武汉永璨生物科技有限公司
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Cas号索引 1
- 1240299-33-5 | AZD-3514 (Catalog# : 1810251)AZD-3514是一种具有潜在抗癌活性的雄激素受体下调因子。
- 1698055-85-4 | ARS-1620 (Catalog# : 1810222)ARS-1620是一种具有理想药代动力学的阿托品选择性KRAS-G12C抑制剂。
- 1175526-27-8 | AM211 (Catalog# : 1810173)AM-211是前列腺素D2受体2型的一种新型强效拮抗剂。
- 1190217-35-6 | ASP7663 (Catalog# : 187123)ASP7663是口服生物可利用选择性TRPA1激活剂。
- 1188890-28-9 | ABT 702盐酸盐 (Catalog# : 18791)ABT 702二盐酸盐是一种强效的非核苷腺苷激酶抑制剂，对腺甘酸相
- 1346623-17-3 | Avacopan (Catalog# : 18761)Avacopan也被称为CCX168，是一种口服活性、选择性和有效的C5aR抑制剂
- 133550-35-3 | AG-494 (Catalog# : 186273)AG-494，也被称为Tyrphostin AG- 494,是表皮生长因子受体激酶的抑制剂
- 1869912-39-9 | AZD5153 (Catalog# : 186254)AZD5153是一种有效的双价三唑吡啶溴化和外治(BET)抑制剂。
- 1818885-28-7 | ARV-825 (Catalog# : 185253)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
- 1637771-14-2 | Alobresib (Catalog# : 185222)Alobresib是抗肿瘤药物的候选药物。
- 1467013-03-3 | Adavivint (Catalog# : 185221)Adavivint是一种Wnt通道抑制剂和免疫调制剂药物候选者。
- 1889279-16-6 | A-485 (Catalog# : 185211)A-485是一种有效且具有选择性的p300/CBP在体外的HAT抑制剂。
- 1883727-34-1 | AMG-176 (Catalog# : 185185)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
- 1217201-17-6 | A-350619盐酸盐 (Catalog# : 185183)A-350619盐酸盐是可溶性的胍基环酶(sGC)的激活剂。
- 1253573-53-3 | AMG-511 (Catalog# : 18542)AMG-511是一种有效的选择性的泛型I PI3K抑制剂。
- 1186206-79-0 | ALW-II-41-27 (Catalog# : 1842813)ALW-II-41-27是一种Eph受体酪氨酸激酶抑制剂。
- 1321514-06-0 | AZD4635 (Catalog# : 184289)AZD-4635，也叫HTL-1071，是一种口服的小分子腺苷A2A受体拮抗剂。
- 1229453-99-9 | Acrizanib (Catalog# : 184181)Acrizanib，又名LHA510，是一种有效的选择性血管生成抑制剂和VEGFR -
- 1032570-98-1 | 2-amino-3-methoxy-4-(3-morpholin-4-ylpropoxy)benzonitrile (Catalog# : 184163)2-amino-3-methoxy-4-(3-morpholin-4-ylpropoxy)benzonitrile是一种药物中间体。
- 1058156-90-3 | 安罗替尼 (Catalog# : 184132)安罗替尼，又名AL3818，是一种受体酪氨酸激酶(RTK)抑制剂，具有潜
- 1125758-85-1 | A-804598 (Catalog# : 184125)A-804598是一种P2X7选择性、竞争性的拮抗剂。
- 185991-07-5 | AMD3465 HCl salt (Catalog# : 184310)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
- 1220646-23-0 | AVN-492 (Catalog# : 18425)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
- 1173154-32-9 | ALB-127158A (Catalog# : 18424)ALB-127158A, also known as ALB-127158(a), is a MCH1 antagonist for the treatment of o
- 1492952-76-7 | Asciminib ( ABL001 ) (Catalog# : 1711222)Asciminib, 也叫ABL001，是一种有效的BCR-ABL的变构抑制剂。ABL001在与尼
- 1644443-47-9 | Autophinib (Catalog# : 17101617)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
- 1124197-79-0 | Adarigiline (Catalog# : 1710167)adarigiline是单胺氧化酶B抑制剂的候选药物。
- 1613589-09-5 | Adafosbuvir (Catalog# : 1710166)Adafosbuvir是一种抗病毒药物。
- 1869912-40-2 | AZD-5153 HNT salt (Catalog# : 1710161)AZD-5153 HNT盐，是AZD-5153的6-hydroxy-2-naphthoic酸盐。AZD-5153对抗血液系
- 1675-66-7 | 阿地米屈 (Catalog# : 179151)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
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
- -- Antibody-drug Conjugate/ADC Related
- -- 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
- 266359-83-5 | Reparixin (Catalog# : 25050)Reparixin is an inhibitor of CXCR2 function, which attenuates inflammatory responses
- 229005-80-5 | TAK-779 (Catalog# : 25049)TAK-779 is a C-C chemokine receptor type 5 (CCR5) receptor antagonist potentially for
- 1402608-02-9 | BAY-1125976 (Catalog# : 25048)BAY-1125976 is a potent and selective allosteric AKT1/2 inhibitor. BAY-1125976 exhibi
- 1628606-05-2 | Vimseltinib free base (Catalog# : 25047)Vimseltinib, also known as DCC-3014, is a potent and orally active inhibitor of the t
- 2128698-24-6 | 2-Propynamide, 3-[(3Z)-3-[[[4-[(dimethylamino)methyl]phenyl]amino]phenylmethylene]-2,3-dihydro-2-oxo-1H-indol-6-yl]-N-ethyl- (Catalog# : 25046)
- 1371587-51-7 | Cavosonstat (Catalog# : 25045)Cavosonstat, alos known as N91115) an orally bioavailable inhibitor of S-nitrosogluta
- 259657-09-5 | Ivospemin Hydrochloride (Catalog# : 25044)Ivospemin is an antineoplastic spermine analogue.
- 2805997-46-8 | Survodutide (Catalog# : 25043)
- 2595308-10-2 | XRD-0394 (Catalog# : 25042)XRD-0394 is a DNA-PKcs inhibitor. XRD-0394 selectively targets, binds to and inhibits
- 1621999-82-3 | CC-90003 (Catalog# : 25041)CC-90003 is an orally available inhibitor of extracellular signal-regulated kinase (E