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抑制剂/受体激动剂
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Epigenetics
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Angiogenesis
Apoptosis
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MAPK
Cytoskeletal Signaling
Cell Cycle
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DNA Damage
Stem Cells & Wnt
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Metabolism
Anti-infection
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others
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Anilines
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Bromides
Carboxes
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Chiral Compounds
Deuterated
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Indoles and Oxindoles
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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
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
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定制合成
工艺研发
订购信息
联系我们
公司简介
联系我们
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Cas号索引 1
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Cas号索引 1
1233231-30-5 | DSP-2230
(Catalog# : 2071525)
DSP-2230 is a selective Nav1.7/Nav1.8 blocker.
1547757-91-4 | 1,4-diazaspiro[5.5]undecan-3-one
(Catalog# : 2071601)
1174321-06-2 | 5-(difluoromethyl)pyrazine-2-carboxylic acid
(Catalog# : 202326)
169194-80-3 | 1-(1,1-dimethyl-prop-2-ynyl)-4-methyl-piperazine
(Catalog# : 2062314)
106635-87-4 | 2-(4-((2,6-dimethoxy-4-methyl-5-(3-(trifluoromethyl)phenoxy)quinolin-8-yl)amino)pentyl)isoindoline-1,3-dione
(Catalog# : 2062309)
1922200-81-4 | 4-(3-(4-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxy-3-nitrophenoxy)propyl)morpholine
(Catalog# : 2062021)
106635-86-3 | 2,6-DIMETHOXY-4-METHYL-5-[3-(TRIFLUOROMETHYL)PHENOXY]QUINOLIN-8-AMINE
(Catalog# : 2062013)
1174047-06-3 | 2,3-Dichloro-4-hydroxypyridine
(Catalog# : 2062012)
1442472-39-0 | DCC-2618 ( Ripretinib )
(Catalog# : 1811121)
Ripretinib,又名DCC-2618,是一种有效的、口服活性和选择性KIT/PDGFR抑
1234356-69-4 | Derazantinib
(Catalog# : 189273)
Derazantinib又名ARQ-087,是一种口服生物有效的成纤维细胞生长因子
1224606-06-7 | D-Lin-MC3-DMA
(Catalog# : 18942)
D-Lin-MC3-DMA是为脂质纳米颗粒(LNPs)传递siRNA而合成的最有效的阳离子
1799711-21-9 | dBET1
(Catalog# : 186261)
dBET1是BET bromodomains的竞争性拮抗剂,其目的是劫持Cereblon E3泛素连
144707-18-6 | 2-D08
(Catalog# : 186231)
2-D08是一种合成黄酮类物质,可以抑制类间酰化。2-D08显示抗聚集
181223-80-3 | DEL-22379
(Catalog# : 186155)
DEL-22379是一种有效的选择性二聚反应抑制剂。
189279-58-1 | 德拉沙星
(Catalog# : 18612)
德拉沙星,也被称为ABT-492, RX-3341和WQ-3034,是一种非锌离子氟喹诺
1219707-39-7 | Delpazolid
(Catalog# : 18611)
Delpazolid,又称LCB01-0371,是一种新型的环胺唑酮恶唑啉酮。
1616690-16-4 | Desidustat
(Catalog# : 185231)
Desidustat是一种抗贫血药。
1104874-94-3 | Defensamide
(Catalog# : 184212)
Defensamide, also known as MHP and methyl caprooyl tyrosinate, is an activator of sph
1032571-01-9 | 6-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxy-3-[3-(morpholin-4-yl)propoxy]aniline
(Catalog# : 2017080116)
6-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxy-3-(3-morpholin-4-ylpropoxy)aniline
1073154-85-4 | Defactinib
(Catalog# : 120111)
Defactinib是一种有效的FAK磷酸化抑制剂;通过依赖AKT的途径克服抵抗
138148-68-2 | DM1-SMe
(Catalog# : 16122935)
DM1-SMe is a potent maytansinoid microtubular inhibitor and an unconjugated DM1 as a
1228105-51-8 | DM1-SMCC
(Catalog# : 16122934)
DM1-SMCC is DM1 with a reactive linker SMCC, which can react with antibody to make an
104821-25-2 | Dihydroethidium
(Catalog# : 16122931)
Dihydroethidium, also known as Hydroethidine and PD-MY 003, is a cell-permeable blue
1073160-26-5 | Defactinib
(Catalog# : 16122929)
Defactinib, also known as VS-6063 and PF04554878, is an orally bioavailable, small-mo
1265229-25-1 | Debio-1347
(Catalog# : 16122928)
Debio-1347, also known as FF284 and CH5183284, is an orally bioavailable inhibitor of
1009119-64-5 | Daclatasvir
(Catalog# : 16122926)
Daclatasvir (USAN), also known as BMS-790052 and EBP-883 (trade name Daklinza), is NS
171500-79-1 | Dalbavancin HCl
(Catalog# : 16122808)
Dalbavancin is a novel second-generation lipoglycopeptide antibiotic. It belongs to t
1195768-06-9 | Dabrafenib mesylate
(Catalog# : 16122807)
Dabrafenib mesylate, also known as GSK 2118436B, is a potent and orally active B-raf
1051375-19-9 | Dolutegravir Sodium
(Catalog# : 16122764)
Dolutegravir is a HIV integrase inhibitor with IC50 of 2.7 nM.Dolutegravir(S/GSK13495
13419-46-0 | DCVC
(Catalog# : 6111408)
DCVC inhibits pathogen-stimulated TNF- in human extra placental membranes in vitro.
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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).