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PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
JAK/STAT
MAPK
Cytoskeletal Signaling
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TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
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Neuronal Signaling
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Fluorides
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Indoles and Oxindoles
Iodos
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Oxazoles
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Phenols
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+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
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Amino Acids
Anilines
Boronic Acids
Bromides
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Deuterated
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Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
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Pyridines
Pyrimidines
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Cas Index 5
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Cas Index 5
596817-06-0 | (2S,4S)-1-(2-chloroacetyl)-4-fluoropyrrolidine-2-carbonitrile
(Catalog# : 82714)
Coming soon!
54857-86-2 | TOFA ( RMI14514; MDL14514)
(Catalog# : 20376)
TOFA ( RMI14514; MDL14514) is an allosteric inhibitor of acetyl-CoA carboxylase-α (A
5560-78-1 | Teclozan
(Catalog# : 20279)
Teclozan is an antiprotozoal agent. It is a dichloroacetamide.
519055-62-0 | Tasisulam
(Catalog# : 2121222)
Tasisulam, also known as LY573636, is an acyl-sulfonamide with potential antineoplast
55094-52-5 | 2,3,5-Tri-O-benzyl-D-ribonolactone
(Catalog# : 2062011)
594839-88-0 | Tafamidis
(Catalog# : 193182)
Tafamidis, Tafamidis, also known as Fx-1006 or PF-06291826, is a drug for the amelior
507475-17-4 | TPCA-1
(Catalog# : 17031308)
TPCA-1 is a potent IKK-2 inhibitor. TPCA-1 is also an effective inhibitor of STAT3 ph
58880-19-6 | Trichostatin A
(Catalog# : 17031306)
Trichostatin A, also known as TSA, is a HDAC inhibitor. TSA inhibits the eukaryotic c
52-24-4 | Thiotepa
(Catalog# : 17031304)
Thiotepa is a polyfunctional, organophosphorus alkylating agent and a stable derivati
530141-72-1 | T-5224
(Catalog# : 16070909)
T-5224 is a selective inhibitor of c-Fos/activator protein-1. T-5224 ameliorates live
58-46-8 | Tetrabenazine
(Catalog# : 010501)
Tetrabenazine is a VMAT-inhibitor used for treatment of hyperkinetic movement disorde
58-22-0 | Testosterone
(Catalog# : 010405)
Testosterone is a steroid hormone from the androgen group and is found in mammals, re
56090-54-1 | Triglycerol
(Catalog# : 120417)
Coming soon!
53473-36-2 | 3-[4-(Trifluoromethyl)phenyl]propionic Acid
(Catalog# : 90704)
Coming soon!
571189-16-7 | tert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylate
(Catalog# : 82711)
Coming soon!
577778-58-6 | Topiroxostat
(Catalog# : 52711)
Topiroxostat(FYX-051) is a novel and potent xanthine oxidoreductase (XOR) inhibitor w
548486- 59-5 | Ulodesine
(Catalog# : 60634)
565460-15-3 | URB602
(Catalog# : 17030711)
URB602 is a selective inhibitor of monoglycerol lipase (MGL), exhibiting an IC50 of 2
58970-76-6 | Ubenimex
(Catalog# : 17030602)
Ubenimex, also known as NK 421 and Bestatin, is a CD13 inhibitor. Ubenimex attenuates
537672-41-6 | UF-010
(Catalog# : 16122842)
UF-010 is a Class I HDAC inhibitor (IC50 values are 0.06, 0.1, 0.5 and 1.5 M for HDAC
518303-20-3 | UMI-77
(Catalog# : 010426)
UMI-77 is a novel selective Mcl-1 SMI inhibitor. UMI-77 binds to the BH3 binding groo
5428-80-8 | Vacquinol-1
(Catalog# : 20435)
Vacquinol-1, also known as NSC 13316, is an activator of MKK4-dependent macropinocyto
599179-03-0 | Vicriviroc maleate
(Catalog# : 185214)
Vicriviroc, also known as SCH 417690 and SCH-D, is a potent, orally active and select
541503-81-5 | Vicriviroc Malate
(Catalog# : 122219)
Vicriviroc Malate is a potent inhibitor of HIV-1 entry into target cells, with a mean
5428-80-8 | Vacquinol-1
(Catalog# : 111906)
Vacquinols are a new class of quinine-derivatives that stimulate death in glioblastom
554403-49-5 | WAY-181187
(Catalog# : 31002)
WAY-181187 is a potent and selective 5-HT6 receptor agonist with Ki value of 2.2 nM.
50892-23-4 | Wy-14643
(Catalog# : 122825)
Wy-14643 is a moderate agonist of PPAR and PPAR with IC50 of 36.5 M and 53.7 M, respe
56776-32-0 | 盐酸依替福辛
(Catalog# : 1712142)
盐酸依替福辛,又称HOE 36801和etafenoxine,是Hoechst在上世纪60年代开
5633-14-7 | 盐酸苄替米特
(Catalog# : 1712141)
盐酸苄替米特,也称为EINECS 227-072-8,Spasmentral,和Dioxatrine毒蕈碱的乙
557782-81-7 | ZINC00881524 (ROCK inhibitor)
(Catalog# : 17021304)
ZINC00881524 is a ROCK inhibitor.
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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
-- 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
-- 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
-- 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
-- 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
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
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
1393466-87-9 | PLX8394
(Catalog# : 20613)
PLX8394 is an orally bioavailable inhibitor of serine/threonine-protein kinase B-raf
2365193-22-0 | Zelasudil
(Catalog# : 24014)
Zelasudil is a potent, highly selective and orally-active inhibitor that targets Rho-
2134675-36-6 | Ziftomenib ( KO-539 )
(Catalog# : 24013)
Ziftomenib is an oral, potent, and selective small molecule inhibitor that targets th
1640282-42-3 | Zunsemetinib
(Catalog# : 24012)
Zunsemetinib is an investigational oral mitogen-activated protein kinase-activated pr
2728667-27-2 | Zongertinib
(Catalog# : 24011)
Zongertinib [BI 1810631] is a human epidermal growth factor receptor 2 (HER2) inhibit
2272904-53-5 | Zasocitinib
(Catalog# : 24010)
Zasocitinib is under development for the treatment of moderate to severe plaque psori
2503036-46-0 | RNK-05047
(Catalog# : 24008)
RNK-05047 is a PROTAC degrader of BRD4 which displays significant tumor growth inhibi
1001288-58-9 | Asengeprast (FT011)
(Catalog# : 24009)
Asengeprast (FT011) is an anti-fibrotic agent thatreduces mRNA expression of collagen
2490431-16-6 | ERAS-801 ( JGK-068S )
(Catalog# : 20635)
ERAS-801 ( JGK-068S ) is a potent EGFR inhibitor.
209746-59-8 | T-1095
(Catalog# : 24004)
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs).