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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
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TGF-beta/Smad
DNA Damage
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Cas号索引 1
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Cas号索引 1
1792180-81-4 | Ritlecitinib ( PF-06651600 )
(Catalog# : 18435)
Ritlecitinib ( PF-06651600 )是一种有效的选择性JAK3抑制剂,是一种具有
1174018-99-5 | Relebactam
(Catalog# : 1712156)
Relebactam, also known as MK-7655, a potent and selective β-lactamase inhibitor.
158681-13-1 | 盐酸利莫那班
(Catalog# : 179137)
利莫那班,又名SR141716,是一种抑制食欲的减肥药。它是为大麻素
147254-64-6 | 雷尼司他
(Catalog# : 178118)
雷尼司他,也被称为AS-3201、SX-3201,是一种醛糖还原酶抑制剂,由Dai
1449598-06-4 | RG7800 ( RO6885247 )
(Catalog# : 174192)
RG7800(RO6885247)是一种小分子改变生存运动神经元2的拼接。
1628838-42-5 | RAF709
(Catalog# : 17030605)
RAF709是一种Raf激酶抑制剂。
1211443-80-9 | Ribociclib HCl
(Catalog# : 17011305)
Ribociclib HCl是一种有效且可口服的细胞周期蛋白依赖性激酶(CDK)抑
112887-68-0 | 雷替曲塞
(Catalog# : 17011303)
雷替曲塞,也称为ZD 1694, 是1998年以来用于治疗结直肠癌的一种抗代
150812-13-8 | 瑞替加滨
(Catalog# : 17011108)
瑞替加滨是一种新型的抗惊厥剂,具有活动范围广泛的癫痫模型。
1446790-62-0 | RO9021
(Catalog# : 17109007)
RO9021能有效抑制SYK激酶活性,平均IC50为5.6 nM,抑制b细胞受体信号
1043797-53-0 | RU-SKI 43
(Catalog# : 6111503)
RU-SKI 43 is a small molecule inhibitor of Hhat(Hedgehog acyltransferase), the enzyme
1070773-09-9 | RK-33
(Catalog# : 611909)
RK-33 is an RNA helicase inhibitor against DDX3, and inhibit its helicase activity.RK
1309684-94-3 | RO8994
(Catalog# : 1673101)
RO8994 is a potent and selective spiroindolinone MDM2 inhibitor for cancer therapy.
1219810-16-8 | RSL 3
(Catalog# : 16070103)
RSL 3
127500-84-9 | Ro41-1049(HCl)
(Catalog# : 166154)
Ro 41-1049 is an inhibitor of the enzyme monoamine oxidase type A(MAO-A).
138489-18-6 | RO31-8220 mesylate
(Catalog# : 16060303)
Ro 31-8220 is a PKC-inhibitor, which inhibits stimulated fluid pinocytosis of human P
150725-87-4 | Ro 46-2005
(Catalog# : 031001)
Ro 46-2005 is a novel synthetic non-peptide endothelin receptor antagonist, inhibits
1182367-47-0 | RAD140
(Catalog# : 030909)
Coming soon!
169758-66-1 | Robalzotan tartrate hydrate
(Catalog# : 011907)
Coming soon!
1037624-75-1 | R428
(Catalog# : 123010)
R428 is a potent and selective small-molecule inhibitor(IC50=14 nM), blocks the activ
1303533-81-4 | Ravidasvir hydrochloride
(Catalog# : 122904)
Ravidasvir is a second-generation, orally active, potent and selective HCV NS5A prote
162011-90-7 | Rofecoxib
(Catalog# : 122837)
Rofecoxib is a synthetic, nonsteroidal derivative of phenyl-furanone with antiinflamm
1622921-15-6 | Remodelin hydrobromide
(Catalog# : 122823)
Remodelin HBr salt is a novel potent and selective inhibitor of the acetyl-transferas
1474034-05-3 | RTA-408
(Catalog# : 122808)
RTA-408 is a synthetic triterpenoid that potently activates the antioxidative transcr
1254205-52-1 | RQ 00203078
(Catalog# : 122521)
RQ-00203078 is a highly selective, potent and orally available TRPM8 antagonist (IC50
117976-90-6 | Rabeprazole sodium
(Catalog# : 122403)
Rabeprazole sodium is an antiulcer drug in the class of proton pump inhibitors.
132907-72-3 | Ramosetron(Hydrochloride)
(Catalog# : 5121408)
Ramosetron (INN) is a serotonin 5-HT3 receptor antagonist for the treatment of nausea
162401-32-3 | Roflumilast
(Catalog# : 121419)
Roflumilast is a drug which acts as a selective, long-acting inhibitor of the enzyme
1396841-57-8 | RGFP966
(Catalog# : 111005)
RGFP966 is a potent and selective histone deacetylase 3 (HDAC3) inhibitor (IC₅₀ =
168273-06-1 | Rimonabant
(Catalog# : 110222)
Rimonabant is a selective central cannabinoid (CB1) receptor inverse agonist with Ki
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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