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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
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分子砌块
Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
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Deuterated
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Peg Linkers
Phenols
Piperidines
Pyridines
Pyrimidines
Quinolines
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Cas号索引 1
1809336-39-7 | Valemetostat
(Catalog# : 192141)
Valemetostat是一种抗肿瘤药物。
1360457-46-0 | Vaborbactam
(Catalog# : 181253)
Vaborbactam,也称为RPX7009, 是一种有效且具有选择性的β-内酰胺酶抑
1391737-01-1 | VU0463271
(Catalog# : 1810151)
VU0463271抑制协同转运蛋白KCC2。
1357362-02-7 | Vafidemstat
(Catalog# : 18891)
Vafidemstat又称ORY 2001,是一种赖氨酸特异性组蛋白去甲基化酶(LSD1)
129497-78-5 | Verteporfin
(Catalog# : 187201)
Verteporfin,也被称为苯卟啉衍生物A或BPD-MA,是一种苯卟啉衍生物,
1352792-74-5 | Verinurad
(Catalog# : 18583)
Verinurad,也称为RDEA3170,是一种有机阴离子转运体URAT1 (SLC22A12)抑制
1451993-15-9 | VU0467154
(Catalog# : 18576)
VU0467154 is a positive allosteric modulator of theM4 muscarinic acetylcholine recept
1535212-07-7 | Voxilaprevir
(Catalog# : 18572)
Voxilaprevir是一种丙型肝炎病毒(HCV)非结构蛋白3/4A蛋白酶抑制剂。
1025504-45-3 | Valbenazine
(Catalog# : 1783010)
Valbenazine,也叫 NBI- 98854和MT - 5199,是一种有效的选择性的VMAT2抑制
1000023-04-0 | Voruciclib
(Catalog# : 178306)
Voruciclib,又称P1446A-05,是一种蛋白质激酶抑制剂,专门针对细胞
1446321-46-5 | Voxelotor(GBT440, GTX011)
(Catalog# : 178916)
Voxelotor(GBT440,GTX011)是一种新的小分子化合物,它能增加血红蛋白与
1350653-20-1 | 维利西呱
(Catalog# : 2017886)
维利西呱,也称为BAY1021189或BAY10-21189, 是一种有效和口服活性sGC刺
1562396-65-9 | VX-984 (M9831)
(Catalog# : 2017879)
VX-984, 也称为M9831,是一种ATP-竞争性抑制剂,依赖蛋白激酶(DNA-PK)的
1383716-46-8 | VPS34抑制剂1
(Catalog# : 17031001)
VPS34抑制剂1(化合物19, PIK-III类似物)是VPS34的有效和选择性抑制剂,
1377049-84-7 | 维帕他韦
(Catalog# : 17022808)
维帕他韦(VEL, GS-5816)是一种新的泛基因型丙型肝炎病毒(HCV)非结构
149647-78-9 | 伏立诺他
(Catalog# : 17022704)
伏立诺他(SAHA)是IC50为10nm的HDAC1 / 3抑制剂。
1000025-07-9 | Vadadustat ( AKB-6548 )
(Catalog# : 6121401)
Vadadustat (AKB-6548), a novel, titratable, oral hypoxia-inducible factor prolyl hydr
1431280-51-1 | VLX1570
(Catalog# : 611932)
VLX1570 is a competitive inhibitor of proteasome DUB activity with IC50 ranging from
1523404-29-6 | Vsp34-IN-1
(Catalog# : 011115)
Coming soon!
1232410-49-9 | VE-821
(Catalog# : 122817)
VE-821 is a potent and selective ATP competitive inhibitor of ATR with Ki/IC50 of 13
1246086-78-1 | VU 0364439
(Catalog# : 122401)
VU 0364439 is a mGlu4 positive allosteric modulator, with EC50 of 19.8 nM.
163521-12-8 | Vilazodone
(Catalog# : 122208)
Vilazodone is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A rece
163521-08-2 | Vilazodone Hydrochloride
(Catalog# : 121808)
Vilazodone Hcl is a combined serotonin specific reuptake inhibitor (SSRI) and 5-HT1A
1624602-30-7 | VR23
(Catalog# : 120423)
VR23 is a small molecule that potently inhibited the activities of trypsin-like prote
1383716-33-3 | VPS34-IN1
(Catalog# : 111016)
VPS34-IN1 is a selective inhibitor of Vps34.
1616113-45-1 | VRT-1353385
(Catalog# : 101912)
Coming soon!
1257044-40-8 | Venetoclax(ABT-199)
(Catalog# : 60101)
Venetoclax, formerly known as ABT-199(GDC-0199), is a Bcl-2-selective inhibitor with
1246560-33-7 | VS-5584
(Catalog# : 52530)
VS-5584 (SB2343) is a potent and selective dual PI3K/mTOR inhibitor for mTOR, PI3K///
1232416-25-9 | VE-822 ( Berzosertib )
(Catalog# : 51607)
VE-822(Berzosertib), an analogue of VE-821 with increased potency and selectivity aga
107355-45-3 | WIN54954
(Catalog# : 20280)
WIN54954 is a broad-spectrum antipicornavirus drug.
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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
-- 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
----
Reactive-Oxygen-Species-ROS
-- 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
-- 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)
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
-- 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
----
Lipase
-- 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
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
204005-46-9 | Semaxanib (SU5416)
(Catalog# : 51803)
Semaxanib (SU5416) is a potent and selectiveVEGFR(Flk-1/KDR) inhibitor withIC50of 1.2
845959-55-9 | Mitoquinol mesylate (MitoQ)
(Catalog# : 26A042)
Mitoquinol mesylate (MitoQ) 是一种线粒体靶向抗氧化剂,具体而言,它
1246960-09-7 | SPG-601 ( VSN-16R )
(Catalog# : 24042)
SPG-601(原名VSN-16R)是一种口服给药、同类首创的小分子药物,是
1421438-81-4 | LY3039478 ( Crenigacestat )
(Catalog# : 17021601)
LY3039478 ( Crenigacestat ) 是一种选择性 NOTCH1 抑制剂,通过阻断 VEGFA/
72882-78-1 | PF-9366
(Catalog# : 184107)
PF-9366是一种新型的人蛋氨酸腺苷转移酶2A (Mat2A),肝外同种型。
2925330-18-1 | MAT2A-IN-22
(Catalog# : 26A021)
MAT2A-IN-22 (Compound 29-1) 是一种可透过血脑屏障的和口服有效的 MAT2A
| Pantothenate kinase-IN-3
(Catalog# : 26A041)
泛酸激酶-IN-3(亦称化合物21,https://doi.org/10.1021/acs.jmedchem.5c03452)
2361124-03-8 | Claziprotamidum ( Claziprotamide ; BBP-671 )
(Catalog# : 26A040)
Claziprotamidum(Claziprotamide;BBP-671)是一种强效、口服有效且能透过
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。
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,