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产品名字索引 A
- AM281 (Catalog# : 19315, Cas# : 202463-68-1)AM281是一种合成大麻素CB1受体拮抗剂。
- ASP9521 (Catalog# : 19312, Cas# : 1126084-37-4)ASP9521是日常的，选择性,口服生物利用率17β-羟甾类脱氢酶的抑制
- AZD0364 (Catalog# : 192275, Cas# : 2097416-76-5)AZD0364是一种用于治疗癌症的ERK1和/或ERK2激酶。ERK1和ERK2激酶是广泛
- ATF6-活化剂-147 (Catalog# : 192212, Cas# : 393121-74-9)ATF6-activator-147是一种ATF6模拟器，它作为一种前体药物，通过一种
- AZD1152 (Catalog# : 192156, Cas# : 722543-31-9)AZD1152是Barasertib-hQPA的前药，是一种高选择性极光B抑制剂，在无细
- AZD3229 (Catalog# : 191287, Cas# : 2248003-60-1)AZD3229是治疗胃肠道间质瘤的一种有效的pan-kit突变抑制剂。AZD3229在
- AM095钠 (Catalog# : 191251, Cas# : 1345614-59-6)AM095是一个强有力的LPA1受体拮抗剂,因为它抑制GTPγS绑定中国仓鼠
- AZD4573 (Catalog# : 191212, Cas# : 2057509-72-3)AZD-4573是一种选择性的丝氨酸/苏氨酸依赖性激酶9 (CDK9)的短期抑制
- AR-9281 (Catalog# : 191146, Cas# : 913548-29-5)AR-9281是一种可溶性环氧化物水解酶(s-EH)抑制剂，有望用于高血压
- ARRY-797 (ARRY-371797) (Catalog# : 191112, Cas# : 1036404-17-7)ARRY-797(CAS1036404-17-7) is an oral, selective p38 mitogen-activated protein kinase
- 艾维替尼 (Catalog# : 19141, Cas# : 1557267-42-1)艾维替尼，又称AC0010和Avitinib，是酪氨酸激酶抑制剂，抗肿瘤药物
- AZD7507 (Catalog# : 1812294, Cas# : 1041852-85-0)AZD7507是一种有效的选择性CSF-1R抑制剂(32 nM 细胞活性)， AZD7507被认
- Auranofin (Catalog# : 1812281, Cas# : 34031-32-8)Auranofin又称Ridaura和SKF-39162，是一种治疗类风湿性关节炎的口服大
- AX-024盐酸盐 (Catalog# : 181254, Cas# : 1704801-24-0)AX-024是一种口服的TCR-Nck相互作用抑制剂，选择性地抑制TCR-触发的
- AG 879 (Catalog# : 1811303, Cas# : 148741-30-4)AG-879是一种酪氨酸磷酸化抑制剂复合物，可抑制PC-12细胞中依赖神
- Avagacestat (Catalog# : 1811283, Cas# : 1146699-66-2)Avagacestat,也称为BMS- 708163是一种口服GSI用于选择性抑制Aβ合成，目
- AS1842856 (Catalog# : 1811265, Cas# : 836620-48-5)AS1842856是一种细胞可渗透的Foxo1抑制剂，IC50为33 nM，阻断Foxo1的转
- Anlotinib HCl ( AL-3818 ) (Catalog# : 1811211, Cas# : 1360460-82-7)Anlotinib也被称为AL3818，是一种受体酪氨酸激酶(RTK)抑制剂，具有潜
- Avatrombopag maleate (Catalog# : 5141902, Cas# : 677007-74-8)Avatrombopag maleate 是一种口服生物可用的小分子血栓生成素受体激动
- AZD-3514 (Catalog# : 1810251, Cas# : 1240299-33-5)AZD-3514是一种具有潜在抗癌活性的雄激素受体下调因子。
- AZ32 (Catalog# : 1810223, Cas# : no)AZ32 是一种口服可利用的，可穿透血脑屏障的 ATM 抑制剂，IC50<6
- ARS-1620 (Catalog# : 1810222, Cas# : 1698055-85-4)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。
- AGL-2263 (Catalog# : 1810175, Cas# : 638213-98-6)AGL-2263是一种新型的胰岛素受体抑制剂。
- AM211 (Catalog# : 1810173, Cas# : 1175526-27-8)AM-211是前列腺素D2受体2型的一种新型强效拮抗剂。
- Arimoclomol maleate (Catalog# : 188281, Cas# : 289893-26-1)Arimoclomol，也被称为BRX-220，能够潜在有用的治疗Niemann-Pick疾病C型
- ASP7663 (Catalog# : 187123, Cas# : 1190217-35-6)ASP7663是口服生物可利用选择性TRPA1激活剂。
- Aldoxorubicin盐酸盐 (Catalog# : 187111, Cas# : 480998-12-7)Aldoxorubicin,也称为INNO-206和Doxo-EMCH，是蒽醌类抗生素类霉素的6-马来
- ABT 702盐酸盐 (Catalog# : 18791, Cas# : 1188890-28-9)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
- Avacopan (Catalog# : 18761, Cas# : 1346623-17-3)Avacopan也被称为CCX168，是一种口服活性、选择性和有效的C5aR抑制剂
- AEW-541 (Catalog# : 18753, Cas# : 475489-16-8)AEW541, 也称为NVP-AEW541,是一种有日常有效的IGF-IR激酶抑制剂。
产品分类
- ---- VEGFR
- ---- JAK
- ---- EGFR
- ---- PDGFR
- ---- FLT3
- ---- FGFR
- ---- Src
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- ---- Syk
- ---- HIF
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- ---- HSV
- ---- Influenza Virus
- ---- RSV
- ---- SARS-CoV
- ---- 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
- ---- 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
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- -- Antibody-drug Conjugate/ADC Related
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- ---- PKK
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- ---- Estrogen Receptor/ERR
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- ---- Newest added products
- -- Aldehydes
- -- Amines
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- -- Anilines
- -- Boronic Acids
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- -- Chiral Compounds
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- -- 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，