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Apoptosis
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MAPK
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Bromides
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联系我们
+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
Vitamin D Related
PROTAC
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Microbiology
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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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产品名字索引 D
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产品名字索引 D
2,3-dimethyl-2,5-cyclohexadiene-1,4 dione
(Catalog# : 17011908, Cas# :
526-86-3
)
2,5-Cyclohexadiene-1,4-dione,2,3-dimethyl-
4,5-Dihydro-2-(Methylthio)-1H-iMidazole-1-carboxylic Acid Methyl Ester
(Catalog# : 17011907, Cas# :
60546-77-2
)
It is a new drug
Doxapram
(Catalog# : 16122937, Cas# :
309-29-5
)
Doxapram is a respiratory stimulant. Administered intravenously, doxapram stimulates
Dobutamine HCl
(Catalog# : 16122936, Cas# :
34368-04-2
)
Dobutamine is a sympathomimetic drug used in the treatment of heart failure and cardi
DM1-SMe
(Catalog# : 16122935, Cas# :
138148-68-2
)
DM1-SMe is a potent maytansinoid microtubular inhibitor and an unconjugated DM1 as a
DM1-SMCC
(Catalog# : 16122934, Cas# :
1228105-51-8
)
DM1-SMCC is DM1 with a reactive linker SMCC, which can react with antibody to make an
Dimethylenastron
(Catalog# : 16122932, Cas# :
863774-58-7
)
Dimethylenastron is an inhibitor of mitotic motor kinesin Eg5 (IC50 = 200 nM). Dimeth
Dihydroethidium
(Catalog# : 16122931, Cas# :
104821-25-2
)
Dihydroethidium, also known as Hydroethidine and PD-MY 003, is a cell-permeable blue
Delamanid (OPC-67683)
(Catalog# : 16122930, Cas# :
681492-22-8
)
Delamanid, also known as OPC-67683, is a drug for the treatment of multi-drug-resista
Defactinib
(Catalog# : 16122929, Cas# :
1073160-26-5
)
Defactinib, also known as VS-6063 and PF04554878, is an orally bioavailable, small-mo
Debio-1347
(Catalog# : 16122928, Cas# :
1265229-25-1
)
Debio-1347, also known as FF284 and CH5183284, is an orally bioavailable inhibitor of
Darinaparsin
(Catalog# : 16122927, Cas# :
69819-86-9
)
Darinaparsin, also know as ZIO-101 is a small-molecule organic arsenical with potenti
Daclatasvir
(Catalog# : 16122926, Cas# :
1009119-64-5
)
Daclatasvir (USAN), also known as BMS-790052 and EBP-883 (trade name Daklinza), is NS
D-64131
(Catalog# : 16122925, Cas# :
74588-78-6
)
D-64131 is a potent and selective tubulin inhibitor. D-64131 inhibits tumor cell prol
Dalbavancin HCl
(Catalog# : 16122808, Cas# :
171500-79-1
)
Dalbavancin is a novel second-generation lipoglycopeptide antibiotic. It belongs to t
Dabrafenib mesylate
(Catalog# : 16122807, Cas# :
1195768-06-9
)
Dabrafenib mesylate, also known as GSK 2118436B, is a potent and orally active B-raf
Dolutegravir Sodium
(Catalog# : 16122764, Cas# :
1051375-19-9
)
Dolutegravir is a HIV integrase inhibitor with IC50 of 2.7 nM.Dolutegravir(S/GSK13495
DCVC
(Catalog# : 6111408, Cas# :
13419-46-0
)
DCVC inhibits pathogen-stimulated TNF- in human extra placental membranes in vitro.
Danirixin
(Catalog# : 16111111, Cas# :
954126-98-8
)
Danirixin is a small molecule, non-peptide, high affinity (IC50 for CXCL8 binding = 1
Defactinib
(Catalog# : 6111019, Cas# :
1345713-71-4
)
Defactinib(VS-6063, PF-04554878)
2,3-dimethoxybenzonitrile
(Catalog# : 6111003, Cas# :
5653-62-3
)
2,3-dimethoxybenzonitrile
10-Deacetyl-7-xylosyl paclitaxel
(Catalog# : 611946, Cas# :
90332-63-1
)
10-Deacetyl-7-xylosyl paclitaxel is a Paclitaxel derivative with improved pharmacolog
Debio 0932
(Catalog# : 611938, Cas# :
1061318-81-7
)
Debio 0932 ( CUDC-305 ) is a novel heat shock protein 90 (HSP90) inhibitor trong affi
DUBs-IN-3
(Catalog# : 611929, Cas# :
924296-17-3
)
DUBs-IN-3 is a potent deubiquitinase enzyme inhibitor with IC50s of 3.1 uM for USP8;
DUBs-IN-1
(Catalog# : 611928, Cas# :
924296-18-4
)
DUBs-IN-1 is a potent deubiquitinase enzyme inhibitor with IC50s of 18 uM/0.71 uM for
DMAT
(Catalog# : 611913, Cas# :
749234-11-5
)
DMAT is a potent and specific CK2 inhibitor with an IC50 of 0.13 uM.
Dovitinib
(Catalog# : 16071106, Cas# :
405169-16-6
)
Dovitinib, also known as TKI-258 or CHIR-258, is an orally bioavailable FGFR3 inhibit
Dasotraline
(Catalog# : 16071017, Cas# :
675126-05-3
)
Dasotraline, also known as SEP-225,289, is a serotonin-norepinephrine-dopamine reupta
DeBio-1143 (AT-406)
(Catalog# : 16070501, Cas# :
1071992-99-8
)
 DeBio-1143, also known as AT-406, ARRY-334543and SM-406, is an orally bioavaila
Danoprevir
(Catalog# : 16070107, Cas# :
850876-88-9
)
Danoprevir, also known as ITMN-191 and RG-7227, is under development by InterMune Inc
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产品分类
信号通路
-- 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
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
NSD1 抑制剂 BT5
(Catalog# : 25207, Cas# :
2351225-46-0
)
BT5可有效抑制NSD1,与细胞中的SET结构域结合,并降低H3K36me2水平。
MA242 TFA
(Catalog# : 25206, Cas# :
1049704-18-8
)
MA242是一种MDM2和NFAT1双重抑制剂,可诱导MDM2自泛素化及降解,并抑
Dabogratinib ( TYRA-300 )
(Catalog# : 24073, Cas# :
2800223-30-5
)
Dabogratinib ( TYRA-300 )是一种口服选择性成纤维细胞生长因子受体3(
AF710B
(Catalog# : 25205, Cas# :
N/A
)
AF710B 是一种高效、选择性变构 M1 毒蕈碱和 σ1 受体激动剂。 AF710
MAT2A inhibitor 5
(Catalog# : 25204, Cas# :
2957874-18-7
)
MAT2A抑制剂5具有抑制MAT2A的高效力和对MTAP缺失的癌症细胞系的显著
(Rac)-AF710B
(Catalog# : 24083, Cas# :
1235733-73-9
)
AF-710B 是 σ 和 M1 毒蕈碱受体的激动剂;AF710B 是 AF710 的对映体。
Flurpiridaz-nonradiolabeled
(Catalog# : 25203, Cas# :
863888-33-9
)
Flurpiridaz是一种有前景的新型心脏PET成像示踪剂,是通过用氟-18放
Flurpiridaz-Precursor
(Catalog# : 25202, Cas# :
863888-32-8
)
现货
KL1333
(Catalog# : 25201, Cas# :
1800405-30-4
)
KL1333是一种口服的小有机分子,与NAD(P)H:醌氧化还原酶1(NQO1)
Palupiprant ( E7046 )
(Catalog# : 24055, Cas# :
1369489-71-3
)
E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece