武汉永璨生物科技有限公司
+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
JAK/STAT
MAPK
Cytoskeletal Signaling
Cell Cycle
TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
Ubiquitin
Neuronal Signaling
NF-κB
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
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
+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
JAK/STAT
MAPK
Cytoskeletal Signaling
Cell Cycle
TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
Ubiquitin
Neuronal Signaling
NF-κB
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
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
搜索
首页
网站地图
产品名字索引 L
按首字母搜索
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
1
2
3
4
5
6
7
8
9
«
1
2
3
4
5
6
»
产品名字索引 L
Lanifibranor
(Catalog# : 184177, Cas# :
927961-18-0
)
Lanifibranor,也叫IVA-337,是一种过氧化物酶体激活受体(PPAR)激动剂
LX-2343
(Catalog# : 184131, Cas# :
333745-53-2
)
LX-2343是一种治疗阿尔茨海默病的神经保护剂。
Lazertinib
(Catalog# : 512194, Cas# :
1903008-80-9
)
Description:Lazertinib is a an orally available third-generation, selective inhibi
LYN-1604
(Catalog# : 18493, Cas# :
2088939-99-3
)
LYN-1604是一种新型的ULK1激活剂,诱导细胞死亡,参与ATF3、RAD21和c
LB42708
(Catalog# : 18443, Cas# :
226929-39-1
)
LB42708是一种有效的、口服活性和选择性的非肽基转移酶抑制剂(FT
LLY-283
(Catalog# : 184314, Cas# :
2040291-27-6
)
LLY-283是一种有效、选择的针对PRMT5的SAM-竞争性化学探针。
L-778123
(Catalog# : 1711249, Cas# :
183499-57-2
)
L-778,123 is an inhibitor of FPTase and GGPTase-I.
LW6
(Catalog# : 17101618, Cas# :
934593-90-5
)
LW6减少HIF-1alpha蛋白表达不影响hif-1beta表达。
LF3
(Catalog# : 1710164, Cas# :
664969-54-4
)
LF3是一种特异的、对经典Wnt信号通路抑制剂,通过破坏β-catenin和
LTURM-34
(Catalog# : 1710138, Cas# :
1879887-96-3
)
LTURM-34是一种新的有效的和选择性的DNA-PK抑制剂,可减轻体外对多
LY2606368 dihydrochloride
(Catalog# : 1710137, Cas# :
1234015-54-3
)
Prexasertib (LY2606368)是一个与ATP竞争的CHK1抑制剂带Ki值0.9 nmol/L。对于
LDC1267
(Catalog# : 179301, Cas# :
1361030-48-9
)
LDC1267显著降低小鼠乳腺癌和黑色素瘤转移依赖NK细胞。TAM酪氨酸激
N-(2,5-二羟基苄基)-5-氨基水杨酸
(Catalog# : 1791119, Cas# :
125697-93-0
)
Lavendustin C,也被称为HDBA和NSC 666251,是一种有效的表皮生长因子(
乐伐替尼(E7080)
(Catalog# : 52025, Cas# :
417716-92-8
)
乐伐替尼,又名E7080,是一种合成的、可口服的血管内皮生长因子
LXS-196
(Catalog# : 1781108, Cas# :
1874276-76-2
)
<span style="color:#34495E;font-family:"font-size:14px;background-color:
LDC4297(LDC044297)
(Catalog# : 178902, Cas# :
1453834-21-3
)
LDC4297也称为LCD044297,是一种有效、具有选择性的CDK7抑制剂。
LY3214996
(Catalog# : 2017887, Cas# :
1951483-29-6
)
LY-3214996是一种有效且具有选择性的,可用于口服的细胞外信号的
LTX-315
(Catalog# : 20178218, Cas# :
1345407-05-7
)
LTX-315是一种两性分子的阳离子肽可能用于治疗黑色素瘤、乳腺癌
LY 344864
(Catalog# : 20178212, Cas# :
186544-26-3
)
LY344864是一种选择性5-HT1F受体激动剂,在最近克隆的5 - HT1F受体上
盐酸LY 344864
(Catalog# : 2017828, Cas# :
1217756-94-9
)
LY344864 hydrochloride is a potent and selective 5-HT1F receptor agonist. It has an E
Lys05 trihydrochloride
(Catalog# : 17030102, Cas# :
1391426-24-6
)
Lys05, 或Lys01三盐酸化物,是一种有效的水溶性溶酶体自噬抑制剂。
拉帕替尼
(Catalog# : 17022807, Cas# :
231277-92-2
)
拉帕替尼(GW-572016) 是一种有效的EGFR和ErbB2抑制剂,IC50分别为10.8和
雷西那德
(Catalog# : 17022706, Cas# :
878672-00-5
)
雷西那德(RDEA594),是URAT1的一日一次抑制剂,是肾脏中调节尿酸排泄
LY3039478 ( Crenigacestat )
(Catalog# : 17021601, Cas# :
1421438-81-4
)
LY3039478 ( Crenigacestat ) 是一种选择性 NOTCH1 抑制剂,通过阻断 VEGFA/
LCI699
(Catalog# : 17021314, Cas# :
928134-65-0
)
LCI699(Osilodrostat)是一种强有力的抑制剂11β-羟化酶,酶催化合成皮质
lumateperone(Tosylate)
(Catalog# : 17012102, Cas# :
1187020-80-9
)
Lumateperone (ITI-722/ITI-007)是一种新型的双5HT2A受体拮抗剂/多巴胺磷蛋
Lys05
(Catalog# : 16123043, Cas# :
1391426-22-4
)
Lys05 is a potent lysosomal autophagy inhibitor. Lys05 is a previously undescribed di
LY-3177833
(Catalog# : 16123042, Cas# :
1627696-51-8
)
LY-3177833 is a potent and selective inhibitor of CDC7 (Cell Division Cycle 7-related
LY3009120
(Catalog# : 16123041, Cas# :
1454682-72-4
)
LY3009120, also known as DP-4978, is potent and selective pan-RAF inhibitor with pote
LY2334737
(Catalog# : 16123040, Cas# :
892128-60-8
)
LY2334737 is an orally available valproic acid ester of gemcitabine, a broad-spectrum
«
1
2
3
4
5
6
»
产品分类
信号通路
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- 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
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Bcr-Abl
----
Src
----
ALK
----
Syk
----
FAK
----
BTK
----
HIF
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Cytoskeletal Signaling
----
Akt
----
Bcr-Abl
----
PKC
----
FAK
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
-- TGF-beta/Smad
----
Bcr-Abl
----
PKC
----
ROCK
----
TGF-beta/Smad
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
-- 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
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
----
Sigma Receptor
----
Ras
----
mAChR
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
-- 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
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
-- 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
-- Vitamin D Related
----
VD/VDR
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
-- PROTAC
----
Molecular Glues
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
TRPM4-IN-2
(Catalog# : 24147, Cas# :
667411-04-3
)
TRPM4-IN-2 (NBA) is a potent transient receptor potential melastatin 4 (TRPM4) inhibi
Isolithocholic Acid
(Catalog# : 24146, Cas# :
1534-35-6
)
Isolithocholic acid is a bile acid that is formed via microbial metabolism of lithoch
H2-Gamendazole
(Catalog# : 24145, Cas# :
877768-84-8
)
H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
CPI-455 HCl
(Catalog# : 24144, Cas# :
2095432-28-1
)
CPI-455 is a potent and selective inhibitor of KDM5 demethylases which reduces surviv
KH-3
(Catalog# : 24143, Cas# :
1215115-03-9
)
KH-3 is a potent RNA-binding protein Hu antigen R (HuR) inhibitor with an IC50 value
Stafib-2
(Catalog# : 24142, Cas# :
2097938-74-2
)
Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b, with
TCRS-417
(Catalog# : 24141, Cas# :
2032123-28-5
)
TCRS-417 (T417) is a small molecule compound capable of docking to the interface betw
PST3 1a
(Catalog# : 24140, Cas# :
1096144-06-7
)
PST3 1a is a Novel selective inhibitor of the N-acetylglucosamine glycosyltransferase
YTX-465
(Catalog# : 24139, Cas# :
2225824-53-1
)
YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
CAY10566
(Catalog# : 10403, Cas# :
944808-88-2
)
Coming soon!