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| | FMOC-LYS(TNM)-OH Basic information |
| Product Name: | FMOC-LYS(TNM)-OH | | Synonyms: | Fmoc-Lys(1,5-dioxaspiro[5.5]undecane-3-nitro-3-met;N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[[(3-nitro-1,5-dioxaspiro[5.5]undec-3-yl)methoxy]carbonyl]-L-lysine;Fmoc-L-Lys(Tnm)-OH;FMOC-N-EPSILON-(TRISHYDROXYMETHYLNITROMETHANE CATALYZED WITH CYCLOHEXANONE)-L-LYSINE;FMOC-LYS(TNM)-OH;FMOC-LYSINE(TNM)-OH;FMOC-LYS(1,5-DIOXASPIRO[5.5]UNDECANE-3-NITRO-3-METHOXYCARBONYL)-OH;FMOC-LYS(1,5-DIOXOSPIRO[5,5]UNDECANE-3-NITRO-3-METHOXYCARBONYL)-OH | | CAS: | 251316-95-7 | | MF: | C32H39N3O10 | | MW: | 625.67 | | EINECS: | | | Product Categories: | | | Mol File: | 251316-95-7.mol |  |
| | FMOC-LYS(TNM)-OH Chemical Properties |
| Boiling point | 850.7±65.0 °C(Predicted) | | density | 1.36 | | storage temp. | -15°C | | pka | 3.88±0.21(Predicted) |
| | FMOC-LYS(TNM)-OH Usage And Synthesis |
| Definition | ChEBI: Camptothecin is a pyranoindolizinoquinoline that is pyrano[3',4':6,7]indolizino[1,2-b]quinoline which is substituted by oxo groups at positions 3 and 14, and by an ethyl group and a hydroxy group at position 4 (the S enantiomer). It has a role as an EC 5.99.1.2 (DNA topoisomerase) inhibitor, an antineoplastic agent, a genotoxin and a plant metabolite. It is a pyranoindolizinoquinoline, a tertiary alcohol, a delta-lactone and a quinoline alkaloid. |
| | FMOC-LYS(TNM)-OH Preparation Products And Raw materials |
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