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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
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
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Cas Index 3
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Cas Index 3
312636-16-1 | SKI II
(Catalog# : 6111526)
SKI-II is a synthetic inhibitor of sphingosine kinase (SK) activity with IC50 of 78 M
305834-79-1 | SC79
(Catalog# : 161009025)
Akt Activator II, SC79, CAS 305834-79-1, is a cell-permeable compound that interacts
380899-24-1 | SB-649868
(Catalog# : 011815)
Coming soon!
379231-04-6 | Saracatinib
(Catalog# : 122913)
Saracatinib is an orally available 5-, 7-substituted anilinoquinazoline with anti-inv
356559-20-1 | SB 525334
(Catalog# : 102205)
SB 525334 is a potent and selective inhibitor of TGF_beta_ receptor I (ALK5) with IC5
321429-48-5 | (1S)-1-(3-fluorophenyl)ethanamine,hydrochloride
(Catalog# : 90726)
Coming soon!
325145-35-5 | (S)-1-Boc-2-Ethylpiperazine
(Catalog# : 81901)
Coming soon!
314741-40-7 | (S)-1-Boc-3-(Hydroxymethyl)piperazine
(Catalog# : 81825)
Coming soon!
330161-87-0 | SU6656
(Catalog# : 52754)
SU 6656 is a selective inhibitor of Src kinases, Including Src, Yes, Lyn, and Fyn (IC
377090-84-1 | SU9516
(Catalog# : 52579)
SU-9516 is a selective CDK2 inhibtor with IC50 of 22 nM; less potent for CDK1/CDK4(IC
301836-41-9 | SB431542
(Catalog# : 52312)
SB431542 is a potent and selective inhibitor ofALK5withIC50of 94 nM, 100-fold more se
345627-80-7 | SNS-032 ( BMS-387032 )
(Catalog# : 52105)
SNS-032 has firstly been described as a selective inhibitor ofCDK2withIC50of 48 nM an
3117940-39-0 | TRI-611
(Catalog# : 26A033)
TRI-611 is an Oral ALK Molecular Glue Degrader.
3107291-07-3 | Tert-butyl 4-((2-(methylamino)-6-(2,2,2-trifluoroethyl)thieno[2,3-d]pyrimidin-4-yl)amino)piperidine-1-carboxylate
(Catalog# : 26B007)
3024657-88-0 | Tert-butyl 6,11-dioxo-6,11-dihydro-5H-benzo[b]carbazole-2-carboxylate
(Catalog# : 24002)
Tert-butyl 6,11-dioxo-6,11-dihydro-5H-benzo[b]carbazole-2-carboxylate, CAS 3024657-88
359629-19-9 | tert-Butyl 4-(1-oxoisoindolin-2-yl-methyl)piperidine-1-carboxylate
(Catalog# : 2062034)
313520-94-4 | TH-263
(Catalog# : 2061303)
TH-263 is an inactive analog control for the type III allosteric LIM-kinase (LIMK) in
31274-51-8 | 2,4,6-tris(4-phenylphenyl)-1,3,5-triazine
(Catalog# : S-204158)
309915-12-6 | Talmapimod HCl
(Catalog# : 181252)
Talmapimod, also known as SCIO-469, is an orally bioavailable, small-molecule, p38 mi
303162-79-0 | TAK-715
(Catalog# : 187202)
TAK-715 is a potent p38 MAPK inhibitor. which displays potent inhibitory activity and
305860-41-7 | tert-butyl ((1H-benzo[d][1,2,3]triazol-1-yl)methyl)carbamate
(Catalog# : 183214)
tert-butyl (1H-benzo[d][1,2,3]triazol-1-yl)methylcarbamate是一种药物中间体。
328898-40-4 | Tildipirosin
(Catalog# : 17011904)
Tildipirosin (TIP) is a novel 16-membered-ring macrolide authorized for the treatment
372523-75-6 | TCS-OX2-29
(Catalog# : 61117)
TCS-OX2-29 is a potent and selective OX2 receptor antagonist with IC50 of 40 nM. Disp
327036-89-5 | TDZD-8
(Catalog# : 161009029)
TDZD-8 protects the brain against I/R injury by inhibiting GSK-3beta activity. TDZD-8
35943-35-2 | Triciribine
(Catalog# : 161009022)
Triciribine inhibits the phosphorylation, activation, and signalling of Akt-1, -2, an
387867-13-2 | Tandutinib
(Catalog# : 123015)
Tandutinib is a potent FLT3 antagonist with IC50 of 0.22 M, also inhibits PDGFR and c
385367-47-5 | Tarafenacin
(Catalog# : 122215)
Tarafenacin(SVT-40776) is a highly selective M3 muscarinic receptor antagonist (Ki= 0
332012-40-5 | Telatinib
(Catalog# : 121432)
Telatinib is a potent inhibitor of VEGFR2/3, c-Kit and PDGFR with IC50 of 6 nM/4 nM,
300801-52-9 | TG003
(Catalog# : 110226)
TG003 is a novel benzothiazole compound that demonstrates potent inhibition of Clk1/S
398489-26-4 | tert-Butyl 3-oxoazetidine-1-carboxylate
(Catalog# : 110213)
Coming soon!
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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)
----
NEKs
-- 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
----
Methionine Adenosyltransferase (MAT)
-- 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
----
GLP Receptor
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- 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
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
-- 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)
----
CGRP-Receptor
----
TRP-Channel
-- 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)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- 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
-- Nuclear Receptor
----
Androgen Receptor(AR)
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
435327-40-5 | Avasopasem manganese (GC-4419; M-40419)
(Catalog# : 25108)
Avasopasem manganese, also known as GC-4419; M 40419 and SC-72325A, is amimetic of th
1421936-85-7 | Iclepertin (BI-425809)
(Catalog# : 24084)
Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
4727-31-5 | Kartogenin ( KGN )
(Catalog# : 52215)
Kartogenin (KGN) is a synthetic small molecule that stimulates chondrogenic cellular
218791-21-0 | Imisopasem manganese ( M40403; GC4403 )
(Catalog# : 72602)
Imisopasem manganese ( M40403; GC4403 ) is a stable non-peptidyl mimetic of MnSOD tha
2311863-36-0 | Apecotrep (BI 764198)
(Catalog# : 26A048)
Apecotrep (BI 764198) is a potential first-in-class, oral, selective TRPC6 inhibitor.
902614-04-4 | Pantothenate kinase-IN-2
(Catalog# : 26A038)
Pantothenate kinase-IN-2 is a pantothenate kinase inhibitor with IC50 values of 92 nM
3062177-59-4 | BH-30643
(Catalog# : 26A047)
BH-30643 is a novel, orally available, non-covalent, macrocyclic, mutant selective OM
2446929-86-6 | Gridegalutamide
(Catalog# : 26A044)
gridegalutamide is an orally bioavailable androgen receptor (AR) degrader, with poten
2446928-30-7 | BMS-986365 (Synonyms: CC-94676 )
(Catalog# : 25138)
BMS-986365, also known as CC-94676, is an orally bioavailable androgen receptor (AR)
681159-27-3 | CBR-5884
(Catalog# : 24109)
CBR 5884 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor which was able to inhi