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Deuterated
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+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
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Membrane Transporter/Ion Channel
others
PROTAC
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Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
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Catalysts
Chiral Compounds
Deuterated
Fluorides
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Pyrimidines
Quinolines
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Cas号索引 1
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Cas号索引 1
1052147-86-0 | LP-211
(Catalog# : 1811302)
LP-211是血清素5-HT7受体的选择性激动剂。
1800398-38-2 | LXH254游离
(Catalog# : 1811213)
LXH254是所有丝氨酸/苏氨酸蛋白激酶Raf家族成员的口服有效抑制剂
1231220-79-3 | LY2828360
(Catalog# : 181172)
LY2828360是一种新的有效的、选择性的、有效的CB2激动剂。
1040526-12-2 | LP-533401盐酸盐
(Catalog# : 1810262)
LP-533401 HCl是色氨酸羟化酶-1 (Tph-1)的抑制剂,Tph-1是内脏衍生血清
1454808-95-7 | LP-922761
(Catalog# : 188101)
LP-922761是一种强有力的和选择性AAK1抑制剂,在体外的IC50值为4.8±
1898283-02-7 | LY-3200882
(Catalog# : 186278)
LY-3200882是一种口服TGFbeta抑制剂。LY3200882目标转化生长因子-beta (T
1610954-97-6 | LX2761
(Catalog# : 186275)
LX2761是一种局部作用的SGLT1抑制剂,体外强效,延缓体内肠道葡萄
120408-07-3 | Lometrexol disodium
(Catalog# : 186151)
Lometrexol是一种具有抗肿瘤活性的叶酸模拟抗代谢产物。
1632032-53-1 | LB-100
(Catalog# : 185312)
LB-100是一种蛋白磷酸酶2A(PP2A)抑制剂。
1292290-38-0 | LY2881835
(Catalog# : 185252)
LY2881835是一种有效的选择性GPR40激动剂,可能用于治疗2型糖尿病。
1903008-80-9 | Lazertinib
(Catalog# : 512194)
Description:Lazertinib is a an orally available third-generation, selective inhibi
183499-57-2 | L-778123
(Catalog# : 1711249)
L-778,123 is an inhibitor of FPTase and GGPTase-I.
1879887-96-3 | LTURM-34
(Catalog# : 1710138)
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
1234015-54-3 | LY2606368 dihydrochloride
(Catalog# : 1710137)
Prexasertib (LY2606368)是一个与ATP竞争的CHK1抑制剂带Ki值0.9 nmol/L。对于
1361030-48-9 | LDC1267
(Catalog# : 179301)
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
125697-93-0 | N-(2,5-二羟基苄基)-5-氨基水杨酸
(Catalog# : 1791119)
Lavendustin C,也被称为HDBA和NSC 666251,是一种有效的表皮生长因子(
1874276-76-2 | LXS-196
(Catalog# : 1781108)
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1453834-21-3 | LDC4297(LDC044297)
(Catalog# : 178902)
LDC4297也称为LCD044297,是一种有效、具有选择性的CDK7抑制剂。
1951483-29-6 | LY3214996
(Catalog# : 2017887)
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
1345407-05-7 | LTX-315
(Catalog# : 20178218)
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
186544-26-3 | LY 344864
(Catalog# : 20178212)
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
1217756-94-9 | 盐酸LY 344864
(Catalog# : 2017828)
LY344864 hydrochloride is a potent and selective 5-HT1F receptor agonist. It has an E
1391426-24-6 | Lys05 trihydrochloride
(Catalog# : 17030102)
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。
1421438-81-4 | LY3039478 ( Crenigacestat )
(Catalog# : 17021601)
LY3039478 ( Crenigacestat ) 是一种选择性 NOTCH1 抑制剂,通过阻断 VEGFA/
1187020-80-9 | lumateperone(Tosylate)
(Catalog# : 17012102)
Lumateperone (ITI-722/ITI-007)是一种新型的双5HT2A受体拮抗剂/多巴胺磷蛋
1391426-22-4 | Lys05
(Catalog# : 16123043)
Lys05 is a potent lysosomal autophagy inhibitor. Lys05 is a previously undescribed di
1627696-51-8 | LY-3177833
(Catalog# : 16123042)
LY-3177833 is a potent and selective inhibitor of CDC7 (Cell Division Cycle 7-related
1454682-72-4 | LY3009120
(Catalog# : 16123041)
LY3009120, also known as DP-4978, is potent and selective pan-RAF inhibitor with pote
187164-19-8 | Luliconazole
(Catalog# : 16123038)
Luliconazole is an azole antifungal drug. As a 1% topical cream, luliconazole is indi
1223403-58-4 | LOXO-101 (ARRY-470)
(Catalog# : 16123036)
Larotrectinib, also known as ARRY-470 and LOXO-101, is an orally bioavailable, potent
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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
----
Ketohexokinase
-- 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
--
Antibody-drug Conjugate/ADC Related
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
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。
2671128-05-3 | FHD-286
(Catalog# : 20471)
FHD-286 is an oral, small-molecule, selective, allosteric inhibitor of BRG1 and BRM i
3002056-30-3 | NST-628
(Catalog# : 24058)
NST-628 是具有血脑屏障渗透性的 MAPK 通路分子胶,能够抑制 RAF 磷
2893778-31-7 | PHGDH-IN-3
(Catalog# : 25077)
PHGDH-IN-3 is an orally active phosphoglycerate dehydrogenase (PHGDH) inhibitor.
2882165-79-7 | CFT1946
(Catalog# : 25078)
CFT1946 是一种口服生物可利用的小分子降解剂,可降解实体瘤中的
68238-36-8 | 异硫蓝
(Catalog# : 178017)
Isosulfan blue 是一种用于淋巴管造影中淋巴管识别的蓝色染料。Isos
2803470-63-3 | HC-7366
(Catalog# : 25076)
HC-7366 is a potent and selective activator of the general control nonderepressible 2
2226636-04-8 | Soquelitinib ( CPI-818 )
(Catalog# : 20671)
Soquelitinib(CPI-818)是一种高度选择性的共价白细胞介素-2诱导的T
2230263-60-0 | Crelosidenib
(Catalog# : 24101)
Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor. It is an antineoplast
1260247-42-4 | LLL12
(Catalog# : 25075)
LLL12 is a potent STAT3 inhibitor. LLL12 inhibits colony formation and cell migration