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Membrane Transporter/Ion Channel
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Proteases
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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
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Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolism
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NF-κB
Protein Tyrosine Kinase
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Cas Index 1
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Cas Index 1
1603845-32-4 | TX1-85-1
(Catalog# : 17030713)
TX1-85-1 is ErbB3 inhibitor. TX2-121-1 may exert Her3-dependent pharmacology through
183204-72-0 | Tipiracil HCl
(Catalog# : 17030710)
Tipiralacil, also known as TPI, is a thymidine phosphorylase inhibitor (TPI). Tipirac
1234365-97-9 | Tenapanor HCl
(Catalog# : 17030113)
Tenapanor, also known as AZD-1722 and RDX 5791, is an inhibitor of the sodium-proton
150915-40-5 | Tirofiban HCl hydrate
(Catalog# : 17030103)
Tirofiban is an antiplatelet drug. It belongs to a class of antiplatelet named glycop
135598-68-4 | TAS-109
(Catalog# : 17022810)
TAS-109, also known as DFP-10917 and CNDAC, is an analogue of the nucleoside deoxycyt
1256037-58-7 | TRX818
(Catalog# : 17022401)
TRX-818 is an orally bioavailable agent with potential antineoplastic and anti-vascul
15421-84-8 | Trapidil
(Catalog# : 17021310)
Trapidil is a PDGF antagonist that can inhibit the proliferation of the PDGF-producin
1439901-97-9 | Tirabrutinib HCl
(Catalog# : 17012103)
ONO-4059 is a selective and novel inhibitor of BTK with IC50 2.2 nm, ONO-4059 binds t
113942-30-6 | Temozolomide Acid
(Catalog# : 17011905)
Temozolomide Acid, also known as TMZA, is a metabolite of temozolomide (TMZ) with dem
1609960-31-7 | TH588
(Catalog# : 17011728)
TH588 is a potent inhibitor of human 7,8-Dihydro-8-oxoguaninetriphosphatase MTH1 (NUD
1415716-58-3 | TG6-10-1
(Catalog# : 17011727)
TG6-10-1 is a potent and selective antagonist for the prostaglandin E2 receptor subty
1033805-22-9 | Telotristat ethyl
(Catalog# : 17011722)
Telotristat ethyl, also known as LX 1032 or LX 1606, is an oral serotonin synthesis i
161715-24-8 | Tebipenem pivoxil
(Catalog# : 17011721)
Tebipenem pivoxil, also known as ME1211 and TBM-PI, is a novel oral carbapenem antibi
193620-69-8 | TAS-301
(Catalog# : 17011719)
TAS-301 is a potent and selective constrictive remodeling regulator on renarrowing af
174634-08-3 | TAS-103
(Catalog# : 17011718)
TAS-103, also known as BMS-247615, is a quinoline derivative that displays antitumor
150080-09-4 | Talabostat mesylate
(Catalog# : 17011717)
Talabostat, also known as PT-100, is dipeptidyl peptidase inhibitor with antineoplast
1312691-41-0 | TAK-659 HCl
(Catalog# : 17011716)
TAK-659 is an inhibitor of spleen tyrosine kinase (syk), with potential anti-inflamma
106463-17-6 | Tamsulosin hydrochloride
(Catalog# : 17109008)
Tamsulosin is a potent and selective α1a adrenergic receptor antagonist. Tamsulosin
1033040-23-1 | TPO agonist 1
(Catalog# : 6111515)
TPO agonist 1 can increase production of platelets by stimulating the TPO receptor in
1604810-83-4 | THZ1
(Catalog# : 6111013)
THZ1 is a novel selective and potent covalent CDK7 inhibitor with IC50(binding affini
1002789-86-7 | TZ9
(Catalog# : 611934)
TZ9 is a novel inhibitor of Rad6 ubiquitin conjugating enzyme(E2 enzyme); inhibits MD
1621523-07-6 | THZ1-R
(Catalog# : 611926)
THZ1-R is a non-cysteine reactive analog, which displays diminished activity for CDK7
1532533-78-0 | TGR-1202 hydrochloride
(Catalog# : 611905)
TGR-1202 hydrochloride is an orally available, next generation PI3Kdelta inhibitor, i
1532533-67-7 | TGR-1202
(Catalog# : 611904)
TGR-1202 is an orally available, next generation PI3Kdelta inhibitor, inhibits PI3K a
104987-11-3 | Tacrolimus
(Catalog# : 161009006)
It is also used in a topical preparation in the treatment of atopic dermatitis (eczem
103300-74-9 | Taltirelin
(Catalog# : 16071029)
Taltirelin
1314891-22-9 | TMP-195
(Catalog# : 16071020)
TMP-195
1621175-65-2 | TC-G 1008
(Catalog# : 16071003)
TC-G 1008,
1258861-20-9 | Taladegib
(Catalog# : 121414)
Taladegib is a potent Hedgehog inhibitor with potential anticancer activity, which in
1096708-71-2 | TAK-580 (MLN2480)
(Catalog# : 16062203)
TAK-580, also known as MLN2480, BIIB024, and AMG 2112819, is an oral, selective pan-R
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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
-- 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
-- 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
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
-- 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
-- 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
2750001-23-9 | AZD0095
(Catalog# : 237072)
AZD0095 is a Selective Inhibitor of Monocarboxylate Transporter 4 (MCT4) for Oncology.
2101538-28-5 | 2-MNG
(Catalog# : 24129)
2-MNG is a new potent melanogenesis inhibitor, which exhibits a unique mode of action
2439277-80-0 | MAT2A-IN-9
(Catalog# : 25147)
MAT2A-IN-9 (compound 167), a 2-oxoquinazoline derivative, is a potent MAT2A (methioni
1898206-17-1 | Safusidenib
(Catalog# : 25149)
Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl
2669009-92-9 | Atebimetinib
(Catalog# : 25148)
Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1
2242751-53-5 | Acoramidis hydrochloride
(Catalog# : 24068)
Acoramidis is an oral, potent, and highly selective small molecule transthyretin (TTR
2230263-60-0 | Crelosidenib
(Catalog# : 24101)
Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor.
2833703-74-3 | LOXO-435
(Catalog# : 25080)
LOXO-435 is a selective small molecule inhibitor of FGFR3. It is active against both
2446928-30-7 | Gridegalutamide
(Catalog# : 25138)
Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
1256349-48-0 | Chiauranib
(Catalog# : 25146)
Chiauranib also known as orally available, small molecule inhibitor of select serine-