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- 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
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Cas号索引 2
- 2375840-87-0 | NDI-091143 (Catalog# : 24057)NDI-091143 is a novel potent inhibitor of human ATP-citrate lyase, indirectly disrupt
- 2354321-33-6 | NMD670 (Catalog# : 24050)NMD670 is an orally bioavailable skeletal muscle-specific chloride ion channel (ClC-1
- 2739866-40-9 | NVL-655 ( ALK-IN-27 ) (Catalog# : 24003)NVL-655是一种新型脑渗透性ALK选择性抑制剂，旨在解决目前可用的
- 2244614-14-8 | Navacaprant (Catalog# : 23122601)Navacaprant (NMRA-335140, BTRX-140) 是一种口服、选择性、可逆的 kappa 阿
- 2254741-41-6 | Ninerafaxstat (Catalog# : 20608)Ninerafaxstat is a biochemical that decreases fatty acid oxidation and improves mitoc
- 2154406-04-7 | NBI-921352 (Catalog# : 20602)NBI-921352 is a potent, highly selective Nav1.6 sodium channel inhibitor being develo
- 2143096-93-7 | Navitoclax-piperazine (Catalog# : 20559)Navitoclax-piperazine, also known as ABT-263-piperazine, is a Navitoclax derative and
- 2411819-82-2 | NBD-14270 (Catalog# : 20448)
- 2055599-51-2 | NTP42 (Catalog# : 2051509)NTP42 is a novel antagonist of the thromboxane prostanoid receptor (TP), currently in
- 2349367-89-9 (free base) | NVS-ZP7-4 (Catalog# : 204506)NVS-ZP7-4 is a potent ZIP7 Inhibitor, which inhibits Notch signaling with IC50 of 0.1
- 2231098-99-8 | NCT-506 (Catalog# : 19354)NCT-506是一种口服生物可利用醛脱氢酶1A1 (ALDH1A1)抑制剂，IC50为7nm。
- 2231079-74-4 | NCT-505 (Catalog# : 1810261)NCT-505是一种口服生物有效醛脱氢酶1A1 (ALDH1A1)抑制剂，具有较强的
- 221244-14-0 | 1NM-PP1 (Catalog# : 184174)1NM-PP1 是一种有效的突变激酶抑制剂。
- 209410-46-8 | Neflamapimod (Catalog# : 1791317)Neflamapimod，也称为VX-745，VRT-031745和VD-31745，是高度有效的和选择性
- 22621-41-6 | 3-Nitrosalicylic Acid Methyl Ester (Catalog# : 178224)3-Nitrosalicylic Acid Methyl Ester
- 209219-38-5 | Nastorazepide (Catalog# : 6111110)Nastorazepide (Z-360) is a selective, orally available, 1,5-benzodiazepine-derivative
- 2070015-09-5 | NU6300 (Catalog# : 611923)NU6300 is a non-covalent ATP-competitive CDK2 inhibitor (IC50 = 0.16 mM). NU6300
- 2158-14-7 | N-(4-azidosulfonylphenyl)acetamide (Catalog# : 110206)Coming soon!
- 274693-55-9 | N,N'-DISALICYLIDENE-1,3-PROPANEDIAMINE (Catalog# : 91829)Coming soon!
- 24623-25-4 | 4-Nitro-1-indanone (Catalog# : 81939)Coming soon!
- 217806-26-3 | 3-N-Boc-Aminoazetidine hydrochloride (Catalog# : 81913)Coming soon!
- 212779-48-1 | NG 52 (Catalog# : 52563)NG 52 (Compound 52 ) is a potent, cell-permeable, reversible, selective, and ATP-comp
- 2257492-95-6 | OPN expression inhibitor 1 (Catalog# : 25060)OPN expression inhibitor 1 (Compound 11) is an osteopontin (OPN) expression inhibitor
- 2231294-96-3 | Opevesostat (Catalog# : 24047)Opevesostat is cholesterol side-chain cleavage enzyme (CYP11A1) inhibitor.
- 2146132-73-0 | OATD-02 (Catalog# : 20642)OATD-02 是一种口服双精氨酸酶抑制剂（ARG1 和 ARG2），目前在 Molecu
- 2212020-52-3 | orforglipron (Catalog# : 20537)Orforglipron, also known as LY3502970, and OWL-833, is a Novel Non-Peptidyl Oral Gluc
- 2244520-98-5 | OUN20985v (Catalog# : 2091912)OUN20985, also known as Homo-PROTAC cereblon degrader 1, is a cereblon degrader. OUN2
- 2088453-21-6 | OATD-01 (GLPG-4716) (Catalog# : 208191)OATD-01 (GLPG-4716)是一种有效的酸性哺乳动物几丁质酶（AMCase）和壳
- 253426-24-3 | 奥瑞布林盐酸盐 (Catalog# : 186291)奥瑞布林是一种合成的水溶性类似物，与combrestyatin A4类似，源自
- 204697-65-4 | Olcegepant (Catalog# : 185285)Olcegepant，又称BIBN-4096或BIBN-4096BS，是降钙素基因相关肽1 (CGRP1)受体
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
- 2991818-13-2 | MGD-28 (Catalog# : 25073)MGD-28 is a potent molecular glue degrader that demonstrates significant in vitro eff
- | TG101209 analog 1 (Catalog# : 25072)TG101209 analog 1 (Compound 8h) is an inhibitor of BUB1B with an IC50 of 10.36 μ M.
- 2170729-29-8 | AT-007 (Catalog# : 25071)AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase in
- 1358751-06-0 | TAK-653 (Catalog# : 25070)TAK-653 is a novel AMPA receptor potentiator, strictly potentiating a glutamate-induc
- 1801344-14-8 | Emavusertib (Catalog# : 25069)Emavusertib, also known as CA-4948 is a potent IRAK4/FLT3 inhibitor with anti-tumor a
- 1305267-37-1 | Roginolisib (Catalog# : 25068)Roginolisib, also known as MSC2360844 and IOA-244, is a potent, orally active and sel
- 1198078-60-2 | NT219 (Catalog# : 25067)NT219 is a novel inhibitor of the insulin/igf signaling cascade (iis), mediating a lo
- 858128-57-1 | SPB linker (Catalog# : 25066)SPB is a agent-linker conjugate for ADC with potent anti-inflammatory activity by usi
- 1404380-58-0 | JTE-151 (Catalog# : 20594)JTE-151 是一种 RORγ 抑制剂，可通过抑制与 Th17 细胞活化相关的 ROR
- 112108-01-7 | Ecopipam ( SCH 39166 ) (Catalog# : 25065)Ecopipam (SCH 39166) 是一种有效的、选择性、具有口服活性的多巴胺