武汉永璨生物科技有限公司
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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
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- Chiral Compounds
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- 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
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产品名字索引 B
- benzyl 4-(methylamino)piperidine-1-carboxylate (Catalog# : 81808, Cas# : 405057-75-2)Coming soon!
- benzyl N-piperidin-4-ylcarbamate,hydrochloride (Catalog# : 81806, Cas# : 207296-89-7)Coming soon!
- Benzyl 4-(aminomethyl)piperidine-1-carboxylate hydrochloride (Catalog# : 81803, Cas# : 172348-57-1)Coming soon!
- benzyl 3-(aminomethyl)piperidine-1-carboxylate (Catalog# : 81802, Cas# : 315717-76-1)Coming soon!
- benzyl N-(piperidin-2-ylmethyl)carbamate (Catalog# : 81801, Cas# : 184044-09-5)Coming soon!
- Benzyl pyrrolidin-3-ylcarbamate hydrochloride (Catalog# : 81736, Cas# : 553672-38-1)Coming soon!
- benzyl N-(2-aminoethyl)carbamate,hydrochloride (Catalog# : 81733, Cas# : 18807-71-1)Coming soon!
- Benzyl (trans-4-aminocyclohexyl)carbamate hydrochloride (Catalog# : 81732, Cas# : 1217664-37-3)Coming soon!
- 1-Boc-3-Methylaminopiperidine (Catalog# : 81729, Cas# : 392331-89-4)Coming soon!
- 1-Boc-4-Ethylaminopiperidine (Catalog# : 81728, Cas# : 264905-39-7)Coming soon!
- 3-Boc-Aminomethyl-Azetidine Hydrochloride (Catalog# : 81722, Cas# : 1170108-38-9)Coming soon!
- 3-(Boc-amino)piperidine (Catalog# : 81702, Cas# : 172603-05-3)Coming soon!
- 3-(Bromomethyl)-2-cyclopropyl-4-(4-fluorophenyl)quinoline (Catalog# : 81306, Cas# : 154057-56-4)Related API & intermediates:Cas#147526-32-7 Pitavastatin CalciumCas# 24922-02-9 E
- 1-Boc-3-(aminomethyl)piperidine (Catalog# : 81032, Cas# : 162167-97-7)Coming soon!
- 2-(Boc-Aminomethyl)-Piperidine (Catalog# : 81027, Cas# : 141774-61-0)Coming soon!
- 4-(Boc-aminomethyl)piperidine (Catalog# : 81026, Cas# : 135632-53-0)Coming soon!
- 1-Boc-piperazine (Catalog# : 81025, Cas# : 143238-38-4)Coming soon!
- 1-Boc-hexahydro-1,4-diazepine (Catalog# : 81024, Cas# : 112275-50-0)Coming soon!
- 3-Bromo-4-(trifluoromethoxy)benzoic acid (Catalog# : 81014, Cas# : 85373-96-2)Coming soon!
- 3-Bromo-4-(tert-butyl)benzoic acid (Catalog# : 81009, Cas# : 38473-89-1)Coming soon!
- 3-bromo-4-(dimethylamino)benzoic acid (Catalog# : 81008, Cas# : 220844-83-7)Coming soon!
- Benzyl-2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside (Catalog# : 80301, Cas# : 13343-63-0)Coming Soon
- b-AP15 (Catalog# : 73106, Cas# : 1009817-63-3)b-AP15 is a specific inhibitor of the deubiquitinating enzymes Uch37 and Usp14 of the
- Bikinin (Catalog# : 61002, Cas# : 188011-69-0)Bikinin(Abrasin) is a potent inhibitor of plant GSK-3/Shaggy-like kinase; activates B
- BLU9931 (Catalog# : 60303, Cas# : 1538604-68-0)BLU9931 is a potent and irreversible small-molecule inhibitor of FGFR4, as a targeted
- BS-181 (Catalog# : 52755, Cas# : 1092443-52-1)BS-181 is a highly selective CDK7 inhibitor with IC50 of 21 nM. ; >40-fold selecti
- BAY 11-7082 (Catalog# : 52713, Cas# : 19542-67-7)BAY 11-7082 is aNF-Binhibitor, inhibits TNF-inducedIBphosphorylation withIC50of 10 M
- Bay 11-7085 (Catalog# : 52712, Cas# : 196309-76-9)BAY 11-7085 is an irreversible inhibitor of TNF-inducedIBphosphorylation withIC50of 1
- BMS-599626 (Catalog# : 52703, Cas# : 714971-09-2)AC480 (BMS-599626) is a selective and efficacious inhibitor of HER1 and HER2 with IC5
- BI 2536 (Catalog# : 52616, Cas# : 755038-02-9)BI2536 is a potent Plk1 inhibitor with IC50 of 0.83 nM, BI2536 shows 4- and 11-fold g
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
- -- 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
- STX-478 (Catalog# : 20633, Cas# : 2883540-92-7)STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
- Iclepertin (BI-425809) (Catalog# : 24084, Cas# : 1421936-85-7)Iclepertin（BI-425809）是一种口服的GlyT-1小分子抑制剂，用于治疗与
- Bomedemstat (Catalog# : 24001, Cas# : 1990504-34-1)Bomedemstat 是一种口服的、不可逆的赖氨酸特异性去甲基酶 1 (LSD1)
- PLX-4545 (Catalog# : 24111, Cas# : 2892065-45-9)PLX-4545 是一种口服生物可利用的 IKZF2 分子胶降解剂，旨在破坏高
- VVD-130037 ( BAY-3605349 ) (Catalog# : 24110, Cas# : 3034880-93-5)VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
- CBR-5884 (Catalog# : 24109, Cas# : 681159-27-3)CBR 5884 是一种磷酸甘油酸脱氢酶 (PHGDH) 抑制剂，能够抑制过度表达
- JHU-083 (Catalog# : 24108, Cas# : 1998725-11-3)JHU-083 选择性阻断大脑 CD11b+ 细胞中的谷氨酰胺酶活性，并防止慢
- LXH-3-71 (Catalog# : 24107, Cas# : 2251753-65-6)LXH-3-71是一种新型“分子胶”，可诱导PHGDH和DDB1-CUL4泛素连接酶之
- CC-92480 ( Mezigdomide ) (Catalog# : 20510, Cas# : 2259648-80-9)CC-92480 是一种有效的新型 CELMoD 化合物，旨在快速最大程度地降解
- Adrixetinib ( Q-702 ) (Catalog# : 20617, Cas# : 2394874-66-7)Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag