武汉永璨生物科技有限公司
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分子砌块
Aldehydes
Amines
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Anilines
Boronic Acids
Bromides
Carboxes
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Deuterated
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Indoles and Oxindoles
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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
技术服务
定制合成
工艺研发
订购信息
联系我们
公司简介
联系我们
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产品名字索引 S
(2S)-4-[(2-methylpropan-2-yl)oxycarbonyl]piperazine-2-carboxylic acid
(Catalog# : 81816, Cas# :
848482-93-9
)
Coming soon!
(S)-Benzyl 2-methylpiperazine-1-carboxylate hydrochloride
(Catalog# : 81813, Cas# :
1217720-49-4
)
Coming soon!
(S)-4-N-Boc-2-methylpiperazine
(Catalog# : 81731, Cas# :
147081-29-6
)
Coming soon!
(S)-Piperazine-2-carboxylic acid dihydrochloride
(Catalog# : 81718, Cas# :
158663-69-5
)
Coming soon!
(1S)-1-(4-chloro-3-methylphenyl)ethanamine
(Catalog# : 81017, Cas# :
943760-74-5
)
Coming soon!
(1S)-1-(4-fluoro-3-methoxyphenyl)ethanamine
(Catalog# : 81015, Cas# :
870849-59-5
)
Coming soon!
SR9243
(Catalog# : 80701, Cas# :
1613028-81-1
)
SR9243 is a LXR inverse agonist that induces LXR-corepressor interaction, which shows
Sapitinib(AZD8931)
(Catalog# : 60301, Cas# :
848942-61-0
)
AZD8931(Sapitinib)is a novel potent reversible small molecule epidermal growth factor
SU6656
(Catalog# : 52754, Cas# :
330161-87-0
)
SU 6656 is a selective inhibitor of Src kinases, Including Src, Yes, Lyn, and Fyn (IC
SBE13 Hydrochloride
(Catalog# : 52751, Cas# :
1052532-15-6
)
SBE13 Hcl is a potent and selective PLK1 with IC50 of 0.2 nM; no inhibition om Aurora
SGI-1027
(Catalog# : 52737, Cas# :
1020149-73-8
)
SGI-1027 is a potent and selective inhibitor of DNA methyltransferase (DNMT) with IC5
SB225002
(Catalog# : 52714, Cas# :
182498-32-4
)
SB225002 is a potent and selective non-peptide inhibitor of CXCR2 with IC50 of 22 nM;
SU9516
(Catalog# : 52579, Cas# :
377090-84-1
)
SU-9516 is a selective CDK2 inhibtor with IC50 of 22 nM; less potent for CDK1/CDK4(IC
SCH900776
(Catalog# : 52575, Cas# :
891494-63-6
)
SCH900776 is a potent, selective and orally bioavailable inhibitor of checkpoint kina
Selumetinib
(Catalog# : 52571, Cas# :
606143-52-6
)
Selumetinib (AZD6244; ARRY-142886) is a potent, highly selective MEK1 inhibitor with
Siramesine hydrochloride
(Catalog# : 52549, Cas# :
224177-60-0
)
Siramesine(Lu 28-179) Hcl is a selective sigma-2 receptor agonist, which has been sho
Siramesine
(Catalog# : 52548, Cas# :
147817-50-3
)
Siramesine(Lu 28-179) is a selective sigma-2 receptor agonist, which has been shown t
S1RA
(Catalog# : 52546, Cas# :
878141-96-9
)
S1RA(E-52862) is a potent and selective sigma-1 receptor(1R, Ki=17 nM) antagonist, sh
SMI-4a
(Catalog# : 52537, Cas# :
438190-29-5
)
SMI-4a is a selective ATP-competitive Pim-1 kinase inhibitor with an IC50 of 21 nM fo
SKLB610
(Catalog# : 52536, Cas# :
1125780-41-7
)
SKLB610, a novel multi-targeted inhibitor, inhibits angiogenesis-related tyrosine kin
StemRegenin 1
(Catalog# : 52531, Cas# :
1227633-49-9
)
StemRegenin 1(SR1) is an antagonist of the aryl hydrocarbon receptor.SR1 is the first
S0859
(Catalog# : 52507, Cas# :
1019331-10-2
)
S0859, an N-cyanosulphonamide compound, reversibly inhibit NBC-mediated pH(i) recover
SRPIN340
(Catalog# : 52210, Cas# :
218156-96-8
)
SRPIN340 is a serine/arginine-rich protein kinase (SRPK)-specific inhibitor with an I
5S rRNA modificator
(Catalog# : 52243, Cas# :
1415238-77-5
)
5S rRNA modificator is a suitable electrophile for 2-hydroxyl acylation on structured
SB431542
(Catalog# : 52312, Cas# :
301836-41-9
)
SB431542 is a potent and selective inhibitor ofALK5withIC50of 94 nM, 100-fold more se
Salirasib
(Catalog# : 52106, Cas# :
162520-00-5
)
Salirasib(S-Farnesylthiosalicylic aci) is an S-farnesyl cysteine analog that interfer
SNS-032 ( BMS-387032 )
(Catalog# : 52105, Cas# :
345627-80-7
)
SNS-032 has firstly been described as a selective inhibitor ofCDK2withIC50of 48 nM an
SNS-314 Mesylate
(Catalog# : 52102, Cas# :
1057249-41-8
)
SNS-314 Mesylate is a potent and selective inhibitor ofAurora A,Aurora BandAurora Cwi
Semaxanib (SU5416)
(Catalog# : 51803, Cas# :
204005-46-9
)
Semaxanib (SU5416) is a potent and selectiveVEGFR(Flk-1/KDR) inhibitor withIC50of 1.2
SSR128129E
(Catalog# : 51608, Cas# :
848318-25-2
)
SSR128129E is an orally-active and allostericFGFR1inhibitor withIC50of 1.9 M, while n
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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
-- 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
-- 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)
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
-- 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
CT1812 ( Zervimesine )
(Catalog# : 193283, Cas# :
1802632-22-9
)
CT-1812是一种同类首创的、可口服的sigma-2/PGRMC1拮抗剂(αβ寡聚体
BLU-808
(Catalog# : 26A024, Cas# :
3041025-10-6
)
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
Zedoresertib
(Catalog# : 26A023, Cas# :
2243882-74-6
)
Zedoresertib(Debio 0123)是一种脑渗透剂,高选择性WEE1激酶抑制剂。
BEN-28010
(Catalog# : 26A022, Cas# :
3033961-38-2
)
BEN-28010是一种自由脑渗透剂,强效且具有选择性的CHK1抑制剂。
4-((2-(甲氨基)-6-(2,2,2-三氟乙基)噻吩并[2,3-d]嘧啶-4-基)氨基)哌啶-1-甲酸叔丁酯
(Catalog# : 26B007, Cas# :
3107291-07-3
)
Muvalaplin
(Catalog# : 20528, Cas# :
2565656-70-2
)
Muvalaplin是一种小分子,通过干扰载脂蛋白(a)与载脂蛋白B100的结合
MAT2A-IN-22
(Catalog# : 26A021, Cas# :
2925330-18-1
)
MAT2A-IN-22 (Compound 29-1) 是一种可透过血脑屏障的和口服有效的 MAT2A
AD-8007
(Catalog# : 26A018, Cas# :
1497439-74-3
)
AD-8007是一种选择性且可穿透血脑屏障的乙酰辅酶A合成酶2(ACSS2)
ZY-444
(Catalog# : 26A020, Cas# :
1802650-31-2
)
ZY-444是一种通过抑制PC活性发挥抗癌作用的药物。
AD-5584
(Catalog# : 26A019, Cas# :
2306525-79-9
)
AD-5584是一种新型脑渗透性ACSS2抑制剂。