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These samples were dried, reconstituted in 20 l of loading buffer (0.1% TFA, 1% acetonitrile), and stored at 20C for subsequent mass spectrometry (MS) analysis

The peptide received FDA approval in June 2019 under the brand name Vyleesi for treatment of acquired, generalized hypoactive sexual desire disorder in premenopausal women, establishing it as a first-in-class medication with a novel mechanism distinct from all previous sexual dysfunction treatments

Proangiogenic effects : BPC 157 may also promote angiogenesis (new blood vessel formation)