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Cas号索引 2

• 2227304-19-8 | CP-506 ( Synonyms: SN-36506 ) (Catalog# : 20645)CP-506 (SN-36506) 是一种缺氧激活的 DNA 烷基化氮芥化合物前药，能够
• 209986-17-4 | Compound E (Catalog# : 20575)Compound E is a cell-permeable, potent, selective inhibitor of ɣ-secretase and Notch
• 20217-22-5 | COH1 inhibitor (Catalog# : 20555)COH1 is a ribonucleotide reductase (RR) inhibitor.
• 2259648-80-9 | CC-92480 ( Mezigdomide ) (Catalog# : 20510)CC-92480 是一种有效的新型 CELMoD 化合物，旨在快速最大程度地降解
• 218457-67-1 | CB-103 (Catalog# : 20322)CB-103 is a γ-secretase inhibitor. CB-103 inhibits Notch signaling in primary human
• 2316817-88-4 | CB-6644 (Catalog# : 41788)CB-6644 acts as a noncompetitive ATPase inhibitor. Additionally, it can inhibit RUVBL
• 21815-91-8 | 3-chloro-1-benzothiophene-2-carbonyl chloride (Catalog# : 2062306)
• 23982-76-5 | 10-Cl-BBQ (Catalog# : 1810161)10-Cl-BBQ是芳烃受体(AhR)配体。
• 218600-44-3 | CDDO (Catalog# : 92304)CDDO是一种合成的齐墩果烷型三萜阻断诱导型一氧化氮合酶和诱导
• 282526-98-1 | Cetilistat (Catalog# : 16122918)Cetilistat, also known as ATL-962, is a drug designed to treat obesity. It acts in th
• 289499-45-2 | Canertinib (Catalog# : 16122909)Canertinib dihydrochloride is the hydrochloride salt of an orally bio-available quina
• 28755-03-5 | 3 CAI (Catalog# : 611801)3CAI is a potent allosteric and specific AKT inhibitor, which exerts efficacy in vitr
• 252917-06-9 | CHIR-99021 (Catalog# : 16062904)CHIR-99021, also known as CT99021, is a glycogen synthase kinase 3 (GSK3) inhibitor t
• 252935-94-7 | CHIR-98014 (Catalog# : 5121103)CHIR98014 is a reversible, cell-permeable activator of the WNT pathway, through inhib
• 267243-28-7 | Canertinib (Catalog# : 120109)Canertinib is an orally bioavailable irreversible Pan-erbB tyrosine kinase inhibitor,
• 202591-23-9 | CPI-203 (Catalog# : 110605)CPI203 is a novel potent, selective and cell permeable inhibitor of the bromodomain a
• 200484-11-3 | CHS-828 (Catalog# : 100904)CHS-828, also known as GMX-1778, is a potent and selective NAMPT inhibitor. CHS-828 i
• 2019-34-3 | 3-(4-Chlorophenyl)propanoic acid (Catalog# : 90615)Coming soon!
• 288383-20-0 | Cediranib (Catalog# : 52779)Cediranib (AZD2171) is a highly potent VEGFR(KDR) inhibitor with IC50 of <1 nM, al
• 285986-88-1 | CCG-1423 (Catalog# : 52502)CCG-1423 is a novel inhibitor of RhoA/C-mediated gene transcription that is capable o
• 2230198-02-2 | Danuglipron (Catalog# : 20538)Danuglipron, also known as PF-06882961 is a potent, orally bioavailable agonist of th
• 2413428-36-9 | DSN28369 (Catalog# : 20498)DSN28369 is a heterobifunctional linker, and useful to make antibody drug conjuate (A
• 2105905-46-0 | 4,6-二氯-1H-吡唑并[3,4-B]吡啶 (Catalog# : 20434)
• 2407725-14-6 | 4,6-dimethylpyrazolo[1,5-a]pyrazine-2-carbaldehyde (Catalog# : 20361)
• 2413256-25-2 | Difelikefalin 盐酸盐 (Catalog# : 21922)Difelikefalin, also known CR-845; MR-13A-9; MR-13A9, is a novel and potent kappa opio
• 2138299-34-8 | diABZI STING agonist-1 trihydrochloride (Catalog# : 2112802)
• 2365172-42-3 | DT-2216 (Catalog# : 20111802)DT2216 is a selective B-cell lymphoma extra large (BCL-XL) proteolysis-targeting chim
• 2007975-22-4 | DSR-141562 (Catalog# : 20792)DSR-141562是新型的PDE1 抑制剂，用于治疗与精神分裂症相关的阳性症
• 24241-18-7 | 3,5-dibromopyrazin-2-amine (Catalog# : 2062016)2-Amino-3,5-dibromopyrazine is used in the preparation of conjugated polymers for neu
• 290304-24-4 | Daun02 (Catalog# : 18793)Daun02是一种细胞生存能力抑制剂和DNA分析抑制剂，IC50值分别为1.5