugating enzyme (E
353262-04-1 | NS6180
(Catalog# : 011118)
NS6180 is a novel potent and selective KCa3.1 channel inhibitor(IC50= 9 nM) prevents
300842-64-2 | NVP-ACC-789
(Catalog# : 010432)
Coming soon!
362003-83-6 | NVP 231
(Catalog# : 122833)
NVP-231 is a potent, specific, and reversible CerK inhibitor(IC50=122 nM) that compet
348575-88-2 | Optovin
(Catalog# : 102609)
Optovin is a reversible photoactive TRPA1 activator; stimulates human TRPA1 channels
313706-15-9 | 1-O-tert-butyl 3-O-methyl (3S)-pyrrolidine-1,3-dicarboxylate
(Catalog# : 83131)
Coming soon!
314741-39-4 | 1-O-tert-butyl 3-O-methyl (3S)-piperazine-1,3-dicarboxylate
(Catalog# : 81820)
Coming soon!
3036158-98-9 | PF-07853578
(Catalog# : 25155)
PF-07853578 is a Patatin-Like Phospholipase Domain-Containing 3 Protein (PNPLA3) modu
3076487-66-3 | PBAS-499
(Catalog# : 25135)
321688-88-4 | Poloxin
(Catalog# : L20349)
Poloxin is the first small-molecule inhibitor specifically targeting the function of
377727-87-2 | Preladenant
(Catalog# : 2061707)
Preladenant, also known as SCH 420814, is a potent and selective antagonist at the ad
312905-21-8 | Piperazine, 1-[(1aR,10bS)-1,1-difluoro-1,1a,6,10b-tetrahydrodibenzo[a,e]cyclopropa[c]cyclohepten-6-yl]-, hydrochloride (1:1), rel-
(Catalog# : S-204141)
31645-39-3 | Palifosfamide
(Catalog# : 192272)
Palifosfamide, also known as ZIO201, is a synthetic mustard compound with potential a
346688-38-8 | Pridopidine
(Catalog# : 18673)
Pridopidine, also known as ACR16, is a dopamine stabilizer, which improves motor perf
309739-67-1 | PP2 Analog
(Catalog# : 185147)
PP2 Analog is an analog of PP2 that acts as a protein trafficking modulator.
330786-25-9 | PCI-29732
(Catalog# : 184101)
PCI-29732 is a BTK inhibitor. It acts by blocking B cell antigen receptor (BCR)-media
31083-55-3 | PRT4165
(Catalog# : 1791515)
PRT4165 is a small molecule inhibitor of polycomb repressive complex 1, which inhibit
372196-67-3 | PIK-75
(Catalog# : 17030913)
PIK-75 was developed as part of a PI 3-kinase drug discovery program. PIK75 attenuate
301353-96-8 | P7C3
(Catalog# : 16122837)
P7C3 is a proneurogenic, neuroprotective agent. P7C3 protects newborn neurons from ap
396091-73-9 | Pasireotide
(Catalog# : 61115)
Pasireotide(SOM 230) is a stable cyclohexapeptide somatostatin mimic that exhibits un
371935-74-9 | PI-103
(Catalog# : 160926002)
It inhibits ATR and ATM only at much higher concentrations (IC50= 850 and 920 nM, res
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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
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)
1260247-42-4 | LLL12
(Catalog# : 25075)
LLL12 is a potent STAT3 inhibitor.
2758659-09-3 | ECC-5004
(Catalog# : 26A015)
ECC5004 (AZD5004) is a novel small-molecule GLP-1 RA for use as an oral therapy for c