Cancer Biology
Cancer Biology(癌症生物学)
Cancer Biology 相关产品(682)
- GP10057Amyloid β-Peptide (10-20) (human)CAS: 152286-31-2
Amyloid β-Peptide (10-20) (human) 是 Amyloid-β 的片段；肽，可用于神经系统疾病的研究。
- GC13840Stachydrine (hydrochloride)CAS: 4136-37-2纯度: >97.00%
A pyrrolidine betaine with anticancer and cardioprotective effects
- GC15555Farnesyl Thiosalicylic Acid AmideCAS: 1092521-74-8纯度: >96.00%
A potent Ras inhibitor with anti-cancer activity
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GP10057 | Amyloid β-Peptide (10-20) (human) | 152286-31-2 | - | |
Amyloid β-Peptide (10-20) (human) 是 Amyloid-β 的片段；肽，可用于神经系统疾病的研究。 | ||||
| GA20357 | 1,2-Dimyristoyl-rac-glycerol | 20255-94-1 | >98.00% | |
A diacylglycerol | ||||
| GA21046 | Boc-Leu-Leu-OH | 73401-65-7 | - | |
A peptide building block | ||||
| GC10612 | BQU57 | 1637739-82-2 | >99.50% | |
An inhibitor of RalA and RalB | ||||
| GC10906 | RBC8 | 361185-42-4 | >98.00% | |
A Ral inhibitor | ||||
| GC11189 | AI-10-49 | 1256094-72-0 | >99.00% | |
AI-10-49 是一种蛋白质-蛋白质相互作用抑制剂，选择性结合 CBFβ-SMMHC 并破坏其与 RUNX1 的结合，FRET IC50 为 0.26 uM。 | ||||
| GC12604 | Fumonisin B1 | 116355-83-0 | >98.00% / >95.00% | |
A mycotoxin | ||||
| GC12876 | ML-097 | 743456-83-9 | - | |
A pan activator of Ras-related GTPases | ||||
| GC12948 | CID-1067700 | 314042-01-8 | >98.00% | |
CID-1067700是Rab GTPases的抑制剂，特别是对Rab2和Rab7具有显著的抑制作用。 | ||||
| GC13315 | ML-098 | 878978-76-8 | >99.50% | |
A selective Rab7 activator | ||||
| GC13460 | 2-Hydroxyestradiol | 362-05-0 | >95.00% | |
A natural metabolite of estradiol | ||||
| GC13840 | Stachydrine (hydrochloride) | 4136-37-2 | >97.00% | |
A pyrrolidine betaine with anticancer and cardioprotective effects | ||||
| GC14676 | Pacritinib (SB1518) | 937272-79-2 | - | |
An equipotent inhibitor of FLT3 and JAK2 | ||||
| GC14778 | tetramethyl Nordihydroguaiaretic Acid | 24150-24-1 | >95.00% | |
A tumor growth inhibitor | ||||
| GC15555 | Farnesyl Thiosalicylic Acid Amide | 1092521-74-8 | >96.00% | |
A potent Ras inhibitor with anti-cancer activity | ||||
| GC15594 | PX 12 | 141400-58-0 | >98.00% | |
An irreversible inhibitor of thioredoxin-1 | ||||
| GC16236 | Fucoidan | 9072-19-9 | >98.00% | |
A sulfated polysaccharide with diverse biological activities | ||||
| GC16331 | Misonidazole | 13551-87-6 | >95.00% | |
A nitroimidazole that targets hypoxic cells | ||||
| GC16722 | CE3F4 | 143703-25-7 | >98.00% | |
An uncompetitive inhibitor of Epac1 | ||||
| GC16765 | ML-099 | 496775-95-2 | - | |
A pan activator of Ras-related GTPases | ||||
| GC17093 | VLX600 | 327031-55-0 | >99.00% | |
An anticancer compound | ||||
| GC18254 | DM1-SMe | 138148-68-2 | - | |
A mertansine analog | ||||
| GC18271 | Polmacoxib | 301692-76-2 | - | |
An inhibitor of COX-2 and carbonic anhydrase | ||||
| GC18290 | Chrysomycin A | 82196-88-1 | - | |
An antibiotic with antitumor properties | ||||