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抑制剂/受体激动剂
Angiogenesis
Anti-infection
Apoptosis
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Cytoskeleton
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Membrane Transporter/Ion Channel
Metabolism
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Protein Tyrosine Kinase
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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
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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
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
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On Sale
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联系我们
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Cas号索引 8
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Cas号索引 8
877387-37-6 (free base) | GSK5182
(Catalog# : 20375)
GSK5182 is a specific inverse agonist for estrogen-related receptor γ.
881639-98-1 | G-1
(Catalog# : 206103)
G-1 is a selective agonist for GPER. It acts by blocking tubulin polymerization.
827319-43-7 | GW-870086
(Catalog# : 1811263)
GW-870086是一种糖皮质激素受体激动剂,有望用于哮喘和特应性皮炎
880635-03-0 | GW6471
(Catalog# : 181151)
GW6471是一种PPARα拮抗剂(IC50 = 0.24μM)。GW6471提高SMRT和NCoR的蛋白质亲
817194-38-0 | GSK180736A (GSK180736)
(Catalog# : 178901)
GSK180736A是一种有效的、具有选择性的IC50 0.77 M25的GRK2抑制剂,比其
844903-58-8 | GSK163090
(Catalog# : 6111015)
GSK163090 is a potent, selective, and orally active 5-HT1A/B/D receptor antagonist wi
863513-91-1 | GRT-6005
(Catalog# : 16071110)
Cebranopadol is a potent nociceptin/orphanin FQ peptide (NOP) and opioid receptor ago
873652-48-3 | GDC-0152
(Catalog# : 16071101)
GDC-0152 is a second mitochondrial activator of caspases (Smac) mimetic inhibitor of
839706-07-9 | GNF-7
(Catalog# : 16060604)
BenzaMide
870483-87-7 | GW2580
(Catalog# : 122524)
GW2580 is an orally bioavailable inhibitor of c-FMS kinase; completely inhibited huma
850664-21-0 | GSK269962A
(Catalog# : 102206)
GSK269962A(CAS 850664-21-0) is a potent ROCK inhibitor (IC50 values are 1.6 and 4 nM
851983-85-2 | Galeterone
(Catalog# : 62003)
Galeterone(VN/124-1,TOK001) is a highly selective, multi-targeted, oral small molecul
864082-47-3 | GSK429286A
(Catalog# : 52629)
GSK429286A is a selective inhibitor of ROCK1 and ROCK2 with IC50 of 14 nM and 63 nM,
888216-25-9 | Ganetespib(STA-9090)
(Catalog# : 52021)
Ganetespib blocked the ability of HSP90 to bind to biotinylated geldanamycin and disr
877768-84-8 | H2-Gamendazole
(Catalog# : 24145)
H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
86227-47-6 | Icosapent ethyl
(Catalog# : 24045)
Icosapent ethyl is used for the treatment of hypertriglyceridemia.
851870-24-1 | 4-iodo-2-isopropyl-1-Methyl-1H-iMidazole
(Catalog# : 2062023)
887401-93-6 | INCB3284甲磺酸盐
(Catalog# : 191143)
INCB3284是一种有效的、选择性的、可口服的hCCR2拮抗剂。
835619-41-5 | Indeglitazar
(Catalog# : 1812131)
Indeglitazar,也称为PPM-204和PLX-204,是一个可口服的过氧化物酶体增
832115-62-5 | ISX-9
(Catalog# : 17022713)
ISX-9 is a neurogenic agent. Isx-9 promotes neurogenesis in vivo, enhancing the proli
873225-46-8 | IKK-16
(Catalog# : 16123017)
IKK-16 is a potent and slective inhibitor of IB kinase (IKK) (IC50 values are 40, 70
866927-10-8 | IC87201
(Catalog# : 16122820)
IC87201 is a nNOS-PDZ/PSD-95-PDZ inhibitor. IC87201 showed great promise in cellular
851870-28-5 | 5-Iodo-2-isopropyl-1-methyl-1H-imidazole
(Catalog# : 021701)
Coming soon!
857679-55-1 | INCB8761 (PF-4136309)
(Catalog# : 92210)
INCB8761(PF-4136309) is a potent, selective, and orally bioavailable CCR2 antagonist.
879-37-8 | Indole-3-Acetamide
(Catalog# : 81920)
Coming soon!
873054-44-5 | Ivacaftor
(Catalog# : 52805)
Ivacaftor (VX-770) is a potentiator of CFTR targeting G551D-CFTR and F508del-CFTR wit
878489-28-2 | JNJ 303
(Catalog# : 122938)
Coming soon!
881202-45-5 | JNJ-26854165 (Serdemetan)
(Catalog# : 52522)
JNJ-26854165 (Serdemetan) acts as a HDM2 ubiquitin ligase antagonist and also induces
888032-58-4 | KPI-10
(Catalog# : 20277)
KPI-10 is a new compound currently being studied for its efficacy in the treatment of
845932-30-1 | KU59403
(Catalog# : 19123)
KU59403是一种有效的选择性ATM(共济失调毛细血管扩张突变)抑制剂,
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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
-- 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
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,
2488609-21-6 | DS68591889
(Catalog# : 25158)
DS68591889 (PTDSS1i) 特异性抑制 PTDSS1,而 PTDSS1 可催化丝氨酸掺入 PC。
944808-88-2 | CAY 10566
(Catalog# : 10403)
CAY 10566是一种强效的选择性SCD-1抑制剂。
2308520-97-8 | Cadefrecitinib (GLPG-3667)
(Catalog# : 20509)
Cadefrecitinib(GLPG-3667)是一种口服小分子TYK2激酶抑制剂,目前正处
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
2377000-84-3 | Dencatistat (STP938)
(Catalog# : 25177)
Dencatistat 是一种口服生物可利用的小分子胞苷三磷酸合酶 1 (CTPS1)
1898207-64-1 | DS-1001b
(Catalog# : 25178)
DS-1001 是一种口服的脑渗透性突变 IDH1 选择性抑制剂。
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
2416095-06-0 | CBR-470-1
(Catalog# : 25192)
CBR-470-1 是诱导 Nrf2 活性的糖酵解酶 PGK1 的抑制剂。
1898206-17-1 | Safusidenib
(Catalog# : 25149)
Safusidenib,也称为DS-1001,是一种口服异柠檬酸脱氢酶[NADP]细胞质(