武汉永璨生物科技有限公司
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抑制剂/受体激动剂
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Epigenetics
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Angiogenesis
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Cytoskeletal Signaling
Cell Cycle
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Neuronal Signaling
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Metabolism
Anti-infection
Proteases
Immunology & Inflammation
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others
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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
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技术服务
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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 S
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产品名字索引 S
SAR-405
(Catalog# : 2017882, Cas# :
1523406-39-4
)
SAR-405是一种有效且选择性的PIK3C3/Vps34抑制剂,防止自噬和协同MTO
雷帕霉素(钠盐)
(Catalog# : 20177313, Cas# :
148554-65-8
)
雷帕霉素是第一个体内open-ring代谢物,不影响mTOR的雷帕霉素抑制Ch
SU5402
(Catalog# : 174191, Cas# :
215543-92-3
)
SU5402是一种纤维母细胞生长因子受体(FGFR)-特异性酪氨酸激酶抑制
SAR-020106
(Catalog# : 17031004, Cas# :
1184843-57-9
)
SAR-020106是一种 ATP -竞争性、强效和选择性的CHK1抑制剂,其IC50为1
SH5-07
(Catalog# : 17031002, Cas# :
1456632-41-9
)
SH5-07是一种健壮的氧肟抗酸的STAT3抑制剂,它能在体外诱导抗肿瘤
SUN11602
(Catalog# : 17030603, Cas# :
704869-38-5
)
SUN11602是一种新型的苯胺类化合物,它模仿了碱性成纤维细胞生长
Sardomozide HCl
(Catalog# : 17030306, Cas# :
138794-73-7
)
Sardomozide,又名SAM486A或CGP48664,是第二代多胺合成抑制剂,它抑制
钠盐沙库必曲
(Catalog# : 17030108, Cas# :
149690-05-1
)
沙库必曲,也被称为AHU377,是血管紧张素受体神经内肽酶抑制剂被
SHP099游离
(Catalog# : 17030107, Cas# :
1801747-42-1
)
<SHP099是强有力的,选择性,具有口服生物利用率,是一种IC50 = 0.07μM的
司马西特
(Catalog# : 17022802, Cas# :
425386-60-3
)
司马西特(LY450139) 是一种针对Aβ42的γ-分泌酶阻断剂, Aβ40和Aβ38的
泰地唑胺杂质 A
(Catalog# : 17021402, Cas# :
1431699-67-0
)
泰地唑胺杂质 A是磷酸四唑磷酸酯活跃的一部分,对革兰氏阳性菌
STO-609
(Catalog# : 17021319, Cas# :
52029-86-4
)
STO-609是一个特定抑制剂。
S49076
(Catalog# : 17021309, Cas# :
1265965-22-7
)
S49076是一种新型的、能有效抑制IC50值低于20 nmol/ L的MET、AXL / MER和
SRT2183
(Catalog# : 17021306, Cas# :
1001908-89-9
)
SRT2183是sirtuin子型SIRT1的小分子激活剂,目前由Sirtris制药公司开发
SW044248
(Catalog# : 17011714, Cas# :
522650-83-5
)
SW044248是一个强有力的和选择性拓扑异构酶抑制剂。SW044248杀死大
舒更葡糖钠
(Catalog# : 17011713, Cas# :
343306-79-6
)
舒更葡糖钠是治疗神经肌肉阻滞的药物。
链脲菌素
(Catalog# : 17011712, Cas# :
18883-66-4
)
链脲菌素是一种从链球菌中分离出来的甲基亚硝基脲类抗肿瘤抗生
Sotagliflozin
(Catalog# : 17011711, Cas# :
1018899-04-1
)
Sotagliflozin,也称为LX4211,是一种口服活性和双SGLT1 / SGLT2抑制剂,在
索利霉素
(Catalog# : 17011710, Cas# :
760981-83-7
)
索利霉素,也称为CEM-101和OP-1068, 是一种用于治疗社区获得性肺炎(C
SMER28
(Catalog# : 17011709, Cas# :
307538-42-7
)
SMER28是一种自噬的小分子调制器,在哺乳动物细胞中独立于雷帕霉
SKF-38393盐酸盐
(Catalog# : 17011707, Cas# :
62717-42-4
)
SKF-38393, 也称为(+/-)-SKF-38393, 是苯偶氮化学类的合成化合物,作为
西他沙星
(Catalog# : 17011706, Cas# :
127254-12-0
)
西他沙星是一种新型的广谱口服氟喹诺酮,它对许多革兰氏阳性、
SHP099盐酸盐
(Catalog# : 17011704, Cas# :
1801747-11-4
)
SHP099是一个强有力的、选择性、口服生物利用率和有效的IC50 = 0.0
6-姜烯酚
(Catalog# : 17011703, Cas# :
555-66-8
)
6-姜烯酚, 是姜的一种辛辣成分,类似于姜酚的化学结构。
SGC707
(Catalog# : 17011702, Cas# :
1687736-54-4
)
SGC707是一种强效、选择性和细胞活性的蛋白质精氨酸甲基转移酶3
SC66
(Catalog# : 17011701, Cas# :
871361-88-5
)
SC66是一种新型的有效的AKT抑制剂,在一定剂量和时间依赖性的方
SBI0206965
(Catalog# : 71161, Cas# :
1884220-36-3
)
SBI0206965是一种有效的选择性自噬激酶ULK1抑制剂。许多肿瘤变得沉
SB-743921盐酸盐
(Catalog# : 17011609, Cas# :
940929-33-9
)
SB-743921是一种具有潜在抗肿瘤性质的合成小分子。
Sardomozide
(Catalog# : 17011607, Cas# :
149400-88-4
)
Sardomozide,也叫SAM486A或CGP48664,是一种第二代聚胺合成抑制剂,抑制
SAR407899 HCl
(Catalog# : 17011606, Cas# :
923262-96-8
)
SAR407899是一种具有良好的抗高血压活性的强效和选择性的激酶抑制
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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!