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+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
PROTAC
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Amines
Amino Acids
Anilines
Boronic Acids
Bromides
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Fluorides
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Pyridines
Pyrimidines
Quinolines
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Cas号索引 1
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Cas号索引 1
1383716-46-8 | VPS34抑制剂1
(Catalog# : 17031001)
VPS34抑制剂1(化合物19, PIK-III类似物)是VPS34的有效和选择性抑制剂,
1377049-84-7 | 维帕他韦
(Catalog# : 17022808)
维帕他韦(VEL, GS-5816)是一种新的泛基因型丙型肝炎病毒(HCV)非结构
149647-78-9 | 伏立诺他
(Catalog# : 17022704)
伏立诺他(SAHA)是IC50为10nm的HDAC1 / 3抑制剂。
1000025-07-9 | Vadadustat ( AKB-6548 )
(Catalog# : 6121401)
Vadadustat (AKB-6548), a novel, titratable, oral hypoxia-inducible factor prolyl hydr
1431280-51-1 | VLX1570
(Catalog# : 611932)
VLX1570 is a competitive inhibitor of proteasome DUB activity with IC50 ranging from
1523404-29-6 | Vsp34-IN-1
(Catalog# : 011115)
Coming soon!
1232410-49-9 | VE-821
(Catalog# : 122817)
VE-821 is a potent and selective ATP competitive inhibitor of ATR with Ki/IC50 of 13
1246086-78-1 | VU 0364439
(Catalog# : 122401)
VU 0364439 is a mGlu4 positive allosteric modulator, with EC50 of 19.8 nM.
163521-12-8 | Vilazodone
(Catalog# : 122208)
Vilazodone is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A rece
163521-08-2 | Vilazodone Hydrochloride
(Catalog# : 121808)
Vilazodone Hcl is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A
1624602-30-7 | VR23
(Catalog# : 120423)
VR23 is a small molecule that potently inhibited the activities of trypsin-like prote
1383716-33-3 | VPS34-IN1
(Catalog# : 111016)
VPS34-IN1 is a selective inhibitor of Vps34.
1616113-45-1 | VRT-1353385
(Catalog# : 101912)
Coming soon!
1257044-40-8 | Venetoclax(ABT-199)
(Catalog# : 60101)
Venetoclax, formerly known as ABT-199(GDC-0199), is a Bcl-2-selective inhibitor with
1246560-33-7 | VS-5584
(Catalog# : 52530)
VS-5584 (SB2343) is a potent and selective dual PI3K/mTOR inhibitor for mTOR, PI3K///
1232416-25-9 | VE-822 ( Berzosertib )
(Catalog# : 51607)
VE-822(Berzosertib), an analogue of VE-821 with increased potency and selectivity aga
107355-45-3 | WIN54954
(Catalog# : 20280)
WIN54954 is a broad-spectrum antipicornavirus drug.
1214265-56-1 | WZ-3146
(Catalog# : 19191)
WZ-3146是一种对EGFR T790M的共价或不可逆的嘧啶基EGFR抑制剂。WZ-3146
1350752-07-6 | 5WKS
(Catalog# : 1812252)
5WKS,又称ZINC97756584,是一种生物化学物质。
1206731-57-8 | WT161
(Catalog# : 184315)
WT161是一种新型高效、选择性和可生物利用的HDAC6抑制剂。
1431866-33-9 | WEHI-539
(Catalog# : 17101613)
WEHI-539是一种高效和选择性的BCL-XL 抑制剂。促生存BCL-2家族蛋白BC
1354825-58-3 | WEHI-345
(Catalog# : 1781007)
WEHI-345是一种有效的、有选择性的波动抑制因子,它能显示NOD信号
1214265-58-3 | WZ4003
(Catalog# : 17030203)
WZ4003是一种选择性抑制剂,可以抑制LKB1 -肿瘤-抑制-激活的NUAK激酶
1243243-89-1 | Wnt-C59
(Catalog# : 16122846)
Wnt-C59 is a potent porcupine (PORCN) inhibitor. Wnt-C59 inhibits PORCN activity in v
1421227-52-2 | WS3
(Catalog# : 16122747)
WS3 is a cell proliferation inducer via modulation of Erb3 binding protein-1 (EBP1)
153437-55-9 | WHI-P180 hydrochloride
(Catalog# : 611927)
WHI-P180 hydrochloride is a potent EGFR and Cdk2 inhibitors with IC50 of 4.0 and 1.0
1062159-35-6 | WAY-600
(Catalog# : 161009014)
WAY-600 is a potent, ATP-competitive and selective inhibitor of mTOR with IC50 of 9 n
1062161-90-3 | WYE-687
(Catalog# : 1610912)
WYE-687 is a potent and ATP-competitive and selective inhibitor of mTOR with IC50 of
1144068-46-1 | WYE-125132
(Catalog# : 161009008)
WYE-132 inhibited mTORC1 and mTORC2 in diverse cancer models in vitro and in vivo. Im
1062169-56-5 | WYE-354
(Catalog# : 1610101)
WYE-354 is a potent cell-permeable inhibitor of mTOR (IC50 = 4.3 nM) which blocks sig
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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
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
-- 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
----
RXFP 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
----
UGT
----
MMP
----
ATP Citrate Lyase
-- 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
----
Glutaminase
-- 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
-- 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
----
Potassium Channel
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
-- PROTAC
----
Molecular Glues
--
Antibody-drug Conjugate/ADC Related
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
2375779-31-8 | GP130 modulator-1
(Catalog# : 25062)
GP130 modulator-1 (compound A33) 是一种GP130信号通路调节剂。GP130 modulato
877459-36-4 | TGN 073
(Catalog# : 25061)
TGN 073 is a facilitator of aquaporin-4 (AQP4), an astroglial water channel. The rats
2257492-95-6 | OPN expression inhibitor 1
(Catalog# : 25060)
OPN expression inhibitor 1 (Compound 11) is an osteopontin (OPN) expression inhibitor
3036109-10-8 | SDU-071
(Catalog# : 25059)
SDU-071 is a potent and orally active inhibitor of BRD4-p53 inhibitor. SDU-071 suppre
2644662-83-7 | BBC0403
(Catalog# : 25058)
BBC0403 is a selective BRD2 inhibitor. BBC0403 inhibits the progression of osteoarthr
694488-83-0 | MFI8
(Catalog# : 25057)
MFI8 is a Mitochondrial Fusion Inhibitor
146255-66-5 | DHPG
(Catalog# : 25056)
DHPG, also known as (RS)-3,5-DHPG, is a selective agonist for group I metabotropic gl
2413020-56-9 | BAY-593 free base
(Catalog# : 25055)
BAY-593 is an orally active inhibitor of geranylgeranyltransferase-I (GGTase-I) that
188425-85-6 | Boscalid
(Catalog# : 25054)
Boscalid is a broad spectrum fungicide used in agriculture to protect crops from fung
690681-65-3 | SABA1
(Catalog# : 25053)
SABA1 is an antibacterial agent against Pseudomonas aeruginosa and Escherichia coli.