武汉永璨生物科技有限公司
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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
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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
+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
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产品名字索引 P
PF 1022A
(Catalog# : 1811232, Cas# :
133413-70-4
)
PF1022A是一种新型的驱虫药,与嗜乳激素样跨膜受体结合,对线虫
普拉曲沙
(Catalog# : 1811221, Cas# :
146464-95-1
)
普拉曲沙是二氢叶酸还原酶(DHFR)的一种叶酸模拟抑制剂,对叶酸还
PF-05231023
(Catalog# : 1811162, Cas# :
1037589-69-7
)
PF-05231023是一种长效FGF21仿生产品。PF-05231023可以减轻非人类灵长类
PA-8
(Catalog# : 1810254, Cas# :
878437-15-1
)
PA-8是PAC1受体的小分子拮抗剂。
Pyronaridine Tetraphosphate
(Catalog# : 1810242, Cas# :
76748-86-2
)
Pyronaridine Tetraphosphate是一种抗疟药,能阻断b -血凝素的形成,抑制
PH-002
(Catalog# : 1810234, Cas# :
1311174-68-1
)
PH-002是一种新型的载脂蛋白(apo) E4分子内区域相互作用的神经细胞
Pemigatinib (INCB054828)
(Catalog# : 1810164, Cas# :
1513857-77-6
)
Pemigatinib是一种酪氨酸激酶抑制剂,也是一种抗肿瘤药物候选药物
Pelitrexol
(Catalog# : 189131, Cas# :
446022-33-9
)
Pelitrexol是GARFT抑制剂,也是具有抗增殖活性的水溶性抗叶酸。
PCI-33380
(Catalog# : 18943, Cas# :
1022899-36-0
)
PCI-33380是基于ibrutinib支架设计的,已被用于细胞和体内研究,证实
Perastine
(Catalog# : 187164, Cas# :
4960-10-5
)
Perastine是一种生物化学药。
PCO371
(Catalog# : 187125, Cas# :
1613373-33-3
)
PCO371是一种有效的、选择性的PTHR1激动剂,用于治疗低甲状旁腺功
PQR530
(Catalog# : 18756, Cas# :
1927857-61-1
)
PQR530是一种高效的日常pan-PI3K/mTORC1/2抑制剂。
Pyrotinib
(Catalog# : 18731, Cas# :
1269662-73-8
)
Pyrotinib,又称SHR -1258,是一种口服生物利用的双激酶抑制剂,是表
PX20606反式消旋体
(Catalog# : 186274, Cas# :
1268244-85-4
)
PX20606, 也称为PX-102, 是一种FXR激动剂。
PF-05180999
(Catalog# : 186153, Cas# :
1394033-54-5
)
PF-05180999是一个强有力的和选择性PDE2a抑制剂(PDE2a的IC50 = 0.001μM,
Pritelivir甲磺酸盐
(Catalog# : 186152, Cas# :
1428333-96-3
)
Pritelivir,又名AIC-316和BAY 57-1293,是一种有效的螺旋酶抑制剂。
Pridopidine
(Catalog# : 18673, Cas# :
346688-38-8
)
Pridopidine也被称为ACR16,是一种多巴胺稳定剂,它可以改善运动表
Pamiparib
(Catalog# : 185233, Cas# :
1446261-44-4
)
Pamiparib是高选择性PARP-1/2抑制剂。临床试验中表现出良好的抗肿瘤
PAC 14028
(Catalog# : 185223, Cas# :
1005168-10-4
)
PAC-14028是高效的选择性的瞬时受体电位香草酸亚型1 (TRPV1) 拮抗剂
PE859
(Catalog# : 185157, Cas# :
1402727-29-0
)
PE859是一个强有力的IC50值分别为0.66和1.2μM的tau和Aβ聚合抑制剂。
PD 168 077
(Catalog# : 185156, Cas# :
190383-31-4
)
PD168077是一种多巴胺D4受体激动剂,对记忆巩固有促进作用。
PF-06462894
(Catalog# : 185155, Cas# :
1622291-66-0
)
PF-06462894是一种形态学上的mGlu5 (mGlu5 Ki = 6nm)。
PF-06291874
(Catalog# : 185154, Cas# :
1393124-08-7
)
PF-06291874是一种胰高血糖素受体拮抗剂,对2型糖尿病患者有效。
Poseltinib
(Catalog# : 185153, Cas# :
1353552-97-2
)
Poseltinib, 也称为HM-71224和LY3337641,一种酪氨酸激酶抑制剂。
Pibrentasvir
(Catalog# : 185148, Cas# :
1353900-92-1
)
Pibrentasvir,也被称为ABT-530,是一种蛋白酶抑制剂,可用于治疗丙
PP2 Analog
(Catalog# : 185147, Cas# :
309739-67-1
)
PP2 Analog是一种PP2类似物,它发挥蛋白质交易调制器的作用。
PP2
(Catalog# : 185146, Cas# :
172889-27-9
)
PP2,也被称为AG 1879,是一种经常被用于癌症研究的物质,作为src
PP1
(Catalog# : 185145, Cas# :
172889-26-8
)
PP1是一种有效的选择性Src家族蛋白酪氨酸激酶抑制剂。
Pocapavir
(Catalog# : 185144, Cas# :
146949-21-5
)
Pocapavir,也被称为SCH -48973和V-073,是一种强效、选择性的抗肠道病
PSMA617 TFA
(Catalog# : 185143, Cas# :
1702967-37-0
)
PSMA-617是一种配体,用于制造177Lu -PSMA-617,这是一种用于对抗癌症
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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!