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- 抑制剂/受体激动剂
- PI3K/Akt/mTOR
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产品名字索引 H
- 6-溴-1,3-二甲基-1H-吲唑 (Catalog# : 25036, Cas# : 1095539-84-6)
- HC-5404 抑制剂 (Catalog# : 25001, Cas# : 2247396-91-2)HC-5404 是一种新型、高选择性、有效的PERK抑制剂。
- H2-Gamendazole (Catalog# : 24145, Cas# : 877768-84-8)H2-Gamendazole is a derivative of Lonidamine that reduces cyst formation in polycysti
- HTL14242 (Catalog# : 24115, Cas# : 1644645-32-8)HTL14242 is a mGlu5 Negative Allosteric Modulator. Metabotropic glutamate receptors (
- HC-5404-FU (Catalog# : 24112, Cas# : 3034479-99-4)HC-5404-FU 是一种新型、高选择性、有效的PERK抑制剂。
- HH-0043 (Catalog# : 24077, Cas# : 2922069-42-7)
- HFY-4A (Catalog# : 20661, Cas# : 2094810-82-7)HFY-4A is a HDAC inhibitor. HFY-4A inhibits breast cancer cell proliferation, migrati
- Hynic-TOC (Catalog# : 20658, Cas# : 257943-19-4)Hynic-TOC is a ligand for making 99mTc-Hynic-TOC as an imaging agent in the diagnosti
- HDAC-IN-58 (Catalog# : 20568, Cas# : 2071224-39-8)HDAC-IN-58 is a HDAC inhibitor.
- 4,5-二碘-1H-1H-1,2,3-三氮唑 (Catalog# : 20521, Cas# : 28194-09-4)
- HM43239 (Catalog# : 20517, Cas# : 2569527-64-4)HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibit
- 5-溴-6-环丙基嘧啶-4-醇 (Catalog# : 20482, Cas# : 27192-20-7)
- 2(1H)-Pyridinone, 5,6-dihydro-4-(4-methylphenyl)-3-(2H-tetrazol-5-yl)-6-[4-(4,4,4-trifluorobutoxy)phenyl]-6-(trifluoromethyl)-, (6S)- (Catalog# : 20430, Cas# : 1441057-15-3)
- 1H-Indazole-1-acetic acid, 3-acetyl-5-bromo-, 1,1-dimethylethyl ester (Catalog# : 20422, Cas# : 2086183-72-2)
- 4-氯-1-[三(甲基乙基)硅酯]-1H-吡咯并[2,3-B]吡啶 (Catalog# : 20410, Cas# : 651744-48-8)
- 4-hydroxybiphenyl-4-carboxamide (Catalog# : 20404, Cas# : 182318-78-1)
- 1H-吡咯并[2,3-B]吡啶-2-羧酸乙酯 (Catalog# : 20388, Cas# : 221675-35-0)
- 6-羟基-3,4-二氢-1H-2-萘酮 (Catalog# : 20371, Cas# : 52727-28-3)
- HISPOLON(P) (Catalog# : 210201, Cas# : 173933-40-9)
- HMPL-523 (Catalog# : 20123101, Cas# : 1415792-84-5)HMPL-523 is a novel, highly selective and potent small molecule oral inhibitor target
- 5-Hydroxymethyldeoxyuridine (Catalog# : 2091910, Cas# : 5116-24-5)5-Hydroxymethyldeoxyuridine is a nucleoside analog with anticancer and antiviral acti
- 2,4-二甲基-5-羟基嘧啶 (Catalog# : 2091204, Cas# : 412003-95-3)我们可以生产公斤级的2,4-二甲基-5-羟基嘧啶 （CAS 412003-95-3）。
- H-BETA-ALA-AMC TFA (Catalog# : 2071633, Cas# : 201847-54-3)
- HC-070 (Catalog# : 206104, Cas# : 1628291-95-1)HC-070 is a potent inhibitor of TRPC4 and TRPC5, leading to anxiolytic and antidepres
- Hydroxyfasudil HCl (Catalog# : 204610, Cas# : 155558-32-0 (HCl))Hydroxyfasudil, aslo known as HA1100, is a cell-permeable hydroxylated metabolite of
- HBX-41108 (Catalog# : 19317, Cas# : 924296-39-9)HBX 41108是泛素特异性蛋白酶(USP) 7的抑制剂。HBX 41108通过IC(50)在亚
- HS-1371 (Catalog# : 192223, Cas# : 2158197-70-5)HS-1371是一种新型的RIP3-介导坏死性凋亡激酶抑制剂。HS-1371以ATP-竞
- HZ-1157 (Catalog# : 19182, Cas# : 1009734-33-1)HZ-1157是一种丙肝病毒(HCV)抑制剂，对HCV NS3/4A蛋白酶有抑制作用。
- H 151 (Catalog# : 1811022, Cas# : 941987-60-6)H 151是一种诱捕拮抗剂，共价结合在Cys91上，阻断棕榈酰化和防止
- HC-056456 (Catalog# : 1810171, Cas# : 7733-96-2)HC-056456是CatSper的通道调制器。
产品分类
- ---- 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
- -- Antibody-drug Conjugate/ADC Related
- -- 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
最新产品
- Reparixin (Catalog# : 25050, Cas# : 266359-83-5)Reparixin is an inhibitor of CXCR2 function, which attenuates inflammatory responses
- TAK-779 (Catalog# : 25049, Cas# : 229005-80-5)TAK-779 is a C-C chemokine receptor type 5 (CCR5) receptor antagonist potentially for
- BAY-1125976 (Catalog# : 25048, Cas# : 1402608-02-9)BAY-1125976 is a potent and selective allosteric AKT1/2 inhibitor. BAY-1125976 exhibi
- Vimseltinib free base (Catalog# : 25047, Cas# : 1628606-05-2)Vimseltinib, also known as DCC-3014, is a potent and orally active inhibitor of the t
- 2-Propynamide, 3-[(3Z)-3-[[[4-[(dimethylamino)methyl]phenyl]amino]phenylmethylene]-2,3-dihydro-2-oxo-1H-indol-6-yl]-N-ethyl- (Catalog# : 25046, Cas# : 2128698-24-6)
- Cavosonstat (Catalog# : 25045, Cas# : 1371587-51-7)Cavosonstat, alos known as N91115) an orally bioavailable inhibitor of S-nitrosogluta
- Ivospemin Hydrochloride (Catalog# : 25044, Cas# : 259657-09-5)Ivospemin is an antineoplastic spermine analogue.
- Survodutide (Catalog# : 25043, Cas# : 2805997-46-8)
- XRD-0394 (Catalog# : 25042, Cas# : 2595308-10-2)XRD-0394 is a DNA-PKcs inhibitor. XRD-0394 selectively targets, binds to and inhibits
- CC-90003 (Catalog# : 25041, Cas# : 1621999-82-3)CC-90003 is an orally available inhibitor of extracellular signal-regulated kinase (E