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
«
48
49
50
51
52
53
54
55
56
57
»
Cas号索引 1
1415792-84-5 | Sovleplenib
(Catalog# : 25107)
Sovleplenib is a tyrosine kinase inhibitor. It is also an antineoplastic agent.
1394808-20-8 | SUVN-G3031 HCl
(Catalog# : 25087)
SUVN-G3031 is a Histamine H3 receptor antagonist, which is potentially useful for tre
160162-42-5 | SR-11302
(Catalog# : 24153)
SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor.
1150153-86-8 | SR 16584
(Catalog# : 24137)
SR 16584 is an antagonist of the α3β4 nAChR subtype (IC50 = 10.2 μM).
1262873-06-2 | Sepetaprost
(Catalog# : 24119)
Sepetaprost is a prodrug of ONO-AG-367. It has been used in trials studying the treat
152121-30-7 | SB-202190
(Catalog# : 24106)
SB-202190 is a highly selective, potent and cell-permeable inhibitor of p38 MAP kinas
1648843-04-2 | SX-682
(Catalog# : 24082)
SX-682 is a potent and selective Cxcr1/2 inhibitor potentially useful for castration-
1933514-13-6 | Sebetralstat free base
(Catalog# : 24048)
Sebetralstat(KVD-900),一种口服血浆激肽释放酶抑制剂。
1878218-66-6 | SY-008 乙酸盐
(Catalog# : 24016)
SY-008 是一种钠葡萄糖转运蛋白 1 (SGLT1) 抑制剂。
1480443-32-0 | SY-008
(Catalog# : 24021)
SY-008 是一种钠葡萄糖转运蛋白 1 (SGLT1) 抑制剂。
194032-32-1 | (S)-1-BOC-2-甲基-[1,4]二氮杂环庚烷
(Catalog# : 20541)
131690-60-3 | (S)-3-氨基-3-(4-氯苯基)-丙酸
(Catalog# : 20516)
1980023-96-8 | (S)-1-(6-(4-氟-1H-吡唑-1-甲基)吡啶-3-甲基)乙胺
(Catalog# : 20396)
100874-08-6 | SB-4 agonist
(Catalog# : G20378)
SB 4 is a potent BMP4 agonist.
1310422-41-3 (HCl) | SEP-363856 盐酸盐
(Catalog# : 822222)
SEP-363856 是一种新型微量胺受体 1 (TAAR1) 激动剂,具有血清素 5-HT1
1629138-41-5 | SRI-011381
(Catalog# : L20355)
SRI-011381 is an agonist of the TGF-beta signaling pathway for treatment of Alzheimer
1449597-34-5 | SMN-C3 抑制剂
(Catalog# : 20344)
SMN-C3 是一种口服活性 SMN2 剪接调节剂。可用于脊椎肌肉萎缩 (SMA)
1619931-27-9 | Seralutinib
(Catalog# : 21238)
Seralutinib,也称为 PK-10571 和 GB002,是一种新型吸入性 Pdgfr 激酶抑
1446712-19-1 | SNG-1153
(Catalog# : 21228)
SNG-1153 is a modulator of estrogen receptor ER-alpha36.
1293281-49-8 | Seltorexant
(Catalog# : 81498)
Seltorexant, also known as JNJ-42847922 and MIN-202, is a selective orexin-2 receptor
1415792-84-5 | Samelisant
(Catalog# : 20123101)
Samelisantis a novel, highly selective and potent small molecule oral inhibitor targe
1401682-78-7 | Senaparib
(Catalog# : 20103002)
Senaparib (IMP4297) is a novel agent targeting PARP (poly-ADP ribose polymerase) with
1433953-83-3 | SAR131675
(Catalog# : 2091901)
SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine
18298-32-4 | SB 225002
(Catalog# : 2071510)
1369767-20-3 | ((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2-diyl)dimethanol
(Catalog# : 202331)
我们可以提供公斤级定制合成。((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2
1393477-72-9 (free base) | Selinexor free base
(Catalog# : 2051501)
Selinexor, also known as KPT-330, is an orally bioavailable, potent and selective XPO
1330782-76-7 | Simurosertib
(Catalog# : 2041504)
Simurosertib, also known as TAK-931, is an orally bioavailable inhibitor of cell divi
1821908-48-8 (free base) | SGC2085 free base
(Catalog# : 204609)
SGC2085 is a Potent and Selective Coactivator Associated Arginine Methyltransferase 1
164991-89-3 | Segetalin B
(Catalog# : 204501)
Segetalin B is natural product isolated from Seeds of Vaccaria Segetalis. Segetalin B
1392816-46-4 | SI-113
(Catalog# : 111896)
SI113 is a specific inhibitor of the Sgk1 kinase activity, counteracting cancer cell
«
48
49
50
51
52
53
54
55
56
57
»
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
1616385-51-3 | Bezuclastinib
(Catalog# : 25198)
Bezuclastinib是KIT D816V突变体以及其他KIT外显子17突变体激酶活性的口
2649400-34-8 | Bexobrutideg ( NX-5948 )
(Catalog# : 25197)
Bexobrutideg(NX-5948)是一种BTK降解剂。
1039760-91-2 , 2074613-88-8 [ALTERNATIVE] | Rosolutamide ( AJ-201 ; ASC-JM17 )
(Catalog# : 25196)
Rosolutamide (formerly known as AJ-201, ASC-JM-17 or ALZ-002) 是一种姜黄素类似
1020634-41-6 | Soclenicant (BNC-210 ; IW-2143)
(Catalog# : 25195)
Soclenicant (BNC-210;IW-2143)是一种新型的α7烟碱型乙酰胆碱受体负
2506273-81-8 | VT-3989
(Catalog# : 25194)
VT3989是一种首创的强效口服TEAD棕榈酰化抑制剂,可阻断YAP转录活
1532533-67-7 | Umbralisib
(Catalog# : 25085)
Umbralisib, also known as TGR1202 and RP5264 , is a highly specific, orally available
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
1820812-16-5 | TAK-071
(Catalog# : 186269)
TAK-071 是一种毒蕈碱 M1 受体正变构调节剂。
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