武汉永璨生物科技有限公司
+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
工艺研发
订购信息
联系我们
公司简介
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
工艺研发
订购信息
联系我们
公司简介
联系我们
搜索
首页
网站地图
Cas号索引 1
按首字母搜索
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
1
2
3
4
5
6
7
8
9
«
3
4
5
6
7
8
9
10
11
12
»
Cas号索引 1
1333714-43-4 | Benpyrine racemate
(Catalog# : 2091907)
(Rac)-Benpyrine is a racemate of Benpyrine. (Rac)-Benpyrine is a potent and orally ac
1660117-38-3 | BI-894999
(Catalog# : 2091902)
BI-894999 is a potent and selective BET inhibitor potentially useful for the Treatmen
1628264-07-2 | 6-BROMO-2-ETHYL-N,8-DIMETHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE
(Catalog# : 2091201)
1818314-88-3 | BMS-1166
(Catalog# : 2073102)
BMS-1166是一种有效的PD-1 / PD-L1相互作用抑制剂,IC50为1.4 nM,可拮抗
1891087-61-8 | BAY-1816032
(Catalog# : 2071615)
BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazole
1301708-12-2 | BMVC-8C3O
(Catalog# : 2071550)
BMVC-8C3O is a DNA G-quadruplexe (G4) ligand which can induce topological conversion
1699717-32-2 | BAY-545
(Catalog# : 2071532)
BAY-545 is a potent and selective antagonist of the A2B adenosine receptor.
1549360-60-2 | 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine
(Catalog# : 2062328)
1628263-43-3 | 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine hydrochloride
(Catalog# : 202327)
1083325-87-4 | 7-bromo-2-(1-methyl-1H-pyrazol-4-yl)-quinoxaline
(Catalog# : 2062028)
101155-02-6 | BW-A 78U
(Catalog# : 2051512)
BW-A 78U is a PDE4 inhibitor with an IC50 of 3 μM.
1802637-39-3 | BB-Cl-Amidine
(Catalog# : 204505)
BB-Cl-A是一种通过激活内质网应激途径治疗犬和猫乳腺癌的新型疗
195615-83-9 | Blarcamesine ( AVex-73 ; AE-37 )
(Catalog# : 6111902)
ANAVEX2-73 (blacamesine) 是一种 Sigma-1 受体激动剂和毒蕈碱受体调节剂
1059630-11-3 | 6-bromo-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride
(Catalog# : ITI007_1)
Sun-shine Chemical is a supplier ofLumateperone, we may provideLumateperone and its i
1622180-31-7 | BMS-986104
(Catalog# : 193285)
BMS-986104是一种强效的选择性S1P1受体调节剂,具有配体偏倚信号转
1613264-40-6 | BAY-1316957
(Catalog# : 193263)
BAY-1316957是一种高效、选择性、口服的人前列腺素E2受体亚型4 (hEP
1800340-40-2 | BMS-986158
(Catalog# : 193255)
BMS-986158是一种有效的选择性BET抑制剂。BMS-986158与BET蛋白BRD中的乙
1801151-09-6 | BMS-986163
(Catalog# : 193207)
BMS-986163是GluN2B的负变构调节剂,在重度抑郁症中具有潜在的应用
1009583-20-3 | BMS-816336
(Catalog# : 19351)
BMS-816336是一种口服活性、有效和选择性的11β-HSD1抑制剂。BMS- 8163
1446113-23-0 | Belvarafenib
(Catalog# : 19341)
Belvarafenib,又名GDC-5573、HM95573、RG6185,是RAF家族激酶的选择性抑制
1191450-19-7 | Burixafor HBr
(Catalog# : 192221)
Burixafor,又名TG-0054,是CXC趋化因子受体4 (CXCR4)的口服生物利用抑
1643368-58-4 | BMS-986142
(Catalog# : 191284)
BMS-986142是一种高效、选择性、可逆的BTK抑制剂。
1564268-08-1 | BAY1238097
(Catalog# : 191257)
BAY1238097是一种有效的选择性BET抑制剂。BAY1238097与BET蛋白BRD上乙酰
166977-43-1 | BMS-189453
(Catalog# : 191253)
BMS-189453也被称为BMS453,是一个强有力的和选择性RARβ受体激动剂和
1093108-50-9 | BI-671800
(Catalog# : 191213)
BI-671800是一种治疗哮喘患者的CRTH2拮抗剂。BI 671800与症状控制单纯
1912445-55-6 | BMS-986195
(Catalog# : 1811264)
BMS-986195是一种有效,共价,Bruton’s酪氨酸激酶的不可逆抑制剂(B
1609392-27-9 | BMS-986165
(Catalog# : 1810163)
BMS-986165是具有选择性、强效、变构抑制剂的酪氨酸激酶2 (Tyk2)。
1611493-60-7 | Bictegravir
(Catalog# : 187181)
Bictegravir,也称为GS - 9883,是一个强有力的,无助推的每日一次HIV- 1整
1034442-21-1 | Basimglurant
(Catalog# : 187121)
Basimglurant,又称RO 4917523和RG-7090,是一种新型的mGlu5阴性变构调制
1923833-60-6 | BMS-986205
(Catalog# : 185314)
BMS-986205是一种抗癌药物。
«
3
4
5
6
7
8
9
10
11
12
»
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
----
DUB
-- 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
2351225-46-0 | NSD1 抑制剂 BT5
(Catalog# : 25207)
BT5可有效抑制NSD1,与细胞中的SET结构域结合,并降低H3K36me2水平。
1049704-18-8 | MA242 TFA
(Catalog# : 25206)
MA242是一种MDM2和NFAT1双重抑制剂,可诱导MDM2自泛素化及降解,并抑
2800223-30-5 | Dabogratinib ( TYRA-300 )
(Catalog# : 24073)
Dabogratinib ( TYRA-300 )是一种口服选择性成纤维细胞生长因子受体3(
N/A | AF710B
(Catalog# : 25205)
AF710B 是一种高效、选择性变构 M1 毒蕈碱和 σ1 受体激动剂。 AF710
2957874-18-7 | MAT2A inhibitor 5
(Catalog# : 25204)
MAT2A抑制剂5具有抑制MAT2A的高效力和对MTAP缺失的癌症细胞系的显著
1235733-73-9 | (Rac)-AF710B
(Catalog# : 24083)
AF-710B 是 σ 和 M1 毒蕈碱受体的激动剂;AF710B 是 AF710 的对映体。
863888-33-9 | Flurpiridaz-nonradiolabeled
(Catalog# : 25203)
Flurpiridaz是一种有前景的新型心脏PET成像示踪剂,是通过用氟-18放
863888-32-8 | Flurpiridaz-Precursor
(Catalog# : 25202)
现货
1800405-30-4 | KL1333
(Catalog# : 25201)
KL1333是一种口服的小有机分子,与NAD(P)H:醌氧化还原酶1(NQO1)
1369489-71-3 | Palupiprant ( E7046 )
(Catalog# : 24055)
E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece