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抑制剂/受体激动剂
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Epigenetics
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Angiogenesis
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Cytoskeletal Signaling
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Metabolism
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others
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分子砌块
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Amino Acids
Anilines
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Bromides
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Deuterated
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Indoles and Oxindoles
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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
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产品名字索引 E
Ensifentrine ( RPL554 )
(Catalog# : 61726, Cas# :
1884461-72-6
)
Ensifentrine (RPL554) is an investigational, first-in-class, inhaled dual inhibitor o
Enarodustat ( JTZ-951 )
(Catalog# : 2073104, Cas# :
1262132-81-9
)
Enarodustat ( JTZ-951 ) is an orally-active HIF-PH inhibitor with an EC50 of 0.22 Μm
Empesertib
(Catalog# : 2071554, Cas# :
1443763-60-7
)
Empesertib, also known as BAY1161909, is an orally bioavailable, selective inhibitor
EIDD-1931
(Catalog# : 2071537, Cas# :
3258-02-4
)
EIDD-1931 is a promising COVID-19 inhibitor. EIDD-1931 has broad spectrum antiviral a
ethyl 2-(2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)acetate
(Catalog# : 2062030, Cas# :
2107880-93-1
)
Ethacrynic acid
(Catalog# : 2061703, Cas# :
58-54-8
)
Etharcrynic Acid is a compound that inhibits symport of sodium, potassium, and chlori
EB-3D
(Catalog# : 2061302, Cas# :
1839150-63-8(溴化物
)
EB-3D is a novel potent and selective choline kinase ChoKα inhibitor. EB-3D Induces
Elexacaftor
(Catalog# : 2052801, Cas# :
2216712-66-0
)
Elexacaftor, also known as VX-445 and WHO 11180, is a next-generation cystic fibrosis
EC-5026
(Catalog# : 2051508, Cas# :
1809885-32-2
)
EC5026, also known as BPN-19186, is a first-in-class, potent and orally active solubl
恩替替尼二盐酸盐
(Catalog# : 1843212, Cas# :
2137030-98-7
)
Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k
Evenamide HCl
(Catalog# : 112594, Cas# :
1092977-06-4
)
Evenamide HCl ( CAS 1092977-06-4) ,a sodium channel blocker, shows efficacy in a broa
Evenamide
(Catalog# : 112593, Cas# :
1092977-61-1
)
venamide is a sodium and/or calcium channel modulator. Evenamide may be potentia usef
2-乙酰基-4-溴苯甲酸乙酯
(Catalog# : 95071, Cas# :
182567-89-1
)
2-乙酰基-4-溴苯甲酸乙酯
Ertapenem
(Catalog# : 19318, Cas# :
153832-46-3
)
Ertapenem是一种肠外碳青霉烯类药物,对多种-内酰胺酶失活具有高
依普沙坦
(Catalog# : 192182, Cas# :
133040-01-4
)
依普沙坦是一种具有竞争性和可逆性的血管紧张素受体拮抗剂,用
EX-229游离酸
(Catalog# : 192153, Cas# :
1219739-36-2
)
EX-229,又称AMPK激活剂991,是一种新型的AMPK激活剂,能增加小鼠骨
依克立达盐酸盐
(Catalog# : 19121, Cas# :
143851-98-3
)
依克立达盐酸盐,又称GF120918A,是一种p -糖蛋白(P-gp)抑制剂,已作
E7820
(Catalog# : 1812293, Cas# :
289483-69-8
)
E7820是一种小分子芳香磺胺衍生物,具有潜在的抗血管生成和抗肿
EMD638683
(Catalog# : 1810253, Cas# :
1181770-72-8
)
EMD638683是一种有效的SGK1抑制剂, IC50值为3 μM。
E2012
(Catalog# : 1810231, Cas# :
870843-42-8
)
E2012是γ-secretase分泌酶调制器(GSM)。
EBI-2511
(Catalog# : 1810165, Cas# :
2098546-05-3
)
EBI-2511是非霍奇金淋巴瘤有效的口服活性EZH2抑制剂。
Entasobulin
(Catalog# : 186293, Cas# :
501921-61-5
)
Entasobulin是一种β-tubulin聚合抑制剂,具有潜在的抗癌活性。
环氧丙烷D
(Catalog# : 186292, Cas# :
189453-10-9
)
环氧丙烷D是从纤维素粘液杆菌中分离出来的一种天然聚酮化合物
EZM2302
(Catalog# : 186272, Cas# :
1628830-21-6
)
EZM2302是一种有效的,选择性的,可口服的精氨酸甲基转移酶CARM1抑
依沙替康甲磺酸盐
(Catalog# : 186271, Cas# :
169869-90-3
)
依沙替康也叫DX 8951,是一种半合成的水溶性喜树碱衍生物,具有
艾菲康唑
(Catalog# : 186213, Cas# :
164650-44-6
)
艾菲康唑是一种三唑类抗真菌药。它被批准用于加拿大和美国作为
Erteberel
(Catalog# : 186157, Cas# :
533884-09-2
)
Erteberel,也称为LY500307,选择性雌激素受体β受体激动剂(ERβ)是治疗良
Edonerpic maleate
(Catalog# : 18671, Cas# :
519187-97-4
)
Edonerpic,也被称为T-817,是一种神经保护剂。
内昔芬 E-异构体盐酸盐
(Catalog# : 184124, Cas# :
1197194-61-8
)
内昔芬 E-异构体是一种他莫昔芬的代谢物和有效的选择性雌激素反
Ensartinib ( X396 )
(Catalog# : 184321, Cas# :
1370651-20-9
)
Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k
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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
TRPM4-IN-2
(Catalog# : 24147, Cas# :
667411-04-3
)
TRPM4-IN-2 (NBA) is a potent transient receptor potential melastatin 4 (TRPM4) inhibi
Isolithocholic Acid
(Catalog# : 24146, Cas# :
1534-35-6
)
Isolithocholic acid is a bile acid that is formed via microbial metabolism of lithoch
H2-Gamendazole
(Catalog# : 24145, Cas# :
877768-84-8
)
H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
CPI-455 HCl
(Catalog# : 24144, Cas# :
2095432-28-1
)
CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
KH-3
(Catalog# : 24143, Cas# :
1215115-03-9
)
KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
Stafib-2
(Catalog# : 24142, Cas# :
2097938-74-2
)
Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b, with
TCRS-417
(Catalog# : 24141, Cas# :
2032123-28-5
)
TCRS-417 (T417) is a small molecule compound capable of docking to the interface betw
PST3 1a
(Catalog# : 24140, Cas# :
1096144-06-7
)
PST3 1a is a Novel selective inhibitor of the N-acetylglucosamine glycosyltransferase
YTX-465
(Catalog# : 24139, Cas# :
2225824-53-1
)
YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
CAY10566
(Catalog# : 10403, Cas# :
944808-88-2
)
Coming soon!