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抑制剂/受体激动剂
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分子砌块
Aldehydes
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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
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联系我们
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Cas号索引 1
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Cas号索引 1
1005491-05-3 | Tirasemtiv
(Catalog# : 52238)
Tirasemtiv(CK 2017357) is a a small-molecule fast-skeletal-troponin activator, which
1223001-51-1 | Torin 2
(Catalog# : 52311)
Torin 2 is a potent and selectivemTORinhibitor withIC50of 0.25 nM; 800-fold greater s
1616632-77-9 | TIC10 ( ONC201 )
(Catalog# : 51802)
ONC201 / TIC10是人类TRAIL基因的新型小分子诱导剂,可改善重组TRAIL的
1532533-67-7 | Umbralisib
(Catalog# : 25085)
Umbralisib, also known as TGR1202 and RP5264 , is a highly specific, orally available
1632002-28-8 | URAT1 inhibitor 7
(Catalog# : 20573)
URAT1 inhibitor 7 (compound 10f) is a potent URAT1 inhibitor.
1448440-52-5 | UAMC-1110
(Catalog# : 21249)
UAMC-1110, also known as SP-13786, is a novel potent and selective inhibitor of fibro
1616413-96-7 | UCB9608
(Catalog# : 2071515)
UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr
142878-12-4 | U-73343
(Catalog# : 112591)
U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p
1612782-86-1 | UNC2541
(Catalog# : 6111901)
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit
1890169-95-5 | UPGL00004
(Catalog# : 193251)
UPGL00004是谷氨酰胺酶C (GAC)的有效抑制剂。
1387560-01-1 | Umibecestat游离
(Catalog# : 193223)
Umibecestat,也被称为CNP-520,是一种β分泌酶抑制剂,是预防阿尔茨
1333218-50-0 | Upacicalcet ( 别名 SK-1403 ; AJT240)
(Catalog# : 192142)
Upacicalcet(别名 SK-1403/AJT240)是一种新型非肽拟钙剂,作为钙敏感
1229582-33-5 | URMC-099
(Catalog# : 1810252)
URMC-099是一种口服生物可用的、脑内渗透混合谱系激酶(MLK)抑制剂
1184136-10-4 | UNC-926游离
(Catalog# : 18584)
UNC-926是一种L3MBTL1域抑制剂. UNC-926联结L3MBTL1蛋白的MBT域。(Kd = 3.9
1310726-60-3 | 乌帕替尼
(Catalog# : 184105)
乌帕替尼,也被称为ABT-494,是一种强力和选择性的JAK抑制剂,用
1048371-03-4 | UPF-1069
(Catalog# : 1791520)
UPF-1069是一种选择性的强效PARP2抑制剂。UPF-1069诱导细胞凋亡。UPF-
1956366-10-1 | Ulixertinib HCl
(Catalog# : 179153)
Ulixertinib,也称为BVD-523和VRT752271,是ERK蛋白激酶抑制剂。对ERK蛋白
1872382-47-2 | UNC3866
(Catalog# : 17011102)
UNC3866是一种强力拮抗剂,对多梳型CBX和CDY家族染色体组的阅读功
126784-99-4 | Ulipristal acetate
(Catalog# : 16122843)
Ulipristal acetate, also known as CDB-2914, is a selective progesterone receptor modu
152273-12-6 | U-93631
(Catalog# : 16122841)
U-93631 is a GABAA receptor antagonist. U-93631 causes rapid decay of gamma-aminobuty
1381291-36-6 | USP7-IN-1
(Catalog# : 611931)
USP7-IN-1 is a novel selective and reversible inhibitor of USP7 with IC50 of 33 uM; l
1481677-78-4 | UNC0642
(Catalog# : 16071013)
UNC0642 is a potent, selective inhibitor of G9a/GLP with improved PK properties. UNC0
1047634-65-0 | Uprosertib (GSK2141795)
(Catalog# : 16070901)
Uprosertib (GSK2141795) is a selective, ATP-competitive, and orally bioavailableAktin
178870-32-1 | UC-781
(Catalog# : 011311)
UC-781 is a thiocarboxanilide non-nucleoside reverse transcriptase inhibitor. It is a
1415800-43-9 | UNC1215
(Catalog# : 011123)
UNC1215 is a potent and selective chemical probe for the methyllysine (Kme) reading f
178606-66-1 | U-104
(Catalog# : 010440)
U-104 is a potent carbonic anhydrase (CA) inhibitor for CA IX and CA XII with Ki of 4
1431612-23-5 | UNC1999
(Catalog# : 111901)
UNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 wit
112648-68-7 | U73122
(Catalog# : 102201)
U73122 is a potent phospholipase C (PLC) inhibitor, which reduces agonist-induced Ca2
1197196-48-7 | UNC0224
(Catalog# : 82404)
UNC0224 is a potent and selective G9a inhibitor with IC50 of 15 nM in the G9a Thioglo
1255580-76-7 | UNC0638
(Catalog# : 82403)
UNC0638 is an inhibitor of G9a and GLP with excellent potency and selectivity over a
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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
85622-93-1 | Temozolomide
(Catalog# : 25209)
替莫唑胺是一种烷化剂。
2035010-37-6 | ALT-007
(Catalog# : 25157)
ALT-007 是一种口服生物可利用的 SPT 抑制剂,比多球菌素更有效,
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim(BHV-7000)是Kv7.2/7.3钾通道(KCNQ2/3)的口服小分子激活剂,
2102501-84-6 | PF-06835919 ( MDK-1846 )
(Catalog# : 193264)
MDK1846是一种强效的酮己糖激酶(KHK)抑制剂。
2271348-04-8 | MK256
(Catalog# : 25208)
MK256是一种新型CDK8抑制剂,通过下调STAT通路在急性髓系白血病(
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