武汉永璨生物科技有限公司
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- 抑制剂/受体激动剂
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产品名字索引 A
- AMD-070盐酸盐 (Catalog# : 18741, Cas# : 880549-30-4)AMD11070，也称为 AMD070, X4P-001和mavorixafor, 是一种有效的口服生物活
- AG-494 (Catalog# : 186273, Cas# : 133550-35-3)AG-494，也被称为Tyrphostin AG- 494,是表皮生长因子受体激酶的抑制剂
- AZD5153 (Catalog# : 186254, Cas# : 1869912-39-9)AZD5153是一种有效的双价三唑吡啶溴化和外治(BET)抑制剂。
- 阿莫奈韦 (Catalog# : 186252, Cas# : 841301-32-4)阿莫奈韦是一种 helicase-primase 抑制剂，对 HSVs 具有强效的抗病毒活
- A22盐酸盐 (Catalog# : 186211, Cas# : 22816-60-0)A22是一种MreB的抑制剂，是一种类似actin样的细菌蛋白，已经被证明
- AST487 (Catalog# : 186158, Cas# : 630124-46-8)AST487, 也称为NVP- AST487, 是一种RET激酶抑制剂/FLT3抑制剂。
- ARV-825 (Catalog# : 185253, Cas# : 1818885-28-7)ARV-825是一种保护蛋白(蛋白酶-靶向嵌合体)。ARV-825与溴域抑制剂(B
- 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
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)
- -- 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
- ---- 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
- ---- 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
- ---- 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
- -- Microbiology
- -- Others
- ---- PKK
- ---- Others modulator
- ---- Estrogen Receptor/ERR
- ---- ChoKα
- ---- Newest added products
- -- 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
- 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，