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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
PROTAC
Antibody-drug Conjugate/ADC Related
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
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On Sale
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Ordering
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About Us
Contact Us
+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
PROTAC
Antibody-drug Conjugate/ADC Related
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
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Services
Custom Synthesis
Process Development
Ordering
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Name Index T
Takinib
(Catalog# : 18672, Cas# :
1111556-37-6
)
Takinib is a selective TAK1 inhibitor that induces apoptosis following TNF-α stimula
TMP269
(Catalog# : 185254, Cas# :
1314890-29-3
)
TMP269 is a highly potent, selective and cell-permeable class IIa HDAC inhibitor with
Trilaciclib (G1T28)
(Catalog# : 185235, Cas# :
1374743-00-6
)
TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A
TAPI-1
(Catalog# : 185181, Cas# :
171235-71-5
)
TAPI-1 is and inhibitor of TACE. It inhibits the cleavage of TNF-a, TNFRI (p60), and
TG100572 HCl
(Catalog# : 185175, Cas# :
867331-64-4
)
TG-100572 is a potent and selective VEGFR2/Src kinase inhibitor.
TLN-232
(Catalog# : 18594, Cas# :
158899-10-6
)
TLN-232, also known as CAP-232, is a synthetic cyclic heptapeptide with potential ant
TRC051384
(Catalog# : 18593, Cas# :
867164-40-7
)
TRC051384 is a inducer of heat shock protein Hsp70.
Triptorelin Acetate
(Catalog# : 18592, Cas# :
140194-24-7
)
Triptorelin is a gonadotropin-releasing hormone agonist (GnRH agonist) used as the ac
Tropifexor
(Catalog# : 18591, Cas# :
1383816-29-2
)
Tropifexor, also known as LJN452, is a farnesoid X receptor agonist for the Treatment
THZ531
(Catalog# : 184172, Cas# :
1702809-17-3
)
THZ531 is a covalent CDK12 and CDK13 covalent inhibitor. Cyclin-dependent kinases 12
Tofogliflozin
(Catalog# : 184311, Cas# :
903565-83-3
)
Tofogliflozin, also known as CSG 452, is a potent and high selective SGLT2 inhibitor
TPX-0005
(Catalog# : 18423, Cas# :
1802220-02-5
)
TPX-0005 is a Src/FAK/Janus kinase 2 (JAK2) inhibitor. TPX-0005 plus EGFR TKI suppres
tert-butyl ((1H-benzo[d][1,2,3]triazol-1-yl)methyl)carbamate
(Catalog# : 183214, Cas# :
305860-41-7
)
tert-butyl (1H-benzo[d][1,2,3]triazol-1-yl)methylcarbamate是一种药物中间体。
Timapiprant
(Catalog# : 1712152, Cas# :
851723-84-7
)
Timapiprant,又名OC000459,是一种强效、选择性和口服的CRTH2拮抗剂。
TUG-770
(Catalog# : 1791519, Cas# :
1402601-82-4
)
TUG-770 is a Highly Potent Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonist for Treatm
TH-2120
(Catalog# : 179157, Cas# :
81686-22-8
)
TH-2120, also known as Sodium ionophore III, is a ionophore. Ionophore is suitable fo
Thiomyristoyl
(Catalog# : 1791113, Cas# :
1429749-41-6
)
Thiomyristoyl is a potent and specific SIRT2 inhibitor with an IC50 of 28 nM. IC50 &
TC-O9311
(Catalog# : 179828, Cas# :
444932-31-4
)
TC-O9311 is a potent GPR139 agonist (EC50 = 39 nM in CHO-K1 cells expressing human GP
Trelagliptin succinate
(Catalog# : 179811, Cas# :
1029877-94-8
)
Trelagliptin, also known as SYR-472, is a long acting dipeptidyl peptidase-4 (DPP-4)
TUG-891
(Catalog# : 1783014, Cas# :
1374516-07-0
)
TUG-891 is a potent and selective agonist of the free fatty acid receptor 4 (FFA4/GPR
TP-3654
(Catalog# : 178303, Cas# :
1361951-15-6
)
TP-3654 is a Pim-1 and Pim-3 kinase inhibitor potentially for the treatment of prosta
TAK1 INHIBITOR
(Catalog# : 1791412, Cas# :
1326712-16-6
)
TAK1 inhibitor is discontinued.
TPCA-1
(Catalog# : 17031308, Cas# :
507475-17-4
)
TPCA-1 is a potent IKK-2 inhibitor. TPCA-1 is also an effective inhibitor of STAT3 ph
Trichostatin A
(Catalog# : 17031306, Cas# :
58880-19-6
)
Trichostatin A, also known as TSA, is a HDAC inhibitor. TSA inhibits the eukaryotic c
Thiotepa
(Catalog# : 17031304, Cas# :
52-24-4
)
Thiotepa is a polyfunctional, organophosphorus alkylating agent and a stable derivati
Tirabrutinib free base ( ONO-4059 )
(Catalog# : 17031303, Cas# :
1351636-18-4
)
Tirabrutinib, also known as ONO-4059 is a potent and orally active Bruton agammaglobu
TCS-OX2-29 HCl
(Catalog# : 17031302, Cas# :
1610882-30-8
)
TCS-OX2-29 or TCS OX2 29 , also known as TCSOX229 and TCS-OX229, is a selective OX2 r
TX1-85-1
(Catalog# : 17030713, Cas# :
1603845-32-4
)
TX1-85-1 is ErbB3 inhibitor. TX2-121-1 may exert Her3-dependent pharmacology through
Tipiracil HCl
(Catalog# : 17030710, Cas# :
183204-72-0
)
Tipiralacil, also known as TPI, is a thymidine phosphorylase inhibitor (TPI). Tipirac
Turofexorate isopropyl
(Catalog# : 17030707, Cas# :
629664-81-9
)
Turofexorate isopropyl, also known as WAY-362450 and XL335, is a highly potent, selec
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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
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
-- 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
----
RXFP 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
----
UGT
----
MMP
----
ATP Citrate Lyase
-- 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
----
Glutaminase
-- 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
-- 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
----
Potassium Channel
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
-- PROTAC
----
Molecular Glues
--
Antibody-drug Conjugate/ADC Related
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
Soquelitinib ( CPI-818 )
(Catalog# : 20671, Cas# :
2226636-04-8
)
Soquelitinib is an oral interleukin-2-inducible T cell kinase (ITK) inhibitor.
Crelosidenib
(Catalog# : 24101, Cas# :
2230263-60-0
)
Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor. It is an antineoplast
LLL12
(Catalog# : 25075, Cas# :
1260247-42-4
)
LLL12 is a potent STAT3 inhibitor. LLL12 inhibits colony formation and cell migration
RMC-6236
(Catalog# : 25074, Cas# :
2765081-21-6
)
Daraxonrasib, also known as RMC-6236 and RAS-IN-2, is a potent and selective RAS(ON)
MGD-28
(Catalog# : 25073, Cas# :
2991818-13-2
)
MGD-28 is a potent molecular glue degrader that demonstrates significant in vitro eff
TG101209 analog 1
(Catalog# : 25072)
TG101209 analog 1 (Compound 8h) is an inhibitor of BUB1B with an IC50 of 10.36 μ M.
AT-007
(Catalog# : 25071, Cas# :
2170729-29-8
)
AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase in
TAK-653
(Catalog# : 25070, Cas# :
1358751-06-0
)
TAK-653 is a novel AMPA receptor potentiator, strictly potentiating a glutamate-induc
Emavusertib
(Catalog# : 25069, Cas# :
1801344-14-8
)
Emavusertib, also known as CA-4948 is a potent IRAK4/FLT3 inhibitor with anti-tumor a
Roginolisib
(Catalog# : 25068, Cas# :
1305267-37-1
)
Roginolisib, also known as MSC2360844 and IOA-244, is a potent, orally active and sel