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Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
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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
Antibody-drug Conjugate/ADC Related
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
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联系我们
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+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
Antibody-drug Conjugate/ADC Related
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
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On Sale
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Cas号索引 1
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Cas号索引 1
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
1033805-28-5 | Telotristat
(Catalog# : 120421)
Telotristat is the active metabolite of LX1606(Telotristat etiprate), which is an ora
1310693-92-5 | Tubastatin A HCl
(Catalog# : 110228)
Tubastatin A is a potent and selective HDAC6 inhibitor. Demonstrates 1093-fold select
1252003-15-8 | Tubastatin A
(Catalog# : 110225)
Tubastatin A is a potent HDAC6 inhibitor with an IC50 value of 15 nM. Comparatively,
1415379-56-4 | T-807( AV1451)
(Catalog# : 102910)
T807( AV1451) 是一种在阿尔茨海默病治疗中新颖的tau蛋白靶向PET示踪
1374107-54-6 | THK-5107
(Catalog# : 102909)
Coming soon!
1374107-64-8 | THK5105
(Catalog# : 102906)
Coming soon!
1573029-17-0 | THK-523
(Catalog# : 102905)
Coming soon!
174634-09-4 | TAS-103 dihydrochloride
(Catalog# : 101904)
TAS-103, also known as BMS-247615, is a quinoline derivative that displays antitumor
1341200-45-0 | TP-0903(Dubermatinib)
(Catalog# : 101207)
TP-0903 is a potent and selective Axl kinase inhibitor with IC50 of 27 nM.
162635-04-3 | Temsirolimus
(Catalog# : 101205)
Temsirolimus is a recently developed mTOR inhibitor. with improved aqueous solubility
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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
----
Ketohexokinase
-- 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
--
Antibody-drug Conjugate/ADC Related
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
2521285-05-0 | Sevabertinib ( 别名:BAY-2927088 )
(Catalog# : 25079)
Sevabertinib ( BAY-2927088 )是一种口服非共价酪氨酸激酶受体抑制剂(
2387898-69-1 | ATH434 mesylate
(Catalog# : 20638)
ATH434 是一种口服药物,旨在抑制与神经变性有关的病理蛋白的聚
2833703-74-3 | LOXO-435
(Catalog# : 25080)
LOXO-435是FGFR3的选择性小分子抑制剂。它对野生型和致癌激活的FGF
2790567-82-5 | AMG-193
(Catalog# : 24017)
AMG-193是安进公司开发的一种口服小分子甲硫腺苷协同PRMT5酶抑制剂
2102501-84-6 | PF-06835919 ( MDK-1846 )
(Catalog# : 193264)
MDK1846是一种强效的酮己糖激酶(KHK)抑制剂。
2671128-05-3 | FHD-286
(Catalog# : 20471)
FHD-286 is an oral, small-molecule, selective, allosteric inhibitor of BRG1 and BRM i
3002056-30-3 | NST-628
(Catalog# : 24058)
NST-628 是具有血脑屏障渗透性的 MAPK 通路分子胶,能够抑制 RAF 磷
2893778-31-7 | PHGDH-IN-3
(Catalog# : 25077)
PHGDH-IN-3 is an orally active phosphoglycerate dehydrogenase (PHGDH) inhibitor.
2882165-79-7 | CFT1946
(Catalog# : 25078)
CFT1946 是一种口服生物可利用的小分子降解剂,可降解实体瘤中的
68238-36-8 | 异硫蓝
(Catalog# : 178017)
Isosulfan blue 是一种用于淋巴管造影中淋巴管识别的蓝色染料。Isos