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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
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GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
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Cas号索引 7
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Cas号索引 7
778277-15-9 | GNF-5
(Catalog# : 52216)
GNF-5, an analogue of GNF-2 with improved pharmacokinetic properties, is a selective
778270-11-4 | GNF-2
(Catalog# : 52301)
GNF-2 is a highly selective non-ATP competitive inhibitor of oncogenic Bcr-Abl activi
700874-72-2 | Galunisertib(LY2157299)
(Catalog# : 52017)
Galunisertib (LY2157299)isselective TGF- receptor kinase inhibitor. Galunisertib was
7733-96-2 | HC-056456
(Catalog# : 1810171)
HC-056456是CatSper的通道调制器。
79551-86-3 | 20-HETE
(Catalog# : 185283)
20-HETE是一种细胞色素P450 (CYP450)代谢产物,在脑血管和肾血管中扮
70500-72-0 | 7-hydroxy-1H-quinolin-2-one
(Catalog# : 91706)
Coming soon!
71759-88-1 | 5-碘-1-甲基咪唑
(Catalog# : 1712292)
5-碘-1-甲基咪唑是一种分子砌块。
75567-37-2 | Ingenol Mebutate
(Catalog# : 16123020)
Ingenol mebutate, also known as ingenol-3-angelate, is a substance found in the sap o
78919-13-8 | Iloprost
(Catalog# : 16123018)
Iloprost is a drug used to treat pulmonary arterial hypertension (PAH), scleroderma,
775351-65-0 | Imeglimin
(Catalog# : 611811)
Imeglimin(EMD-387008) is the first in a new tetrahydrotriazine-containing class of or
780757-88-2 | ICG-001
(Catalog# : 122801)
ICG-001 is a potent, specific inhibitor of the canonical Wnt signaling pathway in can
761423-87-4 | Ipragliflozin
(Catalog# : 82604)
Ipragliflozin (ASP1941) is a highly potent and selective SGLT2 inhibitor with IC50 of
72795-01-8 | ICI118551(HCl)
(Catalog# : 60809)
Highly selective 2 adrenoceptor antagonist (Ki values are 1.2, 120 and 257 nM at 2, 1
729-46-4 | JX06
(Catalog# : 25199)
JX06 是一种有效的,选择性的,共价的 PDK 抑制剂。
749886-87-1 | JSH-23
(Catalog# : 52729)
JSH-23 is an inhibitor of NF-B transcriptional activity with IC50 of 7.1 M.
796874-99-2 | KYP-2047
(Catalog# : 187124)
KYP-2047是一种非常有效的、选择性的Prolyl寡肽酶(POP)抑制剂,也被
774549-97-2 | KM11060
(Catalog# : 17031301)
KM11060是一种突变的F508del囊性纤维化跨膜电导调节器(CFTR)。CFTR基因
72926-24-0 | K-858
(Catalog# : 16122824)
K-858 is a novel inhibitor of mitotic kinesin Eg5 and antitumor agent, induces cell d
74381-53-6 | Leuprolide Acetate
(Catalog# : 192261)
Leuprolide Acetate是一种合成的类似促性腺激素释放激素的非肽类似物
700874-71-1 | LY2109761
(Catalog# : 16123039)
LY2109761 is a novel transforming growth factor beta receptor type I and type II dual
79558-09-1 | L-165041
(Catalog# : 011316)
Coming soon!
79794-75-5 | Loratadine
(Catalog# : 010435)
Loratadine is a selective inverse peripheral histamine H1-receptor agonist with an IC
796967-16-3 | Linifanib
(Catalog# : 121416)
Linifanib is a novel, potent ATP-competitive VEGFR/PDGFR inhibitor for KDR, CSF-1R, F
747412-49-3 | Luminespib ( NVP-AUY922 ; VER-52296 )
(Catalog# : 51703)
NVP-AUY922 is an experimental drug candidate for the treatment of cancer. It was disc
706820-79-3 | 3-溴-5-甲酰基-4-羟基苯甲酸甲酯
(Catalog# : 20363)
794572-10-4 | ML184
(Catalog# : 192214)
ML184,也称为CID2440433,是一种有效的GPR55合成受体激动剂(EC50 = 0.26µM
78351-75-4 | MY 5445
(Catalog# : 191211)
MY 5445是一种潜在的血小板聚集抑制剂。
761438-38-4 | MDK-8384
(Catalog# : 1812254)
MDK-8384,也称为ALK抑制剂2,是一种有效且具有选择性的ALK抑制剂。
71203-35-5 | ML-141
(Catalog# : 179152)
ML-141,也称为CID2950007,是Cdc42抑制剂(EC50 = 2.1μm)。
70476-82-3 | 盐酸米托蒽醌
(Catalog# : 179827)
盐酸米托蒽醌是一种蒽醌抗生素,具有抗肿瘤活性的盐酸盐。米托
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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)
-- 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
-- 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)
-- 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
--
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--
Indoles and Oxindoles
--
Iodos
--
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--
Oxazoles
--
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--
Phenols
--
Piperidines
--
Pyridines
--
Pyrimidines
--
Quinolines
--
Sulfonamides
--
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--
Trifluoroborates
--
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--
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On Sale
新产品
天然化合物
最新产品
2351225-46-0 | NSD1 抑制剂 BT5
(Catalog# : 25207)
BT5可有效抑制NSD1,与细胞中的SET结构域结合,并降低H3K36me2水平。
1049704-18-8 | MA242 TFA
(Catalog# : 25206)
MA242是一种MDM2和NFAT1双重抑制剂,可诱导MDM2自泛素化及降解,并抑
2800223-30-5 | Dabogratinib ( TYRA-300 )
(Catalog# : 24073)
Dabogratinib ( TYRA-300 )是一种口服选择性成纤维细胞生长因子受体3(
N/A | AF710B
(Catalog# : 25205)
AF710B 是一种高效、选择性变构 M1 毒蕈碱和 σ1 受体激动剂。 AF710
2957874-18-7 | MAT2A inhibitor 5
(Catalog# : 25204)
MAT2A抑制剂5具有抑制MAT2A的高效力和对MTAP缺失的癌症细胞系的显著
1235733-73-9 | (Rac)-AF710B
(Catalog# : 24083)
AF-710B 是 σ 和 M1 毒蕈碱受体的激动剂;AF710B 是 AF710 的对映体。
863888-33-9 | Flurpiridaz-nonradiolabeled
(Catalog# : 25203)
Flurpiridaz是一种有前景的新型心脏PET成像示踪剂,是通过用氟-18放
863888-32-8 | Flurpiridaz-Precursor
(Catalog# : 25202)
现货
1800405-30-4 | KL1333
(Catalog# : 25201)
KL1333是一种口服的小有机分子,与NAD(P)H:醌氧化还原酶1(NQO1)
1369489-71-3 | Palupiprant ( E7046 )
(Catalog# : 24055)
E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece