| Bioactivity | Bilaid A1e (Compound 1e) is a tetrapeptide agonist of the µ-opioid receptor (Ki = 750 nM). Bilaid 1e can be isolated from an Australian estuarine isolate of Penicillium sp. Bilaid 1e can be used for pain research[1]. |
| CAS | 2393866-02-7 |
| Sequence | Phe-{d-Val}-Val-{d-Phe}-NH2 |
| Shortening | F-{d-Val}-V-{d-Phe}-NH2 |
| Formula | C28H39N5O4 |
| Molar Mass | 509.64 |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
| Reference | [1]. Dekan Z, et al. A tetrapeptide class of biased analgesics from an Australian fungus targets the µ-opioid receptor. Proc Natl Acad Sci U S A. 2019 Oct 29;116(44):22353-22358. |
Bilaid A1e
CAS: 2393866-02-7 F: C28H39N5O4 W: 509.64
Bilaid A1e (Compound 1e) is a tetrapeptide agonist of the µ-opioid receptor (Ki = 750 nM). Bilaid 1e can be isolated fr
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