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Angiogenesis
Anti-infection
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Autophagy
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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
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Bromides
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Iodos
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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
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
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Amino Acids
Anilines
Boronic Acids
Bromides
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Deuterated
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Iodos
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Name Index B
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Name Index B
Bexagliflozin(EGT1442)
(Catalog# : 1673102, Cas# :
1118567-05-7
)
EGT1442, a potent and selective SGLT2 inhibitor, attenuates blood glucose and HbA(1c)
BCX-1777
(Catalog# : 16071105, Cas# :
209799-67-7
)
BCX-1777
BYK204165
(Catalog# : 16071031, Cas# :
1104546-89-5
)
BYK204165 is a potent and selective poly(ADP-ribose) polymerase (PARP)-1 inhibitor (p
BMS-3
(Catalog# : 16071026, Cas# :
1338247-30-5
)
BMS-3 is a LIM kinase 1 (LIMK1) inhibitor. LIMK inhibition with 1 M BMS-3 damaged MTO
BAM 7
(Catalog# : 16071006, Cas# :
331244-89-4
)
BAM 7 is a Bax activator (EC50 = 3.3 M). BCL-2 family proteins are key regulators of
BTZ043
(Catalog# : 16071005, Cas# :
957217-65-1
)
BTZ043 racemate is adecaprenylphosphoryl--D-ribose 2'-epimerase (DprE1)inhibitor acti
Bromosporine
(Catalog# : 16070108, Cas# :
1619994-69-2
)
Bromosporine is a broad spectrum inhibitor for bromodomains and as such will be very
BMS-582949
(Catalog# : 16062903, Cas# :
623152-17-0
)
BMS-582949 is a potent and selective P38 mitogen-activated protein kinase (P38 MAPK)
BAY1217389
(Catalog# : 16060801, Cas# :
1554458-53-5
)
BAY1217389 is an orally bioavailable, selective inhibitor of the serine/threonine kin
6-bromo-2,3,4,4a(S),5,9b(R)-hexahydropyrido[4,3-b]indole
(Catalog# : 633001, Cas# :
1059630-07-7
)
6-bromo-2,3,4,4a(S),5,9b(R)-hexahydropyrido[4,3-b]indole;CAS#1059630-07-7 provide cus
BMS-833923
(Catalog# : 032512, Cas# :
1059734-66-5
)
Coming soon!
1-benzyl-4-bromobenzene
(Catalog# : 032510, Cas# :
2116-36-1
)
Coming soon!
3-Bromo-2-iodopyridine
(Catalog# : 032507, Cas# :
408502-43-2
)
Coming soon!
2,4-bis(benzyloxy)-5-isopropylbenzaldehyde
(Catalog# : 032504, Cas# :
959466-51-4
)
Coming soon!
1-bromophenanthrene
(Catalog# : 032502, Cas# :
51958-51-1
)
Coming soon!
Bibs-39
(Catalog# : 031004, Cas# :
133085-33-3
)
Coming soon!
BET bromodomain inhibitor
(Catalog# : 030301, Cas# :
1505453-59-7
)
Coming soon!
Butacarb
(Catalog# : 020301, Cas# :
2655-19-8
)
Coming soon!
Burixafor
(Catalog# : 012003, Cas# :
1191448-17-5
)
Burixafor is an orally bioavailable inhibitor of CXC chemokine receptor 4 (CXCR4) wit
BAY 87-2243
(Catalog# : 011920, Cas# :
1227158-85-1
)
BAY 87-2243 is a highly potent and selective inhibitor of hypoxia-induced gene activa
BMS-433796
(Catalog# : 011914, Cas# :
935525-13-6
)
BMS-433796 is a gamma-secretase inhibitor.
Bucillamine
(Catalog# : 011315, Cas# :
65002-17-7
)
Bucillamine is an antirheumatic agent developed from tiopronin.
BLZ945
(Catalog# : 011314, Cas# :
953769-46-5
)
BLZ945 is a highly selective and brain-penetrant inhibitor of CSF1R with IC50 of 1 nM
Bindarit
(Catalog# : 011116, Cas# :
130641-38-2
)
Bindarit, a CCL2, CCL7 and CCL8 inhibitor, is an anti-inflammatory agent.
BMS-690514
(Catalog# : 011102, Cas# :
859853-30-8
)
BMS-690514 is a potent and selective inhibitor of epidermal growth factor receptor (E
BMS-536924
(Catalog# : 010818, Cas# :
468740-43-4
)
BMS-536924 is an ATP-competitive IGF-1R/IR inhibitor with IC50 of 100 nM/73 nM.
BMS-911543
(Catalog# : 010817, Cas# :
1271022-90-2
)
BMS-911543 is a potent and selective small-molecule inhibitor of JAK2; displayes pote
BMS 5
(Catalog# : 010611, Cas# :
1338247-35-0
)
This product is for custom synthesis.
BGT-226 free base
(Catalog# : 123014, Cas# :
915020-55-2
)
BGT226 is a phosphatidylinositol 3-kinase (PI3K) inhibitor with potential antineoplas
Bafetinib
(Catalog# : 122947, Cas# :
859212-16-1
)
Bafetinib is a potent and selective dual Bcr-Abl/Lyn inhibitor with IC50 of 5.8 nM/19
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Products Catalog
Signaling Pathway
-- 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
-- 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
-- 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
-- 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
-- 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
Inhibitors & Agonists
Intermediates
Building Blocks
--
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
New Products
Natural Compounds
Latest Products
Safusidenib
(Catalog# : 25149, Cas# :
1898206-17-1
)
Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl
HC-7366
(Catalog# : 25076, Cas# :
2803470-63-3
)
HC-7366 is a potent and selective activator of the general control nonderepressible 2
Dencatistat
(Catalog# : 25177, Cas# :
2377000-84-3
)
Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
Flavopiridol ( Alvocidib )
(Catalog# : 237071, Cas# :
146426-40-6
)
Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
AG-270
(Catalog# : 25176, Cas# :
2201056-66-6
)
MAT2A Inhibitor AG-270 is an orally available small molecule inhibitor of methionine
AZD-5904
(Catalog# : 181121, Cas# :
618913-30-7
)
AZD5904 is a potent orally bioavailable MPO inhibitor. In preclinical studies, AZD590
ALT-007
(Catalog# : 25157, Cas# :
2035010-37-6
)
ALT-007 is an orally bioavailable SPT inhibitor that is more potent than myriocin, sa
Nizubaglustat ( Synonyms: AZ-3102 )
(Catalog# : 25175, Cas# :
1633666-49-5
)
Nizubaglustat (AZ-3102) is an oral small molecule which inhibits glucosylceramide syn
Catadegbrutinib (Synonyms: BGB-16673; BTK-IN-29)
(Catalog# : 25174, Cas# :
2736508-60-2
)
Anatibant (Synonyms: LF 16-0687; XY-2405)
(Catalog# : 25173, Cas# :
209733-45-9
)