Structure | Cat No. | Product Name | CAS No. | Product description |
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V39377 | DBCO-PEG3-TCO | DBCO-PEG3-TCO is a non-cleavable (non-degradable) ADC linker containing 3 Polyethylene glycol (PEG) units, which may be utilized to prepare Antibody-drug conjugates (ADC). | |
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V0633 | GW2580 (SC203877) | 870483-87-7 | GW2580 (also known as SC-203877)is a novel, potent, selective, and orally bioavailable c-Fms kinaseCSF-1R inhibitor with potential antineoplastic activity. |
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V47750 | 15-去甲-14-氧代赖百当-8(17),12-二烯-18-酸 | 1039673-32-9 | 15-Nor-14-oxolabda-8(17),12E-Diene-18-oic acid (compound 9) is a compound extracted from Chloranthus spicatus. |
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V30349 | 刺囊酸 | 510-30-5 | Echinocystic acid is a naturally occurringpentacyclic triterpene found in the fruits of Gleditsia sinensis Lam with antioxidant, anti-inflammatory and anticancer pactivities. |
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V20571 | 延命草醇 | 28957-06-4 | Enmenol is a novel and potent bioactive compound |
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V0522 | 司马沙尼 | 204005-46-9 | Semaxanib (also known as SU5416) is a novel, potent and selective VEGFR (Flk-1/KDR) inhibitor with potential anticancer activity. |
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V0411 | (+)-JQ1 | 1268524-70-4 | (+)-JQ1 is a novel, potent and highly specific BET (Bromodomain and extra terminal domain) bromodomain inhibitor with antineoplastic activity. |
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V52787 | Carbazole-d8 (咔唑-d8) | 38537-24-5 | Carbazole-d8 is the deuterated form of Carbazole (HY-D0204). |
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V0075 | AZD-1390 | 2089288-03-7 | AZD1390 (AZD-1390) is a novel, potent, selective, first-in-class orally bioavailable and CNS penetrant inhibitor of Ataxia-telangiectasia mutated (ATM) kinase with potential anticancer activity. |
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V51454 | KRA-533 | 10161-87-2 | KRA-533 is a selective KRAS agonist. |
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V35046 | Ditiocarb (Diethyldithiocarbamic acid) | 147-84-2 | Ditiocarb (Diethyldithiocarbamic acid) is a copper reagent that reacts with Cu2+ solution to form a complex, which increases the copper replacement precipitation rate. |