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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 1
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Cas Index 1
1419949-20-4 | NVP-TNKS656
(Catalog# : 010408)
NVP-TNKS656 is a highly potent, selective, and orally active TNKS2 inhibitor with IC5
121032-29-9 | Nelarabine
(Catalog# : 010404)
Nelarabine is a Nucleoside Metabolic Inhibitor. The mechanism of action of nelarabine
104206-65-7 | Nitisinone
(Catalog# : 122526)
Nitisinone is a Hydroxyphenyl-Pyruvate Dioxygenase Inhibitor.
131060-14-5 | NB-598
(Catalog# : 121405)
NB-598 is a potent competitive inhibitor of squalene epoxidase (SE), which suppresses
101385-93-7 | N-Boc-3-Pyrrolidinone
(Catalog# : 90714)
Coming soon!
16642-79-8 | 3-(4-Nitrophenyl)propanoic acid
(Catalog# : 90618)
Coming soon!
1131594-82-5 | 1-N-Boc-Amino-1-N-methyl-3-N-Cbz-aminopropane
(Catalog# : 90602)
Coming soon!
148404-28-8 | N-Boc-Hexahydro-5-oxocyclopenta[c]pyrrole
(Catalog# : 82802)
Coming soon!
17400-34-9 | N-CARBOBENZOXY-1,3-DIAMINOPROPANE HYDROCHLORIDE
(Catalog# : 81734)
Coming soon!
129799-15-1 | N-Boc-Piperazine-2-Carboxylic Acid Methyl Ester
(Catalog# : 81725)
Coming soon!
157115-85-0 | Noopept
(Catalog# : 52813)
Noopept (GVS-111) is a medication promoted and prescribed in Russia and neighbouring
1312445-63-8 | NVP-BKM120 Hydrochloride
(Catalog# : 52775)
Also see <a href="http://www.sun-shinechem.com/Details/BKM120(NVP-BKM120,%20B
1384426-12-3 | NT-157
(Catalog# : 51508)
NT157 is a small-molecule tyrphostin targeting human IRSes.
1245537-68-1 | NVP-BGT226
(Catalog# : 52633)
NVP-BGT226(BGT 226) is a novel class I PI3K/mTOR inhibitor for PI3K// with IC50 of 4
1270138-40-3 | NSI-189
(Catalog# : 52558)
NSI-189 is an experimental drug being studied by Neuralstem, Inc. Research into NSI-1
1418013-75-8 | NMS-873
(Catalog# : 52553)
NMS-873 is a potent, selective allosteric VCP/p97 inhibitor with IC50 value of 20 nM
1402836-58-1 | NLG919(GDC0919)
(Catalog# : 52246)
NLG919 isa promisingandpotent direct enzymatic inhibitor of IDO,In preclinical models
1403783-31-2 | Nexturastat A
(Catalog# : 51503)
Nexturastat A is a potent and selective HDAC6 inhibitor with IC50 of 5 nM; no inhibit
195371-52-9 | NSC 42834
(Catalog# : 52403)
NSC 42834(JAK2 Inhibitor V, Z3), a novel specific inhibitor of Jak2, inhibits Jak2-V6
1655504-04-3 | Orelabrutinib
(Catalog# : 25116)
Orelabrutinib, also known as ICP-022, is a potent, orally active, and irreversible Br
1440796-75-7 (HCl) | Opiranserin HCl
(Catalog# : 25040)
Opiranserin HCl is a glycine transporter inhibitor and serotonin receptor antagonist.
1359969-24-6 | Ocedurenone
(Catalog# : 24091)
Ocedurenone is a non-steroidal mineralocorticoid receptor antagonist.
1257628-77-5 | Olverembatinib (GZD824)
(Catalog# : 24046)
Olverembatinib, also known as GZD824, is a novel orally bioavailable inhibitor agains
1353546-86-7 | Orismilast ( LEO-32731 )
(Catalog# : 20625)
Orismilast is a phosphodiesterase type 4 (PDE4) inhibitor.
1474034-05-3 | omaveloxolone
(Catalog# : 20530)
Omaveloxolone, also known as RTA-408, is a member of the synthetic oleanane triterpen
160492-56-8 (free base) | Osanetant
(Catalog# : 20505)
Osanetant is a tachykinin NK3 antagonist potentially for the treatment of schizophren
1638178-82-1 | ONC201 HCl
(Catalog# : 20305)
ONC-201, also known as TIC10 and imipridone, is a potent, orally active, and stable s
1261289-04-6 | O304
(Catalog# : 2071504)
O-304 is a pan-activator of AMP-activated protein kinase (AMPK). It increases levels
1887014-12-1 | Olutasidenib
(Catalog# : 20791)
Olutasidenib (FT-2102) is a potent mutant-selective IDH1 inhibitor. Olutasidenib (FT-
1340593-59-0 | Oteseconazole
(Catalog# : 111895)
Oteseconazole, also known as VT-1161,is the first Approved Orally Bioavailable and Se
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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