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抑制剂/受体激动剂
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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
Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
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Cas号索引 1
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Cas号索引 1
1364488-67-4 | YH239-EE
(Catalog# : 192213)
YH239-EE是一种高效的p53-MDM2拮抗剂。
199433-58-4 | Y-39983游离
(Catalog# : 185172)
Y-39983 (游离),也被称为Y-33075,是一种有效的、选择性的ROCK家族抑
1339058-04-6 | YL-0919
(Catalog# : 18578)
YL-0919是一种日常5-HT1A受体拮抗剂,具有选择性的 5 -羟色胺再摄取
1943733-16-1 | YU-238259
(Catalog# : 1710139)
YU238259表现出有效的合成致死性设置中的DNA损伤反应和DNA修复缺陷
143984-17-2 | Y-29794 甲苯磺酸酯
(Catalog# : 1791521)
Y-29794甲苯磺酸酯是一种口服有效的,强有力的和特定的非肽脯氨
173897-44-4 | Y-39983盐酸盐
(Catalog# : 17021305)
Y-39983是一种选择性的与之相关的蛋白激酶(ROCK)抑制剂,其IC50为3.
1236188-16-1 | 740 Y-P (PDGFR 740Y-P)
(Catalog# : 17021302)
740 Y-P是PI3K的细胞渗透磷肽激活剂。
163769-88-8 | YM-90709
(Catalog# : 16122849)
YM-90709 is an interleukin-5 receptor antagonist. YM-90709 inhibits the binding of IL
129184-48-1 | Y-29794 Tosylate
(Catalog# : 16122848)
Y-29794 Tosylate is an orally active, potent and specific non-peptide prolyl endopept
1346753-00-1 | YHO-13351
(Catalog# : 6111512)
YHO-13351 is the water-soluble prodrug of YHO-13177, which is a potent and specific i
1273323-67-3 | YLF-466D
(Catalog# : 611813)
YLF-466D is an allosteric AMPK activator.YLF466D activated recombinant human 111, 211
146986-50-7 | Y27632(free base)
(Catalog# : 16070918)
Y27632 is a selective ROCK inhibitor, which inhibits ET-1-induced increases in natriu
1370003-76-1 | YK11
(Catalog# : 030910)
Coming soon!
129830-38-2 | Y-27632 dihydrochloride
(Catalog# : 010421)
Y-27632 2Hcl is a selective ROCK1 (p160ROCK) inhibitor with Ki of 140 nM, exhibits &g
1802650-31-2 | ZY-444
(Catalog# : 26A020)
ZY-444是一种通过抑制PC活性发挥抗癌作用的药物。
1016340-64-9 | Z57346765
(Catalog# : 25191)
Z57346765 是一种 PGK1 特异性抑制剂,可降低 PGK1 糖酵解中代谢酶的
167354-41-8 | Zosuquidar ( LY-335979 )
(Catalog# : 25127)
Zosuquidar是P-糖蛋白介导的多药耐药性的有效调节剂。
1640282-42-3 | Zunsemetinib
(Catalog# : 24012)
Zunsemetinib是一种在研口服丝裂原活化蛋白激酶活化蛋白激酶2(MK2
1606974-33-7 | Zatolmilast
(Catalog# : 20651)
Zatolmilast is a phosphodiesterase IV inhibitor.
1851412-93-5 | Zavondemstat
(Catalog# : 20610)
Zavondemstat 是一种 KDM4 抑制剂,具有抗肿瘤药物的潜力。
1438280-73-9 | 1Z105
(Catalog# : 20567)
1Z105 is a TLR4/MD2 ligand, significantly reducing the IL-6 secretion by subsequent c
1211825-25-0 | ZINC40099027 (ZN27)
(Catalog# : 20513)
ZINC40099027 (ZN27) 是一种特异性粘着斑激酶 (FAK) 激活剂,可促进缺血
1661854-97-2 | Zipalertinib
(Catalog# : 20317)
Zipalertinib, also known as TAS6417, CLN-081, is a Novel EGFR Inhibitor Targeting Exo
1713240-67-5 | Zegocractin ( CM-4620 )
(Catalog# : 204504)
Zegocractin (CM-4620, Auxora(TM)) 是钙释放激活钙通道蛋白 1(CRAC 通道,
1080028-80-3 | Zamicastat
(Catalog# : 189271)
Zamicastat是一个强有力的和选择性的多巴胺β-mono-oxygenase抑制剂。
101975-10-4 | 扎达维林
(Catalog# : 185186)
扎达维林是一种磷酸二酯酶3/4抑制剂。
1691249-45-2 | Zanubrutinib
(Catalog# : 18577)
Zanubrutinib,也称为BGB-3111, 是一种有效且高选择性的小分子BTK抑制
139180-30-6 | ZM241385
(Catalog# : 17022714)
ZM241385是一种腺苷A2A受体拮抗剂。ZM241385在大鼠CA1海马区缺氧后增
1181226-02-7 | ZL006
(Catalog# : 16122851)
ZL006 is a PSD95-nNOS protein-protein interaction inhibitor. ZL006 (EC50: 12.88 M) di
1780259-94-0 | ZK-756326 dihydrochloride
(Catalog# : 16122850)
ZK-756326 is a potent, selective and non-peptide CCR8 chemokine receptor agonist. ZK
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-- Angiogenesis
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VEGFR
----
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----
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----
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----
FLT3
----
FGFR
----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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
----
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----
Integrin
----
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----
Wnt
----
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----
Gap Junction Protein
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
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----
Topoisomerase
----
DNA-PK
----
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----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
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----
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----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- GPCR & G Protein
----
Histamine Receptor
----
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----
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----
Endothelin Receptor
----
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----
OX Receptor
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-- Immunology & Inflammation
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----
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CD73
----
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----
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-- JAK/STAT
----
JAK
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STAT
----
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----
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)
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
-- Neuronal Signaling
----
COX
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
GABA Receptor
----
OX Receptor
----
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----
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----
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----
mAChR
----
α-Synuclein
----
Tau Protein
----
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----
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----
Melanocortin Receptor
----
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-- NF-κB
----
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IKK
----
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-- Protein Tyrosine Kinase
----
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----
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----
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----
FLT3
----
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----
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----
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----
ALK
----
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----
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----
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----
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----
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----
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----
ULK1
----
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----
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----
ROS Kinase
----
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----
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----
RET
----
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-- Proteases
----
Proteasome
----
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----
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----
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----
DPP4
----
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----
FPTase
----
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----
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
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Microbiology
-- Others
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PKK
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Others modulator
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Estrogen Receptor/ERR
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ChoKα
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Newest added products
抑制剂/受体激动剂
中间体
分子砌块
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Amino Acids
--
Anilines
--
Boronic Acids
--
Bromides
--
Carboxes
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On Sale
新产品
天然化合物
最新产品
1497439-74-3 | AD-8007
(Catalog# : 26A018)
AD-8007是一种选择性且可穿透血脑屏障的乙酰辅酶A合成酶2(ACSS2)
1802650-31-2 | ZY-444
(Catalog# : 26A020)
ZY-444是一种通过抑制PC活性发挥抗癌作用的药物。
2306525-79-9 | AD-5584
(Catalog# : 26A019)
AD-5584是一种新型脑渗透性ACSS2抑制剂。
3079716-11-0 | IDB-003
(Catalog# : 26A017)
IDB-003在体内抑制MDA-MB-231肿瘤生长。
1357362-02-7 | Vafidemstat
(Catalog# : 18891)
Vafidemstat又称ORY 2001,是一种赖氨酸特异性组蛋白去甲基化酶(LSD1)
1260247-42-4 | LLL12
(Catalog# : 25075)
LLL12是一种强效的STAT3抑制剂。LLL12在小鼠异种移植物模型中显示出
2758659-09-3 | ECC-5004
(Catalog# : 26A015)
ECC5004是一款每日一次、低剂量、小分子GLP-1受体激动剂。
2911585-37-8 | SILA-123
(Catalog# : 26A014)
SILA-123是一种II型FLT3抑制剂,对FLT3-WT(IC50=2.1 nM)和FLT3-ITD(IC50=1
1214922-52-7 | Encaleret sulfate
(Catalog# : 26A013)
Encaleret是一种正在研究的钙敏感受体的小分子拮抗剂,用于钙稳态
1431303-72-8 | Iadademstat ( ORY-1001 ) hydrochloride
(Catalog# : 26A011)
Iadademstat(ORY-1001)是一种口服活性、高效和选择性的表观遗传酶