cas: 183133-96-2 — see every product listed under this CAS number, including other names
Cabazitaxel (CAS 183133-96-2) is a chemical reagent available from Chemat. Available pack sizes: on request, 250mg, 10mg, 100mg, 25mg, 5mg, 10mM (in 1ml dmso), 50mg. Offered by: Chemat Brand, Mikromol, GLPBio, Biosynth.
| brand | Chemat Brand |
|---|---|
| catalog number | ULC942 |
| cas | 183133-96-2 |
| size | on request |
| availability | Do potwierdzenia przez Chemat|To be confirmed by Chemat |
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| brand | size | price | |
|---|---|---|---|
| Chemat Brand | on request | price on request | |
| Mikromol | 250mg | price on request | |
| GLPBio | 10mg | 625.12 Pln | |
| GLPBio | 100mg | 1046.37 Pln | |
| GLPBio | 25mg | 845.11 Pln | |
| GLPBio | 5mg | 536.19 Pln | |
| GLPBio | 10mM (in 1ml dmso) | 634.48 Pln | |
| GLPBio | 50mg | 751.50 Pln | |
| Biosynth | 1g | price on request | |
| Biosynth | 0,5g | price on request | |
| Biosynth | 2g | price on request | |
| Biosynth | 10g | price on request | |
| Biosynth | 5g | price on request |
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Cabazitaxel is a tetracyclic diterpenoid that is 10-deacetylbaccatin III having O-methyl groups attached at positions 7 and 10 as well as an O-(2R,3S)-3-[(tert-butoxycarbonyl)amino]-2-hydroxy-3-phenylpropanoyl group attached at position 13. Acts as a microtubule inhibitor, binds tubulin and promotes microtubule assembly and simultaneously inhibits disassembly. It has a role as an antineoplastic agent and a microtubule-stabilising agent. It is functionally related to a 10-deacetylbaccatin III.
Source: ChEBI
| Molecular formula | C45H57NO14 |
|---|---|
| Molecular weight | 835.9 g/mol |
| IUPAC name | [(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4-acetyloxy-1-hydroxy-15-[(2R,3S)-2-hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoyl]oxy-9,12-dimethoxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate |
| InChIKey | BMQGVNUXMIRLCK-OAGWZNDDSA-N |
| SMILES | CC1=C2[C@H](C(=O)[C@@]3([C@H](C[C@@H]4[C@]([C@H]3[C@@H]([C@@](C2(C)C)(C[C@@H]1OC(=O)[C@@H]([C@H](C5=CC=CC=C5)NC(=O)OC(C)(C)C)O)O)OC(=O)C6=CC=CC=C6)(CO4)OC(=O)C)OC)C)OC |
Computed by PubChem (NCBI)