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| Product | Description | |
|---|---|---|
| Phortress | Phortress, a lysyl amide prodrug of the benzothiazole 5-fluoro 203, is an apoptosis stimulant potentially for the treatment of solid tumours. Phortress had no effect on HUVEC and MRCV cell proliferation and survival. Unlike paclitaxel and fumagillin, Phortress did not inhibit endothelial tube differentiation. Synonyms: (2S)-2,6-Diamino-N-[4-(5-fluoro-2-benzothiazolyl)-2-methylphenyl]hexanamide dihydrochloride; Phortress; NSC 710305; NSC710305; NSC-710305; 5F-DF-203-L-lysinamide; 5FDF 203Llysinamide. Grades: ≥98% by HPLC. CAS No. 328087-38-3. Molecular formula: C20H23FN4OS.2HCl. Mole weight: 459.41. |  |
| Phortress | Phortress. Group: Biochemicals. Grades: Purified. CAS No. 328087-38-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| Phortress | Phortress is a high affinity AhR ligand that elicits antitumor activity by inducing transcription of CYP1A1 [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NSC 710305. CAS No. 328087-38-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103223. |  |
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