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Epigenetics
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Apoptosis
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MAPK
Cytoskeletal Signaling
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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
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Cas Index 2
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Cas Index 2
285986-88-1 | CCG-1423
(Catalog# : 52502)
CCG-1423 is a novel inhibitor of RhoA/C-mediated gene transcription that is capable o
2230198-02-2 | Danuglipron
(Catalog# : 20538)
Danuglipron, also known as PF-06882961 is a potent, orally bioavailable agonist of th
2413428-36-9 | DSN28369
(Catalog# : 20498)
DSN28369 is a heterobifunctional linker, and useful to make antibody drug conjuate (A
2105905-46-0 | 4,6-dichloro-1H-pyrazolo[3,4-b]pyridine
(Catalog# : 20434)
2407725-14-6 | 4,6-dimethylpyrazolo[1,5-a]pyrazine-2-carbaldehyde
(Catalog# : 20361)
2413256-25-2 | Difelikefalin HCl
(Catalog# : 21922)
Difelikefalin, also known CR-845; MR-13A-9; MR-13A9, is a novel and potent kappa opio
2138299-34-8 | diABZI STING agonist-1 trihydrochloride
(Catalog# : 2112802)
2365172-42-3 | DT-2216
(Catalog# : 20111802)
DT2216 is a selective B-cell lymphoma extra large (BCL-XL) proteolysis-targeting chim
2007975-22-4 | DSR-141562
(Catalog# : 20792)
DSR-141562 is novel Phosphodiesterase 1 Inhibitor for the Treatment of Positive Sympt
24241-18-7 | 3,5-dibromopyrazin-2-amine
(Catalog# : 2062016)
2-Amino-3,5-dibromopyrazine is used in the preparation of conjugated polymers for neu
290304-24-4 | Daun02
(Catalog# : 18793)
Daun02 is a Cell viability inhibitor and DNA synthisis inhibitor with IC50 values of
20830-81-3 | Daunorubicin free base
(Catalog# : 186212)
Daunorubicin exhibits cytotoxic activity through topoisomerase-mediated interaction w
2097334-16-0 | 2-(4-(((2,4-dimethylbenzoyl)oxy)methyl)phenyl)acetic acid
(Catalog# : 183215)
2-(4-(((2,4-dimethylbenzoyl)oxy)methyl)phenyl)acetic acid是一种药物中间体。
261926-09-4 | 3,5-Dichloro-N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosine methyl ester
(Catalog# : 178222)
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220551-92-8 | DAA-1106
(Catalog# : 16062205)
DAA-1106
23541-50-6 | Daunorubicin Hydrochloride
(Catalog# : 122506)
Daunorubicin Hcl inhibits both DNA and RNA synthesis and inhibits DNA synthesis with
211513-37-0 | Dalcetrapib
(Catalog# : 122203)
Dalcetrapib is a rhCETP inhibitor with IC50 of 0.2 M that increases the plasma HDL ch
201530-41-8 | Deferasirox
(Catalog# : 120711)
Deferasirox is an oral iron chelator, which is mainly used to reduce chronic iron ove
2587-02-2 | 2,6-dichloropyridin-4-amine
(Catalog# : 110205)
Coming soon!
2591-17-5 | D-Luciferin
(Catalog# : 101210)
D-Luciferin is a substrate for firefly luciferase with a Km of approx 2 _mu_M.
244767-67-7 | Dapivirine
(Catalog# : 52549)
Dapivirine(TMC 120, TMC 120 R147681) is a NNRTI for HIV reverse transcriptase with IC
208255-80-5 | DAPT(GSI-IX)
(Catalog# : 52202)
DAPT (GSI-IX) is a novel-secretaseinhibitor, which inhibits A production withIC50of 2
2490431-16-6 | ERAS-801 ( JGK-068S )
(Catalog# : 20635)
ERAS-801 ( JGK-068S ) is a potent EGFR inhibitor.
2408839-73-4 | Edecesertib
(Catalog# : 20636)
Edecesertib is a serine/threonine kinase inhibitor and anti-inflammatory. Edecesertib
2359650-50-1 | ethyl 5-chloro-6-fluoropyrazolo[1,5-a]pyrimidine-3-carboxylate
(Catalog# : 20480)
2186700-33-2 | Ervogastat (PF-06865571)
(Catalog# : 20449)
Ervogastat (PF-06865571), a systemically acting diacylglycerol acyltransferase (DGAT2
2239273- 34-6 | Etrumadenant
(Catalog# : 20443)
Etrumadenant, also known as AB928, is a dual antagonist of the A2aR and A2bR adenosin
2239273-34-6 | Etrumadenant
(Catalog# : 171455)
Etrumadenant, also known as AB928, is a dual antagonist of the A2aR and A2bR adenosin
2411748-50-8 | EZM0414
(Catalog# : 171652)
EZM0414 is a potent, selective, and orally bioavailable inhibitor of SETD2.
2701520-23-0 | ethyl 3-bromo-4-ethoxy-5-formylbenzoate
(Catalog# : 20365)
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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
-- 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
-- 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
-- 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
-- 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
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
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
1393466-87-9 | PLX8394
(Catalog# : 20613)
PLX8394 is an orally bioavailable inhibitor of serine/threonine-protein kinase B-raf
2365193-22-0 | Zelasudil
(Catalog# : 24014)
Zelasudil is a potent, highly selective and orally-active inhibitor that targets Rho-
2134675-36-6 | Ziftomenib ( KO-539 )
(Catalog# : 24013)
Ziftomenib is an oral, potent, and selective small molecule inhibitor that targets th
1640282-42-3 | Zunsemetinib
(Catalog# : 24012)
Zunsemetinib is an investigational oral mitogen-activated protein kinase-activated pr
2728667-27-2 | Zongertinib
(Catalog# : 24011)
Zongertinib [BI 1810631] is a human epidermal growth factor receptor 2 (HER2) inhibit
2272904-53-5 | Zasocitinib
(Catalog# : 24010)
Zasocitinib is under development for the treatment of moderate to severe plaque psori
2503036-46-0 | RNK-05047
(Catalog# : 24008)
RNK-05047 is a PROTAC degrader of BRD4 which displays significant tumor growth inhibi
1001288-58-9 | Asengeprast (FT011)
(Catalog# : 24009)
Asengeprast (FT011) is an anti-fibrotic agent thatreduces mRNA expression of collagen
2490431-16-6 | ERAS-801 ( JGK-068S )
(Catalog# : 20635)
ERAS-801 ( JGK-068S ) is a potent EGFR inhibitor.
209746-59-8 | T-1095
(Catalog# : 24004)
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs).