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Epigenetics
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Angiogenesis
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Cytoskeletal Signaling
Cell Cycle
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DNA Damage
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Metabolism
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Catalysts
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Deuterated
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+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
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Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
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Chiral Compounds
Deuterated
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Pyridines
Pyrimidines
Quinolines
Sulfonamides
Thiazoles
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Other Heterocycles
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联系我们
公司简介
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Cas号索引 8
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Cas号索引 8
882272-97-1 | N,N-dibenzyl-6-chloro-5-nitropyrimidine-4-amine
(Catalog# : 2062033)
839713-36-9 | Nelotanserin
(Catalog# : 191121)
Nelotanserin( APD125) is a potent and selective human 5-hydroxytryptamine2A inverse a
890129-26-7 | NVP-BGG463
(Catalog# : 1810233)
NVP-BGG463是一种新型的II型激酶抑制剂,靶向CDK2。
847559-80-2 | NVP-BEP800
(Catalog# : 17030906)
NVP-BEP800, 也称为BEP-800,是一种新型的、完全合成的口服生物可用抑
848354-66-5 | NCH-51
(Catalog# : 17030716)
NCH-51, 也叫PTACH,是一种组蛋白去乙酰化酶(HDAC)抑制剂。NCH-51抑制
82956-11-4 | Nafamostat mesylate
(Catalog# : 16122833)
Nafamostat, also known as FUT-175, is a serine protease inhibitor and an anticoagulan
83280-65-3 | Napabucasin
(Catalog# : 16122708)
Napabucasin is an orally available Stat3 and cancer cell stemness inhibitor.Napabucas
852391-20-9 | Necrostatin 2 S enantiomer
(Catalog# : 6111412)
Necrostatin 2 is a potent necroptosis inhibitor with EC50 of 50 nM.Necrostatin 2 is a
852391-15-2 | Necrostatin 2 racemate
(Catalog# : 6111411)
Necrostatin 2 is a potent necroptosis inhibitor with EC50 of 50 nM.Necrostatin 2 is a
855527-92-3 | NBI-74330
(Catalog# : 6111112)
NBI-74330 is a small molecule antagonist for CXCR3, NBI-74330 demonstrates potent inh
852391-19-6 | Necrostatin 2
(Catalog# : 16070914)
Necrostatin 2
826-62-0 | 5-Norbornene-2,3-Dicarboxylic Anhydride
(Catalog# : 91402)
The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3
872511-34-7 | NVP-BGJ398
(Catalog# : 52743)
NVP-BGJ398(BGJ-398) is a novel selective, pan-specific FGFR inhibitor with IC50 of 0.
853910-02-8 | NVP-BAG956
(Catalog# : 52605)
NVP-BAG956(BAG 956) is a potent, ATP-competitive and selective dual PI3K and PDK1 inh
866399-87-3 | Obicetrapib
(Catalog# : 20314)
Obicetrapib (also known as AMG-899, TA-8995, and DEX-001) is a cholesteryl ester tran
887686-02-4 | OSS-128167
(Catalog# : 184214)
OSS-128167, also known as SIRT6-IN-1, is a potent and selective SIRT 6 inhibitor.
869477-96-3 | 盐酸奥达特罗
(Catalog# : 179824)
盐酸奥达特罗,也称为BI 1744,是一种长效β受体激动剂用于患者吸
855398-58-2 | 6-氧杂螺[4.5]癸烷-9-醇
(Catalog# : 20177315)
6-氧杂螺[4.5]癸烷-9-醇|6-Oxaspiro[4.5]decan-9-ol|15080-A1
865783-95-5 | ON-013100
(Catalog# : 17030902)
ON-013100是一种细胞周期抑制剂,对治疗地幔细胞淋巴瘤有潜在的作
803712-79-0 | 奥巴克拉
(Catalog# : 17022707)
奥巴克拉对Bcl-xL细胞系中的缺乏表现出较低敏感。在 Mcl-1, Bcl-2,和
82571-53-7 | ozagrel
(Catalog# : 120413)
Coming soon!
868049-49-4 | Olodaterol
(Catalog# : 101905)
Olodaterol is a long acting beta-adrenoceptor agonist used as an inhalation for treat
873697-71-3 | Omecamtiv mecarbil (CK-1827452)
(Catalog# : 100901)
Omecamtiv mecarbil is a novel, small-molecule, direct activator of cardiac myosin, th
841205-47-8 | Ostarine
(Catalog# : 52639)
Ostarine(MK-2866; GTX-024)A modulator to human androgen receptor.
83797-69-7 | 6-OAU
(Catalog# : 52217)
6-OAU(GTPL5846; 6-n-octylaminouracil) is a surrogate agonist of GPR84; activates huma
85278-22-4 | p-Aminophenol sulfate
(Catalog# : 2062201)
878437-15-1 | PA-8
(Catalog# : 1810254)
PA-8是PAC1受体的小分子拮抗剂。
848259-27-8 | Pemafibrate
(Catalog# : 179221)
Pemafibrate, also known as K-877 and (R)-K 13675, is a PPAR alpha agonist. (R)-K-1367
875051-72-2 | PF-01247324
(Catalog# : 1781102)
PF-01247324一种新的选择性和口服生物利用率的Nav 1.8通道阻滞剂,能
88069-49-2 | 吡西卡尼盐酸盐
(Catalog# : 17031016)
吡西卡尼,也叫SUN 1165,是日本临床上用来治疗心律失常的一种药
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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
2883540-92-7 | STX-478
(Catalog# : 20633)
STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
1421936-85-7 | Iclepertin (BI-425809)
(Catalog# : 24084)
Iclepertin(BI-425809)是一种口服的GlyT-1小分子抑制剂,用于治疗与
1990504-34-1 | Bomedemstat
(Catalog# : 24001)
Bomedemstat 是一种口服的、不可逆的赖氨酸特异性去甲基酶 1 (LSD1)
2892065-45-9 | PLX-4545
(Catalog# : 24111)
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
3034880-93-5 | VVD-130037 ( BAY-3605349 )
(Catalog# : 24110)
VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
681159-27-3 | CBR-5884
(Catalog# : 24109)
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
1998725-11-3 | JHU-083
(Catalog# : 24108)
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
2251753-65-6 | LXH-3-71
(Catalog# : 24107)
LXH-3-71是一种新型“分子胶”,可诱导PHGDH和DDB1-CUL4泛素连接酶之
2259648-80-9 | CC-92480 ( Mezigdomide )
(Catalog# : 20510)
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
2394874-66-7 | Adrixetinib ( Q-702 )
(Catalog# : 20617)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag