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抑制剂/受体激动剂
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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
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
Vitamin D Related
PROTAC
Antibody-drug Conjugate/ADC Related
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Amino Acids
Anilines
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Deuterated
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Indoles and Oxindoles
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Oxazoles
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Pyrimidines
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产品名字索引 A
ARN-3236
(Catalog# : 193192, Cas# :
1613710-01-2
)
ARN-3236是一种强效、口服活性和选择性的SIK2抑制剂。在攻击- 3236抑
ARN 077
(Catalog# : 193134, Cas# :
1373625-34-3
)
ARN 077是一种强效选择性N -乙酰乙醇胺酸酰胺酶(NAAA)抑制剂,IC50为
阿格列扎
(Catalog# : 193125, Cas# :
475479-34-6
)
阿格列扎, 也称为RG-1439或RO-0728804,是一个过氧物酶体增生激活受
Alvimopan
(Catalog# : 19382, Cas# :
156053-89-3
)
Alvimopan,也称为HSDB-7704和LY246736, 是一种作为一个次要地行动的μ-
Abrocitinib
(Catalog# : 19381, Cas# :
1622902-68-4
)
Abrocitinib(PF-04965842)是Pifzer研发的是一种Janus激酶抑制剂药物,目
AA26-9
(Catalog# : 19372, Cas# :
1312782-34-5
)
AA26-9是一种高效广谱丝氨酸水解酶抑制剂。AA26 -9抑制酶来源于丝
AZD-0284
(Catalog# : 19365, Cas# :
2101291-07-8
)
AZD-0284是一种强有力的、有选择性的反兴奋剂,可以潜在治疗核受
AZ304
(Catalog# : 19363, Cas# :
942507-42-8
)
AZ304是一种ATP-竞争性双BRAF激酶抑制剂,对野生型BRAF、V600E突变型
AZ876
(Catalog# : 19356, Cas# :
898800-26-5
)
AZ876,又称AZ-876,是一种肝脏X受体激动剂。AZ876可预防病理性心肌
AGN-190299
(Catalog# : 19316, Cas# :
118292-41-4
)
Tazarotene是一种视黄醇类前体药物,通过在动物和人体内的快速脱
AM281
(Catalog# : 19315, Cas# :
202463-68-1
)
AM281是一种合成大麻素CB1受体拮抗剂。
ASP9521
(Catalog# : 19312, Cas# :
1126084-37-4
)
ASP9521是日常的,选择性,口服生物利用率17β-羟甾类脱氢酶的抑制
AZD0364
(Catalog# : 192275, Cas# :
2097416-76-5
)
AZD0364是一种用于治疗癌症的ERK1和/或ERK2激酶。ERK1和ERK2激酶是广泛
ATF6-活化剂-147
(Catalog# : 192212, Cas# :
393121-74-9
)
ATF6-activator-147是一种ATF6模拟器,它作为一种前体药物,通过一种
AZD1152
(Catalog# : 192156, Cas# :
722543-31-9
)
AZD1152是Barasertib-hQPA的前药,是一种高选择性极光B抑制剂,在无细
AZD3229
(Catalog# : 191287, Cas# :
2248003-60-1
)
AZD3229是治疗胃肠道间质瘤的一种有效的pan-kit突变抑制剂。AZD3229在
AM095钠
(Catalog# : 191251, Cas# :
1345614-59-6
)
AM095是一个强有力的LPA1受体拮抗剂,因为它抑制GTPγS绑定中国仓鼠
AZD4573
(Catalog# : 191212, Cas# :
2057509-72-3
)
AZD-4573是一种选择性的丝氨酸/苏氨酸依赖性激酶9 (CDK9)的短期抑制
AR-9281
(Catalog# : 191146, Cas# :
913548-29-5
)
AR-9281是一种可溶性环氧化物水解酶(s-EH)抑制剂,有望用于高血压
ARRY-797 (ARRY-371797)
(Catalog# : 191112, Cas# :
1036404-17-7
)
ARRY-797(CAS1036404-17-7) is an oral, selective p38 mitogen-activated protein kinase
艾维替尼
(Catalog# : 19141, Cas# :
1557267-42-1
)
艾维替尼,又称AC0010和Avitinib,是酪氨酸激酶抑制剂,抗肿瘤药物
AZD7507
(Catalog# : 1812294, Cas# :
1041852-85-0
)
AZD7507是一种有效的选择性CSF-1R抑制剂(32 nM 细胞活性), AZD7507被认
Auranofin
(Catalog# : 1812281, Cas# :
34031-32-8
)
Auranofin又称Ridaura和SKF-39162,是一种治疗类风湿性关节炎的口服大
AX-024盐酸盐
(Catalog# : 181254, Cas# :
1704801-24-0
)
AX-024是一种口服的TCR-Nck相互作用抑制剂,选择性地抑制TCR-触发的
AG 879
(Catalog# : 1811303, Cas# :
148741-30-4
)
AG-879是一种酪氨酸磷酸化抑制剂复合物,可抑制PC-12细胞中依赖神
Avagacestat
(Catalog# : 1811283, Cas# :
1146699-66-2
)
Avagacestat,也称为BMS- 708163是一种口服GSI用于选择性抑制Aβ合成,目
AS1842856
(Catalog# : 1811265, Cas# :
836620-48-5
)
AS1842856是一种细胞可渗透的Foxo1抑制剂,IC50为33 nM,阻断Foxo1的转
Anlotinib HCl ( AL-3818 )
(Catalog# : 1811211, Cas# :
1360460-82-7
)
Anlotinib也被称为AL3818,是一种受体酪氨酸激酶(RTK)抑制剂,具有潜
Avatrombopag maleate
(Catalog# : 5141902, Cas# :
677007-74-8
)
Avatrombopag maleate 是一种口服生物可用的小分子血栓生成素受体激动
AZD-3514
(Catalog# : 1810251, Cas# :
1240299-33-5
)
AZD-3514是一种具有潜在抗癌活性的雄激素受体下调因子。
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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
----
Methionine Adenosyltransferase (MAT)
-- 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
----
SSTR
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- 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
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
----
Hemoglobin
-- 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)
----
CGRP-Receptor
----
TRP-Channel
-- 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)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- 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
-- Nuclear Receptor
----
Androgen Receptor(AR)
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
Linafexor (别名: CS-0159)
(Catalog# : 26A089, Cas# :
2765593-43-7
)
Linafexor(同义词:CS-0159)是法尼醇X受体(FXR)的强效非胆汁酸激
Prifetrastat (Synonyms: PF-07248144)
(Catalog# : 26A088, Cas# :
2569008-99-5
)
Prifetrastat (Synonyms: PF-07248144) 是一款首创、选择性、口服活性的
Camonsertib
(Catalog# : 24052, Cas# :
2417489-10-0
)
Camonsertib,也称为RP 3500,是一种新型、强效和选择性的ATR抑制剂,
MRX-2843
(Catalog# : 26A087, Cas# :
1429882-07-4
)
MRX-2843 是一种口服可用的双受体酪氨酸激酶(RTKs)抑制剂,作用
GDC-0134
(Catalog# : 20432, Cas# :
1637394-01-4
)
GDC-0134是一种MAP3K12(DLK)抑制剂。
BI-847325
(Catalog# : 25046, Cas# :
2128698-24-6
)
BI-847325是一种新型的、可口服的、竞争ATP结合位点的Aurora激酶和M
GDD-261
(Catalog# : 26A084, Cas# :
3137699-54-5
)
GDD-261是一种口服活性的磷酸甘油酸脱氢酶变构抑制剂(IC50=61nM)
Atebimetinib
(Catalog# : 25148, Cas# :
2669009-92-9
)
Atebimetinib(IMM-1-104)是一种口服的小分子MEK1和MEK2激酶变构抑制剂
BH-30643
(Catalog# : 26A047, Cas# :
3062177-59-4
)
BH-30643是一种新型、口服、非共价、大环、突变选择性OMNI-EGFR抑制
ERAS-801 ( JGK-068S )
(Catalog# : 20635, Cas# :
2490431-16-6
)
ERAS-801 ( JGK-068S ) 是一种有效的 EGFR 抑制剂。