cas: 5119-48-2 — see every product listed under this CAS number, including other names
Withaferin A (CAS 5119-48-2) is a chemical reagent available from Chemat. Available pack sizes: on request, 10mg, 1mg, 5mg, 10mM (in 1ml dmso), 25mg, 50mg, 250mg. Offered by: Chemat Brand, Dr. Ehrenstorfer, GLPBio, Biosynth.
| brand | Chemat Brand |
|---|---|
| catalog number | ULW011001 |
| cas | 5119-48-2 |
| 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 | |
| Dr. Ehrenstorfer | 10mg | price on request | |
| GLPBio | 1mg | 901.27 Pln | |
| GLPBio | 10mg | 2136.92 Pln | |
| GLPBio | 5mg | 1462.93 Pln | |
| GLPBio | 10mM (in 1ml dmso) | 1500.38 Pln | |
| Biosynth | 25mg | price on request | |
| Biosynth | 10mg | price on request | |
| Thermo Scientific (Acros) | 5MG | 1198.25 Pln | |
| Biosynth | 50mg | price on request | |
| Biosynth | 250mg | price on request | |
| Biosynth | 100mg | price on request | |
| Sigma-Aldrich | 10MG | 2847.00 Pln |
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Withaferin A is a withanolide that is 5,6:22,26-diepoxyergosta-2,24-diene-1,26-dione substituted by hydroxy groups at positions 4 and 27 (the 4beta,5beta,6beta,22R stereoisomer). Isolated from Physalis longifolia, it exhibits cytotoxic activity. It has a role as an antineoplastic agent and an apoptosis inducer. It is an epoxy steroid, a primary alcohol, a delta-lactone, a secondary alcohol, a 27-hydroxy steroid, an ergostanoid, an enone, a 4-hydroxy steroid and a withanolide.
Source: ChEBI
| Molecular formula | C28H38O6 |
|---|---|
| Molecular weight | 470.6 g/mol |
| IUPAC name | (1S,2R,6S,7R,9R,11S,12S,15R,16S)-6-hydroxy-15-[(1S)-1-[(2R)-5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one |
| InChIKey | DBRXOUCRJQVYJQ-CKNDUULBSA-N |
| SMILES | CC1=C(C(=O)O[C@H](C1)[C@@H](C)[C@H]2CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3C[C@@H]5[C@]6([C@@]4(C(=O)C=C[C@@H]6O)C)O5)C)CO |
Computed by PubChem (NCBI)