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抑制剂/受体激动剂
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others
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分子砌块
Aldehydes
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Anilines
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Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
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Indoles and Oxindoles
Iodos
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Quinolines
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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
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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 U
Ulodesine
(Catalog# : 24098, Cas# :
548486-59-5
)
Ulodesine, also known as BCX4208, is a purine nucleoside phosphorylase (PNP) inhibito
UNC5293
(Catalog# : 24094, Cas# :
2226789-82-6
)
UNC5293 is a MERTK -selective and potent inhibitor ( Ki=190 pM).
UJN49930 ( UGT8-IN-1 )
(Catalog# : 20677, Cas# :
2414349-93-0
)
UJN49930 ( UGT8-IN-1 ) 是 UDP-半乳糖神经酰胺半乳糖基转移酶 (UGT8) 的抑
Ulodesine
(Catalog# : 60634, Cas# :
548486- 59-5
)
Usnoflast
(Catalog# : 20629, Cas# :
2455519-86-3
)
Usnoflast is a non-steroidal anti-inflammatory (NSAID).
URAT1 inhibitor 7
(Catalog# : 20573, Cas# :
1632002-28-8
)
URAT1 inhibitor 7 (compound 10f) is a potent URAT1 inhibitor.
UAMC-1110
(Catalog# : 21249, Cas# :
1448440-52-5
)
UAMC-1110, also known as SP-13786, is a novel potent and selective inhibitor of fibro
U-18666A
(Catalog# : 20110401, Cas# :
3039-71-2
)
U-18666A is an inhibitor of cholesterol synthesis. It acts by inhibiting desmosterol
UCB9608
(Catalog# : 2071516, Cas# :
2244989-34-0
)
UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr
UCB9608
(Catalog# : 2071515, Cas# :
1616413-96-7
)
UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr
U-73343
(Catalog# : 112591, Cas# :
142878-12-4
)
U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p
UNC2541
(Catalog# : 6111901, Cas# :
1612782-86-1
)
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit
UPGL00004
(Catalog# : 193251, Cas# :
1890169-95-5
)
UPGL00004是谷氨酰胺酶C (GAC)的有效抑制剂。
Umibecestat游离
(Catalog# : 193223, Cas# :
1387560-01-1
)
Umibecestat,也被称为CNP-520,是一种β分泌酶抑制剂,是预防阿尔茨
UVI3003
(Catalog# : 19343, Cas# :
847239-17-2
)
UVI3003是一种RXR拮抗剂。显示出较高的RXR结合亲和力。UVI3003并不影
Upacicalcet ( 别名 SK-1403 ; AJT240)
(Catalog# : 192142, Cas# :
1333218-50-0
)
Upacicalcet(别名 SK-1403/AJT240)是一种新型非肽拟钙剂,作为钙敏感
UC-1728
(Catalog# : 1812292, Cas# :
948304-40-3
)
UC-1728,又称t-TUCB,是一种可溶性环氧化物水解酶抑制剂。
URMC-099
(Catalog# : 1810252, Cas# :
1229582-33-5
)
URMC-099是一种口服生物可用的、脑内渗透混合谱系激酶(MLK)抑制剂
UM-164
(Catalog# : 186282, Cas# :
903564-48-7
)
UM-164是一种抗癌抑制剂。CAS号为903564-48-7。
UNC-926游离
(Catalog# : 18584, Cas# :
1184136-10-4
)
UNC-926是一种L3MBTL1域抑制剂. UNC-926联结L3MBTL1蛋白的MBT域。(Kd = 3.9
乌帕替尼
(Catalog# : 184105, Cas# :
1310726-60-3
)
乌帕替尼,也被称为ABT-494,是一种强力和选择性的JAK抑制剂,用
UPF-1069
(Catalog# : 1791520, Cas# :
1048371-03-4
)
UPF-1069是一种选择性的强效PARP2抑制剂。UPF-1069诱导细胞凋亡。UPF-
Ulixertinib HCl
(Catalog# : 179153, Cas# :
1956366-10-1
)
Ulixertinib,也称为BVD-523和VRT752271,是ERK蛋白激酶抑制剂。对ERK蛋白
UK-371804
(Catalog# : 1791114, Cas# :
256477-09-5
)
UK-371804是强有力和有选择性的优良酶效价uPA(Ki 10 nm)抑制剂和选
UNC-669
(Catalog# : 178312, Cas# :
314241-44-5
)
UNC-669是L3MBTL领域抑制剂。UNC669是专门针对 IC50 5μM的致死3恶性脑肿
UK-371804 HCl
(Catalog# : 17031008, Cas# :
256476-36-5
)
UK-371804是一种有效的选择性尿激酶型等离子体激活剂(uPA)抑制剂,
URB602
(Catalog# : 17030711, Cas# :
565460-15-3
)
URB602是monoglycerol脂肪酶的选择性抑制剂(MGL),老鼠大脑的酶展现出I
乌苯美司
(Catalog# : 17030602, Cas# :
58970-76-6
)
Ubenimex, also known as NK 421 and Bestatin, is a CD13 inhibitor. Ubenimex attenuates
UNC3866
(Catalog# : 17011102, Cas# :
1872382-47-2
)
UNC3866是一种强力拮抗剂,对多梳型CBX和CDY家族染色体组的阅读功
Ulipristal acetate
(Catalog# : 16122843, Cas# :
126784-99-4
)
Ulipristal acetate, also known as CDB-2914, is a selective progesterone receptor modu
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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
STX-478
(Catalog# : 20633, Cas# :
2883540-92-7
)
STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
Iclepertin (BI-425809)
(Catalog# : 24084, Cas# :
1421936-85-7
)
Iclepertin(BI-425809)是一种口服的GlyT-1小分子抑制剂,用于治疗与
Bomedemstat
(Catalog# : 24001, Cas# :
1990504-34-1
)
Bomedemstat 是一种口服的、不可逆的赖氨酸特异性去甲基酶 1 (LSD1)
PLX-4545
(Catalog# : 24111, Cas# :
2892065-45-9
)
PLX-4545 是一种口服生物可利用的 IKZF2 分子胶降解剂,旨在破坏高
VVD-130037 ( BAY-3605349 )
(Catalog# : 24110, Cas# :
3034880-93-5
)
VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
CBR-5884
(Catalog# : 24109, Cas# :
681159-27-3
)
CBR 5884 是一种磷酸甘油酸脱氢酶 (PHGDH) 抑制剂,能够抑制过度表达
JHU-083
(Catalog# : 24108, Cas# :
1998725-11-3
)
JHU-083 选择性阻断大脑 CD11b+ 细胞中的谷氨酰胺酶活性,并防止慢
LXH-3-71
(Catalog# : 24107, Cas# :
2251753-65-6
)
LXH-3-71是一种新型“分子胶”,可诱导PHGDH和DDB1-CUL4泛素连接酶之
CC-92480 ( Mezigdomide )
(Catalog# : 20510, Cas# :
2259648-80-9
)
CC-92480 是一种有效的新型 CELMoD 化合物,旨在快速最大程度地降解
Adrixetinib ( Q-702 )
(Catalog# : 20617, Cas# :
2394874-66-7
)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag