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联系我们
+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
Ubiquitin
Vitamin D Related
PROTAC
Antibody-drug Conjugate/ADC Related
Microbiology
Others
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
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On Sale
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Cas号索引 5
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Cas号索引 5
558447-26-0 | N'-(1H-苯并咪唑-2-甲基)-N'-((S)-5,6,7,8-四氢喹啉-8-基)丁烷-1,4-二胺
(Catalog# : 20427)
53557-69-0 | 4-氨基-6-碘嘧啶
(Catalog# : 20421)
545395-94-6 | AMG-9810
(Catalog# : 179117)
AMG 9810是对香草类受体1的辣椒素激活竞争性拮抗剂(TRPV1)。此外
52328-98-0 | ASC-J9
(Catalog# : 179816)
ASC-J9,也称为GO-Y025和去甲氧基姜黄素,是一个AR降解剂,ASC-J9通过
5291-32-7 | APR-246 (PRIMA-1MET)
(Catalog# : 17021316)
APR-246, 也称为PRIMA-1MET, 是一种小型的有机分子,已被证明可以恢复
570406-98-3 | Avatrombopag
(Catalog# : 16122860)
Avatrombopag, also known as AKR-501, YM477, AS 1670542 or E5501, is a novel orally-ac
5854-93-3 | Alanosine
(Catalog# : 161227117)
Alanosine, also known as L-alanosine, is an amino acid analogue and antibiotic derive
546-43-0 | Alantolactone
(Catalog# : 161227107)
Alantolactone, a naturally occurring eudesmane-type sesquiterpene lactone (SL), could
50-76-0 | Actinomycin D
(Catalog# : 120110)
Actinomycin D is the most significant member of actinomycines, which are a class of p
51135-91-2 | 4-Amino-2,3-dihydro-1H-inden-1-one
(Catalog# : 81940)
Coming soon!
552325-73-2 | A-674563
(Catalog# : 52617)
A-674563 is a potent selective Akt1 inhibitor with an IC50 of 14 nM; also shows inhib
5072-26-4 | Buthionine Sulphoximine
(Catalog# : 16122907)
Buthionine Sulphoximine, also known as NSC-326231, is a gamma-glutamylcysteine synthe
537034-17-6 | BML-210
(Catalog# : 16122901)
BML-210, also known as CAY10433, is HDAC inhibitor. BML-210 induces growth inhibition
579492-81-2 | Bax inhibitor peptide V5
(Catalog# : 61401)
Bax inhibitor peptide V5 is a peptide inhibitor of Bax translocation to mitochondria.
51958-51-1 | 1-bromophenanthrene
(Catalog# : 032502)
Coming soon!
501437-28-1 | BI-D1870
(Catalog# : 122914)
BI-D1870 is an ATP-competitive inhibitor of S6 ribosome for RSK1/2/3/4 with IC50 of 3
553672-38-1 | Benzyl pyrrolidin-3-ylcarbamate hydrochloride
(Catalog# : 81736)
Coming soon!
56-25-7 | Cantharidine
(Catalog# : 20622)
Cantharidine (free base) is a PP1/2A inhibitor found in Canarthis vesicatoria. It inh
511514-03-7 | 0990CL
(Catalog# : 20562)
0990CL is an inhibitor of heterotrimeric Gαi subunits. 0990CL showed direct interact
55750-05-5 | Caroverine HCl
(Catalog# : 20260)
Caroverine HCl is a nonselective NMDA and AMPA glutamate receptor antagonist, also ac
524-63-0 | 铜色树碱
(Catalog# : S-203042)
52794-97-5 | 卡米诺霉素盐酸盐
(Catalog# : 17914)
卡米诺霉素盐酸盐是一种蒽环类抗肿瘤抗生素类的洋红色马杜拉细
59721-29-8 | Camostat Mesilate
(Catalog# : 16122806)
Camostat Mesilate, also known as FOY 305, is a serine protease inhibitor. Serine prot
55779-48-1 | Coelenterazine
(Catalog# : 6111016)
Coelenterazine
50-22-6 | CORTICOSTERONE
(Catalog# : 010401)
CORTICOSTERONE is an adrenocortical steroid that has modest but significant activitie
587850-67-7 | C-7280948
(Catalog# : 122810)
C-7280948 is a PRMT1 inhibitor.
500863-50-3 | 3-cyanopropyl carbamimidothioate
(Catalog# : 122519)
Coming soon!
556813-39-9 | CHIR98014
(Catalog# : 110601)
CHIR98014 is a reversible, cell-permeable inhibitor of GSK3 and GSK3. It is inactive
524955-09-7 | 3-chloro-4-(pyridin-2-ylmethoxy)aniline
(Catalog# : 82716)
Coming soon!
521937-07-5 | CID755673
(Catalog# : 73104)
CID 755673 is a selective and potent protein kinase D1-D3, PKC, CAK, PLK1 and CAMKII
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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
--
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
85622-93-1 | Temozolomide
(Catalog# : 25209)
Temozolomide is an alkylating agent.
2035010-37-6 | ALT-007
(Catalog# : 25157)
ALT-007 is an orally bioavailable SPT inhibitor that is more potent than myriocin, sa
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim (BHV-7000) is an oral, small-molecule activator of Kv7.2/7.3 potassium chann
2102501-84-6 | PF-06835919 ( MDK-1846 )
(Catalog# : 193264)
MDK1846 is a potent ketohexokinase (KHK) inhibitor.
2271348-04-8 | MK256
(Catalog# : 25208)
MK256 is a novel CDK8 inhibitor with potent antitumor activity in AML through downreg
2351225-46-0 | NSD1 inhibitor BT5
(Catalog# : 25207)
BT5 potently inhibits NSD1, engages the SET domain in cells, and reduces H3K36me2 lev
1049704-18-8 | MA242 TFA
(Catalog# : 25206)
MA242 isMDM2 and NFAT1 dual inhibitorthat induces MDM2 auto-ubiquitination and degrad
2800223-30-5 | Dabogratinib ( TYRA-300 )
(Catalog# : 24073)
Dabogratinib ( TYRA-300 ) is an Oral Selective FGFR3 Inhibitor (IC50 = 11 nM) for the
N/A | AF710B
(Catalog# : 25205)
AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1
2957874-18-7 | MAT2A inhibitor 5
(Catalog# : 25204)
MAT2A inhibitor 5 has a high potency for inhibiting MAT2A and a remarkable selectivit