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MAPK
Membrane Transporter/Ion Channel
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Neuronal Signaling
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Protein Tyrosine Kinase
Proteases
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Deuterated
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Iodos
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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
Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
PI3K/Akt/mTOR
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TGF-beta/Smad
Ubiquitin
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Cas Index 3
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Cas Index 3
343787-29-1 | CP-673451
(Catalog# : 16070704)
CP-673451 is a selective inhibitor of PDGFR/ with IC50 of 10 nM/1 nM in cell-free ass
38628-51-2 | 3-(4-CARBOXYPHENYL)PROPIONIC ACID
(Catalog# : 90617)
Coming soon!
38944-14-8 | 2-(4-Chlorophenyl)pyrrolidine
(Catalog# : 83102)
Coming soon!
370586-05-3 | CID-797718
(Catalog# : 52228)
CID-797718 is a compound with unknown details
301326-22-7 | CH-223191
(Catalog# : 52218)
CH-223191 is a potent and specificaryl hydrocarbon receptor (AhR)antagonist withIC50o
344940-63-2 | Diphenylterazine
(Catalog# : 20324)
Diphenylterazine is a bioluminescence agent. Diphenylterazine alone yields very littl
39589-98-5 | Dimethyl carbate
(Catalog# : 20274)
Dimethyl carbate is an insect repellent. It can be prepared by the Diels–Alder reac
312905-15-0 | 1,1-Difluorocyclopropane-1-dibenzosuberyl Pyrazinium Bromide
(Catalog# : 2062005)
331830-20-7 | 1,4-DPCA
(Catalog# : 204608)
1,4-DPCA is a potent and selective inhibitor of prolyl 4-hydroxylase.
356057-34-6 | Darapladib
(Catalog# : 193202)
Darapladib, also known as SB-480848, is a reversible lipoprotein-associated phospholi
314263-42-8 | DCG04
(Catalog# : 179813)
DCG04 is a multivalent ligand for the mannose-6-phosphate receptor for endolysosomal
309-29-5 | Doxapram
(Catalog# : 16122937)
Doxapram is a respiratory stimulant. Administered intravenously, doxapram stimulates
34368-04-2 | Dobutamine HCl
(Catalog# : 16122936)
Dobutamine is a sympathomimetic drug used in the treatment of heart failure and cardi
301836-43-1 | D4476
(Catalog# : 102611)
D4476, a cell-permeant inhibitor of CK1_delta_ (IC90 <10 uM), suppresses the site-
35018-16-7 | 2-(2,2-diMethylpyrrolidin-1-yl)ethanaMine
(Catalog# : 92201)
Coming soon!
313340-08-8 | 3,5-dichloro-6-ethylpyrazine-2-carboxamide
(Catalog# : 91830)
Coming soon!
312-84-5 | D-Serine
(Catalog# : 90604)
Coming soon!
33301-41-6 | 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate
(Catalog# : 83117)
Coming soon!
36476-86-5 | 1-(Diphenylmethyl)azetidine-3-carbonitrile
(Catalog# : 83112)
Coming soon!
304448-55-3 | Dynasore
(Catalog# : 52514)
Dynasore is a cell-permeable small molecule that inhibits the GTPase activity of dyna
304903-10-4 | 1-ETHYL-1H-PYRAZOLE-4-CARBALDEHYDE
(Catalog# : 20523)
3258-02-4 | EIDD-1931
(Catalog# : 2071537)
EIDD-1931 is a promising COVID-19 inhibitor. EIDD-1931 has broad spectrum antiviral a
388071-27-0 | erythro-N-Boc-L-3,5-difluorophenylalanine epoxide
(Catalog# : 20177314)
ERYTHRO-N-BOC-L-3,5-DIFLUOROPHENYLALANINE EPOXIDE
328998-25-0 | 4E1RCat
(Catalog# : 17011301)
4E1RCat is an inhibitor of the eIF4F translation initiation complex that blocks eIF4E
36589-58-9 | Eprodisate Sodium
(Catalog# : 16122940)
Eprodisate, also known as 3-PDS; NC-503; 3PDS, is an orally available disodium salt f
351994-94-0 | Emeramide ( BDTH2 )
(Catalog# : 16122939)
Emeramide, also known as BDTH2, is a mercury and heavy metal chelator. BDTH2 molecule
36637-19-1 | Etidocaine Hydrochloride
(Catalog# : 16061503)
()-N-(2,6-dimethylphenyl)-2-(ethylpropylamino)butyramide monohydrochloride ;Etidocain
315706-13-9 | 4EGI-1
(Catalog# : 102608)
4EGI-1 is a cell-permeable hydrazone compound that reversibly binds eukaryotic transl
38664-16-3 | 3-(4-ethoxycarbonyl-5-methyl-1H-pyrrol-3-yl)propanoic acid
(Catalog# : 82710)
Coming soon!
33419-42-0 | Etoposide
(Catalog# : 52801)
Etoposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA.
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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