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Inhibitors&Agonists
PI3K/Akt/mTOR
Epigenetics
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Angiogenesis
Apoptosis
Autophagy
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MAPK
Cytoskeletal Signaling
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DNA Damage
Stem Cells & Wnt
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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
JAK/STAT
MAPK
Cytoskeletal Signaling
Cell Cycle
TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
Ubiquitin
Neuronal Signaling
NF-κB
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
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Boronic Acids
Bromides
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Deuterated
Fluorides
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Nitro Compounds
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Cas Index 6
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Cas Index 6
63820-72-4 | Methyl 2,5-dimethylnicotinate
(Catalog# : 16062101)
Methyl 2,5-dimethylnicotinate
603139-19-1 | MK-0822
(Catalog# : 101915)
MK-0822 is an inhibitor of cathepsin K with potential anti-osteoporotic activity. It
610791-05-4 | Methyl 1-Boc-azetidine-3-carboxylate
(Catalog# : 83122)
Coming soon!
606143-89-9 | MEK162
(Catalog# : 52774)
MEK162(ARRY-438162; ARRY-162) is a potent inhibitor of MEK1/2 with IC50 of 12 nM.
667463-62-9 | MLS-2052
(Catalog# : 52582)
6-BIO(6-Bromoindirubin-3'-oxime) is a potent and selective inhibitor of GSK-3 and
6300-44-3 | NSC-45586
(Catalog# : 20483)
NSC-45586 is a pan-PHLPP inhibitor selective for PHLPP1 and PHLPP2.
651734-53-1 | N-Benzyl-2,6-difluoro-3,5-dimethoxyaniline
(Catalog# : 20411)
6097-07-0 | N-(4-PENTYNYL)PHTHALIMIDE 97
(Catalog# : S-204150)
65473-14-5 | Naftifine HCl
(Catalog# : 1791514)
Naftifine is an allylamine antifungal drug for the topical treatment of tinea pedis,
66648-43-9 | N-trans-Feruloyltyramine
(Catalog# : 201708019)
N-Trans-Feruloyltyramine|(E)-3-(4-hydroxy-3-Methoxy-phenyl)-N-[2-(4-hydroxyphenyl)eth
65472-88-0 | Naftifine
(Catalog# : 16122834)
Naftifine is an allylamine antifungal drug for the topical treatment of tinea pedis,
63612-50-0 | Nilutamide
(Catalog# : 122510)
Nilutamide is an Androgen Receptor Inhibitor. The mechanism of action of nilutamide i
69049-73-6 | Nedocromil
(Catalog# : 122201)
Nedocromil is an inhaled anti-inflammatory agent for the preventive management of ast
675576-98-4 | Nutlin-3a
(Catalog# : 121406)
Nutlin-3a is an inhibitor of MDM2 (human homolog of murine double minute 2), which di
6638-79-5 | N,O-Dimethylhydroxylamine hydrochloride
(Catalog# : 90605)
Coming soon!
62965-35-9 | N-Boc-L-tert-Leucine
(Catalog# : 81715)
Coming soon!
6384-92-5 | NMDA
(Catalog# : 52811)
NMDA(N-Methyl-D-aspartic acid) is an amino acid derivative that acts as a specific ag
698387-09-6 | Neratinib
(Catalog# : 52723)
Neratinib (HKI-272) is an orally available, irreversible tyrosine kinase inhibitor wi
6506-37-2 | Nimorazole
(Catalog# : 52512)
Nimorazole is a nitroimidazole anti-infective.
6233-83-6 | Oxytocin acetate
(Catalog# : 1791513)
Oxytocin is a medication and hormone. As a medication, it is used to cause contractio
638132-34-0 | ONO-7300243
(Catalog# : 16122724)
ONO-7300243 is a novel, potent LPA1(Lysophosphatidic Acid Receptor) antagonist with a
686344-29-6 | Otenabant
(Catalog# : 111006)
Otenabant is a recently discovered selective, high affinity, competitive CB1 receptor
686347-12-6 | Otenabant Hydrochloride
(Catalog# : 102603)
Otenabant Hcl (CP-945598) is a recently discovered selective, high affinity, competit
61825-94-3 | Oxaliplatin
(Catalog# : 101918)
Coming soon!
60031-08-5 | 3-oxo-1,2-dihydroindene-5-carboxylic acid
(Catalog# : 81936)
Coming soon!
69975-66-2 | 3-oxo-1,2-dihydroindene-5-carbonitrile
(Catalog# : 81935)
Coming soon!
60899-34-5 | 1-Oxo-2,3-dihydro-1H-indene-4-carbonitrile
(Catalog# : 81932)
Coming soon!
688348-25-6 | PDM-2
(Catalog# : 2061301)
PDM-2 is an analog of resveratrol acting as a potent and selective aryl hydrocarbon r
68238-36-8 | Patent blue violet purified
(Catalog# : 2017080117)
Purification of patent blue purple and isosulfan blue, it is a kind of dye and pigmen
68252-19-7 | Pirmenol
(Catalog# : 17030702)
Pirmenol is an antiarrhythmic agent. Pirmenol inhibits muscarinic acetylcholine recep
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Products Catalog
Signaling Pathway
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- 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
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Bcr-Abl
----
Src
----
ALK
----
Syk
----
FAK
----
BTK
----
HIF
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Cytoskeletal Signaling
----
Akt
----
Bcr-Abl
----
PKC
----
FAK
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
-- TGF-beta/Smad
----
Bcr-Abl
----
PKC
----
ROCK
----
TGF-beta/Smad
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
-- 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
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
----
Sigma Receptor
----
Ras
----
mAChR
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
-- 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
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
-- 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
-- Vitamin D Related
----
VD/VDR
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
-- PROTAC
----
Molecular Glues
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
3034479-99-4 | HC-5404
(Catalog# : 24112)
HC-5404 is a novel, highly selective and potent PERK inhibitor.
2883540-92-7 | STX-478
(Catalog# : 20633)
STX-478 is a second generation, mutant-selective, oral PI3Ka small molecule allosteri
1421936-85-7 | Iclepertin (BI-425809)
(Catalog# : 24084)
Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
1990504-34-1 | Bomedemstat
(Catalog# : 24001)
Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl
2892065-45-9 | PLX-4545
(Catalog# : 24111)
PLX-4545 is an orally bioavailable molecular glue degrader of IKZF2 designed to desta
3034880-93-5 | VVD-130037 ( BAY-3605349 )
(Catalog# : 24110)
VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
681159-27-3 | CBR-5884
(Catalog# : 24109)
CBR 5884 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor which was able to inhi
1998725-11-3 | JHU-083
(Catalog# : 24108)
JHU-083 selectively blocks glutaminase activity in brain CD11b+ cells and prevents de
2251753-65-6 | LXH-3-71
(Catalog# : 24107)
LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH
2259648-80-9 | CC-92480 ( Mezigdomide )
(Catalog# : 20510)
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno