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产品名字索引 B
- 3BDO (Catalog# : 186232, Cas# : 890405-51-3)3BDO，一种丁基内酯衍生物，可以靶向FKBP1A，激活mTOR信号通路。它
- BMS-986205 (Catalog# : 185314, Cas# : 1923833-60-6)BMS-986205是一种抗癌药物。
- Birinapant (Catalog# : 185182, Cas# : 1260251-31-7)Birinapant，也被称为TL32711，是一种合成的小分子，具有潜在的抗肿
- Bryostatin 1 (Catalog# : 18573, Cas# : 83314-01-6)苔藓虫素1是一种有效的蛋白激酶C调制器，从苔藓虫体内分离出来
- BMS-813160 (Catalog# : 1842812, Cas# : 1286279-29-5)BMS-813160是一种有效的选择性CCR2/CCR5拮抗剂，具有潜在的免疫调节
- BRD7116 (Catalog# : 184282, Cas# : 329059-55-4)BRD7116是白血病干细胞(LSC)活性的有效选择性抑制剂(EC50 = 200 nM)。
- 盐酸巴多昔芬 (Catalog# : 18496, Cas# : 198480-56-7)Bazedoxifene，又名WAY-140424，是第三代选择性雌激素受体调节剂(SERM)
- BQR695 (Catalog# : 184218, Cas# : 1513879-21-4)BQR695, also known as NVP-BQR695, is a potent and selective PI4K inhibitor.
- BAY1143572 (Catalog# : 181242, Cas# : 1414943-88-6)Atuveciclib, also known as BAY1143572, is a highly selective, potent and orally avail
- BAY-1436032 (Catalog# : 181181, Cas# : 1803274-65-8)BAY-1436032是一个强有力的,有选择性的，有效的突变异柠檬酸脱氢酶
- BGB-283 (Catalog# : 17101620, Cas# : 1446090-77-2;1446090-79-4)BGB-283，也称为Beigene-283或Lifirafenib，是一种新的有效的和选择性的
- Belizatinib (Catalog# : 17101619, Cas# : 1357920-84-3)Belizatinib，也称为TSR-011，具有受体酪氨酸激酶间变性淋巴瘤激酶（
- Bioymifi (Catalog# : 1710165, Cas# : 1420071-30-2)Bioymifi是DR5的活性剂(Kd = 1.2 µM; IC50 = 2 µM). Bioymifi诱导凋亡的肿瘤
- BLU-554 (Catalog# : 1710162, Cas# : 1707289-21-1)BLU-554是针对肝癌治疗的成纤维细胞生长因子受体4（FGFR4）抑制剂
- BX-517 (Catalog# : 1791314, Cas# : 850717-64-5)BX-517，又名PDK1 inhibitor2，是强有力的和有选择性的PDK1抑制剂。
- BBT-594 (Catalog# : 179133, Cas# : 882405-89-2)BBT594，也称为NVP-BBT594，是强有力的和有选择性的RET和JAK2抑制剂。
- BAY41-4109消旋体 (Catalog# : 1791117, Cas# : 298708-79-9)Bay41-4109消旋体是对Bay41-4109和S-异构体Bay41-4109 R-异构体的混合物。
- BAR-501 (Catalog# : 179821, Cas# : 1632118-69-4)BAR-501是一种选择性GPBAR1激动剂，没有任何的FXR激动剂活性。BAR-50
- Batefenterol(free base) (Catalog# : 179820, Cas# : 743461-65-6)Batefenterol，也称为 GSK961081和TD-5959，是一种毒蕈碱拮抗剂和β2-受体
- BI-847325 (Catalog# : 83101, Cas# : 1207293-36-4)BI-847325是一种口服、具有选择性的日常生物MEK/Aurora激酶抑制剂，
- BAY-598 (Catalog# : 17982, Cas# : 1906919-67-2)BAY-598是一种强效的针对SMYD2中肽-竞争的化学探测器。BAY-598拥有一
- BAY-598 R-异构体 (Catalog# : 17981, Cas# : 1906920-28-2)BAY-598 R-异构体是BAY589 R-异构体。bay-598 R-异构体可以作为一个参照
- 布索芬新 (Catalog# : 17916, Cas# : 171655-91-7)布索芬新是一种充分的单胺再摄取阻滞剂，已被开发用于治疗帕金
- B02 (Catalog# : 1783013, Cas# : 1290541-46-6)B02，也叫RAD51 - in - 02，是一种RAD51抑制剂。B02能增强MM细胞的DOX敏
- BLU-285 (Catalog# : 1781003, Cas# : 1703793-34-3)BLU-285是一种有效、具有选择性的抑制剂。
- BAY-1895344 (Catalog# : 1781002, Cas# : 1876467-74-1)BAY-1895344是一种有效的、具有选择性的ATM抑制剂。
- BIBR1532 (Catalog# : 178813, Cas# : 321674-73-1)BIBR1132对端粒酶的抑制具有很强的选择性，导致肿瘤细胞延迟生长
- BMS-932481 (Catalog# : 2017877, Cas# : 1263871-36-8)BMS-932481调节Aβ肽在血浆和脑脊液的健康志愿者。
- B-1613 (Catalog# : 20178216, Cas# : 214066-78-1)(2S,4S)-4-(氨基甲基)吡咯烷-1,2-二羧酸 1-叔丁酯 2-甲酯；(2S,4S)-1-tert
- Balamapimod (Catalog# : 2017822, Cas# : 863029-99-6)<span style="color:#34495E;font-family:" font-Balamapimod, 也称为MKI-822,是一种
产品分类
- ---- 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
- ---- Methionine Adenosyltransferase (MAT)
- -- 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
- ---- Ras
- ---- Cholecystokinin Receptor
- ---- Melanocortin Receptor
- ---- RXFP Receptor
- ---- Bradykinin Receptor
- ---- GLP Receptor
- -- Immunology & Inflammation
- ---- PD-1
- ---- PD-L1
- ---- COX
- ---- CCR
- ---- Histamine Receptor
- ---- TLR
- ---- CXCR
- ---- MALT
- ---- TDO
- ---- NOS
- ---- IDO
- ---- Thrombopoietin Receptor(TPO)
- ---- NLR inhibitor
- ---- Interleukin Related
- ---- CD73
- ---- Complement System
- ---- Aryl Hydrocarbon Receptor
- ---- Kallikrein
- ---- IRAK
- ---- Reactive Oxygen Species(ROS)
- ---- SOD
- -- 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
- -- Metabolic Enzyme/Protease
- ---- PPAR
- ---- Proteasome
- ---- P450
- ---- Caspase
- ---- HSP
- ---- HIV Protease
- ---- PDE
- ---- MMP
- ---- Factor Xa
- ---- γ-secretase
- ---- Phospholipase
- ---- DPP4
- ---- FAAH
- ---- CETP
- ---- Lipoxygenase
- ---- HMG-CoA Reductase
- ---- Fatty Acid Synthase
- ---- NADPH-oxidase
- ---- FXR
- ---- NAMPT
- ---- TDO
- ---- Carbonic Anhydrase
- ---- Monoamine Oxidase
- ---- IDO
- ---- Mitochondrial Metabolism
- ---- Isocitrate Dehydrogenase (IDH)
- ---- MAGL
- ---- Epoxide Hydrolase
- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- FPTase
- ---- RAR/RXR
- ---- Acetyl-CoA Carboxylase
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- ---- Glutaminase
- ---- Ketohexokinase(KHK)
- ---- Lipase
- ---- Lactate dehydrogenase
- ---- Glyoxalase (GLO)
- ---- E1/E2/E3 Enzyme
- ---- PANK(pantothenate kinase)
- ---- Phosphoglycerate Dehydrogenase (PHGDH)
- -- 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)
- ---- CGRP-Receptor
- ---- TRP-Channel
- -- 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)
- -- PI3K/Akt/mTOR
- ---- PI3K
- ---- Akt
- ---- GSK-3
- ---- S6 Kinase
- ---- AMPK
- ---- DNA-PK
- ---- MELK
- ---- PIKfyve
- ---- PI4K
- ---- PTEN
- ---- mTOR
- ---- ATM
- ---- PDK-1
- ---- ATR
- ---- Vps34
- -- Stem Cells & Wnt
- ---- GSK-3
- ---- JAK
- ---- STAT
- ---- ROCK
- ---- TGF-beta/Smad
- ---- Wnt
- ---- γ-secretase
- ---- β-catenin
- ---- smo
- ---- Notch
- -- 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
- -- Nuclear Receptor
- ---- Androgen Receptor(AR)
- -- 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
- ECI830 (Catalog# : 26A031, Cas# : 3054692-62-2)ECI830是一种实验性的CDK2抑制剂。
- GNE-317 (Catalog# : 52282, Cas# : 1394076-92-6)GNE-317 is a potent, brain-penetrantPI3Kinhibitor
- DPTX-3186 (Catalog# : 26A010, Cas# : 3118994-80-9)DPTX3186 是一种口服的小分子凝聚体调节剂 (c-mod)，可抑制 β-catenin
- Avasopasem manganese (GC-4419; M-40419) (Catalog# : 25108, Cas# : 435327-40-5)Avasopasem manganese, 也称为GC-4419、M 40419和SC-72325A，是超氧化物歧化酶
- 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
- Kartogenin ( KGN ) (Catalog# : 52215, Cas# : 4727-31-5)Kartogenin（KGN）是一种合成小分子，通过激活smad-4/5通路刺激软骨细
- Imisopasem manganese ( M40403; GC4403 ) (Catalog# : 72602, Cas# : 218791-21-0)Imisopasem manganese ( M40403; GC4403 ) 是一种稳定的非肽类 MnSOD 类似物，
- Apecotrep (BI 764198) (Catalog# : 26A048, Cas# : 2311863-36-0)Apecotrep（BI 764198）是一种潜在的同类首创、口服、选择性的TRPC6抑
- Pantothenate kinase-IN-2 (Catalog# : 26A038, Cas# : 902614-04-4)Pantothenate kinase-IN-2是一种泛酸激酶抑制剂，对PanK2的IC50值为92 nM，
- BH-30643 (Catalog# : 26A047, Cas# : 3062177-59-4)BH-30643是一种新型、口服、非共价、大环、突变选择性OMNI-EGFR抑制