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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
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
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中间体
技术服务
定制合成
工艺研发
订购信息
联系我们
公司简介
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
技术服务
定制合成
工艺研发
订购信息
联系我们
公司简介
联系我们
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Cas号索引 4
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Cas号索引 4
458-45-7 | 3-(3-Fluorophenyl)Propionic Acid
(Catalog# : 90610)
Coming soon!
405911-17-3 | GW-3965盐酸盐
(Catalog# : 192251)
GW-3965是一种肝脏X受体激动剂。GW3965抑制小鼠肥大细胞产生促炎细
460330-27-2 | GT 949
(Catalog# : 187182)
GT 949是一种选择EAAT2阳性变构调制器(EC50 = 0.26 nM)。提高谷氨酸的易
413611-93-5 | 10074-G5
(Catalog# : 1791112)
10074-G5是一种c-Myc/Max互动抑制剂。10074-G5类似于10058-F4,具体抑制c
497833-27-9 | Givinostat
(Catalog# : 123008)
Givinostat is an orally bioavailable hydroxymate inhibitor of histone deacetylase (HD
439288-66-1 | GW 627368
(Catalog# : 91003)
GW 627368X is a potent and selective competitive antagonist of the EP4 receptor with
452342-67-5 | GW788388
(Catalog# : 52305)
GW788388 is a potent and selective inhibitor of ALK5 with IC50 of 18 nM, also inhibit
491833-30-8 | Genz-123346
(Catalog# : S1419)
Genz-123346 free base is an inhibitor of GL1 synthase that blocks the conversion of c
412003-95-3 | 2,4-二甲基-5-羟基嘧啶
(Catalog# : 2091204)
我们可以生产公斤级的2,4-二甲基-5-羟基嘧啶 (CAS 412003-95-3)。
422513-13-1 | Hesperadin
(Catalog# : 17011902)
Hesperadin是人类Aurora B的一种抑制剂,它可以阻止IC(50)为40 nM的基质
482-44-0 | Imperatorin
(Catalog# : 16123019)
Imperatorin, aslo known as Pentosalen, Marmelosin, is a furocoumarin and a phytochemi
467459-31-0 | Idalopirdine (Lu AE58054)
(Catalog# : 16122821)
Idalopirdine, also known as Lu AE58054 or Iladopirdine, is a potent and selective 5-H
448906-42-1 | IRAK-1-4 Inhibitor I
(Catalog# : 16062116)
IRAK-1-4 Inhibitor I
459789-99-2 | INT-747
(Catalog# : 122905)
INT-747 is a potent and selective FXR agonist(EC50=99 nM) endowed with anticholestati
461054-93-3 | Ko 143
(Catalog# : 111908)
Ko 143 is a potent and selective breast cancer resistance protein multidrug transport
4727-31-5 | Kartogenin
(Catalog# : 52215)
Kartogenin(KGN) is a small molecule stimulator of chondrogenesis; promotes chondrocyt
436133-68-5 | Kobe0065
(Catalog# : 52237)
Kobe0065 is a novel and effective small-molecule compound inhibiting RasCRaf interact
454453-49-7 | kobe2602
(Catalog# : 52401)
kobe2602 is a novel and effective small-molecule compound inhibiting RasCRaf interact
47142-51-8 | LUN42518
(Catalog# : 2091908)
LUN42518, also known as Phentolamine Analogue 1, is an analogue of phentolamine. Phen
417716-92-8 | 乐伐替尼(E7080)
(Catalog# : 52025)
乐伐替尼,又名E7080,是一种合成的、可口服的血管内皮生长因子
439239-90-4 | Lasmiditan
(Catalog# : 6111006)
Lasmiditan (COL-144; LY573144) is a high-affinity, highly selective 5-HT1F receptor a
460331-61-7 | ML192
(Catalog# : 20464)
ML192, also known as MLS000526305 and CID1434953, is a selective ligands for GPR55. T
442898-34-2 | ML008
(Catalog# : 20112602)
ML008, also known as NCGC00092410, is a potent and selective inhibitor of glucocerebr
476476-54-7 | 4-(2-(6-methylpyridin-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)quinoline-6-carboxylic acid
(Catalog# : 2062320)
400755-41-1 | 3-甲氧基-4-硝基-1H-吡唑
(Catalog# : 5141901)
432001-69-9 | MDK-1699
(Catalog# : 184191)
MDK-1699,也称为Skp2抑制剂C1和SKPinC1,是一种Skp2抑制剂。
474645-27-7 | 单甲基奥立斯丁
(Catalog# : 17022403)
MMAE,又称单甲基奥立斯丁,是一种合成的抗肿瘤药物。
475085-57-5 | MRE-269
(Catalog# : 020106)
MRE-269 is a long-acting and highly selective prostacyclin receptor agonist.
471905-41-6 | MK-0752
(Catalog# : 122949)
MK-0752 is a moderately potent -secretase inhibitor, which reduces A40 production wit
494227-37-1 | Mandyphos SL-M004-1
(Catalog# : 121502)
Coming soon!
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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
921193-28-4 | BTA-EG4 hydrate
(Catalog# : 24157)
BTA-EG4 is a catalase-amyloid interaction inhibitor, which can significantly enhance
2415281-52-4 | CYD19
(Catalog# : 24156)
CYD19 is a potent Snail/HDAC dual target inhibitor.
98570-83-3 | Phylloflavan
(Catalog# : 24155)
Phylloflavan is an antileishmanial agent with an intracellular EC50 of 3.2 nM in RAW
312611-92-0 | VK-28
(Catalog# : 24154)
VK-28, a brain-permeable iron chelator, inhibits both basal and Fe/ascorbate-induced
160162-42-5 | SR-11302
(Catalog# : 24153)
SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor.
2171065-77-1 | AKOS037652256
(Catalog# : 24152)
AKOS037652256 can be used as a TRPML modulator for the treatment of diseases associat
2990506-75-5 | ML353
(Catalog# : 24151)
ML353 is a selective ligand of mGlu5 silent allosteric modulator (SAM).
1208448-95-6 | MIF098
(Catalog# : 24150)
MIF098 is a macrophage migration inhibitory factor (MIF) antagonist.
2319722-53-5 | TM5441sodium
(Catalog# : 24149)
TM-5441, also known as EBP 883 and BMS-790052, is a potent plasminogen activator inhi
2794934-49-7 | RGT-018
(Catalog# : 24148)
RGT-018 is a potent and orally active SOS1 inhibitor with anti-tumor effects.