武汉永璨生物科技有限公司
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抑制剂/受体激动剂
PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
JAK/STAT
MAPK
Cytoskeletal Signaling
Cell Cycle
TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
Ubiquitin
Neuronal Signaling
NF-κB
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
Antibody-drug Conjugate/ADC Related
分子砌块
Aldehydes
Amines
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Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
Fluorides
Imidazoles
Indoles and Oxindoles
Iodos
Nitro Compounds
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Peg Linkers
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Quinolines
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技术服务
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订购信息
联系我们
公司简介
联系我们
+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
JAK/STAT
MAPK
Cytoskeletal Signaling
Cell Cycle
TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
Ubiquitin
Neuronal Signaling
NF-κB
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
Antibody-drug Conjugate/ADC Related
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
中间体
技术服务
定制合成
工艺研发
订购信息
联系我们
公司简介
联系我们
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产品名字索引 B
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产品名字索引 B
BQCA
(Catalog# : 122826, Cas# :
338747-41-4
)
Coming soon!
Balipodect ( TAK-063 )
(Catalog# : 122805, Cas# :
1238697-26-1
)
Balipodect (TAK 063 )is a novel PDE10A inhibitor. It has shown high inhibitory activi
BD-1047 dihydrobromide
(Catalog# : 122520, Cas# :
138356-21-5
)
BD-1047 dihydrobromide is a selective functional antagonist of sigma receptors, shows
BIX 01294 Trihydrochloride
(Catalog# : 122517, Cas# :
1392399-03-9
)
BIX01294 is a potent chemical inhibitor of G9a methyltransferase that catalyzes the m
Bleomycin sulfate
(Catalog# : 122514, Cas# :
9041-93-4
)
Bleomycin is a glycopeptide antibiotic; used as an anticancer agent; Bleomycin acts b
Bicalutamide
(Catalog# : 122507, Cas# :
90357-06-5
)
Bicalutamide is an oral non-steroidal anti-androgen for prostate cancer; binds to the
BIX02188
(Catalog# : 122205, Cas# :
334949-59-6
)
BIX02188 is a selective inhibitor of MEK5 with IC50 of 4.3 nM, also inhibits ERK5 cat
Bilastine
(Catalog# : 121807, Cas# :
202189-78-4
)
Bilastine is a selective histamine H1 receptor antagonist used for treatment of aller
BMS-777607
(Catalog# : 121417, Cas# :
1025720-94-8
)
BMS 777607 是一种 Met-related 抑制剂,能够抑制 c-Met,Axl,Ron 和 Tyro3
Benzyl Dichlorophosphite
(Catalog# : 121411, Cas# :
76101-29-6
)
Coming soon!
BPTES
(Catalog# : 121403, Cas# :
314045-39-1
)
BPTES is a potent and selective allosteric inhibitor of kidney-type glutaminase (GLS)
Belotecan hydrochloride
(Catalog# : 121401, Cas# :
213819-48-8
)
Belotecan Hydrochloride is the hydrochloride salt of the semi-synthetic camptothecin
Belinostat acid
(Catalog# : 120702, Cas# :
866323-87-7
)
Coming soon!
Benazepril
(Catalog# : 120405, Cas# :
86541-75-5
)
Coming soon!
BX471
(Catalog# : 120108, Cas# :
217645-70-0
)
BX471 is a potent, selective non-peptide CCR1 antagonist (Ki = 1 nM for human CCR1);
BMH-21
(Catalog# : 120107, Cas# :
896705-16-1
)
BMH-21 is a small molecule DNA intercalator that binds ribosomal DNA and inhibits RNA
BIX 02189
(Catalog# : 111912, Cas# :
1265916-41-3
)
BIX 02189 is a selective MEK5/ERK5 inhibitor with an IC50 of 59 nM, which was reporte
BAZ2-ICR
(Catalog# : 111907, Cas# :
1665195-94-7
)
BAZ2-ICR is a small molecule inhibitor of BAZ2A (Kd = 109 nM; IC50 = 130 nM) and BAZ2
BMS-863233 HCl
(Catalog# : 111903, Cas# :
1169562-71-3
)
BMS-863233, also known as XL-413, is an orally bioavailable cell division cycle 7 hom
BAY 57-1293
(Catalog# : 111902, Cas# :
348086-71-5
)
BAY 57-1293 is a potent helicase primase inhibitor. BAY 57-1293 inhibits replication
BIX02188
(Catalog# : 111001, Cas# :
1094614-84-2
)
BIX02188 is a MEK5-selective inhibitor with an IC50 of 0.8 1.0 M, which inhibited ca
BMS-754807
(Catalog# : 110908, Cas# :
1001350-96-4
)
BMS-754807 is a potent and reversible inhibitor of IGF-1R/InsR with IC50 of 1.8 nM/1.
BRD4770
(Catalog# : 110227, Cas# :
1374601-40-7
)
BRD4770 is a novel G9a(EHMT2) inhibitor with EC50 of 5 uM (trimethylated H3K9 in PANC
5-Bromo-2-iodopyridine
(Catalog# : 110204, Cas# :
223463-13-6
)
Coming soon!
Blonanserin
(Catalog# : 102612, Cas# :
132810-10-7
)
Blonanserin is a D2/5-HT2 receptor antagonist, atypical antipsychotic.
BRD73954
(Catalog# : 102601, Cas# :
1440209-96-0
)
BRD73954 ia a potent and selective HDAC inhibitor with IC50 of 36 nM and 120 nM for H
BIO-32546
(Catalog# : 101916, Cas# :
1548743-66-3
)
Coming soon!
BIO-acetoxime
(Catalog# : 101401, Cas# :
667463-85-6
)
BIO-Acetoxime is a potent and selective GSK-3a/b inhibitor that reduces invasiveness
BIX01294
(Catalog# : 101203, Cas# :
935693-62-2
)
BIX01294 is an inhibitor of G9a histone methyltransferase with IC50 of 2.7 M.
Bardoxolone methyl
(Catalog# : 92303, Cas# :
218600-53-4
)
Bardoxolone methyl (also known as “RTA 402” and “CDDO-methyl ester”) is an or
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产品分类
信号通路
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- 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
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Bcr-Abl
----
Src
----
ALK
----
Syk
----
FAK
----
BTK
----
HIF
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Cytoskeletal Signaling
----
Akt
----
Bcr-Abl
----
PKC
----
FAK
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
-- TGF-beta/Smad
----
Bcr-Abl
----
PKC
----
ROCK
----
TGF-beta/Smad
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
-- 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
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
----
Sigma Receptor
----
Ras
----
mAChR
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
-- 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
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
-- 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
-- Vitamin D Related
----
VD/VDR
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
-- PROTAC
----
Molecular Glues
--
Antibody-drug Conjugate/ADC Related
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
Reparixin
(Catalog# : 25050, Cas# :
266359-83-5
)
Reparixin is an inhibitor of CXCR2 function, which attenuates inflammatory responses
TAK-779
(Catalog# : 25049, Cas# :
229005-80-5
)
TAK-779 is a C-C chemokine receptor type 5 (CCR5) receptor antagonist potentially for
BAY-1125976
(Catalog# : 25048, Cas# :
1402608-02-9
)
BAY-1125976 is a potent and selective allosteric AKT1/2 inhibitor. BAY-1125976 exhibi
Vimseltinib free base
(Catalog# : 25047, Cas# :
1628606-05-2
)
Vimseltinib, also known as DCC-3014, is a potent and orally active inhibitor of the t
2-Propynamide, 3-[(3Z)-3-[[[4-[(dimethylamino)methyl]phenyl]amino]phenylmethylene]-2,3-dihydro-2-oxo-1H-indol-6-yl]-N-ethyl-
(Catalog# : 25046, Cas# :
2128698-24-6
)
Cavosonstat
(Catalog# : 25045, Cas# :
1371587-51-7
)
Cavosonstat, alos known as N91115) an orally bioavailable inhibitor of S-nitrosogluta
Ivospemin Hydrochloride
(Catalog# : 25044, Cas# :
259657-09-5
)
Ivospemin is an antineoplastic spermine analogue.
Survodutide
(Catalog# : 25043, Cas# :
2805997-46-8
)
XRD-0394
(Catalog# : 25042, Cas# :
2595308-10-2
)
XRD-0394 is a DNA-PKcs inhibitor. XRD-0394 selectively targets, binds to and inhibits
CC-90003
(Catalog# : 25041, Cas# :
1621999-82-3
)
CC-90003 is an orally available inhibitor of extracellular signal-regulated kinase (E