cas: 116355-83-0 — see every product listed under this CAS number, including other names
Fumonisin B1 (CAS 116355-83-0) is a chemical reagent available from Chemat. Available pack sizes: on request, 5mg, 10mg, 1mg, 0,5mg, 2mg. Offered by: Chemat Brand, Dr. Ehrenstorfer, TargetMol, GLPBio.
| brand | Chemat Brand |
|---|---|
| catalog number | ULF110003 |
| cas | 116355-83-0 |
| 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 | |
| Dr. Ehrenstorfer | 5mg | price on request | |
| Dr. Ehrenstorfer | 10mg | price on request | |
| TargetMol | 1mg | 2079.36 Pln | |
| GLPBio | 1mg | 891.91 Pln | |
| GLPBio | 10mg | 3976.36 Pln | |
| GLPBio | 5mg | 2548.81 Pln | |
| Biosynth | 0,5mg | price on request | |
| Biosynth | 1mg | price on request | |
| Biosynth | 2mg | price on request | |
| Biosynth | 5mg | price on request | |
| Biosynth | 10mg | price on request | |
| Sigma-Aldrich | 5MG | 5773.00 Pln |
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Fumonisin B1 is a diester that results from the condensation of the 1-carboxy groups of two molecules of propane-1,2,3-tricarboxylic acid with hydroxy groups at positions 14 and 15 of (2S,3S,5R,10R,12S,14S,15R,16R)-2-amino-12,16-dimethylicosane-3,5,10,14,15-pentol. It has a role as a metabolite and a carcinogenic agent. It is a triol, a fumonisin, a primary amino compound and a diester. It is functionally related to a (2S,3S,5R,10R,12S,14S,15R,16R)-2-amino-12,16-dimethylicosane-3,5,10,14,15-pentol. It is a conjugate acid of a fumonisin B1(3-).
Source: ChEBI
| Molecular formula | C34H59NO15 |
|---|---|
| Molecular weight | 721.8 g/mol |
| IUPAC name | (2R)-2-[2-[(5R,6R,7S,9S,11R,16R,18S,19S)-19-amino-6-[(3R)-3,4-dicarboxybutanoyl]oxy-11,16,18-trihydroxy-5,9-dimethylicosan-7-yl]oxy-2-oxoethyl]butanedioic acid |
| InChIKey | UVBUBMSSQKOIBE-DSLOAKGESA-N |
| SMILES | CCCC[C@@H](C)[C@H]([C@H](C[C@@H](C)C[C@@H](CCCC[C@H](C[C@@H]([C@H](C)N)O)O)O)OC(=O)C[C@@H](CC(=O)O)C(=O)O)OC(=O)C[C@@H](CC(=O)O)C(=O)O |
Computed by PubChem (NCBI)