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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
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Cas号索引 1
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Cas号索引 1
172603-05-3 | 3-(Boc-amino)piperidine
(Catalog# : 81702)
Coming soon!
154057-56-4 | 3-(Bromomethyl)-2-cyclopropyl-4-(4-fluorophenyl)quinoline
(Catalog# : 81306)
Related API & intermediates:Cas#147526-32-7 Pitavastatin CalciumCas# 24922-02-9 E
162167-97-7 | 1-Boc-3-(aminomethyl)piperidine
(Catalog# : 81032)
Coming soon!
141774-61-0 | 2-(Boc-Aminomethyl)-Piperidine
(Catalog# : 81027)
Coming soon!
135632-53-0 | 4-(Boc-aminomethyl)piperidine
(Catalog# : 81026)
Coming soon!
143238-38-4 | 1-Boc-piperazine
(Catalog# : 81025)
Coming soon!
112275-50-0 | 1-Boc-hexahydro-1,4-diazepine
(Catalog# : 81024)
Coming soon!
13343-63-0 | Benzyl-2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside
(Catalog# : 80301)
Coming Soon
1009817-63-3 | b-AP15
(Catalog# : 73106)
b-AP15 is a specific inhibitor of the deubiquitinating enzymes Uch37 and Usp14 of the
188011-69-0 | Bikinin
(Catalog# : 61002)
Bikinin(Abrasin) is a potent inhibitor of plant GSK-3/Shaggy-like kinase; activates B
1538604-68-0 | BLU9931
(Catalog# : 60303)
BLU9931 is a potent and irreversible small-molecule inhibitor of FGFR4, as a targeted
1092443-52-1 | BS-181
(Catalog# : 52755)
BS-181 is a highly selective CDK7 inhibitor with IC50 of 21 nM. ; >40-fold selecti
19542-67-7 | BAY 11-7082
(Catalog# : 52713)
BAY 11-7082 is aNF-Binhibitor, inhibits TNF-inducedIBphosphorylation withIC50of 10 M
196309-76-9 | Bay 11-7085
(Catalog# : 52712)
BAY 11-7085 is an irreversible inhibitor of TNF-inducedIBphosphorylation withIC50of 1
153559-49-0 | Bexarotene
(Catalog# : 52601)
Bexarotene (Targretin) is a selective RXR agonist approved for the treatment of CTCL.
1397219-81-6 | BS-181 HCl
(Catalog# : 52578)
BS-181 HCl is a highly selectiveCDK7inhibitor withIC50of 21 nM. It is more than 40-fo
1174046-72-0 | BMS-794833
(Catalog# : 52205)
BMS-794833 is a potent ATP competitive inhibitor of Met/VEGFR2 with IC50 of 1.7/15 nM
1187594-09-7 | Baricitinib
(Catalog# : 51908)
Baricitinib (also known as LY3009104 or INCB028050) is a novel and potent small molec
1256349-48-0 | Chiauranib
(Catalog# : 25146)
Chiauranib also known as orally available, small molecule inhibitor of select serine-
1371587-51-7 | Cavosonstat
(Catalog# : 25045)
Cavosonstat, alos known as N91115) an orally bioavailable inhibitor of S-nitrosogluta
1621999-82-3 | CC-90003
(Catalog# : 25041)
CC-90003 is an orally available inhibitor of extracellular signal-regulated kinase (E
1403859-14-2 | CC90001 free base
(Catalog# : 24095)
CC-90001 is a potent and selective JNK inhibitor, which is 12.9-fold more potent for
1261451-92-6 | 5-氯-2-甲氧基吡啶-3-磺酰氯
(Catalog# : 24022)
5-氯-2-甲氧基吡啶-3-磺酰氯, CAS 1261451-92-6.
1370032-20-4 | CUR5g
(Catalog# : 20678)
CUR5g is a potent autophagy inhibitor.
1112968-42-9 | Contezolid free base
(Catalog# : 20653)
Contezolid (Youxitai ®), an orally administered oxazolidinone antibacterial agent, i
1610759-22-2 | CFI-402257 free base
(Catalog# : 20626)
CFI-402257 was discontinued for commercial reason.
1345858-76-5 | CYM-50308
(Catalog# : 20488)
CYM 50308 is a novel agonist of SIP4 (EC50 = 56 nM) that displays 37-fold selectivity
1623747-97-6 | CRANAD-28
(Catalog# : 20478)
CRANAD-28 is a blood brain barrier (BBB) penetrable two-photon imaging probe. It acts
1621164-74-6 | Camlipixant ( BLU-5937 )
(Catalog# : 20455)
Camlipixant 是一种在研的每日两次口服 P2X3 受体拮抗剂,用于治疗
127094-58-0 | 6-氯-4-羟基-[1,5]-萘啶-3-羧酸乙酯
(Catalog# : 20423)
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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
-- 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)
-- 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
3054692-62-2 | ECI830
(Catalog# : 26A031)
ECI830是一种实验性的CDK2抑制剂。
1394076-92-6 | GNE-317
(Catalog# : 52282)
GNE-317 is a potent, brain-penetrantPI3Kinhibitor
3118994-80-9 | DPTX-3186
(Catalog# : 26A010)
DPTX3186 是一种口服的小分子凝聚体调节剂 (c-mod),可抑制 β-catenin
435327-40-5 | Avasopasem manganese (GC-4419; M-40419)
(Catalog# : 25108)
Avasopasem manganese, 也称为GC-4419、M 40419和SC-72325A,是超氧化物歧化酶
1421936-85-7 | Iclepertin (BI-425809)
(Catalog# : 24084)
Iclepertin(BI-425809)是一种口服的GlyT-1小分子抑制剂,用于治疗与
4727-31-5 | Kartogenin ( KGN )
(Catalog# : 52215)
Kartogenin(KGN)是一种合成小分子,通过激活smad-4/5通路刺激软骨细
218791-21-0 | Imisopasem manganese ( M40403; GC4403 )
(Catalog# : 72602)
Imisopasem manganese ( M40403; GC4403 ) 是一种稳定的非肽类 MnSOD 类似物,
2311863-36-0 | Apecotrep (BI 764198)
(Catalog# : 26A048)
Apecotrep(BI 764198)是一种潜在的同类首创、口服、选择性的TRPC6抑
902614-04-4 | Pantothenate kinase-IN-2
(Catalog# : 26A038)
Pantothenate kinase-IN-2是一种泛酸激酶抑制剂,对PanK2的IC50值为92 nM,
3062177-59-4 | BH-30643
(Catalog# : 26A047)
BH-30643是一种新型、口服、非共价、大环、突变选择性OMNI-EGFR抑制