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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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Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
Fluorides
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Iodos
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Pyridines
Pyrimidines
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Cas号索引 1
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Cas号索引 1
129799-15-1 | N-Boc-Piperazine-2-Carboxylic Acid Methyl Ester
(Catalog# : 81725)
Coming soon!
157115-85-0 | Noopept
(Catalog# : 52813)
Noopept (GVS-111) is a medication promoted and prescribed in Russia and neighbouring
1312445-63-8 | NVP-BKM120 Hydrochloride
(Catalog# : 52775)
Also see <a href="http://www.sun-shinechem.com/Details/BKM120(NVP-BKM120,%20B
1384426-12-3 | NT-157
(Catalog# : 51508)
NT157 is a small-molecule tyrphostin targeting human IRSes.
1245537-68-1 | NVP-BGT226
(Catalog# : 52633)
NVP-BGT226(BGT 226) is a novel class I PI3K/mTOR inhibitor for PI3K// with IC50 of 4
1270138-40-3 | NSI-189
(Catalog# : 52558)
NSI-189 is an experimental drug being studied by Neuralstem, Inc. Research into NSI-1
1418013-75-8 | NMS-873
(Catalog# : 52553)
NMS-873 is a potent, selective allosteric VCP/p97 inhibitor with IC50 value of 20 nM
1402836-58-1 | NLG919(GDC0919)
(Catalog# : 52246)
NLG919 isa promisingandpotent direct enzymatic inhibitor of IDO,In preclinical models
1403783-31-2 | Nexturastat A
(Catalog# : 51503)
Nexturastat A is a potent and selective HDAC6 inhibitor with IC50 of 5 nM; no inhibit
195371-52-9 | NSC 42834
(Catalog# : 52403)
NSC 42834(JAK2 Inhibitor V, Z3), a novel specific inhibitor of Jak2, inhibits Jak2-V6
1359969-24-6 | Ocedurenone
(Catalog# : 24091)
Ocedurenone is a non-steroidal mineralocorticoid receptor antagonist.
1257628-77-5 | Olverembatinib (GZD824)
(Catalog# : 24046)
Olverembatinib, also known as GZD824, is a novel orally bioavailable inhibitor agains
1474034-05-3 | omaveloxolone
(Catalog# : 20530)
Omaveloxolone, also known as RTA-408, is a member of the synthetic oleanane triterpen
160492-56-8 (free base) | Osanetant
(Catalog# : 20505)
Osanetant is a tachykinin NK3 antagonist potentially for the treatment of schizophren
1638178-82-1 | ONC201 HCl
(Catalog# : 20305)
ONC-201, also known as TIC10 and imipridone, is a potent, orally active, and stable s
1261289-04-6 | O304
(Catalog# : 2071504)
O-304 is a pan-activator of AMP-activated protein kinase (AMPK). It increases levels
1887014-12-1 | olutasidenib
(Catalog# : 20791)
Olutasidenib(FT-2102)是一种有效的突变体选择性IDH1抑制剂。 Olutasi
1340593-59-0 | Oteseconazole
(Catalog# : 111895)
Oteseconazole,也称为 VT-1161,是第一个批准的口服生物利用度和选择
1638178-87-6 | ONC206
(Catalog# : 111891)
ONC206 is a chemical analogue of ONC201. ONC206 is a benzyl-flurobenzyl imipridone th
1309198-71-7 | Ogerin
(Catalog# : 193186)
Ogerin是一种选择性的GPR68 PAM,在野生型小鼠中抑制恐惧条件反射的
1802661-73-9 | ONO-8590580
(Catalog# : 1810162)
ONO-8590580是一个GABAA α5的消极变构调制器。
1807861-48-8 | ONC212
(Catalog# : 185286)
ONC212是一种氟化的ONC201类似物,在黑色素瘤和肝细胞癌模型中显示
131631-89-5 | OPC-21268
(Catalog# : 185163)
OPC-21268是一种血管加压素1受体拮抗剂,可用于治疗心力衰竭和高
1431697-89-0 | OTSSP167游离
(Catalog# : 185161)
OTSSP167,也被称为OTS167,是一种口服有效的抑制母胚胎亮氨酸拉链
1316755-16-4 | Olodanrigan游离酸
(Catalog# : 1842810)
Olodanrigan,又称EMA-401和PD-126055,是一种血管紧张素AT2拮抗剂,可用
1421373-66-1 | Osimertinib mesylate
(Catalog# : 1712154)
Osimertinib, also known as mereletinib and AZD-9291, is a third-generation EGFR inhib
131247-39-8 | ON1231320
(Catalog# : 1791319)
ON1231320,也称为GBO-006,是Plk2抑制剂。
1306760-87-1 | 奥扎莫德
(Catalog# : 110902)
奥扎莫德是一种选择性的鞘氨醇1磷酸受体调节剂和方法,可能在
1353550-13-6 | 奥莫替尼
(Catalog# : 011103)
奥莫替尼是一种有效的布鲁顿酪氨酸激酶(BTK)小分子抑制剂。
1261491-89-7 | Olumacostat Glasaretil
(Catalog# : 732801)
Olumacostat glasaretil是一种新型的用于痤疮治疗的局部皮脂抑制剂。
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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