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Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
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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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others
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Aldehydes
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Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
Chiral Compounds
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Fluorides
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Nitro Compounds
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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
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Amino Acids
Anilines
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Bromides
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Chiral Compounds
Deuterated
Fluorides
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Pyridines
Pyrimidines
Quinolines
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联系我们
公司简介
联系我们
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Cas号索引 6
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Cas号索引 6
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
634907-30-5 | Censavudine
(Catalog# : 20632)
Censavudine, also known as OBP-601, BMS-986001 or festinavir, is a nucleoside reverse
693288-97-0 | CPPHA
(Catalog# : 20467)
CPPHA is a positive allosteric modulator of metabotropic glutamate receptor 5 (mGluR5
647834-15-9 | CMP3a
(Catalog# : 20441)
CMP3a is a NEK2 kinase inhibitor. CMP3a efficiently attenuated GBM growth in a mouse
695205-24-4 | CNS004 抑制剂
(Catalog# : 122622)
CNS004是一种基于谷氨酸浓度增强NMDA受体电流的新型化合物。这种
612501-52-7 | 4-(3-Chloro-2-fluoroanilino)-6-hydroxy-7-methoxyquinazoline
(Catalog# : 2062022)
6340-55-2 | 2-chloro-6-methoxy-4-methylquinoline
(Catalog# : 2062014)
628692-22-8 | 2-Chloro-3-fluoro-4-(trifluoromethyl)pyridine
(Catalog# : 032506)
Coming soon!
670220-88-9 | Crenolanib
(Catalog# : 122406)
Crenolanib is a n orally bioavailable small molecule, targeting the platelet-derived
659731-48-3 | 5-Chloro-2-Fluoro-4-Iodopyridine
(Catalog# : 92205)
5-Chloro-2-Fluoro-4-Iodopyridine
638156-11-3 | CID 2011756
(Catalog# : 52532)
CID-2011756 is a cell-active ATP competitive and specific PKD1 inhibitor that inhibit
651734-54-2 | 2,6-二氟-3,5-二甲氧基苯胺
(Catalog# : 20103004)
2,6-difluoro-3,5-dimethoxybenzeneamine is a key intermeidate ofPemigatinib.1Kg~10Kg s
67197-53-9 | 2,6-二溴苄腈
(Catalog# : 1781502)
2-(2,6-dibroMophenyl)acetonitrile 是有机合成反应中的一个重要合成砌块
60546-77-2 | 4,5-Dihydro-2-(Methylthio)-1H-iMidazole-1-carboxylic Acid Methyl Ester
(Catalog# : 17011907)
It is a new drug
681492-22-8 | Delamanid (OPC-67683)
(Catalog# : 16122930)
Delamanid, also known as OPC-67683, is a drug for the treatment of multi-drug-resista
69819-86-9 | Darinaparsin
(Catalog# : 16122927)
Darinaparsin, also know as ZIO-101 is a small-molecule organic arsenical with potenti
675126-05-3 | Dasotraline
(Catalog# : 16071017)
Dasotraline, also known as SEP-225,289, is a serotonin-norepinephrine-dopamine reupta
6898-97-1 | Diethylstilbestrol
(Catalog# : 122511)
Diethylstilbestrol is used in the treatment of menopausal and postmenopausal disorder
60669-69-4 | Dibutylboron trifluoromethanesulfonate
(Catalog# : 121501)
Coming soon!
628732-11-6 | 4,5-Difluoro-2,3-dihydro-1H-inden-1-one
(Catalog# : 83105)
Coming soon!
69304-47-8 | Daclatasvir
(Catalog# : 52776)
Daclatasvir (BMS-790052; EBP 883) is a first-in-class, highly-selective oral HCV NS5A
677773-32-9 | Etamicastat HCl salt
(Catalog# : 16071009)
Etamicastat, also known as BIA 5-453, is a potent, reversible, peripherally selective
679406-03-2 | Ethyl 4,6-dichloropyridazine-3-carboxylate
(Catalog# : 110209)
Coming soon!
68301-99-5 | ethyl 2-amino-5-oxo-7-propan-2-ylchromeno[2,3-b]pyridine-3-carboxylate
(Catalog# : 91413)
The related API: AmoxanoxThe related intermediates: 4-oxo-6-propan-2-ylchromene-3-car
697761-98-1 | Elvitegravir(GS-9137)
(Catalog# : 52022)
Elvitegravir(EVG, formerlyGS-9137) is anintegrase inhibitorused to treatHIVinfection.
613225-56-2 | 063-0967
(Catalog# : 20315)
F1063-0967 is a novel inhibitor of dual-specificity phosphatase 26 (DUSP26), inducing
648927-86-0 | Firibastat ( QGC-001 )
(Catalog# : 26188)
Firibastat, (originally named QGC001) is the first drug candidate of a new class of c
69123-98-4 | 非阿尿苷
(Catalog# : 184283)
非阿尿苷,又名FIAU, DRG-0098,是一种DNA定向DNA聚合酶抑制剂,可用
658084-64-1 | FK866(APO866,Daporinad)
(Catalog# : 1662306)
FK866 is a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltra
699-99-0 | 4-Fluoro-1-indanone
(Catalog# : 81931)
Coming soon!
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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