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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
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Anti-infection
Apoptosis
Autophagy
Cell Cycle
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DNA Damage
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Immunology & Inflammation
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MAPK
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Cas Index 6
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Cas Index 6
688348-25-6 | PDM-2
(Catalog# : 2061301)
PDM-2 is an analog of resveratrol acting as a potent and selective aryl hydrocarbon r
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
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
690681-65-3 | SABA1
(Catalog# : 25053)
SABA1 is an antibacterial agent against Pseudomonas aeruginosa and Escherichia coli.
64-86-8 | (S)-Colchicine
(Catalog# : 24049)
(S)-Colchicine is a medication most commonly used to treat gout. Colchicine inhibits
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
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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
1820812-16-5 | TAK-071
(Catalog# : 186269)
TAK-071 is a muscarinic M1 receptor positive allosteric modulator.
2750895-97-5 | MTX115325
(Catalog# : 186264)
MTX115325 is a potent, selective, brain-penetrant USP30 inhibitor with good drug-like
2166616-75-5 | LY-3381916
(Catalog# : 193123)
LY-3381916 is a potent, selective and brain penetrated inhibitor of IDO1 activity, bi
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim (BHV-7000) is an oral, small-molecule activator of Kv7.2/7.3 potassium chann
2488609-21-6 | DS68591889
(Catalog# : 25158)
DS68591889 (PTDSS1i) specifically inhibits PTDSS1, which catalyzes serine incorporati
944808-88-2 | CAY 10566
(Catalog# : 10403)
CAY 10566 is a potent selective SCD-1 inhibitor.
2308520-97-8 | Cadefrecitinib (GLPG-3667)
(Catalog# : 20509)
Cadefrecitinib (GLPG-3667) is an oral, small molecule inhibitor of the TYK2 kinase in
1802735-28-9 | QBS10072S
(Catalog# : 25190)
QBS10072S isa blood-brain-barrier (BBB) penetrative agent composed of a cytotoxic che
2377000-84-3 | Dencatistat
(Catalog# : 25177)
Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
1898207-64-1 | DS-1001b
(Catalog# : 25178)
DS-1001 is an oral brain-penetrant mutant IDH1 selective inhibitor.