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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
PROTAC
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Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
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Chiral Compounds
Deuterated
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Oxazoles
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Pyridines
Pyrimidines
Quinolines
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Thiazoles
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Other Azoles
Other Heterocycles
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On Sale
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联系我们
公司简介
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Cas号索引 1
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Cas号索引 1
1011557-82-6 | Tenovin-6
(Catalog# : 52528)
Tenovin-6 is the water soluble analog of Tenovin-1 (HY-13423) and acts as a potent SI
1005491-05-3 | Tirasemtiv
(Catalog# : 52238)
Tirasemtiv(CK 2017357) is a a small-molecule fast-skeletal-troponin activator, which
1223001-51-1 | Torin 2
(Catalog# : 52311)
Torin 2 is a potent and selectivemTORinhibitor withIC50of 0.25 nM; 800-fold greater s
1401031-39-7 | TRV130 ( Oliceridine )
(Catalog# : 51910)
TRV 130 Hcl(Oliceridine)是一种新颖的MOR 激动剂,能够优先激活 G-protei
1616632-77-9 | TIC10 ( ONC201 )
(Catalog# : 51802)
ONC201 / TIC10是人类TRAIL基因的新型小分子诱导剂,可改善重组TRAIL的
1632002-28-8 | URAT1 inhibitor 7
(Catalog# : 20573)
URAT1 inhibitor 7 (compound 10f) is a potent URAT1 inhibitor.
1448440-52-5 | UAMC-1110
(Catalog# : 21249)
UAMC-1110, also known as SP-13786, is a novel potent and selective inhibitor of fibro
1616413-96-7 | UCB9608
(Catalog# : 2071515)
UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr
142878-12-4 | U-73343
(Catalog# : 112591)
U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p
1612782-86-1 | UNC2541
(Catalog# : 6111901)
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit
1890169-95-5 | UPGL00004
(Catalog# : 193251)
UPGL00004是谷氨酰胺酶C (GAC)的有效抑制剂。
1387560-01-1 | Umibecestat游离
(Catalog# : 193223)
Umibecestat,也被称为CNP-520,是一种β分泌酶抑制剂,是预防阿尔茨
1333218-50-0 | Upacicalcet ( 别名 SK-1403 ; AJT240)
(Catalog# : 192142)
Upacicalcet(别名 SK-1403/AJT240)是一种新型非肽拟钙剂,作为钙敏感
1229582-33-5 | URMC-099
(Catalog# : 1810252)
URMC-099是一种口服生物可用的、脑内渗透混合谱系激酶(MLK)抑制剂
1184136-10-4 | UNC-926游离
(Catalog# : 18584)
UNC-926是一种L3MBTL1域抑制剂. UNC-926联结L3MBTL1蛋白的MBT域。(Kd = 3.9
1310726-60-3 | 乌帕替尼
(Catalog# : 184105)
乌帕替尼,也被称为ABT-494,是一种强力和选择性的JAK抑制剂,用
1048371-03-4 | UPF-1069
(Catalog# : 1791520)
UPF-1069是一种选择性的强效PARP2抑制剂。UPF-1069诱导细胞凋亡。UPF-
1956366-10-1 | Ulixertinib HCl
(Catalog# : 179153)
Ulixertinib,也称为BVD-523和VRT752271,是ERK蛋白激酶抑制剂。对ERK蛋白
1872382-47-2 | UNC3866
(Catalog# : 17011102)
UNC3866是一种强力拮抗剂,对多梳型CBX和CDY家族染色体组的阅读功
126784-99-4 | Ulipristal acetate
(Catalog# : 16122843)
Ulipristal acetate, also known as CDB-2914, is a selective progesterone receptor modu
152273-12-6 | U-93631
(Catalog# : 16122841)
U-93631 is a GABAA receptor antagonist. U-93631 causes rapid decay of gamma-aminobuty
1381291-36-6 | USP7-IN-1
(Catalog# : 611931)
USP7-IN-1 is a novel selective and reversible inhibitor of USP7 with IC50 of 33 uM; l
1481677-78-4 | UNC0642
(Catalog# : 16071013)
UNC0642 is a potent, selective inhibitor of G9a/GLP with improved PK properties. UNC0
1047634-65-0 | Uprosertib (GSK2141795)
(Catalog# : 16070901)
Uprosertib (GSK2141795) is a selective, ATP-competitive, and orally bioavailableAktin
178870-32-1 | UC-781
(Catalog# : 011311)
UC-781 is a thiocarboxanilide non-nucleoside reverse transcriptase inhibitor. It is a
1415800-43-9 | UNC1215
(Catalog# : 011123)
UNC1215 is a potent and selective chemical probe for the methyllysine (Kme) reading f
178606-66-1 | U-104
(Catalog# : 010440)
U-104 is a potent carbonic anhydrase (CA) inhibitor for CA IX and CA XII with Ki of 4
1431612-23-5 | UNC1999
(Catalog# : 111901)
UNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 wit
112648-68-7 | U73122
(Catalog# : 102201)
U73122 is a potent phospholipase C (PLC) inhibitor, which reduces agonist-induced Ca2
1197196-48-7 | UNC0224
(Catalog# : 82404)
UNC0224 is a potent and selective G9a inhibitor with IC50 of 15 nM in the G9a Thioglo
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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