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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
1061354-48-0 | AVN-101 HCl
(Catalog# : 2071801)
AVN-101 is a very potent 5-HT7 receptor antagonist (Ki = 153 pM), with slightly
1270084-92-8 | APX-115 freebase
(Catalog# : 2071628)
1949837-12-0 | ARV-771
(Catalog# : 2071539)
ARV-771 is a small-molecule pan-BET degrader. ARV-771 demonstrates dramatically impro
1446817-84-0 | ABX-1431
(Catalog# : 2071517)
ABX-1431 is a covalent, irreversible MGLL inhibitor. ABX-1431 is currently entering c
1572510-80-5 | AB-423
(Catalog# : 2071503)
AB-423 is a novel inhibitor of hepatitis b virus pregenomic rna encapsidation
1542020-25-6 | 2-aminopyrazolo[1,5-a]pyridine-3-carboxylic acid
(Catalog# : 202323)
114985-63-6 | 1-acetyl-5-nitro-3H-indol-2-one
(Catalog# : 2062319)
1035299-32-3 | 8-Acetyl-5-(benzyloxy)-2H-benzo[b][1,4]oxazin-3(4H)-one
(Catalog# : 2062311)
113305-94-5 | 2-Amino-5-cyanopyrazine
(Catalog# : 2062307)
1452226-14-0 | 5-amino-3,4-dimethylthieno[2,3-c]pyridazine-6-carboxylic acid
(Catalog# : 2062025)
1056901-64-4 | AT13148 intermediate(N1)
(Catalog# : 2062009)
177036-94-1 | Ambrisentan
(Catalog# : 2061308)
Ambrisentan, also known as BSF-208075 and LU-208075, is a drug indicated for use in t
186141-75-3 | A134974
(Catalog# : 204605)
A134974 is a bioactive chemical.
1375557-33-7 | A-1293201
(Catalog# : 204604)
A-1293201 is a potent and selective NAMPT inhibitor.
1219624-62-0 | A-1048400
(Catalog# : 204602)
A-1048400 is a potent and selective N-type and T-type calcium channel blocker.
1821-13-2 | A-1062
(Catalog# : 204601)
A-1062 is a resolvase-binding inhibitor. A1062 inhibits resolvase binding to the res
1103522-45-7 | Aprocitentan
(Catalog# : 112191)
Aprocitentan is an orally active, dual endothelin (ET) receptor antagonist developed
1838651-58-3 | ACT-709478
(Catalog# : 193288)
ACT-709478 is a Potent, Selective T-type Calcium Channel Blocker as a Drug Candidate
1893415-00-3 | AZD9567
(Catalog# : 193254)
AZD9567 is an oral differentiated non-steroidal selective glucocorticoid receptor mod
133825-81-7 | ATR-101 HCl
(Catalog# : 193208)
ATR-101, also known as PD-132301 (a free base) or PD-132301-2 (a HCl salt), is in cli
1613710-01-2 | ARN-3236
(Catalog# : 193192)
ARN-3236 is potent, orally active and selective SIK2 inhibitor. ARN-3236 inhibited th
1373625-34-3 | ARN 077
(Catalog# : 193134)
ARN 077 is a potent and selective N-acylethanolamine acid amidase (NAAA) inhibitor wi
156053-89-3 | Alvimopan
(Catalog# : 19382)
Alvimopan, also known as HSDB-7704 and LY246736, is a drug which behaves as a periphe
1622902-68-4 | Abrocitinib
(Catalog# : 19381)
Abrocitinib, Bulk in stock, contact us by email for the quotation. Kg scale intermedi
1312782-34-5 | AA26-9
(Catalog# : 19372)
AA26-9 is a potent and broad-spectrum serine hydrolase inhibitor. AA26-9-inhibited en
118292-41-4 | AGN-190299
(Catalog# : 19316)
Tazarotene is a retinoid prodrug which is converted to its active form, the cognate c
1126084-37-4 | ASP9521
(Catalog# : 19312)
ASP9521 is a novel, selective, orally bioavailable inhibitor of 17β-hydroxysteroid d
1345614-59-6 | AM095 sodium
(Catalog# : 191251)
AM095 is a potent LPA1 receptor antagonist because it inhibited GTPγS binding to Chi
1036404-17-7 | ARRY-797 (ARRY-371797)
(Catalog# : 191112)
ARRY-797 is an oral, selective p38 mitogen-activated protein kinase inhibitor. ARRY-7
1557267-42-1 | Abivertinib
(Catalog# : 19141)
Abivertinib, also known as AC0010 and Avitinib, is a tyrosine kinase inhibitor, antin
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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.