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抑制剂/受体激动剂
PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
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MAPK
Cytoskeletal Signaling
Cell Cycle
TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
Ubiquitin
Neuronal Signaling
NF-κB
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Metabolism
Anti-infection
Proteases
Immunology & Inflammation
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others
PROTAC
分子砌块
Aldehydes
Amines
Amino Acids
Anilines
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Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
Fluorides
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Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
Peg Linkers
Phenols
Piperidines
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Pyrimidines
Quinolines
Sulfonamides
Thiazoles
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联系我们
+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
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
中间体
技术服务
定制合成
工艺研发
订购信息
联系我们
公司简介
联系我们
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产品名字索引 E
按首字母搜索
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产品名字索引 E
Efavirenz
(Catalog# : 16122763, Cas# :
154598-52-4
)
Efavirenz is a synthetic non-nucleoside reverse transcriptase (RT) inhibitor with ant
Epoxomicin
(Catalog# : 16122762, Cas# :
134381-21-8
)
Epoxomicin is a selective proteasome inhibitor with anti-inflammatory activity, inhib
EAI045
(Catalog# : 16122734, Cas# :
1942114-09-1
)
EAI045 is an allosteric inhibitor that targets selected drug-resistant EGFR mutants b
ETC-1002
(Catalog# : 16122703, Cas# :
738606-46-7
)
ETC-1002,also known as Bempedoic acid, is an orally available, once-daily LDL-C lower
ERK5-IN-1
(Catalog# : 6111502, Cas# :
1234479-76-5
)
ERK5-IN-1 exhibits potent inhibition of ERK5 with cellular EC50 values of 0.19 M and
Etretinate
(Catalog# : 61124, Cas# :
54350-48-0
)
Etretinate is an oral aromatic retinoid acid which is effective in psoriasis and othe
EW-7197
(Catalog# : 6111007, Cas# :
1352608-82-2
)
EW-7197 is a highly potent, selective, and orally bioavailable TGF- receptor ALK4/ALK
ETP-46321
(Catalog# : 611825, Cas# :
1252594-99-2
)
ETP-46321 is a potent and orally bioavailable PI3K / inhibitor with IC50 of 2.3/14.2
ETP-46464
(Catalog# : 161009015, Cas# :
1345675-02-6
)
ATR,Bioactive Small Molecule Alphabetical Index,Bioactive Small Molecules,Cell Biolog
EPZ020411
(Catalog# : 16090201, Cas# :
1700663-41-7
)
EPZ020411 is a potent and selective inhibitor of PRMT6 with IC50 of 10 nM, has 10 fol
Elesclomol
(Catalog# : 16071025, Cas# :
488832-69-5
)
Elesclomol, also known as STA-4783, is a HSP-90 Inhibitor, and is a small-molecule bi
Emricasan
(Catalog# : 16071024, Cas# :
254750-02-2
)
Emricasan (IDN-6556, PF-03491390) is a potent irreversible pan-caspaseinhibitor with
EPZ031686
(Catalog# : 16071015, Cas# :
1808011-22-4
)
EPZ031686
Etelcalcetide
(Catalog# : 16071011, Cas# :
1334237-71-6
)
Etelcalcetide, also known as AMG 416 and KAI-4169, is a D-amino peptide calcimimetic
Etamicastat HCl salt
(Catalog# : 16071009, Cas# :
677773-32-9
)
Etamicastat, also known as BIA 5-453, is a potent, reversible, peripherally selective
Entospletinib (GS-9973)
(Catalog# : 16062803, Cas# :
1229208-44-9
)
Entospletinib, also known as GS-9973, is a highly selective and orally efficacious Sy
EL-102(EL102)
(Catalog# : 1661901, Cas# :
1233948-61-2
)
EL102 is a novel toluidine sulphonamide.EL102 has showedthe potential efficacy in pre
Etidocaine Hydrochloride
(Catalog# : 16061503, Cas# :
36637-19-1
)
()-N-(2,6-dimethylphenyl)-2-(ethylpropylamino)butyramide monohydrochloride ;Etidocain
Etbicyphat
(Catalog# : 16061502, Cas# :
1005-93-2
)
Etbicyphat,1,3-Propanediol, 2-ethyl-2-(hydroxymethyl)-, cyclic phosphate
eptapirone
(Catalog# : 16060602, Cas# :
179756-58-2
)
eptapirone
ETC-159
(Catalog# : 16060301, Cas# :
1638250-96-0
)
ETC-159, also known as ETC-1922159, is a potent, selective and orally available PORCN
Eluxadoline
(Catalog# : 012005, Cas# :
864821-90-9
)
Eluxadoline is an orally active mixed opioid receptor (OR) agonist opioid receptor
Evatanepag
(Catalog# : 011922, Cas# :
223488-57-1
)
Coming soon!
Eperezolid
(Catalog# : 011910, Cas# :
165800-04-4
)
Eperezolid is a oxazolidinone antibacterial agent.
Emapunil
(Catalog# : 011303, Cas# :
226954-04-7
)
Emapunil is a translocator protein [TSPO (18 kDa)] ligand.
Enzastaurin
(Catalog# : 011122, Cas# :
170364-57-5
)
Enzastaurin is a potent PKC selective inhibitor with IC50 of 6 nM, 6- to 20-fold sele
EPZ004777
(Catalog# : 010608, Cas# :
1338466-77-5
)
EPZ004777 is a potent, selective DOT1L inhibitor with IC50 of 0.4 nM.
Elbasvir
(Catalog# : 010411, Cas# :
1444832-51-2
)
Elbasvir is a HCV NS5A inhibitor, which is currently in phase 2b clinical trials as
Estradiol
(Catalog# : 010406, Cas# :
50-28-2
)
Estradiol is the 17-beta-isomer of estradiol, an aromatized C18 steroid with hydroxyl
E-4031
(Catalog# : 122940, Cas# :
113559-13-0
)
E-4031 is a benzenesulfonamide antiarrhythmic agent; blocks the ATP-sensitive potassi
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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
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
STX-478
(Catalog# : 20633, Cas# :
2883540-92-7
)
STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
Iclepertin (BI-425809)
(Catalog# : 24084, Cas# :
1421936-85-7
)
Iclepertin(BI-425809)是一种口服的GlyT-1小分子抑制剂,用于治疗与
Bomedemstat
(Catalog# : 24001, Cas# :
1990504-34-1
)
Bomedemstat 是一种口服的、不可逆的赖氨酸特异性去甲基酶 1 (LSD1)
PLX-4545
(Catalog# : 24111, Cas# :
2892065-45-9
)
PLX-4545 是一种口服生物可利用的 IKZF2 分子胶降解剂,旨在破坏高
VVD-130037 ( BAY-3605349 )
(Catalog# : 24110, Cas# :
3034880-93-5
)
VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
CBR-5884
(Catalog# : 24109, Cas# :
681159-27-3
)
CBR 5884 是一种磷酸甘油酸脱氢酶 (PHGDH) 抑制剂,能够抑制过度表达
JHU-083
(Catalog# : 24108, Cas# :
1998725-11-3
)
JHU-083 选择性阻断大脑 CD11b+ 细胞中的谷氨酰胺酶活性,并防止慢
LXH-3-71
(Catalog# : 24107, Cas# :
2251753-65-6
)
LXH-3-71是一种新型“分子胶”,可诱导PHGDH和DDB1-CUL4泛素连接酶之
CC-92480 ( Mezigdomide )
(Catalog# : 20510, Cas# :
2259648-80-9
)
CC-92480 是一种有效的新型 CELMoD 化合物,旨在快速最大程度地降解
Adrixetinib ( Q-702 )
(Catalog# : 20617, Cas# :
2394874-66-7
)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag