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抑制剂/受体激动剂
Angiogenesis
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Apoptosis
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Cytoskeleton
DNA Damage
Epigenetics
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MAPK
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Metabolism
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Proteases
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Aldehydes
Amines
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Anilines
Boronic Acids
Bromides
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Catalysts
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Deuterated
Fluorides
Imidazoles
Indoles and Oxindoles
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Peg Linkers
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联系我们
+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
Vitamin D Related
PROTAC
Antibody-drug Conjugate/ADC Related
Microbiology
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
中间体
技术服务
定制合成
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订购信息
联系我们
公司简介
联系我们
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Cas号索引 2
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Cas号索引 2
2095116-40-6 | brigimadlin
(Catalog# : 20533)
Brigimadlin is an E3 ubiquitin-protein ligase Mdm2 inhibitor with potential as an ant
2607829-38-7 | BDTX-1535
(Catalog# : 20512)
BDTX-1535 是一种突变选择性、不可逆的第四代 EGFR 抑制剂。
2140301-96-6 | Brepocitinib Tosylate
(Catalog# : 232252)
Brepocitinib ( PF-06700841 ) is an orally available, selective inhibitor of non-recep
2098836-45-2 | BRD4 degrader AT1
(Catalog# : 20496)
BRD4 degrader AT1 is an analogue of MZ1. It shows improved selectivity for BRD4 degra
2531244-56-9 | BJJF078
(Catalog# : 20492)
BJJF078 is a potent inhibitor of recombinant human and mouse Transglutaminase enzyme
2760881-74-9 | BRD0639
(Catalog# : 20485)
BRD0639 is a potent PRMT5 inhibitor. BRD0639 engages the target in cells, disrupts PR
2114324-48-8 | BMS-986251
(Catalog# : 20445)
2376257-44-0 | Bexotegrast ( PLN-74809 )
(Catalog# : 171680)
Bexotegrast(同义词:PLN-74809)是一种小分子、双重选择性 αVβ1 / α
2766481-17-6 | BGB 15025 ; BGB-15025 ; BGB15025
(Catalog# : 171452)
BGB-15025 是一种有效的选择性 HPK1 抑制剂,在多种肿瘤模型中作为
2477812-42-1 | N-乙基-2-(4-甲酰基苯基)乙酰胺
(Catalog# : 20419)
2097334-15-9 | Benzeneacetic acid, 4-[[(2,4-dimethylbenzoyl)oxy]methyl]-, methyl ester
(Catalog# : 20391)
2230836-55-0 | BI-3406
(Catalog# : 21234)
BI-3406 is Potent & Selective SOS1::KRAS Inhibitor (IC50=5 nM), which Opens a New
2056261-41-5 | BRD0705
(Catalog# : 202112701)
BRD0705 is a potent, paralog selective and orally active GSK3α inhibitor. BRD0705 ca
2141955-96-4 | BLU-782
(Catalog# : 20121701)
2242464-44-2 | BAY-2416964
(Catalog# : 2091906)
BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist
279262-28-1 | 4-(2-丁氧基乙氧基)苯基硼酸
(Catalog# : 2091203)
2225819-06-5 | BAY-2402234
(Catalog# : 2071553)
BAY-2402234 is a potent and selective dihydroorotate dehydrogenase (DHODH) inhibitor
273404-37-8 | Belnacasan
(Catalog# : 52004)
Belnacasan (VX-765) 是 VRT-043198 的口服生物活性前药,VRT-043198 是有效
2113650-03-4 | BMS-1001
(Catalog# : 2062901)
202865-80-3 | 4-bromo-2-fluoro-1-propan-2-yloxybenzene
(Catalog# : 2062316)
2162982-11-6 | BAY-218
(Catalog# : 204301)
BAY-218, also known as BAY-2335218, is a potent and selective small-molecule AhR inhi
2091135-02-1 | 3-bromo-7-nitro-1-tosyl-1H-indole
(Catalog# : 511191)
2244904-70-7 | BAY-293
(Catalog# : 193121)
BAY-293是一种有效的SOS1抑制剂,通过破坏IC50为21 nM的RAS-SOS1的相互
2097132-94-8 | Blu667
(Catalog# : 191282)
BLU-667是一种有效的选择性 RET 抑制剂, IC50 为0.4 nM,对突变体 RET
2166387-64-8 | BI-3812
(Catalog# : 19124)
BI-3812是BCL6 BTB/POZ区域与多个共抑制因子相互作用的有效抑制剂。
2080306-23-4 | BAY-299
(Catalog# : 1811262)
BAY-299是一种有效且具有选择性的BRD1和TAF1抑制剂(IC50的值分别为
298708-79-9 | BAY41-4109消旋体
(Catalog# : 1791117)
Bay41-4109消旋体是对Bay41-4109和S-异构体Bay41-4109 R-异构体的混合物。
214066-78-1 | B-1613
(Catalog# : 20178216)
(2S,4S)-4-(氨基甲基)吡咯烷-1,2-二羧酸 1-叔丁酯 2-甲酯;(2S,4S)-1-tert
222638-67-7 | BEC HCl
(Catalog# : 17030110)
BEC,也称为S -(2-boronoethyl)-L-cysteine,是一个慢结合和竞争力的精氨酸
209799-67-7 | BCX-1777
(Catalog# : 16071105)
BCX-1777
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产品分类
信号通路
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
----
Eukaryotic Initiation Factor (eIF)
-- Cytoskeleton
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
----
Gap Junction Protein
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- 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
----
Ras
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
----
Bradykinin Receptor
-- 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
----
Kallikrein
----
IRAK
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- 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
----
Proton Pump
----
Potassium Channel
-- 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
----
Mitochondrial Metabolism
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Ketohexokinase(KHK)
-- 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
----
Sigma Receptor
----
mAChR
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
----
Melanocortin Receptor
----
Glucosylceramide Synthase (GCS)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
----
Keap1-Nrf2
-- 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
----
Bcr-Abl
----
FAK
----
RET
----
Phosphoglycerate Kinase (PGK)
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
----
Lipase
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- TGF-beta/Smad
----
PKC
----
ROCK
----
TGF-beta/Smad
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
-- Vitamin D Related
----
VD/VDR
-- PROTAC
----
Molecular Glues
----
PROTACs
--
Antibody-drug Conjugate/ADC Related
--
Microbiology
-- Others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
----
Newest added products
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
2750895-97-5 | MTX115325
(Catalog# : 186264)
MTX115325是一种强效、选择性、脑渗透性USP30抑制剂,具有良好的类
2166616-75-5 | LY-3381916
(Catalog# : 193123)
LY-3381916是一种强效的、选择性的、脑透性的IDO1活性抑制剂,与缺
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim(BHV-7000)是Kv7.2/7.3钾通道(KCNQ2/3)的口服小分子激活剂,
2488609-21-6 | DS68591889
(Catalog# : 25158)
DS68591889 (PTDSS1i) 特异性抑制 PTDSS1,而 PTDSS1 可催化丝氨酸掺入 PC。
944808-88-2 | CAY 10566
(Catalog# : 10403)
CAY 10566是一种强效的选择性SCD-1抑制剂。
2308520-97-8 | Cadefrecitinib (GLPG-3667)
(Catalog# : 20509)
Cadefrecitinib(GLPG-3667)是一种口服小分子TYK2激酶抑制剂,目前正处
1802735-28-9 | QBS10072S
(Catalog# : 25190)
QBS10072S 是一种血脑屏障 (BBB) 渗透剂,由细胞毒性化疗结构域 N-双
2377000-84-3 | Dencatistat (STP938)
(Catalog# : 25177)
Dencatistat 是一种口服生物可利用的小分子胞苷三磷酸合酶 1 (CTPS1)
1898207-64-1 | DS-1001b
(Catalog# : 25178)
DS-1001 是一种口服的脑渗透性突变 IDH1 选择性抑制剂。
1016340-64-9 | Z57346765
(Catalog# : 25191)
Z57346765 是一种 PGK1 特异性抑制剂,可降低 PGK1 糖酵解中代谢酶的