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Angiogenesis
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Cytoskeletal Signaling
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Metabolism
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Catalysts
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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
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Membrane Transporter/Ion Channel
others
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Amino Acids
Anilines
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Pyridines
Pyrimidines
Quinolines
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Cas号索引 9
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Cas号索引 9
912999-49-6 | AT13387
(Catalog# : 52768)
AT13387 is a selective potent Hsp90 inhibitor with IC50 of 18 nM in A375 cells, displ
919351-41-0 | AZD1283
(Catalog# : 52573)
AZD1283 is a potent antagonist of the P2Y12 receptor with EC50 of 3.0 ug/kg/min, TI &
98600-34-1 | 4-溴吲哚-3-甲醛
(Catalog# : 24059)
913611-97-9 | Brexpiprazole
(Catalog# : 20620)
Brexpiprazole, also known as OPC-34712, is a novel D2 dopamine partial agonist called
924759-42-2 | BT44
(Catalog# : 20469)
BT44 is a novel RET agonist for the treatment of experimental neuropathies.
94630-53-2 | 1,10-BIS[4-AZA-1-AZONIABICYCLO[2.2.2]OCTAN-1-YL]DECANE DIBROMIDE
(Catalog# : G20381)
917909-71-8 | BIT225
(Catalog# : 20270)
BIT-225 is a NCp7 zinc finger inhibitor potentially for the treatment of HCV infectio
960293-88-3 | BI605906
(Catalog# : 16122867)
BI605906 is a IKK inhibitor. BI605906 inhibits TNF-dependent IB degradation and expre
945771-74-4 | BNC105
(Catalog# : 6111023)
BNC105 is a tubulin polymerization inhibitor with potent antiproliferative and tumor
909397-54-2 | 3-bromo-1-ethyl-1H-pyrrole-2,5-dione
(Catalog# : 1681202)
3-bromo-1-ethyl-1H-pyrrole-2,5-dione,CAS#909397-54-2
957217-65-1 | BTZ043
(Catalog# : 16071005)
BTZ043 racemate is adecaprenylphosphoryl--D-ribose 2'-epimerase (DprE1)inhibitor acti
959466-51-4 | 2,4-bis(benzyloxy)-5-isopropylbenzaldehyde
(Catalog# : 032504)
Coming soon!
935525-13-6 | BMS-433796
(Catalog# : 011914)
BMS-433796 is a gamma-secretase inhibitor.
953769-46-5 | BLZ945
(Catalog# : 011314)
BLZ945 is a highly selective and brain-penetrant inhibitor of CSF1R with IC50 of 1 nM
915020-55-2 | BGT-226 free base
(Catalog# : 123014)
BGT226 is a phosphatidylinositol 3-kinase (PI3K) inhibitor with potential antineoplas
918505-61-0 | BRAF inhibitor
(Catalog# : 122840)
BRAF inhibitor is a potent BRAF inhibitor.
9041-93-4 | Bleomycin sulfate
(Catalog# : 122514)
Bleomycin is a glycopeptide antibiotic; used as an anticancer agent; Bleomycin acts b
90357-06-5 | Bicalutamide
(Catalog# : 122507)
Bicalutamide is an oral non-steroidal anti-androgen for prostate cancer; binds to the
935693-62-2 | BIX01294
(Catalog# : 101203)
BIX01294 is an inhibitor of G9a histone methyltransferase with IC50 of 2.7 M.
950736-05-7 | B-Raf IN 1
(Catalog# : 51918)
B-Raf IN 1 is a highlt potent and selective B-Raf inhibitor with IC50 of 24 nM; equip
944396-07-0 | BKM120(NVP-BKM120, Buparlisib)
(Catalog# : 52207)
BKM120(NVP-BKM120, Buparlisib) is an orally bioavailable specific oral inhibitor of t
959163-01-0 | 6-氯-4-(乙基氨基)-3-吡啶甲醛
(Catalog# : 20418)
957208-65-0 | 4-氯甲基-1-环戊基-2-三氟甲基苯
(Catalog# : 20308)
90775-01-2 | 1-cyanocyclohexyl 4-methylbenzenesulfonate
(Catalog# : 21075)
1-cyanocyclohexyl 4-methylbenzenesulfonate (CAS 90775-01-2 ) 是有机合成反应中
924012-43-1 | Centanafadine ( free base )
(Catalog# : 21237)
Centanafadine (free base) is a dual norepinephrine-dopamine transporter inhibitor use
923981-14-0 | Centanafadine HCl
(Catalog# : 21236)
Centanafadine, also known as EB-1020, is an adrenergic uptake inhibitor and dopamine
958230-19-8 | 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde
(Catalog# : 20103005)
92953-10-1 | 氯非铵甲苯磺酸盐
(Catalog# : 193181)
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
942947-93-5 | CCT129202
(Catalog# : 1810291)
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
902146-11-6 | CBM 301940
(Catalog# : 1810232)
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
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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
2883540-92-7 | STX-478
(Catalog# : 20633)
STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
1421936-85-7 | Iclepertin (BI-425809)
(Catalog# : 24084)
Iclepertin(BI-425809)是一种口服的GlyT-1小分子抑制剂,用于治疗与
1990504-34-1 | Bomedemstat
(Catalog# : 24001)
Bomedemstat 是一种口服的、不可逆的赖氨酸特异性去甲基酶 1 (LSD1)
2892065-45-9 | PLX-4545
(Catalog# : 24111)
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
3034880-93-5 | VVD-130037 ( BAY-3605349 )
(Catalog# : 24110)
VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
681159-27-3 | CBR-5884
(Catalog# : 24109)
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
1998725-11-3 | JHU-083
(Catalog# : 24108)
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
2251753-65-6 | LXH-3-71
(Catalog# : 24107)
LXH-3-71是一种新型“分子胶”,可诱导PHGDH和DDB1-CUL4泛素连接酶之
2259648-80-9 | CC-92480 ( Mezigdomide )
(Catalog# : 20510)
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
2394874-66-7 | Adrixetinib ( Q-702 )
(Catalog# : 20617)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag