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| Product | Description | |
|---|---|---|
| Cucurbit(8)uril | Cucurbit(8)uril. Group: Polymers. Alternative Names: Cucurbit[8]uril; Curcubit[8]uril; Cucurbit[8]uril (CB[8]) hydrate, 99+%; Cucurbit[8]uril hydrate contains acid of crystalization; Cucurbit[8]uril hydrate; 2, 20:3, 19-Dimethano-2, 3, 4a, 5a, 6a, 7a, 8a, 9a, 10a, 11a, 12a, 13a, 14a, 15a, 16a, 17a, 19, 20, 21a, 22a, 23a, 24a, 25a, 26a, 27a, 28a, 29a, 30a, 31a, 32a, 33a, 34a-dotriacontaazabispentaleno[1, 6:5, 6, 7]cycloocta[1, 2, 3:3, 4]pentaleno[1. CAS No. 259886-51-6. Product ID: 3, 5, 8, 10, 13, 15, 18, 20, 23, 25, 28, 30, 33, 35, 38, 40, 41, 43, 45, 47, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73-dotriacontazapentacosacyclo[35. 3. 3. 36, 7. 311, 12. 316, 17. 321, 22. 326, 27. 331, 32. 22, 41. 236, 43. 13, 40. 15, 8. 110, 13. 115, 18. 120, 23. 125, 28. 130, 33. 135, 38. 145, 51. 147, 73. 153, 55. 157, 59. 161, 63. 165, 67. 169, 71]octacontane-44, 46, 48, 49, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72-hexadecone. Molecular formula: 1329.1g/mol. Mole weight: C48H48N32O16. C1N2C3C4N (C2=O)CN5C6C7N (C5=O)CN8C9C2N (C8=O)CN5C8C%10N (C5=O)CN5C%11C%12N (C5=O)CN5C%13C%14N (C5=O)CN5C%15C%16N (C5=O)CN5C%17C (N1C5=O)N1CN3C (=O)N4CN6C (=O)N7CN9C (=O)N2CN8C (=O)N%10CN%11C (=O)N%12CN%13C (=O)N%14CN%15C (=O)N%16CN%17C1=O. InChI=1S / C48H48N32O16 / c81-33-49-1-50-18-20-54 (34 (50) 82) 4-58-22-24-62 (38 (58) 86) 8-66-26-28-70 (42 (66) 90) 12-74-30-32-78 (46 (74) 94) 15-77-31-29-73 (45 (77) 93) 11-69-27-25-65 (41 (69) 89) 7-61-23-2 |  |
| Cucurbit[8]uril | Cucurbit[8]uril is a potent, low toxicity and orally active supramolecular inducer of protein heterodimerization. Cucurbit[8]uril induces heterodimerization of methylviologen and naphthalene functionalized proteins. Cucurbit[8]uril can induce energy transfer [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 259886-51-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-103689. |  |
| Cucurbit[8]uril | Cucurbit[8]uril is a remarkably versatile host molecule utilized in a diverse range of drug delivery and catalysis applications. Its unique ability to selectively bind various drug and biomolecule targets with high avidity illustrates its significant potential as a candidate for targeted drug delivery. Furthermore, the catalytic efficacy and promising sensor properties of Cucurbit[8]uril make it a valuable asset in the field of chemical synthesis and detection of diverse analytes. Synonyms: CB[8]; Cucurubituril(8). Grades: 95%. CAS No. 259886-51-6. Molecular formula: C48H48N32O16. Mole weight: 1329.10. |  |
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