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+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
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
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Cas号索引 3
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Cas号索引 3
336113-53-2 | Ispinesib
(Catalog# : 52747)
Ispinesib (SB-715992) is a potent, specific and reversible inhibitor of KSP (HsEg5) w
36945-98-9 | Icilin
(Catalog# : 52561)
Icilin(AG 3-5) is a synthetic super-agonist of TRPM8 ion channel.
309271-94-1 | Inauhzin
(Catalog# : 52543)
Inauhzin(INZ) is a novel small molecule that effectively reactivates p53 by inhibitin
314245-33-5 | IU1
(Catalog# : 51637)
IU1 is a reversible and specific inhibitor of proteasome-associating Usp14. It does n
315705-75-0 | JNJ0966
(Catalog# : 193201)
JNJ0966是一种高选择性的基质金属蛋白酶-9 (MMP-9)变构抑制剂。
383150-41-2 | JTE-013
(Catalog# : 184313)
TE-013是一种有效、选择的鞘氨醇-1-磷酸2 (S1P2)受体拮抗剂,分别与
363571-83-9 | Kinesore
(Catalog# : 193203)
Kinesore是肌动蛋白-1在细胞微管动力学调控中的激活因子。它已被
330676-02-3 | KH7
(Catalog# : 19362)
KH7是一种新型的可溶性腺苷酸环化酶(Sac)抑制剂。
342639-96-7 | KRIBB11
(Catalog# : 17031014)
KRIBB11废除了热触觉荧光素酶活动的IC50 1.2μM。它是转录因子热休克
355025-24-0 | Ki16425
(Catalog# : 61121)
Ki16425 is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA3 wit
342777-54-2 | LM22B-10
(Catalog# : 187165)
LM22B-10是TrkB和TrkC激动剂。LM22B-10表现为神经营养活性(EC50 = 200- 300
333745-53-2 | LX-2343
(Catalog# : 184131)
LX-2343是一种治疗阿尔茨海默病的神经保护剂。
333963-40-9 | Lubiprostone
(Catalog# : 16123037)
Lubiprostone, also known as RU-0211, is a medication used in the management of chroni
325970-71-6 | L67
(Catalog# : 16122828)
L67 is a DNA Ligase Inhibitor. L67 inhibited DNA ligases I and III. L67 is a simple c
344897-95-6 | Leukadherin-1
(Catalog# : 161227107)
Leukadherin-1 (LA1) is a small molecule agonist that enhances CD11b/CD18-dependent ce
313368-91-1 | Lumateperone(ITI-007)
(Catalog# : 632801)
ITI-007 is an investigational atypical antipsychotic which is currently under develop
303727-31-3 | L-779450
(Catalog# : 122835)
L-779450 is a potent, selective and ATP-competitive Raf kinase inhibitor (IC50 = 10 n
396129-53-6 | LY-364947
(Catalog# : 52509)
LY364947 is a potent ATP-competitive inhibitor of TGFR-I with IC50 of 59 nM, exhibits
3040122-14-0 | Mutant IDH1/NAMPT-IN-1
(Catalog# : 26A032)
Mutant IDH1/NAMPT-IN-1 (Compound 23h) 是突变的异柠檬酸脱氢酶1 (mutant IDH1
352356-71-9 | 3-甲基-1,2,4-噻二唑-5-羧酸甲酯
(Catalog# : 20459)
35134-07-7 | 3-Methoxythiophene-2-carbaldehyde
(Catalog# : 2062019)
313254-94-3 | MMG-11
(Catalog# : 1932010)
MMG-11是一种高效、选择性的TLR2/1和TLR2/6信号双抑制剂,具有较低的
380449-51-4 | Melphalan flufenamide
(Catalog# : 192279)
Melphalan flufenamide,也称为前药J-1,是一种将烷基化剂美法仑与氟苯
35891-70-4 | Myriocin
(Catalog# : 191283)
多壳球菌素,又称抗生素ISP-1和热莫西丁,是一种非典型氨基酸,
305335-31-3 | MLN-4760
(Catalog# : 1812295)
MLN-4760是一种血管紧张素-转换(ACE2)抑制剂。在huMNCs中,MLN-4760-B检
315698-17-0 | ML311
(Catalog# : 179826)
ML311,也被称为EU-5346,是强有力的和有选择性的Mcl-1和Bim蛋白相互
3659-97-0 | 1-甲基咪唑烷-2,4,5-三酮
(Catalog# : 1781501)
1-甲基咪唑烷-2,4,5-三酮;1-MethyliMidazolidine-2,4,5-Trione
376348-65-1 | 马拉维若
(Catalog# : 17022804)
马拉维若(UK-427857; Selzentry; Celsentri) 是选择性CCR5拮抗剂(IC50 = 6.4 nM
329689-23-8 | Monastrol
(Catalog# : 17021322)
Monastrol是一种细胞可渗透的小分子抑制剂,它对保持半纺锤的分离
374913-63-0 | Madrasin
(Catalog# : 16122830)
Madrasin is a potent and cell penetrant splicing inhibitor that interferes with the e
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产品分类
信号通路
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----
VEGFR
----
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----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
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----
HSV
----
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----
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)
----
NEKs
-- 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
----
Methionine Adenosyltransferase (MAT)
-- GPCR & G Protein
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
Endothelin Receptor
----
SGLT
----
OX Receptor
----
CaSR
----
CXCR
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----
Glucagon Receptor
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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
----
GLP Receptor
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- 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
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
-- 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
----
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----
CGRP-Receptor
----
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-- NF-κB
----
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----
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)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- 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
-- Nuclear Receptor
----
Androgen Receptor(AR)
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
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Trifluoroborates
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On Sale
新产品
天然化合物
最新产品
3054692-62-2 | ECI830
(Catalog# : 26A031)
ECI830是一种实验性的CDK2抑制剂。
1394076-92-6 | GNE-317
(Catalog# : 52282)
GNE-317 is a potent, brain-penetrantPI3Kinhibitor
3118994-80-9 | DPTX-3186
(Catalog# : 26A010)
DPTX3186 是一种口服的小分子凝聚体调节剂 (c-mod),可抑制 β-catenin
435327-40-5 | Avasopasem manganese (GC-4419; M-40419)
(Catalog# : 25108)
Avasopasem manganese, 也称为GC-4419、M 40419和SC-72325A,是超氧化物歧化酶
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
4727-31-5 | Kartogenin ( KGN )
(Catalog# : 52215)
Kartogenin(KGN)是一种合成小分子,通过激活smad-4/5通路刺激软骨细
218791-21-0 | Imisopasem manganese ( M40403; GC4403 )
(Catalog# : 72602)
Imisopasem manganese ( M40403; GC4403 ) 是一种稳定的非肽类 MnSOD 类似物,
2311863-36-0 | Apecotrep (BI 764198)
(Catalog# : 26A048)
Apecotrep(BI 764198)是一种潜在的同类首创、口服、选择性的TRPC6抑
902614-04-4 | Pantothenate kinase-IN-2
(Catalog# : 26A038)
Pantothenate kinase-IN-2是一种泛酸激酶抑制剂,对PanK2的IC50值为92 nM,
3062177-59-4 | BH-30643
(Catalog# : 26A047)
BH-30643是一种新型、口服、非共价、大环、突变选择性OMNI-EGFR抑制