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Metabolic Enzyme/Protease
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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
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
PI3K/Akt/mTOR
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Cas Index 1
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Cas Index 1
1638178-87-6 | ONC206
(Catalog# : 111891)
ONC206 is a chemical analogue of ONC201. ONC206 is a benzyl-flurobenzyl imipridone th
1309198-71-7 | Ogerin
(Catalog# : 193186)
Ogerin is a selective GPR68 PAM, suppressing recall in fear conditioning in wild-type
1802661-73-9 | ONO-8590580
(Catalog# : 1810162)
ONO-8590580 is a GABAA α5 negative allosteric modulator.
1807861-48-8 | ONC212
(Catalog# : 185286)
ONC212 is a fluorinated-ONC201 analogue, shows preclinical efficacy in melanoma and h
131631-89-5 | OPC-21268
(Catalog# : 185163)
OPC-21268 is a vasopressin 1 receptor antagonist potentially for the treatment of hea
1431697-89-0 | OTSSP167 free base
(Catalog# : 185161)
OTSSP167, also known as OTS167, is an orally available inhibitor of maternal embryoni
1316755-16-4 | Olodanrigan free acid
(Catalog# : 1842810)
Olodanrigan, also known as EMA-401 and PD-126055, is an angiotensin AT2 antagonist po
1421373-66-1 | Osimertinib mesylate
(Catalog# : 1712154)
Osimertinib,也被称为Mereletinib和AZD- 9291,是第三代EGFR抑制剂,为晚
131247-39-8 | ON1231320
(Catalog# : 1791319)
ON1231320, also known as GBO-006, is a Polo-like kinase 2 (PLK2) inhibitor.
1306760-87-1 | Ozanimod
(Catalog# : 110902)
Ozanimod is a selective sphingosine 1 phosphate receptor modulators and methods which
1353550-13-6 | Olmutinib
(Catalog# : 011103)
Olmutinib is a potent small molecule inhibitor of Bruton's tyrosine kinase (BTK).
1261491-89-7 | Olumacostat Glasaretil
(Catalog# : 732801)
Olumacostat glasaretil is a novel topical sebum inhibitor in the treatment of acne vu
1338540-63-8 | OTS514
(Catalog# : 17031015)
OTS514 is a highly potent TOPK(T-LAK cell-originated protein kinase) inhibitor with
167305-00-2 | Omapatrilat
(Catalog# : 17030903)
Omapatrilat is a novel antihypertensive agent that inhibits both neutral endopeptidas
1026791-61-6;100044-96-0 | Org-26576
(Catalog# : 17021328)
Org-26576 is an AMPA glutamate receptor modulator potentially for the treatment of de
14698-29-4 | Oxolinic acid
(Catalog# : 16122720)
Oxolinic acid is a quinolone antibiotic, inhibiting the enzyme DNA gyrase and DNA syn
1357470-29-1 | ON123300
(Catalog# : 16122712)
ON123300 is a potent and multi-targeted kinase inhibitor with IC50 of 3.9 nM, 5 nM, 2
1640292-55-2 | Oclacitinib
(Catalog# : 16122705)
Oclacitinib is a novel inhibitor of JAK family members with IC50 ranging from 10 to 9
1801787-56-3 | OICR-9429
(Catalog# : 6111010)
OICR-9429 is a novel small-molecule antagonist of the Wdr5-MLL interaction with IC50
1404231-34-0 | ON 146040
(Catalog# : 611901)
ON 146040 is the first dual PI3K and BCR-ABL inhibitor that targets the STAT3 and STA
193153-04-7 | OtaMixaban
(Catalog# : 16070915)
OtaMixaban
171099-57-3 | Oritavancin
(Catalog# : 16070815)
Oritavancin, also known as LY333328, is a novel semisynthetic glycopeptide antibiotic
1330633-98-1(free base) | ON-01911.Na
(Catalog# : 1662310)
ON-01911.Na is a non-ATP-competitive inhibitor ofPLK1.
183321-86-0 | OSI-420(Desmethyl Erlotinib)
(Catalog# : 166215)
OSI-420 is the active metabolite of Erlotinib which is an orally active EGFR tyrosin
1351635-67-0 | ONO4059-Analog
(Catalog# : 652602)
ONO4059-Analog(CAS#1351635-67-0)is a potent and selective BTK inhibitor.
192564-14-0 | Oritavancin(OC)
(Catalog# : 42510)
Oritavancin (INN, also known as LY333328, Orbactiv) is a novel semisynthetic glycopep
1297538-32-9 | ODM-201(BAY-1841788)
(Catalog# : 123101)
ODM-201(also known as BAY-1841788)is a novel, nonsteroidal, orally active AR inhibito
1086062-66-9 | Omipalisib(GSK2126458,GSK458)
(Catalog# : 121429)
GSK2126458 is a highly selective and potent inhibitor of PI3K with Ki of 0.019 nM/0.1
175135-47-4 | O4I1
(Catalog# : 120813)
O4I1 is as a potent Oct3/4 inducer.
165682-93-9 | O4I2
(Catalog# : 120812)
O4I2 is a potent Oct3/4 inducer in various human cell lines including human fibroblas
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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)
----
NEKs
-- 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
----
Methionine Adenosyltransferase (MAT)
-- 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
----
GLP Receptor
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- 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
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
-- 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)
----
CGRP-Receptor
----
TRP-Channel
-- 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)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- 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
-- Nuclear Receptor
----
Androgen Receptor(AR)
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
3054692-62-2 | ECI830
(Catalog# : 26A031)
ECI830 is a potent and highly selective CDK2 inhibitor.
1394076-92-6 | GNE-317
(Catalog# : 52282)
GNE-317 is a potent, brain-penetrantPI3Kinhibitor
3118994-80-9 | DPTX-3186
(Catalog# : 26A010)
DPTX3186, an orally administered small molecule condensate modulator (c-mod) inhibiti
435327-40-5 | Avasopasem manganese (GC-4419; M-40419)
(Catalog# : 25108)
Avasopasem manganese, also known as GC-4419; M 40419 and SC-72325A, is amimetic of th
1421936-85-7 | Iclepertin (BI-425809)
(Catalog# : 24084)
Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen
4727-31-5 | Kartogenin ( KGN )
(Catalog# : 52215)
Kartogenin (KGN) is a synthetic small molecule that stimulates chondrogenic cellular
218791-21-0 | Imisopasem manganese ( M40403; GC4403 )
(Catalog# : 72602)
Imisopasem manganese ( M40403; GC4403 ) is a stable non-peptidyl mimetic of MnSOD tha
2311863-36-0 | Apecotrep (BI 764198)
(Catalog# : 26A048)
Apecotrep (BI 764198) is a potential first-in-class, oral, selective TRPC6 inhibitor.
902614-04-4 | Pantothenate kinase-IN-2
(Catalog# : 26A038)
Pantothenate kinase-IN-2 is a pantothenate kinase inhibitor with IC50 values of 92 nM
3062177-59-4 | BH-30643
(Catalog# : 26A047)
BH-30643 is a novel, orally available, non-covalent, macrocyclic, mutant selective OM