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+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
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PROTAC
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Aldehydes
Amines
Amino Acids
Anilines
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Cas号索引 1
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Cas号索引 1
1809885-32-2 | EC-5026
(Catalog# : 2051508)
EC5026, also known as BPN-19186, is a first-in-class, potent and orally active solubl
1092977-06-4 | Evenamide HCl
(Catalog# : 112594)
Evenamide HCl ( CAS 1092977-06-4) ,a sodium channel blocker, shows efficacy in a broa
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
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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
-- 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
-- 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
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
-- 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
-- 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
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On Sale
新产品
天然化合物
最新产品
2750001-23-9 | AZD0095
(Catalog# : 237072)
AZD0095 is a Selective Inhibitor of Monocarboxylate Transporter 4 (MCT4) for Oncology.
2101538-28-5 | 2-MNG
(Catalog# : 24129)
2-巯基烟酰甘氨酸是一种新型强效黑素生成抑制剂,具有独特的作
2439277-80-0 | MAT2A-IN-9
(Catalog# : 25147)
MAT2A-IN-9(化合物167)是一种2-氧代喹唑啉衍生物,是一种强效的M
1898206-17-1 | Safusidenib
(Catalog# : 25149)
Safusidenib,也称为DS-1001,是一种口服异柠檬酸脱氢酶[NADP]细胞质(
2669009-92-9 | Atebimetinib
(Catalog# : 25148)
阿替美替尼(IMM-1-104)是一种口服的小分子MEK1和MEK2激酶变构抑制
2242751-53-5 | Acoramidis hydrochloride
(Catalog# : 24068)
Acoramidis是一种口服、强效、高选择性小分子转甲状腺素蛋白(TTR
2230263-60-0 | Crelosidenib
(Catalog# : 24101)
Crelosidenib ( [LY3410738)是一种有效的选择性的具有口服活性的突变
2833703-74-3 | LOXO-435
(Catalog# : 25080)
LOXO-435是FGFR3的选择性小分子抑制剂。它对野生型和致癌激活的FGF
2446928-30-7 | Gridegalutamide
(Catalog# : 25138)
Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
1256349-48-0 | Chiauranib
(Catalog# : 25146)
Chiauranib also known as orally available, small molecule inhibitor of select serine-