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Inhibitors&Agonists
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
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
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Other Azoles
Other Heterocycles
Other Building Blocks
On Sale
Intermediates
Services
Custom Synthesis
Process Development
Ordering
Contact Us
About Us
Contact Us
+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
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
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
Intermediates
Services
Custom Synthesis
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Name Index H
H3B-6527
(Catalog# : 179822, Cas# :
1702259-66-2
)
H3B-6527 is a potent and orally active FGFR4 inhibitor with potential antineoplastic
1H-pyrazolo[3,4-c]pyridine
(Catalog# : 1781503, Cas# :
271-47-6
)
1H-pyrazolo[3,4-c]pyridine
H-89 Dihydrochloride
(Catalog# : 178815, Cas# :
130964-39-5
)
H-89 is a specific adenylyl cyclase inhibitor (DDA) and a cyclic AMP-dependent protei
HDM201
(Catalog# : 2017872, Cas# :
1448867-41-1
)
HDM201 is an orally bioavailable human double minute 2 homolog (HDM2) inhibitor with
HM-61713 (BI-1482694)
(Catalog# : 17022709, Cas# :
1802181-20-9
)
BI-1482694, is a potent small molecule inhibitor of Bruton's tyrosine kinase (BTK).
5-hydroxypyrazine-2-carboxylic acid
(Catalog# : 17021403, Cas# :
34604-60-9
)
5-hydroxypyrazine-2-carboxylic acid , a metabolite of anti-tuberculosis drug pyrazina
Hesperadin
(Catalog# : 17011902, Cas# :
422513-13-1
)
Hesperadin is an inhibitor of human Aurora B, which can prevent the phosphorylation o
HLCL-61 HCl
(Catalog# : 16122819, Cas# :
1158279-20-9
)
HLCL-61 is a potent and selective PRMT5 inhibitor for treatment of acute myeloid leuk
Hexaminolevulinate HCl
(Catalog# : 16122818, Cas# :
140898-91-5
)
Hexaminolevulinate hydrochloride, also known as hexyl 5-aminolevulinate HCl, is the h
HA15
(Catalog# : 16122816, Cas# :
1609402-14-3
)
HA15 displayed anti-cancerous activity on all melanoma cells tested, including cells
Honokiol
(Catalog# : 161009024, Cas# :
35354-74-6
)
Houpu has traditionally been used in Eastern medicine as analgesic and to treat anxie
HS-173
(Catalog# : 161009001, Cas# :
1276110-06-5
)
HS-173 inhibited the PI3K signaling pathway, and showed anti-proliferative effects on
HUHS015
(Catalog# : 16062902, Cas# :
1453097-13-6
)
HUHS015 is a potent PCA-1/ALKBH3 inhibitor both in vitro and in vivo. The bioavailabi
HLCL-61
(Catalog# : 16062204, Cas# :
586395-74-6
)
HLCL-61 is a potent and selective PRMT5 inhibitor for treatment of acute myeloid leuk
1H-Pyrrolo[2,3-B]Pyridine-3-Carboxylic Acid
(Catalog# : 032511, Cas# :
156270-06-3
)
Coming soon!
1H-Indazole-5-boronic acid
(Catalog# : 032503, Cas# :
338454-14-1
)
Coming soon!
HTH-01-015
(Catalog# : 011306, Cas# :
1613724-42-7
)
HTH-01-015 is a potent and selective inhibitor of NUAK1 with IC50 of 100 nM, does not
hydrocortisone
(Catalog# : 010402, Cas# :
50-23-7
)
Hydrocortisone is the main glucocorticoid secreted by the ADRENAL CORTEX. Its synthet
HQL-79
(Catalog# : 121507, Cas# :
162641-16-9
)
Coming soon!
HBED-CC-PSMA ( PSMA-11 )
(Catalog# : 103003, Cas# :
1366302-52-4
)
PSMA-11, also known as HBED-CC-PSMA or Psma-hbed-CC, has potential use as a tracer fo
HBED-CC
(Catalog# : 103002, Cas# :
143557-99-7
)
Coming soon!
6-hydroxy-N-Methylbenzofuran-3-carboxaMide
(Catalog# : 92218)
Coming soon!
7-hydroxy-1H-quinolin-2-one
(Catalog# : 91706, Cas# :
70500-72-0
)
Coming soon!
3-(4-Hydroxyphenyl)propionic acid
(Catalog# : 90608, Cas# :
501-97-3
)
Coming soon!
6-Hydroxy-1-indanone
(Catalog# : 81930, Cas# :
62803-47-8
)
Coming soon!
2H-Isoindole-1-carboxylic acid methyl ester
(Catalog# : 81003, Cas# :
56365-71-0
)
Coming soon!
6H05
(Catalog# : 52732, Cas# :
1469338-01-9
)
6H05 is a selective, and allosteric inhibitor of oncogenic mutant K-Ras(G12C
HMN-214
(Catalog# : 52581, Cas# :
173529-46-9
)
HMN-214(IVX214) is a potent PLK1 inhibitor an average IC50 of 0.12 M.
HPGDS inhibitor 1
(Catalog# : 52535, Cas# :
1033836-12-2
)
HPGDS inhibitor 1 is a novel and selective Hematopoietic Prostaglandin D Synthase (HP
HSP990 (NVP-HSP990)
(Catalog# : 52015, Cas# :
934343-74-5
)
NVP-HSP990 (HSP990) is a novel, potent and selectiveHSP90inhibitor for HSP90/ withIC5
«
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Products Catalog
Signaling Pathway
-- 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
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
HC-5404
(Catalog# : 24112, Cas# :
3034479-99-4
)
HC-5404 is a novel, highly selective and potent PERK inhibitor.
STX-478
(Catalog# : 20633, Cas# :
2883540-92-7
)
STX-478 is a second generation, mutant-selective, oral PI3Ka small molecule allosteri
Iclepertin (BI-425809)
(Catalog# : 24084, Cas# :
1421936-85-7
)
Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
Bomedemstat
(Catalog# : 24001, Cas# :
1990504-34-1
)
Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl
PLX-4545
(Catalog# : 24111, Cas# :
2892065-45-9
)
PLX-4545 is an orally bioavailable molecular glue degrader of IKZF2 designed to desta
VVD-130037 ( BAY-3605349 )
(Catalog# : 24110, Cas# :
3034880-93-5
)
VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2).
CBR-5884
(Catalog# : 24109, Cas# :
681159-27-3
)
CBR 5884 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor which was able to inhi
JHU-083
(Catalog# : 24108, Cas# :
1998725-11-3
)
JHU-083 selectively blocks glutaminase activity in brain CD11b+ cells and prevents de
LXH-3-71
(Catalog# : 24107, Cas# :
2251753-65-6
)
LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH
CC-92480 ( Mezigdomide )
(Catalog# : 20510, Cas# :
2259648-80-9
)
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno