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产品名字索引 A
- 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
- AR-7 (Catalog# : 179158, Cas# : 80306-38-3)AR-7，亦称非典型维甲酸7，是一种有效的和选择性的自噬（CMA）增
- 阿地米屈 (Catalog# : 179151, Cas# : 1675-66-7)阿地米屈是壬二酸的合成酰胺衍生物，具有对称的化学结构。它被
- AZD7545 (Catalog# : 179136, Cas# : 252017-04-2)AZD7545是丙酮酸脱氢酶激酶2抑制剂（pdhk2）（对6.4nm IC50值）用于治
- AMG-9810 (Catalog# : 179117, Cas# : 545395-94-6)AMG 9810是对香草类受体1的辣椒素激活竞争性拮抗剂（TRPV1）。此外
- AS-2444697 HCl (Catalog# : 179832, Cas# : 1287665-60-4)AS-2444697是一种 RAK-4抑制剂。六周重复给药AS2444697（0.3-3mg/kg，一天
- 乙酰卡尼盐酸盐 (Catalog# : 179829, Cas# : 34118-92-8)乙酰卡尼，又名N-乙酰普鲁卡因胺和ASL 601，普鲁卡因胺是N-乙酰化
- ASC-J9 (Catalog# : 179816, Cas# : 52328-98-0)ASC-J9，也称为GO-Y025和去甲氧基姜黄素，是一个AR降解剂，ASC-J9通过
- AMG-009 (Catalog# : 17987, Cas# : 1027847-67-1)AMG 009是一种口服活性小分子CRTH2受体（趋化受体的同源分子表达在
- 5-氨基-2-氟-4-甲基苯腈 (Catalog# : 1781603, Cas# : 1426136-04-0)5-氨基-2-氟-4-甲基苯腈,5-amino-2-fluoro-4-methylbenzonitrile
- 2-azaspiro[3.5]nonan-7-ol hydrochloride (Catalog# : 1781602, Cas# : 1434141-67-9)2-azaspiro[3.5]nonan-7-ol hydrochloride
- AZD3264 (Catalog# : 178910, Cas# : 1609281-86-8)AZD3264是一种新型的小分子IKK2抑制剂。IKK2作为IB激酶的蛋白质亚基
- A-971432 (Catalog# : 178816, Cas# : 1240308-45-5)A - 971432对S1P5具有高度选择性，在临床前口服剂量后，显露出良好
- A-1165442 (Catalog# : 20178812, Cas# : 1221443-94-2)A-1165442是一种中性温度具有止痛功效的瞬时受体电位香草酸亚型1
- AZD4205 (Catalog# : 20178710, Cas# : 2091134-35-7)AZD4205是一种高效JAK1-选择性激酶抑制剂，拥有优秀的临床前药代动
- ACY-775 (Catalog# : 77821, Cas# : 1375466-18-4)ACY-775是一种组蛋白去乙酰化酶6(HDAC6)选择性抑制剂。
- AAI-101 (Catalog# : 1773101, Cas# : 1001404-83-6)AAI101(AAI101)是一种新型的增谱-乳酸酶抑制剂。AAI101(AAI101)与头孢吡
- AV-412甲苯磺酸盐 (Catalog# : 17030105, Cas# : 451493-31-5)AV-412,也称为MP-412,是第二代生物可利用的双激酶抑制剂，具有潜在
- AZD-7594 (Catalog# : 17022812, Cas# : 1196509-60-0)AZD-7594，也叫AZ13189620，是一种吸入选择性糖皮质激素受体(GCCR)调制
- AZD3839 (Catalog# : 17022710, Cas# : 1227163-56-5)AZD3839是一种有效的选择性BACE1抑制剂。AZD3839是治疗阿尔茨海默病
- A-1210477 (Catalog# : 17022404, Cas# : 1668553-26-1)A-1210477是一种有效、选择性的MCL-1抑制剂。
- 阿帕替尼 (Catalog# : 17022301, Cas# : 811803-05-1)阿帕替尼是一种具有生物口服、选择性的IC50为1 nM的VEGFR2 抑制剂。
- 硫酸阿米卡星 (Catalog# : 17021407, Cas# : 39831-55-5)硫酸阿米卡星(BAY416651 硫酸)是一种由卡那霉素a衍生的半合成氨基
- AFN-1252 (Catalog# : 17021406, Cas# : 620175-39-5)AFN-1252(Debio 1452) 是enoyl -酰基载体蛋白还原酶(FabI)的有效抑制剂。
产品分类
- ---- VEGFR
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- -- Autophagy
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- -- Cell Cycle
- ---- CDK
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- ---- Chk
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- ---- APC
- ---- Wee1
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- ---- c-Myc
- ---- Aurora Kinase
- ---- ROCK inhibitor
- ---- Eukaryotic Initiation Factor (eIF)
- -- Cytoskeleton
- ---- HSP
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- ---- Integrin
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- ---- Wnt
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- -- DNA Damage
- ---- PARP
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- ---- Sirtuin
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- ---- Mps1
- -- Epigenetics
- ---- PARP
- ---- JAK
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- ---- Histone Demethylase
- ---- Histone Acetyltransferase
- ---- HDAC
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- ---- Aurora Kinase
- ---- Histone Methyltransferase
- ---- METTL3
- ---- Epigenetic Reader Domain
- -- GPCR & G Protein
- ---- Histamine Receptor
- ---- Dopamine Receptor
- ---- Opioid Receptor
- ---- Endothelin Receptor
- ---- SGLT
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- ---- CaSR
- ---- CXCR
- ---- Vasopressin Receptor
- ---- Glucagon Receptor
- ---- Prostaglandin Receptor
- ---- 5-HT Receptor
- ---- Adrenergic Receptor
- ---- Cannabinoid Receptor
- ---- Sphingosine 1 Phosphate Receptor
- ---- PKA
- ---- Adenosine Receptor
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- ---- Ras
- ---- Cholecystokinin Receptor
- ---- Melanocortin Receptor
- ---- RXFP Receptor
- ---- Bradykinin 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
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- ---- Potassium Channel
- ---- Proton Pump
- -- Metabolism
- ---- PPAR
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- ---- Factor Xa
- ---- Phospholipase
- ---- FAAH
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- ---- 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
- ---- Glucosylceramide Synthase (GCS)
- -- 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)
- -- Proteases
- ---- Proteasome
- ---- Caspase
- ---- HIV Protease
- ---- MMP
- ---- γ-secretase
- ---- DPP4
- ---- Isocitrate Dehydrogenase (IDH)
- ---- FPTase
- ---- Acetyl-CoA Carboxylase
- ---- Glutaminase
- ---- Methionine Adenosyltransferase (MAT)
- ---- Lipase
- -- 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
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- ---- PKK
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- ---- Newest added products
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- -- Chiral Compounds
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- -- Imidazoles
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- -- 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
- Dencatistat (STP938) (Catalog# : 25177, Cas# : 2377000-84-3)Dencatistat 是一种口服生物可利用的小分子胞苷三磷酸合酶 1 (CTPS1)
- DS-1001b (Catalog# : 25178, Cas# : 1898207-64-1)DS-1001 是一种口服的脑渗透性突变 IDH1 选择性抑制剂。
- Z57346765 (Catalog# : 25191, Cas# : 1016340-64-9)Z57346765 是一种 PGK1 特异性抑制剂，可降低 PGK1 糖酵解中代谢酶的
- CBR-470-1 (Catalog# : 25192, Cas# : 2416095-06-0)CBR-470-1 是诱导 Nrf2 活性的糖酵解酶 PGK1 的抑制剂。
- 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（
- HC-7366 (Catalog# : 25076, Cas# : 2803470-63-3)HC-7366 is a potent and selective activator of the general control nonderepressible 2
- Flavopiridol ( 夫拉平度 ) (Catalog# : 237071, Cas# : 146426-40-6)Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
- AG-270 (Catalog# : 25176, Cas# : 2201056-66-6)MAT2A 抑制剂 AG-270 是一种口服的蛋氨酸腺苷转移酶 II α (MAT2A) 小分
- 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
- ALT-007 (Catalog# : 25157, Cas# : 2035010-37-6)ALT-007 是一种口服生物可利用的 SPT 抑制剂，比多球菌素更有效，