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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
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
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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
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
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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 &
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.
913611-97-9 | Brexpiprazole
(Catalog# : 52746)
Brexpiprazole is a novel D2 dopamine partial agonist.
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
-- 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
-- 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
-- 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
-- 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
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
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
1393466-87-9 | PLX8394
(Catalog# : 20613)
PLX8394 is an orally bioavailable inhibitor of serine/threonine-protein kinase B-raf
2365193-22-0 | Zelasudil
(Catalog# : 24014)
Zelasudil 是一种有效的、高选择性的口服活性抑制剂,针对 Rho 相关
2134675-36-6 | Ziftomenib ( KO-539 )
(Catalog# : 24013)
Ziftomenib 是一种口服、有效、选择性的小分子抑制剂,针对 menin 和
1640282-42-3 | Zunsemetinib
(Catalog# : 24012)
Zunsemetinib是一种在研口服丝裂原活化蛋白激酶活化蛋白激酶2(MK2
2728667-27-2 | Zongertinib ( BI 1810631 )
(Catalog# : 24011)
Zongertinib [BI 1810631] 是一种人表皮生长因子受体 2 (HER2) 抑制剂。
2272904-53-5 | Zasocitinib
(Catalog# : 24010)
Zasocitinib是一种作用于非受体酪氨酸蛋白激酶 (TYK2)靶点的抑制
2503036-46-0 | RNK-05047
(Catalog# : 24008)
RNK-05047 为BRD4降解剂,其在小鼠荷瘤异种移植模型中展现出显著抑
1001288-58-9 | Asengeprast (FT011)
(Catalog# : 24009)
Asengeprast (FT011) 是一种抗纤维化剂,降低胶原蛋白 I 和 III 的 mRNA
2490431-16-6 | ERAS-801 ( JGK-068S )
(Catalog# : 20635)
ERAS-801 ( JGK-068S ) 是一种有效的 EGFR 抑制剂。
209746-59-8 | T-1095
(Catalog# : 24004)
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs).