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PI3K/Akt/mTOR
Epigenetics
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Angiogenesis
Apoptosis
Autophagy
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MAPK
Cytoskeletal Signaling
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TGF-beta/Smad
DNA Damage
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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
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Membrane Transporter/Ion Channel
others
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Cas Index 6
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Cas Index 6
68238-36-8 | Patent blue violet purified
(Catalog# : 2017080117)
Purification of patent blue purple and isosulfan blue, it is a kind of dye and pigmen
68252-19-7 | Pirmenol
(Catalog# : 17030702)
Pirmenol is an antiarrhythmic agent. Pirmenol inhibits muscarinic acetylcholine recep
66-97-7 | Psoralen
(Catalog# : 17021307)
Psoralen is a naturally occurring furocoumarin that intercalates with DNA, inhibiting
677338-12-4 | PIK-90
(Catalog# : 160926010)
PIK-90 is a potent PI3K inhibitor with potential anticancer activity.
63208-82-2 | Pifithrin-alpha
(Catalog# : 012011)
Pifithrin- is an inhibitor of p53, inhibiting p53-dependent transactivation of p53-re
688046-61-9 | Pyriofenone
(Catalog# : 011119)
Coming soon!
685847-78-3 | PX-478
(Catalog# : 111307)
PX-478 is HIF-1alpha inhibitor, is also an orally active small molecule with potentia
612547-11-2 | PL-100
(Catalog# : 102616)
PL-100 is a novel HIV-1 protease inhibitor (PI) with a favorable cross-resistance pro
612530-44-6 | PTP1B-IN-1
(Catalog# : 92302)
Coming soon!
6628-74-6 | Pyrrolidin-1-yl-acetic acid hydrochloride
(Catalog# : 92206)
Coming soon!
68497-62-1 | Pramiracetam
(Catalog# : 52817)
Pramiracetam is a nootropic drug derived from piracetam, and is more potent. Pramirac
610318-54-2 | RGX-104 free form
(Catalog# : 19181)
RGX-104, also known as SB 742881, is a liver X receptor beta agonist with potential i
610318-03-1 | RGX-104 HCl
(Catalog# : 186234)
RGX-104 is a liver X receptor beta agonist with potential immunomodulating and antine
65376-05-8 | (1R,2R)-Cyclohexane-1,2-diyldimethanol
(Catalog# : 91407)
The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3
68285-23-4 | (R)-1-(2-Methoxyphenyl)ethylamine
(Catalog# : 91118)
Coming soon!
6150-01-2 | (1R)-1-phenylbutan-1-amine
(Catalog# : 91110)
Coming soon!
625115-55-1 | Riociguat
(Catalog# : 91005)
Riociguat is a stimulator of soluble guanylate cyclase (sGC). At the moment Phase III
65645-32-1 | (R)-4-(1-Aminoethyl)aniline dihydrochloride
(Catalog# : 90721)
Coming soon!
637027-25-9 | (R)-Methyl piperazine-2-carboxylate dihydrochloride
(Catalog# : 81818)
Coming soon!
68252-28-8 | (R)-Oxiracetam
(Catalog# : 52814)
(R)-Oxiracetam is the (R)-enantiomer of the nootropic drug oxiracetam. Oxiracetam (IS
656820-32-5 | Reversine
(Catalog# : 52515)
Reversine, a small synthetic purine analogue (2,6-disubstituted purine), is a potent
68941-21-9 | SKF-91488 HCl
(Catalog# : 20662)
SKF 91488 dihydrochloride is a homolog of dimaprit.
63388-44-3 | SJB2-043
(Catalog# : 2071609)
SJB2-043 is an inhibitor of USP1 target ID1 degradation in leukemic cells.
697235-38-4 | Silvestrol
(Catalog# : 192278)
Silvestrol, a member of flavagline family of natural products from the genus of Aglai
614749-78-9 | SM16
(Catalog# : 192215)
SM16 is a novel Type I TGF-β signaling inhibitor.
62717-42-4 | SKF-38393 hydrochloride
(Catalog# : 17011707)
SKF-38393, aslo known as (+/-)-SKF-38393, is a synthetic compound of the benzazepine
627908-92-3 | SU14813
(Catalog# : 011912)
SU14813 is an oral, multitargeted tyrosine kinase inhibitor (TKI) targeting vascular
627536-09-8 | SD-208
(Catalog# : 011304)
SD-208 is a potent, orally active ATP-competitive transforming growth factor- recepto
62996-74-1 | Staurosporine
(Catalog# : 010601)
Staurosporine is a prototypical potent ATP-competitive kinase inhibitor with IC50 of
676479-06-4 | Sembragiline
(Catalog# : 122921)
Coming soon!
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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).