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Angiogenesis
Apoptosis
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MAPK
Cytoskeletal Signaling
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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
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others
PROTAC
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Cas Index 1
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Cas Index 1
15893-52-4 | 2,4-Dihydroxy-7-methoxy-2H,1,4-benzoxazin-3(4H)one
(Catalog# : 2071630)
1903768-17-1 | Danicopan
(Catalog# : 2071535)
Danicopan, aslo known as ACH-4471 and ACH-0144471, is a highly potent, orally active
1233231-30-5 | DSP-2230
(Catalog# : 2071525)
DSP-2230 is a selective Nav1.7/Nav1.8 blocker.
1547757-91-4 | 1,4-diazaspiro[5.5]undecan-3-one
(Catalog# : 2071601)
1174321-06-2 | 5-(difluoromethyl)pyrazine-2-carboxylic acid
(Catalog# : 202326)
169194-80-3 | 1-(1,1-dimethyl-prop-2-ynyl)-4-methyl-piperazine
(Catalog# : 2062314)
106635-87-4 | 2-(4-((2,6-dimethoxy-4-methyl-5-(3-(trifluoromethyl)phenoxy)quinolin-8-yl)amino)pentyl)isoindoline-1,3-dione
(Catalog# : 2062309)
1922200-81-4 | 4-(3-(4-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxy-3-nitrophenoxy)propyl)morpholine
(Catalog# : 2062021)
106635-86-3 | 2,6-DIMETHOXY-4-METHYL-5-[3-(TRIFLUOROMETHYL)PHENOXY]QUINOLIN-8-AMINE
(Catalog# : 2062013)
1174047-06-3 | 2,3-Dichloro-4-hydroxypyridine
(Catalog# : 2062012)
1442472-39-0 | DCC-2618 ( Ripretinib )
(Catalog# : 1811121)
Ripretinib, also known as DCC-2618, is a potent, orally active and selective KIT/PDGF
1234356-69-4 | Derazantinib
(Catalog# : 189273)
Derazantinib, also known as ARQ-087, is an orally bioavailable inhibitor of the fibro
1224606-06-7 | D-Lin-MC3-DMA
(Catalog# : 18942)
D-Lin-MC3-DMA is the most potent cationic lipid that has been synthesized for Lipid n
1799711-21-9 | dBET1
(Catalog# : 186261)
dBET1 is a competitive antagonist of BET bromodomains to hijack the Cereblon E3 ubiqu
144707-18-6 | 2-D08
(Catalog# : 186231)
2-D08 is a synthetic flavone that inhibits sumoylation. 2-D08 showed anti-aggregatory
181223-80-3 | DEL-22379
(Catalog# : 186155)
DEL-22379 is a potent and selective ERK Dimerization inhibitor.
189279-58-1 | Delafloxacin
(Catalog# : 18612)
Delafloxacin, also known as ABT-492, RX-3341 and WQ-3034, is a non-zwitterionic fluor
1219707-39-7 | Delpazolid
(Catalog# : 18611)
Delpazolid, also known as LCB01-0371, is a new oxazolidinone with cyclic amidrazone.
1616690-16-4 | Desidustat
(Catalog# : 185231)
Desidustat is an antianaemic drug candidate.
1104874-94-3 | Defensamide
(Catalog# : 184212)
Defensamide,也被称为MHP和甲基己酰酪氨酸,是鞘氨醇激酶(SPHK1)的激
1032571-01-9 | 6-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxy-3-[3-(morpholin-4-yl)propoxy]aniline
(Catalog# : 2017080116)
6-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxy-3-(3-morpholin-4-ylpropoxy)aniline
1073154-85-4 | Defactinib
(Catalog# : 120111)
Defactinib is a potent FAK phosphorylation inhibitor; overcomes YB-1Cmediated paclita
138148-68-2 | DM1-SMe
(Catalog# : 16122935)
DM1-SMe is a potent maytansinoid microtubular inhibitor and an unconjugated DM1 as a
1228105-51-8 | DM1-SMCC
(Catalog# : 16122934)
DM1-SMCC is DM1 with a reactive linker SMCC, which can react with antibody to make an
104821-25-2 | Dihydroethidium
(Catalog# : 16122931)
Dihydroethidium, also known as Hydroethidine and PD-MY 003, is a cell-permeable blue
1073160-26-5 | Defactinib
(Catalog# : 16122929)
Defactinib, also known as VS-6063 and PF04554878, is an orally bioavailable, small-mo
1265229-25-1 | Debio-1347
(Catalog# : 16122928)
Debio-1347, also known as FF284 and CH5183284, is an orally bioavailable inhibitor of
1009119-64-5 | Daclatasvir
(Catalog# : 16122926)
Daclatasvir (USAN), also known as BMS-790052 and EBP-883 (trade name Daklinza), is NS
171500-79-1 | Dalbavancin HCl
(Catalog# : 16122808)
Dalbavancin is a novel second-generation lipoglycopeptide antibiotic. It belongs to t
1195768-06-9 | Dabrafenib mesylate
(Catalog# : 16122807)
Dabrafenib mesylate, also known as GSK 2118436B, is a potent and orally active B-raf
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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
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
2394874-66-7 | Adrixetinib ( Q-702 )
(Catalog# : 20617)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag