武汉永璨生物科技有限公司
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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
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
中间体
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定制合成
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订购信息
联系我们
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产品名字索引 S
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产品名字索引 S
SOP1812 (QN-302)
(Catalog# : 20639, Cas# :
2546091-70-5
)
QN-302 是一种 G4选择性转录抑制剂。
SEW2871
(Catalog# : 20604, Cas# :
256414-75-2
)
SEW2871 is a S1P1 agonist (sphingosine-1-phosphate type 1 receptor agonist). SEW2871
STX-721
(Catalog# : 20576, Cas# :
2765525-82-2
)
STX-721 is a next-generation, orally delivered therapy, designed with potential best-
STC-15
(Catalog# : 20549, Cas# :
2648257-56-9
)
STC-15 is a first-in-class inhibitor of RNA modification and is the first ever RNA me
(S)-1-BOC-2-甲基-[1,4]二氮杂环庚烷
(Catalog# : 20541, Cas# :
194032-32-1
)
(S)-5-fluoro-3-methylbenzo[c][1,2]oxaborol-1(3H)-ol
(Catalog# : 20522, Cas# :
2921961-53-5
)
(S)-3-氨基-3-(4-氯苯基)-丙酸
(Catalog# : 20516, Cas# :
131690-60-3
)
Samidorphan
(Catalog# : 20454, Cas# :
852626-89-2
)
Samidorphan, also known as ALKS-33 and RDC-0313, is an opioid modulator with μ-antag
Spiro[cyclohexane-1,9'(6'H)-pyrazino[1',2':1,5]pyrrolo[2,3-d]pyrimidine]-7'(8'H)-carboxylic acid, 2'-(methylthio)-6'-oxo-5'-[[(trifluoromethyl)sulfonyl]oxy]-, 1,1-dimethylethyl ester
(Catalog# : 20412, Cas# :
2170746-98-0
)
(S)-1-(6-(4-氟-1H-吡唑-1-甲基)吡啶-3-甲基)乙胺
(Catalog# : 20396, Cas# :
1980023-96-8
)
SB-4 agonist
(Catalog# : G20378, Cas# :
100874-08-6
)
SB 4 is a potent BMP4 agonist.
SEP-363856 盐酸盐
(Catalog# : 822222, Cas# :
1310422-41-3 (HCl)
)
SEP-363856 是一种新型微量胺受体 1 (TAAR1) 激动剂,具有血清素 5-HT1
SRI-37330 free base
(Catalog# : 1711224, Cas# :
2322245-42-9 (free base)
)
SRI-37330 is a novel inhibitor of TXNIP expression, decreasing glucagon secretion and
Sunvozertinib ( DZD 9008 )
(Catalog# : 20369, Cas# :
2370013-12-8
)
Sunvozertinib,也称为 DZD9008,是一种口服、强效、不可逆和选择性
SHMT-IN-2 抑制剂
(Catalog# : 20368, Cas# :
2102681-49-0
)
SHMT-IN-2 是一种丝氨酸羟甲基转移酶 (SHMT) 抑制剂,可有效抑制人
SRI-011381
(Catalog# : L20355, Cas# :
1629138-41-5
)
SRI-011381 is an agonist of the TGF-beta signaling pathway for treatment of Alzheimer
SJ-172550
(Catalog# : L20353, Cas# :
431979-47-4
)
SJ-172550, also known as MDMX Inhibitor II, is an inhibitor of MDMX that disrupts MDM
SMN-C3 抑制剂
(Catalog# : 20344, Cas# :
1449597-34-5
)
SMN-C3 是一种口服活性 SMN2 剪接调节剂。可用于脊椎肌肉萎缩 (SMA)
Stafia-1
(Catalog# : L20338, Cas# :
2582757-90-0
)
STM2457
(Catalog# : 20321, Cas# :
2499663-01-1
)
STM2457 is a highly potent and selective first-in-class catalytic inhibitor of METTL3
SRI-37330 HCl
(Catalog# : 20306, Cas# :
2322245-49-6
)
SRI-37330 hydrochloride 是一种新型 TXNIP 表达抑制剂,呈剂量依赖性抑
SM-102
(Catalog# : 21252, Cas# :
2089251-47-6
)
SM-102 is an ionizable amino lipid that has been used in combination with other lipid
Seralutinib
(Catalog# : 21238, Cas# :
1619931-27-9
)
Seralutinib,也称为 PK-10571 和 GB002,是一种新型吸入性 Pdgfr 激酶抑
Sonidegib (LDE-225)
(Catalog# : 21232, Cas# :
956697-53-3
)
Sonidegib, also known as, erismodegib, LDE225, NVP-LDE225, is an orally bioavailable
SB-366791
(Catalog# : 21230, Cas# :
472981-92-3
)
SB-366791 is a potent and selective TRPV1 antagonist. SB-366791 inhibits glutamatergi
Scriptaid
(Catalog# : 21229, Cas# :
287383-59-9
)
Scriptaid, also known as GCK 1026, is a HDAC inhibitor. Scriptaid protects against tr
SNG-1153
(Catalog# : 21228, Cas# :
1446712-19-1
)
SNG-1153 is a modulator of estrogen receptor ER-alpha36.
Seltorexant
(Catalog# : 81498, Cas# :
1293281-49-8
)
Seltorexant, also known as JNJ-42847922 and MIN-202, is a selective orexin-2 receptor
Samelisant
(Catalog# : 20123101, Cas# :
1415792-84-5
)
Samelisantis a novel, highly selective and potent small molecule oral inhibitor targe
Senaparib
(Catalog# : 20103002, Cas# :
1401682-78-7
)
Senaparib (IMP4297) is a novel agent targeting PARP (poly-ADP ribose polymerase) with
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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
-- 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
Dencatistat (STP938)
(Catalog# : 25177, Cas# :
2377000-84-3
)
Dencatistat 是一种口服生物可利用的小分子胞苷三磷酸合酶 1 (CTPS1)
DS-1001b
(Catalog# : 25178, Cas# :
1898207-64-1
)
DS-1001 是一种口服的脑渗透性突变 IDH1 选择性抑制剂。
Z57346765
(Catalog# : 25191, Cas# :
1016340-64-9
)
Z57346765 是一种 PGK1 特异性抑制剂,可降低 PGK1 糖酵解中代谢酶的
CBR-470-1
(Catalog# : 25192, Cas# :
2416095-06-0
)
CBR-470-1 是诱导 Nrf2 活性的糖酵解酶 PGK1 的抑制剂。
Safusidenib
(Catalog# : 25149, Cas# :
1898206-17-1
)
Safusidenib,也称为DS-1001,是一种口服异柠檬酸脱氢酶[NADP]细胞质(
HC-7366
(Catalog# : 25076, Cas# :
2803470-63-3
)
HC-7366 is a potent and selective activator of the general control nonderepressible 2
Flavopiridol ( 夫拉平度 )
(Catalog# : 237071, Cas# :
146426-40-6
)
Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
AG-270
(Catalog# : 25176, Cas# :
2201056-66-6
)
MAT2A 抑制剂 AG-270 是一种口服的蛋氨酸腺苷转移酶 II α (MAT2A) 小分
AZD-5904
(Catalog# : 181121, Cas# :
618913-30-7
)
AZD5904是一个有效的口服生物利用率MPO抑制剂。在临床前研究中,AZ
ALT-007
(Catalog# : 25157, Cas# :
2035010-37-6
)
ALT-007 是一种口服生物可利用的 SPT 抑制剂,比多球菌素更有效,