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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
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others
分子砌块
Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
Fluorides
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Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
Peg Linkers
Phenols
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Pyrimidines
Quinolines
Sulfonamides
Thiazoles
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联系我们
+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
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
技术服务
定制合成
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订购信息
联系我们
公司简介
联系我们
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产品名字索引 F
AAG-1 ( FLAG-003 )
(Catalog# : 20640, Cas# :
1614235-14-1
)
FLAG-003 是一种多效水溶性小分子治疗药物,旨在通过两种成熟的作
FC-116
(Catalog# : 20569, Cas# :
2417298-29-2
)
FC-116 is a Tubulin inhibitor that effectively inhibits tumor growth in mice.
F7H inhibitor
(Catalog# : 20556, Cas# :
897109-93-2
)
F7H is a Frizzled receptor FZD7 antagonist.
Flavopiridol ( 夫拉平度 )
(Catalog# : 237071, Cas# :
146426-40-6
)
Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
FHD-286
(Catalog# : 20471, Cas# :
2671128-05-3
)
FHD-286 is an oral, small-molecule, selective, allosteric inhibitor of BRG1 and BRM i
3-氟-6-甲氧基喹啉
(Catalog# : 20433, Cas# :
426842-85-5
)
5-氟喹唑啉-2,4(1H,3H)-二酮
(Catalog# : 20420, Cas# :
192570-33-5
)
4-氟-2-(三氟甲基)苯甲醛
(Catalog# : 20405, Cas# :
90176-80-0
)
Fosgonimeton (ATH-1017)
(Catalog# : 1711225, Cas# :
2093305-05-4
)
Fosgonimeton (ATH-1017) 是一种小分子,旨在增强肝细胞生长因子 (HGF)
Fadraciclib free base
(Catalog# : L20347, Cas# :
1070790-89-4
)
Fadraciclib, also known as CYC065, is an orally bioavailable inhibitor of cyclin depe
063-0967
(Catalog# : 20315, Cas# :
613225-56-2
)
F1063-0967 is a novel inhibitor of dual-specificity phosphatase 26 (DUSP26), inducing
1-[6-(4-fluoro-1H-pyrazol-1-yl)-3-pyridinyl]Ethanone
(Catalog# : 20262, Cas# :
1980023-94-6
)
Firibastat ( QGC-001 )
(Catalog# : 26188, Cas# :
648927-86-0
)
Firibastat, (originally named QGC001) is the first drug candidate of a new class of c
FM-381
(Catalog# : 20122201, Cas# :
2226521-65-7
)
FM-381 is a Chemical Probe For JAK3 and JAK3 specific reversible covalent inhibitor.
FOY-251 mesylate
(Catalog# : 2091911, Cas# :
71079-09-9
)
FOY-251 is a metabolite of Camostat that acts as a pollen protease inhibitor for prev
FG-7142
(Catalog# : 2091909, Cas# :
78538-74-6
)
FG-7142 is a benzodiazepine receptor ligand with anxiogenic and proconvulsant propert
FT113
(Catalog# : 2071557, Cas# :
1630808-89-7
)
FT113 is a novel potent inhibitor of fatty acid synthase (fasn)
Fulacimstat
(Catalog# : 2071514, Cas# :
1488354-15-9
)
Fulacimstat, also known as BAY1142524, is a chymase inhibitor and antifibrotic drug c
FB23-2
(Catalog# : 207102, Cas# :
2243736-45-8
)
FB23-2 is a potent FTO inhibitor. FB23-2 demonstrated the potent inhibitory impact in
2-(3-Fluoro-4-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
(Catalog# : 262324, Cas# :
1350426-06-0
)
2-fluoro-4-methyl-5-nitrobenzoic acid methyl ester
(Catalog# : 2062015, Cas# :
753924-48-0
)
FTI-2148
(Catalog# : 111897, Cas# :
251577-09-0
)
FTI-2148 is a potent farnesyltransferase inhibitor with potential antitumor activity.
FR-190809
(Catalog# : 193253, Cas# :
215589-63-2
)
FR-190809是一种强效、无毒、口服有效的ACAT抑制剂。
FM19G11
(Catalog# : 192211, Cas# :
329932-55-0
)
FM19G11是缺氧诱导因子α的抑制剂(HIFα),据报道,影响干细胞的自我更
Fmk
(Catalog# : 188102, Cas# :
821794-92-7
)
强效不可逆RSK1/2抑制剂(IC50 = 15nm)。灭活C端自激酶域活性。
帕罗西汀 杂质C
(Catalog# : 18794, Cas# :
1841-19-6
)
帕罗西汀 杂质C是一种二苯基丁哌啶典型的抗精神病药物,用于精
Fezolinetant
(Catalog# : 18722, Cas# :
1629229-37-3
)
Fezolinetant,也被称为ESN-364,是一种神经kinin-3 (NK-3)受体拮抗剂,已
FRAX486
(Catalog# : 18721, Cas# :
1232030-35-1
)
FRAX486是一种有效的p21激活激酶(PAK)抑制剂(PAK1、PAK2、PAK3和PAK4的IC
非阿尿苷
(Catalog# : 184283, Cas# :
69123-98-4
)
非阿尿苷,又名FIAU, DRG-0098,是一种DNA定向DNA聚合酶抑制剂,可用
Fonadelpar
(Catalog# : 18445, Cas# :
515138-06-4
)
Fonadelpar是一个强有力的和选择性的过氧物酶体扩散者激活受体δ(
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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
-- 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
-- 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
-- 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
-- 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
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
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
PLX8394
(Catalog# : 20613, Cas# :
1393466-87-9
)
PLX8394 is an orally bioavailable inhibitor of serine/threonine-protein kinase B-raf
Zelasudil
(Catalog# : 24014, Cas# :
2365193-22-0
)
Zelasudil 是一种有效的、高选择性的口服活性抑制剂,针对 Rho 相关
Ziftomenib ( KO-539 )
(Catalog# : 24013, Cas# :
2134675-36-6
)
Ziftomenib 是一种口服、有效、选择性的小分子抑制剂,针对 menin 和
Zunsemetinib
(Catalog# : 24012, Cas# :
1640282-42-3
)
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
Zongertinib ( BI 1810631 )
(Catalog# : 24011, Cas# :
2728667-27-2
)
Zongertinib [BI 1810631] 是一种人表皮生长因子受体 2 (HER2) 抑制剂。
Zasocitinib
(Catalog# : 24010, Cas# :
2272904-53-5
)
Zasocitinib是一种作用于非受体酪氨酸蛋白激酶 (TYK2)靶点的抑制
RNK-05047
(Catalog# : 24008, Cas# :
2503036-46-0
)
RNK-05047 为BRD4降解剂,其在小鼠荷瘤异种移植模型中展现出显著抑
Asengeprast (FT011)
(Catalog# : 24009, Cas# :
1001288-58-9
)
Asengeprast (FT011) 是一种抗纤维化剂,降低胶原蛋白 I 和 III 的 mRNA
ERAS-801 ( JGK-068S )
(Catalog# : 20635, Cas# :
2490431-16-6
)
ERAS-801 ( JGK-068S ) 是一种有效的 EGFR 抑制剂。
T-1095
(Catalog# : 24004, Cas# :
209746-59-8
)
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs).