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抑制剂/受体激动剂
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Epigenetics
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Cytoskeletal Signaling
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Neuronal Signaling
NF-κB
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
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others
PROTAC
分子砌块
Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
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Indoles and Oxindoles
Iodos
Nitro Compounds
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Peg Linkers
Phenols
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Pyridines
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Quinolines
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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
技术服务
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 O
OSS-128167
(Catalog# : 184214, Cas# :
887686-02-4
)
OSS-128167, also known as SIRT6-IN-1, is a potent and selective SIRT 6 inhibitor.
Osimertinib mesylate
(Catalog# : 1712154, Cas# :
1421373-66-1
)
Osimertinib, also known as mereletinib and AZD-9291, is a third-generation EGFR inhib
醋酸催产素
(Catalog# : 1791513, Cas# :
6233-83-6
)
催产素是一种药物和激素。作为一种药物,它被用来引起子宫收缩
ON1231320
(Catalog# : 1791319, Cas# :
131247-39-8
)
ON1231320,也称为GBO-006,是Plk2抑制剂。
盐酸奥达特罗
(Catalog# : 179824, Cas# :
869477-96-3
)
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
奥扎莫德
(Catalog# : 110902, Cas# :
1306760-87-1
)
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
奥莫替尼
(Catalog# : 011103, Cas# :
1353550-13-6
)
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。
OXi-4503钠
(Catalog# : 178308, Cas# :
288847-34-7
)
OXi-4503是一种二磷酸酯类药物,开始是从植物纤维中分离出来的,
6-氧杂螺[4.5]癸烷-9-醇
(Catalog# : 20177315, Cas# :
855398-58-2
)
6-氧杂螺[4.5]癸烷-9-醇|6-Oxaspiro[4.5]decan-9-ol|15080-A1
Olumacostat Glasaretil
(Catalog# : 732801, Cas# :
1261491-89-7
)
Olumacostat glasaretil是一种新型的用于痤疮治疗的局部皮脂抑制剂。
OTS514
(Catalog# : 17031015, Cas# :
1338540-63-8
)
OTS514是一种高效的TOPK(T-LAK胞起源蛋白激酶)抑制剂,IC50值为2.6 nM。
奥马曲拉
(Catalog# : 17030903, Cas# :
167305-00-2
)
奥马曲拉是一种新型的抗高血压药,可抑制中性内肽酶(NEP)和血管
ON-013100
(Catalog# : 17030902, Cas# :
865783-95-5
)
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
ONT-093
(Catalog# : 17030901, Cas# :
216227-54-2
)
ONT-093, 也称为OC-144-093,是一种口服的P-糖蛋白泵抑制剂,用于治疗
催产素
(Catalog# : 17030805, Cas# :
50-56-6
)
催产素是一种药物和荷尔蒙。作为一种药物,它被用来引起子宫收
Orteronel (外消旋)
(Catalog# : 17030610, Cas# :
426219-18-3
)
Orteronel(外消旋)是s - Orteronel和r - Orteronel异构体的混合物。Orteronel
奥巴克拉
(Catalog# : 17022707, Cas# :
803712-79-0
)
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
Org-26576
(Catalog# : 17021328, Cas# :
1026791-61-6;100044-96-0
)
Org-26576是一种AMPA谷氨酸受体调制器,可能用于治疗抑郁症和注意
氧化白藜芦醇
(Catalog# : 17021324, Cas# :
29700-22-9
)
氧化白藜芦醇,一种天然存在的化合物,尤其在Morus alba L中发现。
ONO-7300243
(Catalog# : 16122724, Cas# :
638132-34-0
)
ONO-7300243 is a novel, potent LPA1(Lysophosphatidic Acid Receptor) antagonist with a
Oxolinic acid
(Catalog# : 16122720, Cas# :
14698-29-4
)
Oxolinic acid is a quinolone antibiotic, inhibiting the enzyme DNA gyrase and DNA syn
ON123300
(Catalog# : 16122712, Cas# :
1357470-29-1
)
ON123300 is a potent and multi-targeted kinase inhibitor with IC50 of 3.9 nM, 5 nM, 2
Oclacitinib
(Catalog# : 16122705, Cas# :
1640292-55-2
)
Oclacitinib is a novel inhibitor of JAK family members with IC50 ranging from 10 to 9
Opicapone
(Catalog# : 6111514, Cas# :
923287-50-7
)
Opicapone(BIA 9-1067) is a long-acting, peripherally selective inhibitor of catechol-
OICR-9429
(Catalog# : 6111010, Cas# :
1801787-56-3
)
OICR-9429 is a novel small-molecule antagonist of the Wdr5-MLL interaction with IC50
ON 146040
(Catalog# : 611901, Cas# :
1404231-34-0
)
ON 146040 is the first dual PI3K and BCR-ABL inhibitor that targets the STAT3 and STA
OSI-027 HCl salt
(Catalog# : 161009007, Cas# :
936890-98-1
)
mTOR kinase inhibitor OSI-027 binds to and inhibits both the raptor-mTOR (TOR complex
OtaMixaban
(Catalog# : 16070915, Cas# :
193153-04-7
)
OtaMixaban
Oritavancin
(Catalog# : 16070815, Cas# :
171099-57-3
)
Oritavancin, also known as LY333328, is a novel semisynthetic glycopeptide antibiotic
ON-01911.Na
(Catalog# : 1662310, Cas# :
1330633-98-1(free base)
)
ON-01911.Na is a non-ATP-competitive inhibitor ofPLK1.
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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