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+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
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Pyrimidines
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Cas号索引 1
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Cas号索引 1
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。
1338540-63-8 | OTS514
(Catalog# : 17031015)
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。
167305-00-2 | 奥马曲拉
(Catalog# : 17030903)
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
1026791-61-6;100044-96-0 | Org-26576
(Catalog# : 17021328)
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
14698-29-4 | Oxolinic acid
(Catalog# : 16122720)
Oxolinic acid is a quinolone antibiotic, inhibiting the enzyme DNA gyrase and DNA syn
1357470-29-1 | ON123300
(Catalog# : 16122712)
ON123300 is a potent and multi-targeted kinase inhibitor with IC50 of 3.9 nM, 5 nM, 2
1640292-55-2 | Oclacitinib
(Catalog# : 16122705)
Oclacitinib is a novel inhibitor of JAK family members with IC50 ranging from 10 to 9
1801787-56-3 | OICR-9429
(Catalog# : 6111010)
OICR-9429 is a novel small-molecule antagonist of the Wdr5-MLL interaction with IC50
1404231-34-0 | ON 146040
(Catalog# : 611901)
ON 146040 is the first dual PI3K and BCR-ABL inhibitor that targets the STAT3 and STA
193153-04-7 | OtaMixaban
(Catalog# : 16070915)
OtaMixaban
171099-57-3 | Oritavancin
(Catalog# : 16070815)
Oritavancin, also known as LY333328, is a novel semisynthetic glycopeptide antibiotic
1330633-98-1(free base) | ON-01911.Na
(Catalog# : 1662310)
ON-01911.Na is a non-ATP-competitive inhibitor ofPLK1.
183321-86-0 | OSI-420(Desmethyl Erlotinib)
(Catalog# : 166215)
OSI-420 is the active metabolite of Erlotinib which is an orally active EGFR tyrosin
1351635-67-0 | ONO4059-Analog
(Catalog# : 652602)
ONO4059-Analog(CAS#1351635-67-0)is a potent and selective BTK inhibitor.
192564-14-0 | Oritavancin(OC)
(Catalog# : 42510)
Oritavancin (INN, also known as LY333328, Orbactiv) is a novel semisynthetic glycopep
1297538-32-9 | ODM-201(BAY-1841788)
(Catalog# : 123101)
ODM-201(also known as BAY-1841788)is a novel, nonsteroidal, orally active AR inhibito
1086062-66-9 | Omipalisib(GSK2126458,GSK458)
(Catalog# : 121429)
GSK2126458 is a highly selective and potent inhibitor of PI3K with Ki of 0.019 nM/0.1
175135-47-4 | O4I1
(Catalog# : 120813)
O4I1 is as a potent Oct3/4 inducer.
165682-93-9 | O4I2
(Catalog# : 120812)
O4I2 is a potent Oct3/4 inducer in various human cell lines including human fibroblas
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产品分类
信号通路
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
----
Eukaryotic Initiation Factor (eIF)
----
NEKs
-- Cytoskeleton
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
----
Gap Junction Protein
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- 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
----
Ras
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
----
Bradykinin Receptor
----
GLP Receptor
-- 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
----
Kallikrein
----
IRAK
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- 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
----
Proton Pump
----
Potassium Channel
-- 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
----
Mitochondrial Metabolism
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Ketohexokinase(KHK)
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
-- 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
----
Sigma Receptor
----
mAChR
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
----
Melanocortin Receptor
----
Glucosylceramide Synthase (GCS)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
----
Keap1-Nrf2
-- 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
----
Bcr-Abl
----
FAK
----
RET
----
Phosphoglycerate Kinase (PGK)
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
----
Lipase
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- TGF-beta/Smad
----
PKC
----
ROCK
----
TGF-beta/Smad
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
----
DUB
-- Vitamin D Related
----
VD/VDR
-- PROTAC
----
Molecular Glues
----
PROTACs
--
Antibody-drug Conjugate/ADC Related
--
Microbiology
-- Others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
----
Newest added products
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
1497439-74-3 | AD-8007
(Catalog# : 26A018)
AD-8007是一种选择性且可穿透血脑屏障的乙酰辅酶A合成酶2(ACSS2)
1802650-31-2 | ZY-444
(Catalog# : 26A020)
ZY-444是一种通过抑制PC活性发挥抗癌作用的药物。
2306525-79-9 | AD-5584
(Catalog# : 26A019)
AD-5584是一种新型脑渗透性ACSS2抑制剂。
3079716-11-0 | IDB-003
(Catalog# : 26A017)
IDB-003在体内抑制MDA-MB-231肿瘤生长。
1357362-02-7 | Vafidemstat
(Catalog# : 18891)
Vafidemstat又称ORY 2001,是一种赖氨酸特异性组蛋白去甲基化酶(LSD1)
1260247-42-4 | LLL12
(Catalog# : 25075)
LLL12是一种强效的STAT3抑制剂。LLL12在小鼠异种移植物模型中显示出
2758659-09-3 | ECC-5004
(Catalog# : 26A015)
ECC5004是一款每日一次、低剂量、小分子GLP-1受体激动剂。
2911585-37-8 | SILA-123
(Catalog# : 26A014)
SILA-123是一种II型FLT3抑制剂,对FLT3-WT(IC50=2.1 nM)和FLT3-ITD(IC50=1
1214922-52-7 | Encaleret sulfate
(Catalog# : 26A013)
Encaleret是一种正在研究的钙敏感受体的小分子拮抗剂,用于钙稳态
1431303-72-8 | Iadademstat ( ORY-1001 ) hydrochloride
(Catalog# : 26A011)
Iadademstat(ORY-1001)是一种口服活性、高效和选择性的表观遗传酶