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抑制剂/受体激动剂
Angiogenesis
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Apoptosis
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Metabolism
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Aldehydes
Amines
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Anilines
Boronic Acids
Bromides
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Catalysts
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Deuterated
Fluorides
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Indoles and Oxindoles
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+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
Antibody-drug Conjugate/ADC Related
Microbiology
Others
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
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联系我们
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Cas号索引 5
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Cas号索引 5
501692-44-0 | Odevixibat
(Catalog# : 20600)
Odevixibat, also known as AZD 8294, is a potent, once-daily, non-systemic ileal bile
502887-71-0 | OUN87710
(Catalog# : 2051503)
OUN87710, also known as MMP-9-IN-1 is a specific matrix metalloproteinase-9 (MMP-9) i
579-13-5 | 寡霉素A
(Catalog# : 186154)
寡霉素A,又称 MCH 32,是一种ATP合酶抑制剂。
50-56-6 | 催产素
(Catalog# : 17030805)
催产素是一种药物和荷尔蒙。作为一种药物,它被用来引起子宫收
50743-32-3 | 4-oxo-6-propan-2-ylchromene-3-carbonitrile
(Catalog# : 91412)
The related API: AmoxanoxThe related intermediates: ethyl 2-amino-5-oxo-7-propan-2-yl
56461-20-2 | 1-oxo-2,3-dihydroindene-4-carboxylic acid
(Catalog# : 81937)
Coming soon!
5431-44-7 | 吡啶-2,6-二甲醛
(Catalog# : S-204148)
58-60-6 | Puromycin Aminonucleoside
(Catalog# : 1791310)
嘌呤霉素,也被称为PAN,NSC3056,在人类肾小球疾病的研究和肾小
586379-66-0 | PH-797804
(Catalog# : 17030914)
PH-797804是一种有效的p38 mit原活化蛋白(MAP)激酶的选择性抑制剂。P
5608-24-2 | PRIMA-1
(Catalog# : 16122770)
PRIMA-1 is a mutant p53 reactivator. It induces apoptosis and inhibits growth of huma
593960-11-3 | PIK-93
(Catalog# : 160926009)
PIK-93 is a potent PI3K inhibitor. PIK93 selectively inhibits the type III PI 4-kinas
59566-45-9 | 2-Pyrimidineacetonitrile (9CI)
(Catalog# : 101903)
Coming soon!
571190-30-2 | Palbociclib
(Catalog# : 52001)
Palbociclib (PD-0332991) is an orally available pyridopyrimidine-derived cyclin-depen
57452-98-9 | (R)-Praziquantel
(Catalog# : 20655)
(R)-Praziquantel is an active enantiomer of praziquantel that acts as a potent anthel
592542-59-1 | Rigosertib
(Catalog# : 690120)
Rigosertib(ON-01910) is a multi-kinase inhibitor and a selective anti-cancer agent, w
5552292-08-7 | Rolapitant游离
(Catalog# : 185152)
Rolapitant,也被称为SCH-619734,是一种口服生物可用的,具有中央作
575474-82-7 | R112
(Catalog# : 031003)
R112 is an ATP-competitive inhibitor of Syk kinase with a Ki of 96 nM. R112 inhibits
518048-05-0 | Raltegravir
(Catalog# : 010412)
Raltegravir is a pyrrolidinone derivative and HIV INTEGRASE INHIBITOR that is used in
572924-54-0 | Ridaforolimus
(Catalog# : 123018)
Ridaforolimus is a selective mTOR inhibitor with IC50 of 0.2 nM; while not classified
552292-08-7 | Rolapitant
(Catalog# : 122804)
Rolapitant is a potent, highly selective, long-acting Neurokinin-1 (NK-1) receptor an
500287-72-9 | Rilpivirine
(Catalog# : 111904)
Rilpivirine is a pharmaceutical drug, developed by Tibotec, for the treatment of HIV
57233-86-0 | (R)-alpha-Methyl-4-nitrobenzylamine hydrochloride
(Catalog# : 80320)
Coming soon!
528587-70-4 | (1S,5R)-1-(3-fluorophenyl)-3-oxabicyclo[3.1.0]hexan-2-one
(Catalog# : 2091205)
52029-86-4 | STO-609
(Catalog# : 17021319)
STO-609是一个特定抑制剂。
522650-83-5 | SW044248
(Catalog# : 17011714)
SW044248是一个强有力的和选择性拓扑异构酶抑制剂。SW044248杀死大
555-66-8 | 6-姜烯酚
(Catalog# : 17011703)
6-姜烯酚, 是姜的一种辛辣成分,类似于姜酚的化学结构。
521984-48-5 | SIS3
(Catalog# : 16122721)
SIS3, a novel specific inhibitor of Smad3, inhibits TGF- and activin signaling by sup
53123-88-9 | Sirolimus (Rapamycin)
(Catalog# : 161009003)
In cells, sirolimus binds to the immunophilin FK Binding Protein-12 (FKBP-12) to gene
501951-42-4 | SB-705498
(Catalog# : 011921)
SB-705498 is a potent, selective and orally bioavailable transient receptor potential
502632-66-8 | Sonolisib
(Catalog# : 122944)
Sonolisib is a small-molecule wortmannin analogue inhibitor of the alpha, gamma, and
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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
-- 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
2750895-97-5 | MTX115325
(Catalog# : 186264)
MTX115325是一种强效、选择性、脑渗透性USP30抑制剂,具有良好的类
2166616-75-5 | LY-3381916
(Catalog# : 193123)
LY-3381916是一种强效的、选择性的、脑透性的IDO1活性抑制剂,与缺
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim(BHV-7000)是Kv7.2/7.3钾通道(KCNQ2/3)的口服小分子激活剂,
2488609-21-6 | DS68591889
(Catalog# : 25158)
DS68591889 (PTDSS1i) 特异性抑制 PTDSS1,而 PTDSS1 可催化丝氨酸掺入 PC。
944808-88-2 | CAY 10566
(Catalog# : 10403)
CAY 10566是一种强效的选择性SCD-1抑制剂。
2308520-97-8 | Cadefrecitinib (GLPG-3667)
(Catalog# : 20509)
Cadefrecitinib(GLPG-3667)是一种口服小分子TYK2激酶抑制剂,目前正处
1802735-28-9 | QBS10072S
(Catalog# : 25190)
QBS10072S 是一种血脑屏障 (BBB) 渗透剂,由细胞毒性化疗结构域 N-双
2377000-84-3 | Dencatistat (STP938)
(Catalog# : 25177)
Dencatistat 是一种口服生物可利用的小分子胞苷三磷酸合酶 1 (CTPS1)
1898207-64-1 | DS-1001b
(Catalog# : 25178)
DS-1001 是一种口服的脑渗透性突变 IDH1 选择性抑制剂。
1016340-64-9 | Z57346765
(Catalog# : 25191)
Z57346765 是一种 PGK1 特异性抑制剂,可降低 PGK1 糖酵解中代谢酶的