武汉永璨生物科技有限公司
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抑制剂/受体激动剂
PI3K/Akt/mTOR
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Cytoskeletal Signaling
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others
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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
PROTAC
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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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
FKL-117
(Catalog# : 24087, Cas# :
2740496-44-8
)
Fosmanogepix
(Catalog# : 24072, Cas# :
2091769-17-2
)
Fosmanogepix is a novel antifungal, targeting the conserved Gwt1 enzyme required for
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。
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
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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
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
STX-478
(Catalog# : 20633, Cas# :
2883540-92-7
)
STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
Iclepertin (BI-425809)
(Catalog# : 24084, Cas# :
1421936-85-7
)
Iclepertin(BI-425809)是一种口服的GlyT-1小分子抑制剂,用于治疗与
Bomedemstat
(Catalog# : 24001, Cas# :
1990504-34-1
)
Bomedemstat 是一种口服的、不可逆的赖氨酸特异性去甲基酶 1 (LSD1)
PLX-4545
(Catalog# : 24111, Cas# :
2892065-45-9
)
PLX-4545 是一种口服生物可利用的 IKZF2 分子胶降解剂,旨在破坏高
VVD-130037 ( BAY-3605349 )
(Catalog# : 24110, Cas# :
3034880-93-5
)
VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
CBR-5884
(Catalog# : 24109, Cas# :
681159-27-3
)
CBR 5884 是一种磷酸甘油酸脱氢酶 (PHGDH) 抑制剂,能够抑制过度表达
JHU-083
(Catalog# : 24108, Cas# :
1998725-11-3
)
JHU-083 选择性阻断大脑 CD11b+ 细胞中的谷氨酰胺酶活性,并防止慢
LXH-3-71
(Catalog# : 24107, Cas# :
2251753-65-6
)
LXH-3-71是一种新型“分子胶”,可诱导PHGDH和DDB1-CUL4泛素连接酶之
CC-92480 ( Mezigdomide )
(Catalog# : 20510, Cas# :
2259648-80-9
)
CC-92480 是一种有效的新型 CELMoD 化合物,旨在快速最大程度地降解
Adrixetinib ( Q-702 )
(Catalog# : 20617, Cas# :
2394874-66-7
)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag