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Membrane Transporter/Ion Channel
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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
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Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
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Cas Index 1
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Cas Index 1
1222998-36-8 | Torin 1
(Catalog# : 52820)
Torin 1 is a potent inhibitor of mTORC1/2 with IC50 of 2 nM/10 nM; exhibits 1000-fold
1100598-32-0 | Tepotinib (EMD 1214063)
(Catalog# : 52785)
Tepotinib (EMD 1214063) is a potent and selective c-Met inhibit
1228591-30-7 | TAK-632
(Catalog# : 52562)
TAK-632 is a selective pan-RAF kinase inhibitor with IC50 values of 2.4/1.4 nM for BR
1197300-24-5 | TGR5 Receptor Agonist
(Catalog# : 52557)
TGR5 Receptor Agonist, a potent TGR5(GPCR19) agonist, showed improved potency in the
1011557-82-6 | Tenovin-6
(Catalog# : 52528)
Tenovin-6 is the water soluble analog of Tenovin-1 (HY-13423) and acts as a potent SI
1005491-05-3 | Tirasemtiv
(Catalog# : 52238)
Tirasemtiv(CK 2017357) is a a small-molecule fast-skeletal-troponin activator, which
1223001-51-1 | Torin 2
(Catalog# : 52311)
Torin 2 is a potent and selectivemTORinhibitor withIC50of 0.25 nM; 800-fold greater s
1616632-77-9 | TIC10 ( ONC201 )
(Catalog# : 51802)
TIC10 ( ONC201 ), Bulk in stock, contact us by email for detailed quotation.ONC201/TI
1532533-67-7 | Umbralisib
(Catalog# : 25085)
Umbralisib, also known as TGR1202 and RP5264 , is a highly specific, orally available
1632002-28-8 | URAT1 inhibitor 7
(Catalog# : 20573)
URAT1 inhibitor 7 (compound 10f) is a potent URAT1 inhibitor.
1448440-52-5 | UAMC-1110
(Catalog# : 21249)
UAMC-1110, also known as SP-13786, is a novel potent and selective inhibitor of fibro
1616413-96-7 | UCB9608
(Catalog# : 2071515)
UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr
142878-12-4 | U-73343
(Catalog# : 112591)
U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p
1612782-86-1 | UNC2541
(Catalog# : 6111901)
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit
1890169-95-5 | UPGL00004
(Catalog# : 193251)
UPGL00004 is a potent inhibitor of glutaminase C (GAC).
1387560-01-1 | Umibecestat free base
(Catalog# : 193223)
Umibecestat, also known as CNP-520, is a beta-secretase inhibitor and is a drug candi
1333218-50-0 | Upacicalcet
(Catalog# : 192142)
Upacicalcet (formerly SK-1403/AJT240) is a novel non-peptide calcimimetic agent that
1229582-33-5 | URMC-099
(Catalog# : 1810252)
URMC-099 is an orally bioavailable, brain penetrant mixed lineage kinase (MLK) inhibi
1184136-10-4 | UNC-926 free base
(Catalog# : 18584)
UNC-926 is a L3MBTL1 domain inhibitor. UNC-926 binds to the MBT domain of the L3MBTL1
1310726-60-3 | Upadacitinib
(Catalog# : 184105)
Upadacitinib, also known as ABT-494, is a potent and selective JAK inhibitors in deve
1048371-03-4 | UPF-1069
(Catalog# : 1791520)
UPF-1069 is a selective and potent PARP2 inhibitor. UPF-1069 induces apoptosis. UPF-1
1956366-10-1 | Ulixertinib HCl
(Catalog# : 179153)
Ulixertinib, also known as BVD-523 and VRT752271, is an inhibitors of ERK protein kin
1872382-47-2 | UNC3866
(Catalog# : 17011102)
UNC3866 is a potent antagonist of the methyllysine (Kme) reading function of the Poly
126784-99-4 | Ulipristal acetate
(Catalog# : 16122843)
Ulipristal acetate, also known as CDB-2914, is a selective progesterone receptor modu
152273-12-6 | U-93631
(Catalog# : 16122841)
U-93631 is a GABAA receptor antagonist. U-93631 causes rapid decay of gamma-aminobuty
1381291-36-6 | USP7-IN-1
(Catalog# : 611931)
USP7-IN-1 is a novel selective and reversible inhibitor of USP7 with IC50 of 33 uM; l
1481677-78-4 | UNC0642
(Catalog# : 16071013)
UNC0642 is a potent, selective inhibitor of G9a/GLP with improved PK properties. UNC0
1047634-65-0 | Uprosertib (GSK2141795)
(Catalog# : 16070901)
Uprosertib (GSK2141795) is a selective, ATP-competitive, and orally bioavailableAktin
178870-32-1 | UC-781
(Catalog# : 011311)
UC-781 is a thiocarboxanilide non-nucleoside reverse transcriptase inhibitor. It is a
1415800-43-9 | UNC1215
(Catalog# : 011123)
UNC1215 is a potent and selective chemical probe for the methyllysine (Kme) reading f
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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
-- 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
----
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)
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
-- 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
2243882-74-6 | Zedoresertib
(Catalog# : 26A023)
Zedoresertib (Debio 0123) is a brain-penetrant, highly selective WEE1 kinase inhibito
3033961-38-2 | BEN-28010
(Catalog# : 26A022)
BEN-28010 is a freely brain-penetrant, potent, and selective CHK1 inhibitor.
3107291-07-3 | Tert-butyl 4-((2-(methylamino)-6-(2,2,2-trifluoroethyl)thieno[2,3-d]pyrimidin-4-yl)amino)piperidine-1-carboxylate
(Catalog# : 26B007)
2565656-70-2 | Muvalaplin
(Catalog# : 20528)
Muvalaplin is a small molecule that inhibits formation of Lp(a) by interfering with t
2925330-18-1 | MAT2A-IN-22
(Catalog# : 26A021)
MAT2A-IN-22 (Compound 29-1) is a blood-brain barrier-penetrant and orally active MAT2
1497439-74-3 | AD-8007
(Catalog# : 26A018)
AD-8007 is a selective and brain-penetrant inhibitor of acetyl CoA synthase 2 (ACSS2).
1802650-31-2 | ZY-444
(Catalog# : 26A020)
ZY-444 is an anti-cancer agent by inhibiting PC ( pyruvate carboxylase ) activity.
2306525-79-9 | AD-5584
(Catalog# : 26A019)
AD-5584 is a novel brain-permeable ACSS2 inhibitors.
3079716-11-0 | IDB-003
(Catalog# : 26A017)
IDB-003 inhibits MDA-MB-231 tumor growth in vivo.
1357362-02-7 | Vafidemstat
(Catalog# : 18891)
Vafidemstat, also known as ORY 2001, is a lysine-specific histone demethylase (LSD1)