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Deuterated
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Indoles and Oxindoles
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联系我们
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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 P
Pyridostatin TFA盐
(Catalog# : 185142, Cas# :
1472611-44-1
)
Pyridostatin在细胞中稳定G-四链体(G4s),并通过DNA双链断裂(DSB)的形成
PF-06260933
(Catalog# : 18544, Cas# :
1811510-56-1
)
PF-06260933是一种有效且高选择性MAP4K4抑制剂。
PHA-767491盐酸盐
(Catalog# : 184286, Cas# :
942425-68-5
)
PHA-767491,又名CAY10572,是一种有效的、具有ATP-竞争力的双cdc7/cdk9
PLX51107
(Catalog# : 184285, Cas# :
1627929-55-8
)
PLX51107是一种高效、选择性的BRD4抑制剂或BET抑制剂,其体外和体内
PD 158780
(Catalog# : 184284, Cas# :
171179-06-9
)
PD 158780是表皮生长因子受体(EGFR) (IC50为0.08 nM)的酪氨酸激酶活性的
PZM21
(Catalog# : 184162, Cas# :
1997387-43-5
)
PZM21是强有力Gi活化剂,对μOR和最小β-arrestin-2具有特殊选择性的补
PF-9366
(Catalog# : 184107, Cas# :
72882-78-1
)
PF-9366是一种新型的人蛋氨酸腺苷转移酶2A (Mat2A),肝外同种型。
PFI-2盐酸盐
(Catalog# : 184106, Cas# :
1627607-87-7
)
在其他甲基转移酶和其他非表观遗传靶点上,PFI-2是一种具有IC50为
PCI-29732
(Catalog# : 184101, Cas# :
330786-25-9
)
PCI-29732是BTK抑制剂。它通过阻断B细胞抗原受体(BCR)介导的CD20+ B细
PF-0684000
(Catalog# : 184318, Cas# :
198474-05-4
)
PF-0684000,也称为EOS200271,是强有力的IDO-1抑制剂(IC50 0.15μM)。PF-06
PF-06409577
(Catalog# : 18434, Cas# :
1467057-23-3
)
PF-06409577是一种有效和具有选择的5腺苷酸活化蛋白激酶(AMPK)激活剂
PRN-1371
(Catalog# : 17101614, Cas# :
1802929-43-6
)
PRN-1371是一种共价键,不可逆的,高选择性的纤维母细胞生长因子
PF-5006739
(Catalog# : 17101612, Cas# :
1293395-67-1
)
PF-5006739是一种有效的CK1δ/ε抑制剂。PF-5006739对阿片类药物具有药
PF-04628935
(Catalog# : 17101611, Cas# :
1383719-97-8
)
PF-04628935是一种有效的关于胃肽感受器的拮抗激动剂,生长激素促
PIM447
(Catalog# : 1710134, Cas# :
1210608-43-7
)
PIM447,也称为lgh447,是一种有效的Moloney小鼠白血病(PIM)1, 2,和
PF-562271 HCl
(Catalog# : 179302, Cas# :
939791-41-0
)
PF-562271,也称为PF-562,271 and PF-271,是口服小分子与ATP竞争性粘着斑
Pemafibrate
(Catalog# : 179221, Cas# :
848259-27-8
)
Pemafibrate, also known as K-877 and (R)-K 13675, is a PPAR alpha agonist. (R)-K-1367
Pyridostatin TFA盐
(Catalog# : 1791517, Cas# :
179474-81-8
)
Pyridostatin稳定G-四链体(G4S)在细胞和诱导引起的DNA双链断裂形成
琥珀酸普卡比利
(Catalog# : 1791516, Cas# :
179474-85-2
)
琥珀酸普卡比利,也称为r-108512,是一种选择性、高亲和力的5-羟
PRT4165
(Catalog# : 1791515, Cas# :
31083-55-3
)
PRT4165是一个核心蛋白复合体1的小分子抑制剂,从而抑制泛素蛋白
盐酸普拉克索
(Catalog# : 1791510, Cas# :
104632-25-9
)
普拉克索是一个GαI-联多巴胺受体D2、D3和D4受体激动剂。它是相对
PF-06281355
(Catalog# : 1791312, Cas# :
1435467-38-1
)
PF-06281355,也称为PF-1355,是一种口服有效的、选择性的,有效的机
Puromycin Aminonucleoside
(Catalog# : 1791310, Cas# :
58-60-6
)
嘌呤霉素,也被称为PAN,NSC3056,在人类肾小球疾病的研究和肾小
P7C3-OMe
(Catalog# : 179116, Cas# :
1235481-43-2
)
P7C3-OMe,也称为(R)- P7C3-OMe,是P3C3-A20和P7C3的模拟。减轻C57BL/6J小
PF-CBP1 游离
(Catalog# : 179113, Cas# :
1962928-21-7
)
PF-CBP1,也称为 PF06670910,是强效、高选择性的CREB结合蛋白布罗莫
PF-CBP1盐酸
(Catalog# : 179112, Cas# :
2070014-93-4
)
PF-CBP1,也称为 PF06670910,是强效、高选择性的CREB结合蛋白布罗莫
PF-06650833
(Catalog# : 17988, Cas# :
1817626-54-2
)
PF-06650833是一种白细胞介素-1受体相关激酶4 (IRAK4)抑制剂。IRAK4位于
Prexasertib 甲磺酸
(Catalog# : 17986, Cas# :
1234015-55-4
)
Prexasertib也称为LY2606368,是一种有效,具有选择性的Chk1/Chk2抑制剂
PF-01247324
(Catalog# : 1781102, Cas# :
875051-72-2
)
PF-01247324一种新的选择性和口服生物利用率的Nav 1.8通道阻滞剂,能
PD166866
(Catalog# : 178814, Cas# :
192705-79-6
)
PD166866有明显的抗增殖作用。
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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!