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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
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Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
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Immunology & Inflammation
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MAPK
Membrane Transporter/Ion Channel
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Cas Index 1
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Cas Index 1
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
149488-17-5 | trovirdine
(Catalog# : 16060302)
trovirdine
1021950-26-4 | Tyrosine kinase inhibitor
(Catalog# : 030302)
Coming soon!
1639417-53-0 or 1693773-94-2 | Tenalisib
(Catalog# : 012009)
Tenalisib is a potent and selective dual PI3K/ inhibitor that inhibited growth of B-c
1035555-63-5 | TAK-733
(Catalog# : 010813)
TAK-733 is a potent and selective MEK allosteric site inhibitor for MEK1 with IC50 of
136310-93-5 | Tiotropium Bromide
(Catalog# : 010502)
Tiotropium Bromide is a muscarinic acetylcholine receptor (mAChR) antagonist that blo
139404-48-1 | Tiotropium Bromide
(Catalog# : 010439)
Tiotropium Bromide hydrate is an anticholinergic and bronchodilator and a muscarinic
114899-77-3 | Trabectedin
(Catalog# : 122948)
Trabectedin is a novel antitumour agent of marine origin with potent antitumour activ
1257426-19-9 | TBA-354
(Catalog# : 122934)
TBA-354 is a potent anti-tuberculosis compound; maintains activity against Mycobacter
14636-12-5 | Terlipressin
(Catalog# : 122929)
Terlipressin is an analogue of vasopressin used as a vasoactive drug in the managemen
1234423-95-0 | Tenapanor
(Catalog# : 122919)
Tenapanoris an inhibitor of the sodium-proton exchanger NHE3. Thisantiporter protein
150683-30-0 | Tolvaptan
(Catalog# : 122814)
Tolvaptan is a selective, competitive arginine vasopressin receptor 2 antagonist with
119413-54-6 | Topotecan Hydrochloride
(Catalog# : 122522)
Topotecan Hcl is the first topoisomerase I-directed cytotoxic agent to enter clinical
154-42-7 | 6-Thioguanine
(Catalog# : 122512)
6-Thioguanine belongs to the thiopurine family of drugs that also include mercaptopur
104-06-3 | Thiacetazone
(Catalog# : 122408)
A thiosemicarbazone that is used in association with other antimycobacterial agents i
145733-36-4 | TASOSARTAN
(Catalog# : 121505)
Coming soon!
1092351-67-1 | Torkinib
(Catalog# : 121420)
PP242 is a selective mTOR inhibitor with IC50 of 8 nM; targets both mTOR complexes wi
1033805-28-5 | Telotristat
(Catalog# : 120421)
Telotristat is the active metabolite of LX1606(Telotristat etiprate), which is an ora
1310693-92-5 | Tubastatin A HCl
(Catalog# : 110228)
Tubastatin A is a potent and selective HDAC6 inhibitor. Demonstrates 1093-fold select
1252003-15-8 | Tubastatin A
(Catalog# : 110225)
Tubastatin A is a potent HDAC6 inhibitor with an IC50 value of 15 nM. Comparatively,
1415379-56-4 | T-807( AV1451)
(Catalog# : 102910)
T807( AV1451) is a novel tau positron emission tomography imaging agent for Alzheimer
1374107-54-6 | THK-5107
(Catalog# : 102909)
Coming soon!
1374107-64-8 | THK5105
(Catalog# : 102906)
Coming soon!
1573029-17-0 | THK-523
(Catalog# : 102905)
Coming soon!
174634-09-4 | TAS-103 dihydrochloride
(Catalog# : 101904)
TAS-103, also known as BMS-247615, is a quinoline derivative that displays antitumor
1341200-45-0 | TP-0903(Dubermatinib)
(Catalog# : 101207)
TP-0903 is a potent and selective Axl kinase inhibitor with IC50 of 27 nM.
162635-04-3 | Temsirolimus
(Catalog# : 101205)
Temsirolimus is a recently developed mTOR inhibitor. with improved aqueous solubility
1207283-85-9 | TP-434
(Catalog# : 92216)
Coming soon!
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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
----
Bradykinin 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)
-- 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
85622-93-1 | Temozolomide
(Catalog# : 25209)
Temozolomide is an alkylating agent.
2035010-37-6 | ALT-007
(Catalog# : 25157)
ALT-007 is an orally bioavailable SPT inhibitor that is more potent than myriocin, sa
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim (BHV-7000) is an oral, small-molecule activator of Kv7.2/7.3 potassium chann
2102501-84-6 | PF-06835919 ( MDK-1846 )
(Catalog# : 193264)
MDK1846 is a potent ketohexokinase (KHK) inhibitor.
2271348-04-8 | MK256
(Catalog# : 25208)
MK256 is a novel CDK8 inhibitor with potent antitumor activity in AML through downreg
2351225-46-0 | NSD1 inhibitor BT5
(Catalog# : 25207)
BT5 potently inhibits NSD1, engages the SET domain in cells, and reduces H3K36me2 lev
1049704-18-8 | MA242 TFA
(Catalog# : 25206)
MA242 isMDM2 and NFAT1 dual inhibitorthat induces MDM2 auto-ubiquitination and degrad
2800223-30-5 | Dabogratinib ( TYRA-300 )
(Catalog# : 24073)
Dabogratinib ( TYRA-300 ) is an Oral Selective FGFR3 Inhibitor (IC50 = 11 nM) for the
N/A | AF710B
(Catalog# : 25205)
AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1
2957874-18-7 | MAT2A inhibitor 5
(Catalog# : 25204)
MAT2A inhibitor 5 has a high potency for inhibiting MAT2A and a remarkable selectivit