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Cytoskeletal Signaling
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联系我们
+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
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
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
分子砌块
Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
Fluorides
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Iodos
Nitro Compounds
Oxazoles
Peg Linkers
Phenols
Piperidines
Pyridines
Pyrimidines
Quinolines
Sulfonamides
Thiazoles
Trifluoroborates
Other Azoles
Other Heterocycles
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Cas号索引 1
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Cas号索引 1
106463-17-6 | 盐酸坦索罗辛
(Catalog# : 17109008)
盐酸坦索罗辛是一个强有力的和选择性α1a肾上腺素能受体拮抗剂
1033040-23-1 | TPO agonist 1
(Catalog# : 6111515)
TPO agonist 1 can increase production of platelets by stimulating the TPO receptor in
1604810-83-4 | THZ1
(Catalog# : 6111013)
THZ1 is a novel selective and potent covalent CDK7 inhibitor with IC50(binding affini
1002789-86-7 | TZ9
(Catalog# : 611934)
TZ9 is a novel inhibitor of Rad6 ubiquitin conjugating enzyme(E2 enzyme); inhibits MD
1621523-07-6 | THZ1-R
(Catalog# : 611926)
THZ1-R is a non-cysteine reactive analog, which displays diminished activity for CDK7
1532533-78-0 | TGR-1202 hydrochloride
(Catalog# : 611905)
TGR-1202 hydrochloride is an orally available, next generation PI3Kdelta inhibitor, i
1532533-67-7 | TGR-1202
(Catalog# : 611904)
TGR-1202 is an orally available, next generation PI3Kdelta inhibitor, inhibits PI3K a
104987-11-3 | Tacrolimus
(Catalog# : 161009006)
It is also used in a topical preparation in the treatment of atopic dermatitis (eczem
103300-74-9 | Taltirelin
(Catalog# : 16071029)
Taltirelin
1314891-22-9 | TMP-195
(Catalog# : 16071020)
TMP-195
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
175591-09-0 | Tapentadol hydrochloride
(Catalog# : 010407)
Tapentadol Hcl is a centrally acting oral analgesic with opioid and adrenergic activi
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
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产品分类
信号通路
-- 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
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
-- 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
----
RXFP 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
----
UGT
----
MMP
----
ATP Citrate Lyase
-- 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
----
Glutaminase
-- 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
-- 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
----
Potassium Channel
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
-- PROTAC
----
Molecular Glues
抑制剂/受体激动剂
中间体
分子砌块
--
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
新产品
天然化合物
最新产品
667411-04-3 | TRPM4-IN-2
(Catalog# : 24147)
TRPM4-IN-2 (NBA) is a potent transient receptor potential melastatin 4 (TRPM4) inhibi
1534-35-6 | Isolithocholic Acid
(Catalog# : 24146)
Isolithocholic acid is a bile acid that is formed via microbial metabolism of lithoch
877768-84-8 | H2-Gamendazole
(Catalog# : 24145)
H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
2095432-28-1 | CPI-455 HCl
(Catalog# : 24144)
CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
1215115-03-9 | KH-3
(Catalog# : 24143)
KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
2097938-74-2 | Stafib-2
(Catalog# : 24142)
Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b, with
2032123-28-5 | TCRS-417
(Catalog# : 24141)
TCRS-417 (T417) is a small molecule compound capable of docking to the interface betw
1096144-06-7 | PST3 1a
(Catalog# : 24140)
PST3 1a is a Novel selective inhibitor of the N-acetylglucosamine glycosyltransferase
2225824-53-1 | YTX-465
(Catalog# : 24139)
YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
944808-88-2 | CAY10566
(Catalog# : 10403)
Coming soon!