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+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
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Amino Acids
Anilines
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产品名字索引 C
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产品名字索引 C
CMPD1
(Catalog# : 2061307, Cas# :
41179-33-3
)
CMPD1 is an inhibitor of MK2 activation, primarily inhibiting tubulin polymerisation
CGP52411
(Catalog# : 2061306, Cas# :
145915-58-8
)
CGP52411, also known as DAPH, is a selective inhibitor of the epidermal growth factor
CADD522
(Catalog# : 2051505, Cas# :
199735-88-1
)
CADD522 is a potent inhibitor of runt-related transcription factor-2 (RUNX2)-DNA bind
2-氯-7-氟喹啉-3-甲醛
(Catalog# : S-204160, Cas# :
745830-16-4
)
铜色树碱
(Catalog# : S-203042, Cas# :
524-63-0
)
CC-885
(Catalog# : 2041501, Cas# :
1010100-07-8
)
CC-885 is a potent Cereblon Modulator with potent antitumor activity mediated through
CC-90009
(Catalog# : 203071, Cas# :
1860875-51-9
)
CC-90009 是一种 cereblon (CRBN) E3 连接酶调节剂。CC-90009 与 CRBN 特异性
5-氯-2,6-二甲氧基-4-甲基喹啉
(Catalog# : 4281903, Cas# :
189746-19-8
)
5-氯-2,6-二甲氧基-4-甲基喹啉是一个他非诺喹原料药合成中非常关
Cenicriviroc Mesylate
(Catalog# : S510901, Cas# :
497223-28-6
)
Cenicriviroc(代号TAK-652,TBR-652)是用于治疗HIV感染的实验候选药物
CLP-290
(Catalog# : 193286, Cas# :
1181083-81-7
)
CLP-290是一种新型的KCC2调制器和CLP-257的前药,对KCC2相关的Cl-转运
CT-1812
(Catalog# : 193283, Cas# :
1802632-22-9
)
CT-1812是一类口服的sigma-2/PGRMC1拮抗剂(α-β-低聚物受体拮抗剂),目
氯非铵甲苯磺酸盐
(Catalog# : 193181, Cas# :
92953-10-1
)
氯非铵甲苯磺酸盐是一种K+通道阻滞剂、心脏抑制剂和抗心律失常
Cevipabulin fumarate
(Catalog# : 193124, Cas# :
849550-67-0
)
Cevipabulin fumarate (TTI-237 fumarate) 是一种口服活性微管活性抗肿瘤化
Conteltinib
(Catalog# : 19342, Cas# :
1384860-29-0
)
Conteltinib是一种酪氨酸激酶抑制剂和抗肿瘤药。
C25-140
(Catalog# : 192274, Cas# :
1358099-18-9
)
C25-140是环-E3连接酶(TRAF6) / E2酶(Ubc13)结合的一级蛋白-蛋白相互作用
CCT-137690
(Catalog# : 192192, Cas# :
1095382-05-0
)
CCT137690是一种极光激酶抑制剂CCT137690,是一种高选择性的口服生物
CAY10602
(Catalog# : 191285, Cas# :
374922-43-7
)
CAY10602是SIRT1激活剂。CAY10602是通过高通量筛选增加sirt1介导的特定
Cilofexor ( GS-9674 )
(Catalog# : 19132, Cas# :
1418274-28-8
)
Cilofexor(也称为 GS-9674)是一种非甾体法尼醇 X 受体(FXR)激动剂
CCT241736
(Catalog# : 1812283, Cas# :
1402709-93-6
)
CCT241736是一种有效且具有口服活性的日常FLT3-Aurora抑制剂。
CA-4948
(Catalog# : 1811292, Cas# :
1801343-74-7
)
CA-4948是一种生物活性化学物。
CCT129202
(Catalog# : 1810291, Cas# :
942947-93-5
)
CCT129202是Aurora激酶活性的抑制剂,在临床前研究中表现出良好的抗
CBM 301940
(Catalog# : 1810232, Cas# :
902146-11-6
)
CBM 301940是一种有效的丙二酰辅酶a脱羧酶抑制剂,具有口服生物有
CID16020046
(Catalog# : 1810225, Cas# :
834903-43-4
)
CID16020046是一种选择性GPR55逆激动剂。
10-Cl-BBQ
(Catalog# : 1810161, Cas# :
23982-76-5
)
10-Cl-BBQ是芳烃受体(AhR)配体。
CGP-71683A盐酸盐
(Catalog# : 18792, Cas# :
192322-50-2
)
CGP 71683A是一种有效且高选择性的NPY Y(5)受体的非肽拮抗剂,在肥胖
卡卢莫南钠
(Catalog# : 18752, Cas# :
86832-68-0
)
卡卢莫南钠,也被称为Amasulin和AMA-1080,是一种单异戊巴丁与青霉
CEP-40783
(Catalog# : 186281, Cas# :
1437321-24-8
)
CEP-40783,又称RXDX-106,是AXL和c-Met的一种有效、选择性和口服的抑
CD437
(Catalog# : 185316, Cas# :
125316-60-1
)
CD437合成维生素a是一个RARγ-selective受体激动剂。
CB-1158
(Catalog# : 185315, Cas# :
1345810-21-0
)
CB-1158,又称INCB01158,是一种有效的精氨酸酶抑制剂。
西洛司特
(Catalog# : 185291, Cas# :
153259-65-5
)
西洛司特是一种用于治疗呼吸系统疾病,如哮喘和慢性阻塞性肺病
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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