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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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Protein Tyrosine Kinase
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Cas Index 7
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Cas Index 7
745017-94-1 | MMAF (Monomethyl auristatin F)
(Catalog# : 17030611)
Monomethyl auristatin F (MMAF) is a synthetic antineoplastic agent. It is part of som
7752-54-7 | 7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine
(Catalog# : 17011908)
7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine
75172-81-5 | Migalastat HCl
(Catalog# : 16123048)
Migalastat HCl, also known as AT1001 or GR181413A, is a pharmacological chaperone tha
783348-36-7 | MLN120B
(Catalog# : 16070813)
MLN120B
790299-79-5 | Masitinib
(Catalog# : 121508)
Masitinib is a novel inhibitor for Kit and PDGFR/ with IC50 of 200 nM and 540 nM/800
726169-73-9 | Mocetinostat(MGCD0103)
(Catalog# : 111015)
Mocetinostat is an orally-bioavailable, spectrum-selective HDAC inhibitor. Mocetinost
71695-21-1 | Methyl 3-bromo-4-(dimethylamino)benzoate
(Catalog# : 81011)
Coming soon!
7120-41-4 | Methyl 5-bromo-2-methoxybenzoate
(Catalog# : 80306)
Coming soon!
77086-22-7 | (+)-MK801(maleate)
(Catalog# : 71903)
(+)-MK-801 is an uncompetitive antagonist of the N-Methyl-D-aspartate (NMDA) receptor
790702-57-7 | NGI-1
(Catalog# : 181171)
NGI-1, also knowns ML414, is a a cell-permeable inhibitor of oligosaccharyltransferas
78191-00-1 | N-Methoxy-N-methylacetamide
(Catalog# : 178223)
N-Methoxy-N-methylacetamide
79060-88-1 | NaBARF
(Catalog# : 121503)
Coming soon!
71555-25-4 | NSC319726
(Catalog# : 121409)
NSC319726 is a mutant p53R175 reactivator; inhibits growth of fibroblasts expressing
775288-71-6 | 1-(6-nitropyridin-3-yl)piperazine
(Catalog# : 82726)
Coming soon!
79513-35-2 | N-Boc-Ethylenediamine Hydrochloride
(Catalog# : 81709)
Coming soon!
761439-42-3 | NVP-TAE 684
(Catalog# : 52572)
NVP-TAE684(TAE684) is a highly potent and selective small-molecule ALK inhibitor, whi
79455-30-4 | Nicaraven
(Catalog# : 52508)
Nicaraven is a hydroxyl radical scavenger with antivasospastic and neuroprotective ef
761437-28-9 | NVP-TAE 226
(Catalog# : 52212)
NVP-TAE226 is a potent FAK inhibitor with IC50 of 5.5 nM and modestly potent to Pyk2(
7497-07-6 | NSC 405020
(Catalog# : 52241)
NSC-405020 is a novel small molecule inhibitor of MT1-MMP
79371-39-4 | 2-oxo-5,5-diphenyltetrahydro-4-furancarboxylic acid
(Catalog# : 204123)
728033-96-3 | OSI-930
(Catalog# : 185162)
OSI-930 is a selective thiophene-derived tyrosine kinase inhibitor with potential ant
73323-65-6 | 1-O-tert-butyl 2-O-methyl (2R)-pyrrolidine-1,2-dicarboxylate
(Catalog# : 83132)
Coming soon!
717142-73-9 | PP-001
(Catalog# : 25131)
7038-75-7 | 4-Pyrimidinol, 6-cyclopropyl- (7CI,8CI)
(Catalog# : 20481)
76748-86-2 | Pyronaridine Tetraphosphate
(Catalog# : 1810242)
Pyronaridine Tetraphosphate is an antimalarial agent, blocking B-hematin formation, i
72882-78-1 | PF-9366
(Catalog# : 184107)
PF-9366 is a novel inhibitor of human methionine adenosyltransferase 2A (Mat2A), the
74150-27-9 | Pimobendan
(Catalog# : 17030916)
Pimobendan is a veterinary medication. Pimobendan is both a calcium sensitizer and a
72496-41-4 | Pirarubicin
(Catalog# : 16070806)
Pirarubicin is an anthracycline drug. An analogue of the anthracycline antineoplastic
717906-29-1 | PF-431396
(Catalog# : 122818)
PF-431396 is dual focal adhesion kinase (FAK) and proline-rich tyrosine kinase 2 (PYK
714272-27-2 | Plinabulin
(Catalog# : 52603)
Plinabulin (NPI-2358) is a vascular disrupting agents (VDA) against tubulin-depolymer
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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
----
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)
-- 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
2800223-30-5 | Dabogratinib ( TYRA-300 )
(Catalog# : 24073)
Dabogratinib ( TYRA-300 ) is an Oral Selective FGFR3 Inhibitor (IC50 = 11 nM) for the
N/A | AF710B
(Catalog# : 25205)
AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1
2957874-18-7 | MAT2A inhibitor 5
(Catalog# : 25204)
MAT2A inhibitor 5 has a high potency for inhibiting MAT2A and a remarkable selectivit
1235733-73-9 | (Rac)-AF710B
(Catalog# : 24083)
AF-710B is an agonist of sigma and M1 muscarinic receptors; AF710B is an enantiomer o
863888-33-9 | Flurpiridaz-nonradiolabeled
(Catalog# : 25203)
Flurpiridazis a promising novel cardiac PET imaging tracer formed by the radiolabelin
863888-32-8 | Flurpiridaz-Precursor
(Catalog# : 25202)
Flurpiridaz-Precursor in stock.
1800405-30-4 | KL1333
(Catalog# : 25201)
KL1333 is an orally available, small organic molecule that reacts with NAD(P)H:quinon
1369489-71-3 | Palupiprant ( E7046 )
(Catalog# : 24055)
E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece
2460722-04-5 | Oveporexton ( TAK-861 )
(Catalog# : 25194)
Oveporexton isan oral small molecule selective orexin type-2 receptor (OX2R) agonist.
2506273-81-8 | VT-3989
(Catalog# : 25200)
VT3989, a first-in-class potent oral TEAD palmitoylation inhibitor, disrupts YAP tran