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产品名字索引 A
- Alobresib (Catalog# : 185222, Cas# : 1637771-14-2)Alobresib是抗肿瘤药物的候选药物。
- Adavivint (Catalog# : 185221, Cas# : 1467013-03-3)Adavivint是一种Wnt通道抑制剂和免疫调制剂药物候选者。
- ALX 1393 (Catalog# : 185213, Cas# : 949164-09-4)ALX 1393是一种甘氨酸转运体-2抑制剂。
- A-485 (Catalog# : 185211, Cas# : 1889279-16-6)A-485是一种有效且具有选择性的p300/CBP在体外的HAT抑制剂。
- AS-1517499 (Catalog# : 185187, Cas# : 919486-40-1)AS-1517499是一种有效且具有选择性的STAT6抑制剂。
- AMG-176 (Catalog# : 185185, Cas# : 1883727-34-1)AMG-176是诱导髓系白血病细胞分化蛋白MCL-1(骨髓细胞白血病-1)的抑
- A-350619盐酸盐 (Catalog# : 185183, Cas# : 1217201-17-6)A-350619盐酸盐是可溶性的胍基环酶(sGC)的激活剂。
- ARQ-531 (Catalog# : 185176, Cas# : 2095393-15-8)ARQ-531是一种具有潜在抗肿瘤活性的有效的口服BTK抑制剂。
- ADX-47273 (Catalog# : 185173, Cas# : 851881-60-2)ADX-47273是一种强有力的和选择性mGluR5受体PAM(积极的变构调制器),E
- AMG-511 (Catalog# : 18542, Cas# : 1253573-53-3)AMG-511是一种有效的选择性的泛型I PI3K抑制剂。
- AZD1390 (Catalog# : 18541, Cas# : 2089288-03-7)AZD1390是一种强效和选择性的ATM抑制剂，适合治疗颅内恶性肿瘤，
- ALW-II-41-27 (Catalog# : 1842813, Cas# : 1186206-79-0)ALW-II-41-27是一种Eph受体酪氨酸激酶抑制剂。
- AZD4635 (Catalog# : 184289, Cas# : 1321514-06-0)AZD-4635，也叫HTL-1071，是一种口服的小分子腺苷A2A受体拮抗剂。
- Acrizanib (Catalog# : 184181, Cas# : 1229453-99-9)Acrizanib，又名LHA510，是一种有效的选择性血管生成抑制剂和VEGFR -
- 2-amino-3-methoxy-4-(3-morpholin-4-ylpropoxy)benzonitrile (Catalog# : 184163, Cas# : 1032570-98-1)2-amino-3-methoxy-4-(3-morpholin-4-ylpropoxy)benzonitrile是一种药物中间体。
- 安罗替尼 (Catalog# : 184132, Cas# : 1058156-90-3)安罗替尼，又名AL3818，是一种受体酪氨酸激酶(RTK)抑制剂，具有潜
- A-804598 (Catalog# : 184125, Cas# : 1125758-85-1)A-804598是一种P2X7选择性、竞争性的拮抗剂。
- AMD3465 HCl salt (Catalog# : 184310, Cas# : 185991-07-5)AMD3465是一种新型CXCR4受体拮抗剂，具有潜在的抗癌和抗艾滋病活性
- 阿必鲁肽 (Catalog# : 18438, Cas# : 782500-75-8)阿必鲁肽是一种胰高血糖素-样 肽-1受体激动剂(GLP-1 受体激动剂)。
- AVN-492 (Catalog# : 18425, Cas# : 1220646-23-0)AVN-492是一种有效且具有选择性的5-HT6R拮抗剂。AVN-492具有良好的体
- ALB-127158A (Catalog# : 18424, Cas# : 1173154-32-9)ALB-127158A, also known as ALB-127158(a), is a MCH1 antagonist for the treatment of o
- AZD-5904 (Catalog# : 181121, Cas# : 618913-30-7)AZD5904是一个有效的口服生物利用率MPO抑制剂。在临床前研究中,AZ
- 2-氨基嘧啶-5-羧酸 (Catalog# : 171281, Cas# : 3167-50-8)2-氨基嘧啶-5-羧酸
- Asciminib ( ABL001 ) (Catalog# : 1711222, Cas# : 1492952-76-7)Asciminib, 也叫ABL001，是一种有效的BCR-ABL的变构抑制剂。ABL001在与尼
- Autophinib (Catalog# : 17101617, Cas# : 1644443-47-9)Autophinib是一种新颖有效的自噬抑制剂，抑制通过靶向脂质激酶VPS
- Adarigiline (Catalog# : 1710167, Cas# : 1124197-79-0)adarigiline是单胺氧化酶B抑制剂的候选药物。
- Adafosbuvir (Catalog# : 1710166, Cas# : 1613589-09-5)Adafosbuvir是一种抗病毒药物。
- AZD-5153 HNT salt (Catalog# : 1710161, Cas# : 1869912-40-2)AZD-5153 HNT盐，是AZD-5153的6-hydroxy-2-naphthoic酸盐。AZD-5153对抗血液系
- ABT-100 (Catalog# : 1710131, Cas# : 450839-40-4)abt-100是一种口服的法尼基转移酶抑制剂.
- 阿西鲁司特 (Catalog# : 179159, Cas# : 943764-99-6)阿西鲁司特,也称为ZK322，是强有力的和有选择性的白三烯A4水解酶
产品分类
- ---- VEGFR
- ---- JAK
- ---- EGFR
- ---- PDGFR
- ---- FLT3
- ---- FGFR
- ---- Src
- ---- ALK
- ---- Syk
- ---- HIF
- -- Anti-infection
- ---- CMV
- ---- Filovirus
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- ---- HIV
- ---- HSV
- ---- Influenza Virus
- ---- RSV
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- ---- Antibacterial
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- ---- 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)
- -- 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
- -- 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
- -- 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
- ---- Kallikrein
- ---- IRAK
- -- 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
- -- 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
- ---- Mitochondrial Metabolism
- ---- MAGL
- ---- Epoxide Hydrolase
- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- RAR/RXR
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- ---- Ketohexokinase(KHK)
- -- 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
- -- NF-κB
- ---- NF-κB
- ---- HDAC
- ---- IKK
- -- 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
- -- Proteases
- ---- Proteasome
- ---- Caspase
- ---- HIV Protease
- ---- MMP
- ---- γ-secretase
- ---- DPP4
- ---- Isocitrate Dehydrogenase (IDH)
- ---- FPTase
- ---- Acetyl-CoA Carboxylase
- ---- Glutaminase
- ---- Methionine Adenosyltransferase (MAT)
- -- PI3K/Akt/mTOR
- ---- PI3K
- ---- Akt
- ---- GSK-3
- ---- S6 Kinase
- ---- AMPK
- ---- DNA-PK
- ---- MELK
- ---- PIKfyve
- ---- PI4K
- ---- PTEN
- ---- mTOR
- ---- ATM
- ---- PDK-1
- ---- ATR
- -- Stem Cells & Wnt
- ---- GSK-3
- ---- JAK
- ---- STAT
- ---- ROCK
- ---- TGF-beta/Smad
- ---- Wnt
- ---- γ-secretase
- ---- β-catenin
- ---- smo
- -- TGF-beta/Smad
- ---- PKC
- ---- ROCK
- ---- TGF-beta/Smad
- -- Ubiquitin
- ---- Proteasome
- ---- p97
- ---- Deubiquitinase
- -- Vitamin D Related
- ---- VD/VDR
- -- PROTAC
- ---- Molecular Glues
- ---- PROTACs
- -- Antibody-drug Conjugate/ADC Related
- -- Microbiology
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- ---- Newest added products
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- -- 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
- AZD0095 (Catalog# : 237072, Cas# : 2750001-23-9)AZD0095 is a Selective Inhibitor of Monocarboxylate Transporter 4 (MCT4) for Oncology.
- 2-MNG (Catalog# : 24129, Cas# : 2101538-28-5)2-巯基烟酰甘氨酸是一种新型强效黑素生成抑制剂，具有独特的作
- MAT2A-IN-9 (Catalog# : 25147, Cas# : 2439277-80-0)MAT2A-IN-9（化合物167）是一种2-氧代喹唑啉衍生物，是一种强效的M
- Safusidenib (Catalog# : 25149, Cas# : 1898206-17-1)Safusidenib，也称为DS-1001，是一种口服异柠檬酸脱氢酶[NADP]细胞质（
- Atebimetinib (Catalog# : 25148, Cas# : 2669009-92-9)阿替美替尼（IMM-1-104）是一种口服的小分子MEK1和MEK2激酶变构抑制
- Acoramidis hydrochloride (Catalog# : 24068, Cas# : 2242751-53-5)Acoramidis是一种口服、强效、高选择性小分子转甲状腺素蛋白（TTR
- Crelosidenib (Catalog# : 24101, Cas# : 2230263-60-0)Crelosidenib （ [LY3410738）是一种有效的选择性的具有口服活性的突变
- LOXO-435 (Catalog# : 25080, Cas# : 2833703-74-3)LOXO-435是FGFR3的选择性小分子抑制剂。它对野生型和致癌激活的FGF
- Gridegalutamide (Catalog# : 25138, Cas# : 2446928-30-7)Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
- Chiauranib (Catalog# : 25146, Cas# : 1256349-48-0)Chiauranib also known as orally available, small molecule inhibitor of select serine-