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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
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NF-κB
Protein Tyrosine Kinase
Proteases
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Cas Index 2
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Cas Index 2
2408840-26-4 | Imlunestrant
(Catalog# : 25104)
Imlunestrant is a biochemical
2230974-62-4 | Irpagratinib
(Catalog# : 25089)
Irpagratinib is an orally bioavailable, selective inhibitor of human fibroblast growt
259657-09-5 | Ivospemin Hydrochloride
(Catalog# : 25044)
Ivospemin is an antineoplastic spermine analogue.
2246607-08-7 | Inupadenant
(Catalog# : 24138)
Inupadenant, also known as EOS-850, is a highly selective small molecule antagonist o
2448172-22-1 | Icovamenib
(Catalog# : 24097)
This product was removed for commercial reasons.
2059148-82-0 | IMP-1088
(Catalog# : 24029)
IMP-1088 is a potenthuman N-myristoyltransferases NMT1andNMT2dual inhibitor.
2563892-44-2 | IK-930
(Catalog# : 20656)
IK-930 is a novel, selective, small molecule inhibitor of TEAD that prevents palmitat
2447007-60-3 | Iptacopan hydrochloride hydrate
(Catalog# : 20649)
Iptacopan hydrochloride hydrate is a highly potent and highly selective factor B inhi
21321-89-1 | Itruvone
(Catalog# : 20623)
Itruvone is an antidepressant.
2404604-06-2 | ITK inhibitor 6
(Catalog# : 20591)
2408840-26-4 | Imlunestrant
(Catalog# : 20475)
Imlunestrant is a biochemical
2741-16-4 | 1-ISOPROPOXYBENZENE
(Catalog# : 20406)
2160546-07-4 | IACS-13909
(Catalog# : 822221)
IACS-13909 is a specific and potent allosteric inhibitor of SHP2, that suppresses sig
252870-53-4(free base) | Ispronicline
(Catalog# : 20288)
Ispronicline, also known as AZD3480; TC 1734; TC-0173, and RJR 1734, is a alpha4beta2
2231259-57-5 | IACS-9439
(Catalog# : 20911)
IACS-9439 is a potent, highly selective and orally bioavailable CSF1R inhibitor. IACS
2074607-48-8 | IWP-O1
(Catalog# : 186222)
IWP-O1 is highly potent Porcn inhibitor, is essential for the secretion of Wnt protei
22503-72-6 | IDRA-21
(Catalog# : 179134)
IDRA-21 is a positive AMPA receptor modulator. IDRA-21 inhibits synaptic and extrasyn
23146-22-7 | IQ-1S
(Catalog# : 16123021)
IQ-1S is a potent and selective c-Jun N-Terminal Kinase Inhibitor. IQ-1S inhibits mur
200626-61-5 | ITSA-1 (ITSA1)
(Catalog# : 16122741)
ITSA-1 (ITSA1) is an HDAC activator via TSA suppression, but shows no activity toward
24386-93-4 | 5-Iodotubercidin
(Catalog# : 16122729)
5-Iodotubercidin is a potent adenosine kinase inhibitor with IC50 of 26 nM. It inhibi
219989-84-1 | Ixabepilone
(Catalog# : 122307)
Ixabepilone is an epothilone B analog and nontaxane microtubule-stabilizing compound
241479-67-4 | Isavuconazole
(Catalog# : 120801)
Coming soon!
218791-21-0 | Imisopasem-manganese(M40403)
(Catalog# : 72602)
M40403 is a low molecular weight, synthetic manganese containing superoxide dismutase
2982787-50-6 | JBI-802
(Catalog# : 24116)
2410512-38-6 | JQKD82
(Catalog# : 20285)
JQKD82 is a cell-permeable and selective KDM5 inhibitor (MM.1S cells, IC50 = 0.42 uM)
2110426-27-0 | JNJ-63576253
(Catalog# : 21250)
TRC253, also known as JNJ63576253, is a potent and orally active androgen receptor an
2098890-15-2 | JUN90152
(Catalog# : 21247)
JUN90152, also known as SMS2-IN-1, is a potent and highly selective sphingomyelin syn
2260886-64-2 | JND3229
(Catalog# : 2091904)
JND3229 is a New EGFRC797S Mutant Inhibitor with In Vivo Monodrug Efficacy (IC50 = 5.
2234281-75-3 | JI051
(Catalog# : 2071526)
JI051 is an inhibitor of the cancer-associated transcription factor Hes1 via the PHB2
2086772-26-9 | JNJ-64619178
(Catalog# : 193292)
JNJ-64619178 is an anticancer drug candidate.
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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
----
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
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
1820812-16-5 | TAK-071
(Catalog# : 186269)
TAK-071 is a muscarinic M1 receptor positive allosteric modulator.
2750895-97-5 | MTX115325
(Catalog# : 186264)
MTX115325 is a potent, selective, brain-penetrant USP30 inhibitor with good drug-like
2166616-75-5 | LY-3381916
(Catalog# : 193123)
LY-3381916 is a potent, selective and brain penetrated inhibitor of IDO1 activity, bi
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim (BHV-7000) is an oral, small-molecule activator of Kv7.2/7.3 potassium chann
2488609-21-6 | DS68591889
(Catalog# : 25158)
DS68591889 (PTDSS1i) specifically inhibits PTDSS1, which catalyzes serine incorporati
944808-88-2 | CAY 10566
(Catalog# : 10403)
CAY 10566 is a potent selective SCD-1 inhibitor.
2308520-97-8 | Cadefrecitinib (GLPG-3667)
(Catalog# : 20509)
Cadefrecitinib (GLPG-3667) is an oral, small molecule inhibitor of the TYK2 kinase in
1802735-28-9 | QBS10072S
(Catalog# : 25190)
QBS10072S isa blood-brain-barrier (BBB) penetrative agent composed of a cytotoxic che
2377000-84-3 | Dencatistat
(Catalog# : 25177)
Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
1898207-64-1 | DS-1001b
(Catalog# : 25178)
DS-1001 is an oral brain-penetrant mutant IDH1 selective inhibitor.