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抑制剂/受体激动剂
Angiogenesis
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联系我们
+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
Vitamin D Related
PROTAC
Antibody-drug Conjugate/ADC Related
Microbiology
Others
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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Cas号索引 1
1092977-61-1 | Evenamide
(Catalog# : 112593)
venamide is a sodium and/or calcium channel modulator. Evenamide may be potentia usef
182567-89-1 | 2-乙酰基-4-溴苯甲酸乙酯
(Catalog# : 95071)
2-乙酰基-4-溴苯甲酸乙酯
153832-46-3 | Ertapenem
(Catalog# : 19318)
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
133040-01-4 | 依普沙坦
(Catalog# : 192182)
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
1219739-36-2 | EX-229游离酸
(Catalog# : 192153)
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
143851-98-3 | 依克立达盐酸盐
(Catalog# : 19121)
依克立达盐酸盐,又称GF120918A,是一种p -糖蛋白(P-gp)抑制剂,已作
1181770-72-8 | EMD638683
(Catalog# : 1810253)
EMD638683是一种有效的SGK1抑制剂, IC50值为3 μM。
189453-10-9 | 环氧丙烷D
(Catalog# : 186292)
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
1628830-21-6 | EZM2302
(Catalog# : 186272)
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
169869-90-3 | 依沙替康甲磺酸盐
(Catalog# : 186271)
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
164650-44-6 | 艾菲康唑
(Catalog# : 186213)
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
1197194-61-8 | 内昔芬 E-异构体盐酸盐
(Catalog# : 184124)
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
1370651-20-9 | Ensartinib ( X396 )
(Catalog# : 184321)
Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k
1914078-41-3 | eCF506 ( 别名:NXP 900 )
(Catalog# : 18382)
eCF506靶向一种叫做Src酪氨酸激酶的分子,这是乳腺癌细胞生长和传
1632006-28-0 | Esaxerenone
(Catalog# : 1710121)
Esaxerenone(cs-3150,xl-550)是一种非甾体类抗盐皮质激素Exelixis发现
1616391-65-1 | EPZ015666
(Catalog# : 011309)
EPZ-015666 是一种强效、选择性的口服生物药,PRMT5抑制剂与Ki为5 nm
1346242-81-6 | 厄达替尼(JNJ-42756493)
(Catalog# : 651701)
Erdafitinib(JNJ-42756493) is a potent and selective panfibroblast growth factor recep
13275-31-5 | Ethyl 2-cyclohexyl-2-oxoacetate
(Catalog# : 178157)
Ethyl 2-cyclohexyl-2-oxoacetate
1140964-99-3 | E7449
(Catalog# : 178903)
E7449是一种可口服的小分子抑制剂,核酶聚(ADP-核糖)聚合酶(PARP)1和
1388651-30-6 | Elenbecestat ( E2609 )
(Catalog# : 2017878)
Elenbecestat是一种β-Site淀粉样前体蛋白裂解酶BACE)抑制剂,主要用
117091-64-2 | 依托泊苷磷酸酯
(Catalog# : 20178213)
依托泊苷磷酸盐是一种半合成足叶草毒素的磷酸盐。
1206123-37-6 | Etrasimod
(Catalog# : 17031018)
Etrasimod,也被称为APD334,是一种多功能S1P1受体的功能拮抗剂,用
1849590-01-7 | eFT-508
(Catalog# : 17031010)
eFT-508 (eFT508)是一种有效且选择性的MNK1 / 2抑制剂,可能导致肿瘤细
1234563-16-6 | 盐酸Epetraborole
(Catalog# : 17022806)
盐酸Epetraborole是一种新型的leucyl - trna合成酶(LeuRS)抑制剂。
1693758-51-8 | Eganelisib ( IPI-549 )
(Catalog# : 711401)
Eganelisib (IPI-549) 是一种首创、口服、高选择性 PI3Kγ 抑制剂,单独
124750-92-1 | EXP-3174
(Catalog# : 16122943)
EXP-3174, also known as Losartan Carboxylic Acid, is a physiologically active metabol
179756-85-5 | Eptapirone
(Catalog# : 16122941)
Eptapirone, also known as F11440, is a potent, selective, high efficacy 5-HT1A recept
1349723-93-8 | Elacestrant dihydrochloride
(Catalog# : 16122810)
Elacestrant dihydrochloride, also known as RAD1901, is an orally available, selective
154598-52-4 | Efavirenz
(Catalog# : 16122763)
Efavirenz is a synthetic non-nucleoside reverse transcriptase (RT) inhibitor with ant
134381-21-8 | Epoxomicin
(Catalog# : 16122762)
Epoxomicin is a selective proteasome inhibitor with anti-inflammatory activity, inhib
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产品分类
信号通路
-- 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)
-- 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
-- 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
-- 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
----
Kallikrein
----
IRAK
-- 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
----
Potassium Channel
-- 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
----
Mitochondrial Metabolism
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Ketohexokinase(KHK)
-- 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)
-- 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)
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
----
Lipase
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- 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
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
85622-93-1 | Temozolomide
(Catalog# : 25209)
替莫唑胺是一种烷化剂。
2035010-37-6 | ALT-007
(Catalog# : 25157)
ALT-007 是一种口服生物可利用的 SPT 抑制剂,比多球菌素更有效,
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim(BHV-7000)是Kv7.2/7.3钾通道(KCNQ2/3)的口服小分子激活剂,
2102501-84-6 | PF-06835919 ( MDK-1846 )
(Catalog# : 193264)
MDK1846是一种强效的酮己糖激酶(KHK)抑制剂。
2271348-04-8 | MK256
(Catalog# : 25208)
MK256是一种新型CDK8抑制剂,通过下调STAT通路在急性髓系白血病(
2351225-46-0 | NSD1 抑制剂 BT5
(Catalog# : 25207)
BT5可有效抑制NSD1,与细胞中的SET结构域结合,并降低H3K36me2水平。
1049704-18-8 | MA242 TFA
(Catalog# : 25206)
MA242是一种MDM2和NFAT1双重抑制剂,可诱导MDM2自泛素化及降解,并抑
2800223-30-5 | Dabogratinib ( TYRA-300 )
(Catalog# : 24073)
Dabogratinib ( TYRA-300 )是一种口服选择性成纤维细胞生长因子受体3(
N/A | AF710B
(Catalog# : 25205)
AF710B 是一种高效、选择性变构 M1 毒蕈碱和 σ1 受体激动剂。 AF710
2957874-18-7 | MAT2A inhibitor 5
(Catalog# : 25204)
MAT2A抑制剂5具有抑制MAT2A的高效力和对MTAP缺失的癌症细胞系的显著