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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
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MAPK
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Cas号索引 1
130798-51-5 | MDL-29951
(Catalog# : 52545)
MDL-29951 is a novel glycine antagonist of NMDA receptor activation (Ki=0.14 mM, [3H]
1395084-25-9 | MS436
(Catalog# : 52317)
MS436 is a diazobenzene-based small-molecule inhibitor for the BRD4 bromodomains with
1633666-49-5 | Nizubaglustat ( 同义词: AZ-3102 )
(Catalog# : 25175)
Nizubaglustat(AZ-3102)是一种口服小分子,可抑制阿扎法罗斯开发的
1637542-33-6 | Nedisertib ( peposertib )
(Catalog# : 25094)
Nedisertib,也称为M-3814,MSC2490484A,是一种口服的DNA依赖性蛋白激酶
1198078-60-2 | NT219
(Catalog# : 25067)
NT219 is a novel inhibitor of the insulin/igf signaling cascade (iis), mediating a lo
1256448-47-1 | Nanatinostat
(Catalog# : 25034)
Nanatinostat, also known as Tractinostat, CHR-3996 and VRx-3996, is an orally bioavai
1606996-12-6 | NMS-293 ( NMS-P293 )
(Catalog# : 20514)
NMS-293 是 Nerviano Medical Sciences 处于早期临床开发阶段的 PARP-1 抑制
13728-56-8 | NSC-92828
(Catalog# : 20486)
NSC-92828, also known as 3-Phenanthrenebutyric acid, is a Protein–protein interacti
1693734-80-3 | NXP-800 ( CCT361814 )
(Catalog# : 233141)
NXP800 是一种口服小分子热休克因子 1 (HSF1) 通路抑制剂。 NXP800 可
168021-79-2 | NXY-059 ( Disufenton Sodium )
(Catalog# : 52014)
Disufenton sodium (NXY-059) 是神经保护剂phenylbutynitrone的衍生物,具有极
1628263-77-3 | N-(6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-yl)formamide
(Catalog# : 20402)
1628263-96-6 | N-(6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-yl)-N-methylformamide
(Catalog# : 20401)
1335241-44-5 | N,N-DIETHYL-2,6-CIS-DIMETHYLPIPERIDINIUM IODIDE
(Catalog# : G20383)
1402837-78-8 (free base) | Navoximod free base
(Catalog# : 20290)
1401728-56-0 | NE 52-QQ57
(Catalog# : 21233)
NE52-QQ57 is an orally available GPR4 antagonist with an IC50 of 70 nM. NE 52-QQ57 si
1783816-74-9 | NVS-PAK1-1
(Catalog# : 21231)
NVS-PAK1-1 is a a specific allosteric PAK1 inhibitor.
1613220-15-7 | Niraparib tosylate hydrate
(Catalog# : 2021115)
Niraparib, also know as MK-4827, is an inhibitor of poly (ADP-ribose) polymerase (PAR
1346133-39-8 | N-(3,5-dimethoxyphenyl)-3-(1-methyl-1H-pyrazol-4-yl)quinoxalin-6-amine
(Catalog# : 2062032)
120173-57-1 | N-Fmoc-O-[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-α-D-galactopyranosyl]-L-serine
(Catalog# : 2061601)
1019115-13-9 | N-benzyl-2,4-dichloropyrimidine-5-carboxamide
(Catalog# : 197101)
1263373-43-8 | NVP-2
(Catalog# : 193205)
NVP-2是细胞周期蛋白依赖性激酶CDK9的抑制剂。
1566-81-0 | NS-1652
(Catalog# : 19361)
NS-1652是一种阴离子电导抑制剂。
1434639-57-2 | ND-646
(Catalog# : 191102)
ND-646是ACC酶ACC1和ACC2的变构抑制剂,可阻止ACC亚基二聚化,在体内
1434635-54-7 | ND-630
(Catalog# : 19133)
ND-630,也称为GS-0976, NDI-010976和firsocostat, 是一种有效的ACC抑制剂。
1448232-80-1 | Naquotinib游离
(Catalog# : 1812297)
Naquotinib,又称ASP8273,是一种口服、不可逆、第三代、突变选择、
1208315-24-5 | N6022
(Catalog# : 1811304)
N6022是一种有效、选择性、可逆性和有效性的s -亚硝基谷胱甘肽还
1253584-84-7 | NMS-E973
(Catalog# : 1810293)
NMS-E973是一种新型、选择性和强效的热休克蛋白90 (Hsp90)抑制剂。
153587-01-0 | NS1619
(Catalog# : 1810227)
NS1619是一种Bkca开启工具或大电导Ca2+活化钾(Bkca, KCa1.1)通道激活器
1452458-86-4 | Nacubactam
(Catalog# : 185169)
Nacubactam, 也称为RG-6080, FPI-1459, 和OP-0595, 是一种β-内酰胺酶抑制剂
108852-90-0 | Nemorubicin
(Catalog# : 185167)
Nemorubicin,又名PNU152243A,是一种不同于其母体药物的doxorubicin衍生
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-- Angiogenesis
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----
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----
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----
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----
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----
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----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
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CMV
----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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
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Vasopressin Receptor
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Glucagon Receptor
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----
5-HT Receptor
----
Adrenergic Receptor
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LPL Receptor
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Ras
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Cholecystokinin Receptor
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Melanocortin Receptor
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RXFP Receptor
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GLP Receptor
-- Immunology & Inflammation
----
PD-1
----
PD-L1
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MALT
----
TDO
----
NOS
----
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----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
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Aryl Hydrocarbon Receptor
----
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----
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
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Adrenergic Receptor
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NMDA Receptor
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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
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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
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Microbiology
-- Others
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PKK
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Others modulator
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Estrogen Receptor/ERR
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ChoKα
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Newest added products
抑制剂/受体激动剂
中间体
分子砌块
--
Aldehydes
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Amines
--
Amino Acids
--
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Boronic Acids
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--
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Chiral Compounds
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On Sale
新产品
天然化合物
最新产品
1802632-22-9 | CT1812 ( Zervimesine )
(Catalog# : 193283)
CT-1812是一种同类首创的、可口服的sigma-2/PGRMC1拮抗剂(αβ寡聚体
3041025-10-6 | BLU-808
(Catalog# : 26A024)
BLU-808是一种针对肥大细胞疾病的野生型c-KIT的强效且具有选择性的
2243882-74-6 | Zedoresertib
(Catalog# : 26A023)
Zedoresertib(Debio 0123)是一种脑渗透剂,高选择性WEE1激酶抑制剂。
3033961-38-2 | BEN-28010
(Catalog# : 26A022)
BEN-28010是一种自由脑渗透剂,强效且具有选择性的CHK1抑制剂。
3107291-07-3 | 4-((2-(甲氨基)-6-(2,2,2-三氟乙基)噻吩并[2,3-d]嘧啶-4-基)氨基)哌啶-1-甲酸叔丁酯
(Catalog# : 26B007)
2565656-70-2 | Muvalaplin
(Catalog# : 20528)
Muvalaplin是一种小分子,通过干扰载脂蛋白(a)与载脂蛋白B100的结合
2925330-18-1 | MAT2A-IN-22
(Catalog# : 26A021)
MAT2A-IN-22 (Compound 29-1) 是一种可透过血脑屏障的和口服有效的 MAT2A
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。