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Membrane Transporter/Ion Channel
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+86-17702719238
sales@sun-shinechem.com
Home
Inhibitors&Agonists
Angiogenesis
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
1041852-85-0 | AZD7507
(Catalog# : 1812294)
AZD7507 is a potent and selective CSF-1R inhibitor (32 nM cell activity), AZD7507 is
1704801-24-0 | AX-024 HCl
(Catalog# : 181254)
AX-024 is an orally available inhibitor of the TCR-Nck interaction that selectively i
148741-30-4 | AG 879
(Catalog# : 1811303)
AG-879 is a tyrphostin compound that inhibits nerve growth factor-dependent TrkA tyro
1146699-66-2 | Avagacestat
(Catalog# : 1811283)
Avagacestat, also known as BMS-708163, is an oral GSI designed for selective inhibiti
1360460-82-7 | Anlotinib HCl ( AL-3818 )
(Catalog# : 1811211)
Anlotinib is a novel oral tyrosine kinase inhibitor (TKI) targeting c-kit, platelet-d
1240299-33-5 | AZD-3514
(Catalog# : 1810251)
AZD-3514 is a potent androgen receptor downregulator with potential anticancer cancer
1698055-85-4 | ARS-1620
(Catalog# : 1810222)
ARS-1620 is an atropisomeric selective KRAS-G12C inhibitor with desirable pharmacokin
1175526-27-8 | AM211
(Catalog# : 1810173)
AM-211 is a novel and potent antagonist of the prostaglandin D2 receptor type 2.
1190217-35-6 | ASP7663
(Catalog# : 187123)
ASP7663 is an orally bioavailable selective TRPA1 activator.
1188890-28-9 | ABT 702 Dihydrochloride
(Catalog# : 18791)
ABT 702 Dihydrochloride is a potent non-nucleoside adenosine kinase inhibitor, select
1346623-17-3 | Avacopan
(Catalog# : 18761)
Avacopan, also known as CCX168, is an orally active, selective and potent C5aR inhibi
133550-35-3 | AG-494
(Catalog# : 186273)
AG-494, also known as Tyrphostin AG-494, is an inhibitor of epidermal growth factor r
1869912-39-9 | AZD5153
(Catalog# : 186254)
AZD5153 is a potent bivalent triazolopyridazine based Bromodomain and Extraterminal (
1818885-28-7 | ARV-825
(Catalog# : 185253)
ARV-825 is a PROTAC (proteolysis-targeting chimera). ARV-825 exerts superior lethal a
1637771-14-2 | Alobresib
(Catalog# : 185222)
Alobresib is an antineoplastic drug candidate.
1467013-03-3 | Adavivint
(Catalog# : 185221)
Adavivint is a Wnt pathway inhibitor and immunomodulator drug candidate.
1889279-16-6 | A-485
(Catalog# : 185211)
A-485 is a potent and selective HAT inhibitor of p300/CBP in vitro with an IC50 of 10
1883727-34-1 | AMG-176
(Catalog# : 185185)
AMG-176 is an inhibitor of induced myeloid leukemia cell differentiation protein MCL-
1217201-17-6 | A-350619 HCI
(Catalog# : 185183)
A-350619 hydrochloride is an activator of soluble guanylyl cyclase (sGC).
1253573-53-3 | AMG-511
(Catalog# : 18542)
AMG-511 is a potent and selective pan class I PI3K inhibitor.
1186206-79-0 | ALW-II-41-27
(Catalog# : 1842813)
ALW-II-41-27 is a Eph receptor tyrosine kinase inhibitor.
1321514-06-0 | AZD4635
(Catalog# : 184289)
AZD-4635, also known as HTL-1071, is an orally available, small molecule adenosine A2
1229453-99-9 | Acrizanib
(Catalog# : 184181)
Acrizanib, also known as LHA510, is a potent and selective angiogenesis inhibitor and
1032570-98-1 | 2-amino-3-methoxy-4-(3-morpholin-4-ylpropoxy)benzonitrile
(Catalog# : 184163)
2-amino-3-methoxy-4-(3-morpholin-4-ylpropoxy)benzonitrile is a drug intermediate.
1058156-90-3 | Anlotinib
(Catalog# : 184132)
Anlotinib, also known as AL3818, is a receptor tyrosine kinase (RTK) inhibitor with p
1125758-85-1 | A-804598
(Catalog# : 184125)
A-804598 is a P2X7 selective, competitive antagonist.
185991-07-5 | AMD3465 HCl salt
(Catalog# : 184310)
AMD3465 is a novel CXCR4 receptor antagonist with potential anticancer and anti-HIV a
1220646-23-0 | AVN-492
(Catalog# : 18425)
AVN-492 is a potent and selective 5-HT6R Antagonist. AVN-492 demonstrates good in vit
1173154-32-9 | ALB-127158A
(Catalog# : 18424)
ALB-127158A,又名ALB-127158(a),是治疗肥胖的MCH1拮抗剂。临床前的研
1492952-76-7 | Asciminib ( ABL001 )
(Catalog# : 1711222)
Asciminib, Bulk in stock, contact us by email for the quotation. Kg scale intermediat
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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
-- 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
-- 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
-- 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
-- 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
1898206-17-1 | Safusidenib
(Catalog# : 25149)
Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl
2803470-63-3 | HC-7366
(Catalog# : 25076)
HC-7366 is a potent and selective activator of the general control nonderepressible 2
2377000-84-3 | Dencatistat
(Catalog# : 25177)
Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph
146426-40-6 | Flavopiridol ( Alvocidib )
(Catalog# : 237071)
Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
2201056-66-6 | AG-270
(Catalog# : 25176)
MAT2A Inhibitor AG-270 is an orally available small molecule inhibitor of methionine
618913-30-7 | AZD-5904
(Catalog# : 181121)
AZD5904 is a potent orally bioavailable MPO inhibitor. In preclinical studies, AZD590
2035010-37-6 | ALT-007
(Catalog# : 25157)
ALT-007 is an orally bioavailable SPT inhibitor that is more potent than myriocin, sa
1633666-49-5 | Nizubaglustat ( Synonyms: AZ-3102 )
(Catalog# : 25175)
Nizubaglustat (AZ-3102) is an oral small molecule which inhibits glucosylceramide syn
2736508-60-2 | Catadegbrutinib (Synonyms: BGB-16673; BTK-IN-29)
(Catalog# : 25174)
209733-45-9 | Anatibant (Synonyms: LF 16-0687; XY-2405)
(Catalog# : 25173)