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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- Proteases
- Immunology & Inflammation
- Vitamin D Related
- Membrane Transporter/Ion Channel
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- Piperidines
- Pyridines
- Pyrimidines
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- Other Heterocycles
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产品名字索引 B
- BAY-2402234 (Catalog# : 2071553, Cas# : 2225819-06-5)BAY-2402234 is a potent and selective dihydroorotate dehydrogenase (DHODH) inhibitor
- BMVC-8C3O (Catalog# : 2071550, Cas# : 1301708-12-2)BMVC-8C3O is a DNA G-quadruplexe (G4) ligand which can induce topological conversion
- BAY-545 (Catalog# : 2071532, Cas# : 1699717-32-2)BAY-545 is a potent and selective antagonist of the A2B adenosine receptor.
- Belnacasan (Catalog# : 52004, Cas# : 273404-37-8)Belnacasan (VX-765) 是 VRT-043198 的口服生物活性前药，VRT-043198 是有效
- BMS-1001 (Catalog# : 2062901, Cas# : 2113650-03-4)
- 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine (Catalog# : 2062328, Cas# : 1549360-60-2)
- 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine hydrochloride (Catalog# : 202327, Cas# : 1628263-43-3)
- 4-bromo-2-fluoro-1-propan-2-yloxybenzene (Catalog# : 2062316, Cas# : 202865-80-3)
- 1-bromo-4-propan-2-ylsulfonylbenzene (Catalog# : 2062315, Cas# : 70399-02-9)
- 5-(2,4-bis(benzyloxy)-5-isopropylphenyl)-N-ethyl-4-iodoisoxazole-3-carboxamide (Catalog# : 2062305, Cas# : 741414-22-8)
- 7-bromo-2-(1-methyl-1H-pyrazol-4-yl)-quinoxaline (Catalog# : 2062028, Cas# : 1083325-87-4)
- (3-bromoprop-1-en-2-yl)benzene (Catalog# : 2062001, Cas# : 3360-54-1)
- BW-A 78U (Catalog# : 2051512, Cas# : 101155-02-6)BW-A 78U is a PDE4 inhibitor with an IC50 of 3 μM.
- 9-溴-2-羟基-7-甲基-4H-吡啶并[1,2-a]嘧啶-4-酮 (Catalog# : S-204156, Cas# : 663619-90-7)
- BB-Cl-Amidine (Catalog# : 204505, Cas# : 1802637-39-3)BB-Cl-A是一种通过激活内质网应激途径治疗犬和猫乳腺癌的新型疗
- BAY-218 (Catalog# : 204301, Cas# : 2162982-11-6)BAY-218, also known as BAY-2335218, is a potent and selective small-molecule AhR inhi
- Blarcamesine ( AVex-73 ; AE-37 ) (Catalog# : 6111902, Cas# : 195615-83-9)ANAVEX2-73 (blacamesine) 是一种 Sigma-1 受体激动剂和毒蕈碱受体调节剂
- (6bR,10aS)-3-methyl-2,3,6b,7,8,9,10,10a-octahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline (Catalog# : ITI007_3, Cas# : 313368-85-3)
- (6bR,10aS)-2-oxo-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline-8-carboxylic acid ethyl ester (Catalog# : ITI007_2, Cas# : 313369-16-3)Sun-shine Chemical is a supplier Lumateperone and its intermediate from 100g scale to
- 6-bromo-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride (Catalog# : ITI007_1, Cas# : 1059630-11-3)Sun-shine Chemical is a supplier ofLumateperone, we may provideLumateperone and its i
- 3-bromo-7-nitro-1-tosyl-1H-indole (Catalog# : 511191, Cas# : 2091135-02-1)
- BMS-986104 (Catalog# : 193285, Cas# : 1622180-31-7)BMS-986104是一种强效的选择性S1P1受体调节剂，具有配体偏倚信号转
- BAY-1316957 (Catalog# : 193263, Cas# : 1613264-40-6)BAY-1316957是一种高效、选择性、口服的人前列腺素E2受体亚型4 (hEP
- BMS-986158 (Catalog# : 193255, Cas# : 1800340-40-2)BMS-986158是一种有效的选择性BET抑制剂。BMS-986158与BET蛋白BRD中的乙
- BMS-986163 (Catalog# : 193207, Cas# : 1801151-09-6)BMS-986163是GluN2B的负变构调节剂，在重度抑郁症中具有潜在的应用
- BAY-293 (Catalog# : 193121, Cas# : 2244904-70-7)BAY-293是一种有效的SOS1抑制剂，通过破坏IC50为21 nM的RAS-SOS1的相互
- BMS-816336 (Catalog# : 19351, Cas# : 1009583-20-3)BMS-816336是一种口服活性、有效和选择性的11β-HSD1抑制剂。BMS- 8163
- Belvarafenib (Catalog# : 19341, Cas# : 1446113-23-0)Belvarafenib，又名GDC-5573、HM95573、RG6185，是RAF家族激酶的选择性抑制
- Burixafor HBr (Catalog# : 192221, Cas# : 1191450-19-7)Burixafor，又名TG-0054，是CXC趋化因子受体4 (CXCR4)的口服生物利用抑
- BMS-986142 (Catalog# : 191284, Cas# : 1643368-58-4)BMS-986142是一种高效、选择性、可逆的BTK抑制剂。
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