Structure | Cat No. | Product Name | CAS No. | Product Description |
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V58968 | Antitumor agent-48 | 2917547-29-4 | Antitumor agent-48 (Compound 4a) is a 2,3-dehydrosilybin analogue with anticancer effect. |
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V60957 | Antitumor agent-49 | 2763914-21-0 | Antitumor agent-49 (Compound 10) is a harmine analogue-furan hybrid containing NO donor and has anticancer effect. |
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V57283 | Antitumor agent-50 | 2891985-53-6 | Antitumor agent-50 (compound 1a), a thiazolidinone, is a potent antitumor agent. |
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V59192 | Antitumor agent-67 | 2820146-10-7 | Antitumor agent-67 (compound 3) is a potent antitumor agent. |
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V60162 | Antitumor agent-75 | 2827065-29-0 | Antitumor agent-75 is a new and effective antitumor agent. |
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V61427 | Antitumor agent-90 | 131268-74-1 | Antitumor agent-90 is cytotoxic to PC 14 cells and MKN 45 cells. |
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V60721 | Antiviral agent 27 | 2270947-36-7 | antiviral compound 27 (Compound 12) has anti-Ebola virus activity (EC50= 14 nM). |
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V61078 | Antiviral agent 6 | 2847129-11-5 | antiviral compound 6 displays excellent anti-TSWV activity in vivo with EC50 of 188 mg/L. |
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V59417 | AP-C1 | 2234280-26-1 | AP-C1 is a potent inhibitor of guanosine 3',5'-cyclic monophosphate (cGMP)-dependent protein kinase II (cGKII) with pIC50 of 6.5. |
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V59734 | AP-C3 | 682795-78-4 | AP-C3 is a potent inhibitor of guanosine 3',5'-cyclic monophosphate (cGMP)-dependent protein kinase II (cGKII) with pIC50 of 6.3. |
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V59816 | AP-C4 | 682794-85-0 | AP-C4 is an inhibitor (blocker/antagonist) of guanosine 3',5'-cyclic monophosphate (cGMP)-dependent protein kinase II (cGKII) with pIC50 of 5.2. |
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V59273 | AP-C6 | 2234276-60-7 | AP-C6 is a potent inhibitor of guanosine 3',5'-cyclic monophosphate (cGMP)-dependent protein kinase II (cGKII) with pIC50 of 6.5. |
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V59726 | AP-C7 | 2234275-84-2 | AP-C7 is an inhibitor (blocker/antagonist) of guanosine 3',5'-cyclic monophosphate (cGMP)-dependent protein kinase II (cGKII) with pIC50 of 5.0. |
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V57006 | AP39 | 1429061-80-2 | AP39 is a triphenylphosphine-derived anethole dithiothione and a mitochondria-targeted hydrogen sulfide (H2S) donor. |
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V62301 | APC 366 TFA | 2421110-28-1 | APC 366 (TFA) is an irreversible mast cell trypsin inhibitor. |
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V64451 | APOL1-IN-1 | 2446817-72-5 | KIF18A-IN-1 is an inhibitor (blocker/antagonist) of apolipoprotein L1 APOL1 and may be utilized in the study of focal segmental glomerulosclerosis (FSGS) and non-diabetic kidney disease (NDKD). |
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V58583 | Apyrase | 9000-95-7 | Apyrase is a biochemical compound that can be used as a biomaterial or organic/chemical reagent for biomedical research. |
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V61722 | Arachidonic acid-alkyne | 1219038-32-0 | Arachidonic acid-alkyne is an α-alkynyl lipid substitute for polyunsaturated fatty acids. |
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V61454 | Aranciamycin | 72389-06-1 | Aranciamycin (Compound 1) is a class of anthracycline antibiotics with collagenase inhibitory activity (IC503.7*10-7M). |
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V60584 | ARN 077 (enantiomer) (URB913 (enantiomer)) | 1439366-88-7 | ARN 077 enantiomer (19) is a less active isomer of ARN 077 with IC50 of 3.53 μM for rat NAAA. |