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Epigenetics
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Angiogenesis
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Cytoskeletal Signaling
Cell Cycle
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Neuronal Signaling
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Metabolism
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Proteases
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others
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Anilines
Boronic Acids
Bromides
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Deuterated
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+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
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
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
Antibody-drug Conjugate/ADC Related
分子砌块
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
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On Sale
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Cas号索引 1
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Cas号索引 1
1805787-93-2 | JAK3-IN-1
(Catalog# : 6111506)
JAK3-IN-1 is a potent JAK3 inhibitor with IC50 of 4.8 nM, also inhibits JAK1 (IC50 =
1268524-70-4 | (+)-JQ1
(Catalog# : 16070105)
(+)-JQ1 is a BET potent BET bromodomain Inhibitor. Bromodomain and extra terminal dom
1193383-09-3 | JNJ-42041935
(Catalog# : 031401)
JNJ-42041935 is a potent (pKi = 7.3-7.9), 2-oxoglutarate competitive, reversible, and
1639422-97-1 | JH-VIII-157-02
(Catalog# : 62103)
JH-VIII-157-02, a structural analogue of alectinib, is potent against the G1202R muta
1700693-08-8 | JH-II-127
(Catalog# : 012010)
JH-II-127 is a potent and selective inhibitor of both wild-type and G2019S mutant LRR
1127498-03-6 | JNJ 40411813
(Catalog# : 122939)
JNJ-40411813 is a novel positive allosteric modulator of the metabotropic Glutamate 2
1210004-12-8 | JZL195
(Catalog# : 111007)
JZL195 is a selective and efficacious dual FAAH/MAGL inhibitor with IC50 of 13 nM and
1094873-14-9 | JNJ-31020028
(Catalog# : 100903)
JNJ-31020028 is a selective brain penetrant small molecule antagonist of the neuropep
1146963-51-0 | J-147
(Catalog# : 52505)
J-147 is a broad spectrum neuroprotective phenyl hydrazide compound(EC50=60-115 nM) w
199596-05-9 | JIB-04
(Catalog# : 52225)
JIB-04 is a pan-selective Jumonji histone demethylase inihibitor with IC50 of 230, 34
1215115-03-9 | KH-3
(Catalog# : 24143)
KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
1357164-52-3 | KUS121
(Catalog# : 20676)
KUS-121 是一种过渡内质网 ATP 酶(含缬氨肽蛋白 [VCP];p97)的小分
1596348-16-1 | KDM5-C49
(Catalog# : 20493)
KDM5-C49 is a potent and selective inhibitor of KDM5 (also known as JARID1). KDM5-C49
1771756-32-1 | KUN56321
(Catalog# : 21246)
KUN56321 is a luminescent agent. The application of KUN56321 comprises: coating the f
1695533-89-1 | KO-947
(Catalog# : 20122101)
KO-947 is a potent and selective ERK inhibitor with slow dissociation kinetics. KO-94
1784282-12-7 | KHS101盐酸盐
(Catalog# : 191281)
KHS101 HCl是一种转化酸性卷曲蛋白3 (TACC3)的抑制剂。它的作用是通
1646795-59-6 | KC01
(Catalog# : 1810294)
KC01是ABHD16A的共价抑制剂。ABHD16A是一种磷脂酰丝氨酸(PS)脂肪酶,
18228-17-6 | KG-501
(Catalog# : 1810226)
KG-501是cAMP反应元件结合蛋白(CREB)抑制剂。
1131456-28-4 | KGP-94
(Catalog# : 3291806)
KGP94 is a reversible, time-dependent and competitive inhibitor of human cathepsin L.
1428729-56-9 | KIN-1148
(Catalog# : 184121)
KIN-1148是一个IRF3激动剂。KIN1148诱导剂量依赖性IRF3核易位和特异性
1799974-70-1 | KI-696
(Catalog# : 1710132)
ki-696代表一个优良的低分子量的工具来研究体内Keap1与Nrf2-Nrf2的相
1261113-96-5 | KAF-156
(Catalog# : 20178211)
KAF-156,也称为GNF-156, 是一种可治疗疟疾的抗疟药。
1188890-41-6 | KN-93 phosphate
(Catalog# : 16123029)
KN-93 is a CaMKII inhibitor. KN-93 suppresses ventricular arrhythmia induced by LQT2
191089-59-5 | K-7174
(Catalog# : 16123028)
K-7174 is a novel orally active, potent proteasome inhibitor. K-7174 exerts anti-myel
182004-65-5 | KB-R7943 mesylate
(Catalog# : 16122826)
KB-R7943 is a potent, selective inhibitor of the reverse mode of the Na+/Ca2+ exchang
142273-20-9 | Kenpaullone
(Catalog# : 16122711)
Kenpaullone is an ATP-competitive inhibitor of cyclin-dependent kinases (CDKs). It al
1309444-75-4 | K145
(Catalog# : 6111523)
K145 is a selective SphK2 inhibitor with an IC50 of 4.300.06 M , while no inhibition
1253452-78-6 | KS176
(Catalog# : 6111510)
KS176 is a potent and selective inhibitor of the breast cancer resistance protein (BC
1956356-56-1 | KYA1797K
(Catalog# : 6111416)
KYA1797K is a highly potent and selective Wnt/-catenin inhibitor with IC50 of 0.75 M
1354037-26-5 | KH-CB19
(Catalog# : 611922)
KH-CB19 is a potent and highly specific inhibitor of the CDC2-like kinase isoforms 1
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产品分类
信号通路
-- 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
--
Antibody-drug Conjugate/ADC Related
抑制剂/受体激动剂
中间体
分子砌块
--
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
新产品
天然化合物
最新产品
2375779-31-8 | GP130 modulator-1
(Catalog# : 25062)
GP130 modulator-1 (compound A33) 是一种GP130信号通路调节剂。GP130 modulato
877459-36-4 | TGN 073
(Catalog# : 25061)
TGN 073 is a facilitator of aquaporin-4 (AQP4), an astroglial water channel. The rats
2257492-95-6 | OPN expression inhibitor 1
(Catalog# : 25060)
OPN expression inhibitor 1 (Compound 11) is an osteopontin (OPN) expression inhibitor
3036109-10-8 | SDU-071
(Catalog# : 25059)
SDU-071 is a potent and orally active inhibitor of BRD4-p53 inhibitor. SDU-071 suppre
2644662-83-7 | BBC0403
(Catalog# : 25058)
BBC0403 is a selective BRD2 inhibitor. BBC0403 inhibits the progression of osteoarthr
694488-83-0 | MFI8
(Catalog# : 25057)
MFI8 is a Mitochondrial Fusion Inhibitor
146255-66-5 | DHPG
(Catalog# : 25056)
DHPG, also known as (RS)-3,5-DHPG, is a selective agonist for group I metabotropic gl
2413020-56-9 | BAY-593 free base
(Catalog# : 25055)
BAY-593 is an orally active inhibitor of geranylgeranyltransferase-I (GGTase-I) that
188425-85-6 | Boscalid
(Catalog# : 25054)
Boscalid is a broad spectrum fungicide used in agriculture to protect crops from fung
690681-65-3 | SABA1
(Catalog# : 25053)
SABA1 is an antibacterial agent against Pseudomonas aeruginosa and Escherichia coli.