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Anti-infection
Apoptosis
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Cas号索引 1
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Cas号索引 1
1357164-52-3 | KUS121
(Catalog# : 20676)
KUS-121 是一种过渡内质网 ATP 酶(含缬氨肽蛋白 [VCP];p97)的小分
1596348-16-1 | KDM5-C49
(Catalog# : 20493)
KDM5-C49 is a potent and selective inhibitor of KDM5 (also known as JARID1). KDM5-C49
1771756-32-1 | KUN56321
(Catalog# : 21246)
KUN56321 is a luminescent agent. The application of KUN56321 comprises: coating the f
1695533-89-1 | KO-947
(Catalog# : 20122101)
KO-947 is a potent and selective ERK inhibitor with slow dissociation kinetics. KO-94
1784282-12-7 | KHS101盐酸盐
(Catalog# : 191281)
KHS101 HCl是一种转化酸性卷曲蛋白3 (TACC3)的抑制剂。它的作用是通
1646795-59-6 | KC01
(Catalog# : 1810294)
KC01是ABHD16A的共价抑制剂。ABHD16A是一种磷脂酰丝氨酸(PS)脂肪酶,
18228-17-6 | KG-501
(Catalog# : 1810226)
KG-501是cAMP反应元件结合蛋白(CREB)抑制剂。
1131456-28-4 | KGP-94
(Catalog# : 3291806)
KGP94 is a reversible, time-dependent and competitive inhibitor of human cathepsin L.
1428729-56-9 | KIN-1148
(Catalog# : 184121)
KIN-1148是一个IRF3激动剂。KIN1148诱导剂量依赖性IRF3核易位和特异性
1799974-70-1 | KI-696
(Catalog# : 1710132)
ki-696代表一个优良的低分子量的工具来研究体内Keap1与Nrf2-Nrf2的相
1261113-96-5 | KAF-156
(Catalog# : 20178211)
KAF-156,也称为GNF-156, 是一种可治疗疟疾的抗疟药。
1188890-41-6 | KN-93 phosphate
(Catalog# : 16123029)
KN-93 is a CaMKII inhibitor. KN-93 suppresses ventricular arrhythmia induced by LQT2
191089-59-5 | K-7174
(Catalog# : 16123028)
K-7174 is a novel orally active, potent proteasome inhibitor. K-7174 exerts anti-myel
182004-65-5 | KB-R7943 mesylate
(Catalog# : 16122826)
KB-R7943 is a potent, selective inhibitor of the reverse mode of the Na+/Ca2+ exchang
142273-20-9 | Kenpaullone
(Catalog# : 16122711)
Kenpaullone is an ATP-competitive inhibitor of cyclin-dependent kinases (CDKs). It al
1309444-75-4 | K145
(Catalog# : 6111523)
K145 is a selective SphK2 inhibitor with an IC50 of 4.300.06 M , while no inhibition
1253452-78-6 | KS176
(Catalog# : 6111510)
KS176 is a potent and selective inhibitor of the breast cancer resistance protein (BC
1956356-56-1 | KYA1797K
(Catalog# : 6111416)
KYA1797K is a highly potent and selective Wnt/-catenin inhibitor with IC50 of 0.75 M
1354037-26-5 | KH-CB19
(Catalog# : 611922)
KH-CB19 is a potent and highly specific inhibitor of the CDC2-like kinase isoforms 1
1000669-72-6 | KW-2449
(Catalog# : 16071012)
KW-2449 is a novel multikinase inhibitor, which suppresses the growth of leukemia cel
1431985-92-0 | K02288
(Catalog# : 52728)
K02288 is a novel small molecule inhibitor of ALK1/2/3/6 with IC50s of 1.8/1.1/34.4/6
1233533-04-4 | kb NB 142-70
(Catalog# : 52568)
kb NB 142-70 is a selective protein kinase D (PKD) inhibitor (IC50 values are 28.3, 5
1118807-13-8 | KY02111
(Catalog# : 52212)
KY02111 is a small molecule which can promote differentiation of hPSCs to cardiomyocy
1350622-33-1 | kb-NB77-78
(Catalog# : 51502)
kb-NB77-78 is an analog of CID797718, which is a by-product of the synthesis of the p
191089-60-8 | K-7174 dihydrochloride
(Catalog# : 52002)
K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of
1260247-42-4 | LLL12
(Catalog# : 25075)
LLL12是一种强效的STAT3抑制剂。LLL12在小鼠异种移植物模型中显示出
1934259-00-3 | Limertinib
(Catalog# : 24093)
Limertinib, also known as ASK120067, is an EGFR inhibitor. ASK120067 displayed potent
190791-29-8 | Lasofoxifene tartrate
(Catalog# : 24054)
Lasofoxifene, also known as CP 336156, is a non-steroidal selective estrogen receptor
180916-16-9 | Lasofoxifene
(Catalog# : 24053)
Lasofoxifene, also known as CP 336156, is a non-steroidal selective estrogen receptor
1820940-17-7 | Lorundrostat
(Catalog# : 20654)
Lorundrostat is an aldosterone synthase inhibitor.
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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
----
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----
GnRH
----
LPL Receptor
----
Ras
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
----
Bradykinin Receptor
----
GLP Receptor
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
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----
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
--
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--
Pyridines
--
Pyrimidines
--
Quinolines
--
Sulfonamides
--
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--
Trifluoroborates
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Other Heterocycles
--
Other Building Blocks
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On Sale
新产品
天然化合物
最新产品
1497439-74-3 | AD-8007
(Catalog# : 26A018)
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)
1802650-31-2 | ZY-444
(Catalog# : 26A020)
ZY-444是一种通过抑制PC活性发挥抗癌作用的药物。
2306525-79-9 | AD-5584
(Catalog# : 26A019)
AD-5584是一种新型脑渗透性ACSS2抑制剂。
3079716-11-0 | IDB-003
(Catalog# : 26A017)
IDB-003在体内抑制MDA-MB-231肿瘤生长。
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)
1260247-42-4 | LLL12
(Catalog# : 25075)
LLL12是一种强效的STAT3抑制剂。LLL12在小鼠异种移植物模型中显示出
2758659-09-3 | ECC-5004
(Catalog# : 26A015)
ECC5004是一款每日一次、低剂量、小分子GLP-1受体激动剂。
2911585-37-8 | SILA-123
(Catalog# : 26A014)
SILA-123是一种II型FLT3抑制剂,对FLT3-WT(IC50=2.1 nM)和FLT3-ITD(IC50=1
1214922-52-7 | Encaleret sulfate
(Catalog# : 26A013)
Encaleret是一种正在研究的钙敏感受体的小分子拮抗剂,用于钙稳态
1431303-72-8 | Iadademstat ( ORY-1001 ) hydrochloride
(Catalog# : 26A011)
Iadademstat(ORY-1001)是一种口服活性、高效和选择性的表观遗传酶