![Retinoic acid ene acetate Smiles: CO[C@]1(C)C[C@@H](O[C@@H](C)[C@@]1(O)CNCCC)O[C@H]1[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@](C)(O)C[C@@H](C)CN[C@H](C)[C@@H](O)[C@](C)(O)[C@@H](CC)OC(=O)[C@@H]1C](https://cdn.shopify.com/s/files/1/0389/1897/9723/files/1686733673582.png?v=1686733696)
Retinoic acid ene acetate Smiles: CO[C@]1(C)C[C@@H](O[C@@H](C)[C@@]1(O)CNCCC)O[C@H]1[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@](C)(O)C[C@@H](C)CN[C@H](C)[C@@H](O)[C@](C)(O)[C@@H](CC)OC(=O)[C@@H]1C
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Retinoic acid ene acetate Smiles: CO[C@]1(C)C[C@@H](O[C@@H](C)[C@@]1(O)CNCCC)O[C@H]1[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@](C)(O)C[C@@H](C)CN[C@H](C)[C@@H](O)[C@](C)(O)[C@@H](CC)OC(=O)[C@@H]1CCeanothic acid, the A 1 homologue of betulinic acid, is isolated from Ceanothus americanus. Synthesized compounds from ceanothic acid have been shown to inhibit Epstein Barr virus early antigen activation in anti cancer research. It also demonstrates growth inhibitory effect against Streptococcus mutans, Actinomyces viscosus, Porphyromonas gingivalis, and Prevotella. Product information CAS Number: 302 79 4 Molecular Weight: 300. 44 Formula: C20H28O2
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