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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
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MAPK
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Cas号索引 2
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Cas号索引 2
204697-65-4 | Olcegepant
(Catalog# : 185285)
Olcegepant,又称BIBN-4096或BIBN-4096BS,是降钙素基因相关肽1 (CGRP1)受体
288847-34-7 | OXi-4503钠
(Catalog# : 178308)
OXi-4503是一种二磷酸酯类药物,开始是从植物纤维中分离出来的,
216227-54-2 | ONT-093
(Catalog# : 17030901)
ONT-093, 也称为OC-144-093,是一种口服的P-糖蛋白泵抑制剂,用于治疗
29700-22-9 | 氧化白藜芦醇
(Catalog# : 17021324)
氧化白藜芦醇,一种天然存在的化合物,尤其在Morus alba L中发现。
202590-98-5 | OTX015
(Catalog# : 111012)
OTX-015 is a new potent BRD2/3/4 inhibitor with evident anti-proliferative activity i
270065-52-6 | 1-O-benzyl 2-O-ethyl (2S)-5-oxopyrrolidine-1,2-dicarboxylate
(Catalog# : 90103)
Coming soon!
252990-05-9 | 1-O-tert-butyl 2-O-methyl (2R)-piperazine-1,2-dicarboxylate
(Catalog# : 81726)
Coming soon!
2756333-39-6 | Palacaparib ( Synonyms: AZD-9574 )
(Catalog# : 26A053)
Palacioparib(AZD-9574)是一种口服的中枢神经系统渗透剂PARP-1抑制剂
2170608-85-0 | PZ-3022
(Catalog# : 26A039)
PZ-3022是一种别构型的PanK激活剂,能够抵消C3-CoA的抑制作用。
2759304-23-7 | Pimicotinib hydrochloride
(Catalog# : 26A003)
Pimicotinib (ABSK021) hydrochloride 是一种选择性且具有口服活性的 CSF1R
2128698-24-6 | 2-Propynamide, 3-[(3Z)-3-[[[4-[(dimethylamino)methyl]phenyl]amino]phenylmethylene]-2,3-dihydro-2-oxo-1H-indol-6-yl]-N-ethyl-
(Catalog# : 25046)
2892065-45-9 | PLX-4545
(Catalog# : 24111)
PLX-4545 是一种口服生物可利用的 IKZF2 分子胶降解剂,旨在破坏高
2416875-06-2 | 7-氯-5-(3-戊基)吡唑并[1,5-A]嘧啶
(Catalog# : 24081)
2893778-31-7 | PHGDH-IN-3
(Catalog# : 25077)
PHGDH-IN-3 is an orally active phosphoglycerate dehydrogenase (PHGDH) inhibitor.
2101700-15-4 | Pirtobrutinib
(Catalog# : 20618)
2904682-19-3 | PDS-0330
(Catalog# : 231106)
PDS-0330 是一种特异性、有效的Claudin-1抑制剂。PDS-0330 干扰 claudin-1
2253123-16-7 | Pimicotinib
(Catalog# : 20548)
Pimicotinib是一种新型的 CSF-1R 小分子抑制剂,可口服、高选择性、
260415-63-2 | PD-173955
(Catalog# : 20499)
PD-173955 is a src tyrosine kinase inhibitor. PD173955 inhibited Bcr-Abl-dependent ce
217171-01-2 | PD-173212
(Catalog# : 20468)
PD-173212 is a small molecule N-type calcium channel blocker. PD173212 fully reduced
2172870-89-0 | Paltusotine ( CRN-00808 )
(Catalog# : 20294)
Paltusotine 是一类新型的、口服、选择性、非肽类2型生长抑素受体
26305-03-3 | Pepstatin
(Catalog# : 2071607)
Pepstatin inhibits the aspartic protease endothiapepsin.
2227425-05-8 | PF-06869206
(Catalog# : 2071506)
PF-06869206 is an Orally Bioavailable Selective Inhibitors of the Sodium-Phosphate Co
26033-20-5 | 3-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE
(Catalog# : 2062020)
248282-01-1 | Paquinimod
(Catalog# : 2061706)
Paquinimod, also known as ABR‑215757, is a S100A9 inhibitor preventing S100A9 bindi
2170608-82-7 | PZ-2891
(Catalog# : 193282)
PZ-2891是一种强效的、选择性的、口服活性泛酸激酶(PANK)调制剂,
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。
2185857-97-8 | PF-06873600
(Catalog# : 191145)
PF-06873600是一种口服生物利用的细胞周期蛋白依赖性激酶(CDK)抑制
2070014-93-4 | PF-CBP1盐酸
(Catalog# : 179112)
PF-CBP1,也称为 PF06670910,是强效、高选择性的CREB结合蛋白布罗莫
25606-41-1 | 霜霉威盐酸盐
(Catalog# : 2017080115)
霜霉威盐酸盐是一种高效、广谱、氨基甲酸酯类杀菌剂。
257933-82-7 | 培利替尼
(Catalog# : 17022702)
培利替尼(EKB-569; WAY-EKB 569)是一种有效且不可逆转的IC50为38.5 nM的E
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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)
----
NEKs
-- 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
----
Methionine Adenosyltransferase (MAT)
-- 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
----
GLP Receptor
----
SSTR
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- 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
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
----
Hemoglobin
-- 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)
----
CGRP-Receptor
----
TRP-Channel
-- 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)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- 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
-- Nuclear Receptor
----
Androgen Receptor(AR)
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
--
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On Sale
新产品
天然化合物
最新产品
2417955-18-9 | Osivelotor (别名: GBT-601; GBT-021601)
(Catalog# : 26A061)
Osivelotor(同义词:GBT-601;GBT-021601)是下一代镰状血红蛋白(HbS)
2389060-50-6 | Linvemastat (别名: FP-020)
(Catalog# : 26A060)
Linvemastat(FP-020)是一种高效、选择性口服MMP-12抑制剂。
3041025-10-6 | BLU-808
(Catalog# : 26A024)
BLU-808是一种针对肥大细胞疾病的野生型c-KIT的强效且具有选择性的
1695564-98-7 | SCO-240
(Catalog# : 26A059)
SCO-240是一种研究性、口服活性和选择性生长抑素受体亚型5(SSTR5
2227154-23-4 | N-Methylamisulpride ( 别名: LB-102 )
(Catalog# : 26A058)
N-甲基咪唑胺(同义词:LB-102)是一种多巴胺D2和D3受体拮抗剂和血
1898207-64-1 | Safusidenib Erbumine
(Catalog# : 25178)
DS-1001 是一种口服的脑渗透性突变 IDH1 选择性抑制剂。
2837993-05-0 | Repinatrabit ( 别称: JNT-517 )
(Catalog# : 26A056)
Repinatrabit(JNT-517)是一种针对Phe转运蛋白SLC6A19的研究性、选择性
1361200-34-1 | Privosegtor ( 别名: OCS-05, ACT-01 )
(Catalog# : 26A055)
Privosegtor(OCS-05,ACT-01)是一种小分子拟肽、BDNF/NT-3生长因子受体
2923356-52-7 | ART-6043
(Catalog# : 26A054)
ART-6043是一种口服的DNA聚合酶θ(POLQ)小分子抑制剂。
2756333-39-6 | Palacaparib ( Synonyms: AZD-9574 )
(Catalog# : 26A053)
Palacioparib(AZD-9574)是一种口服的中枢神经系统渗透剂PARP-1抑制剂