| Bioactivity | α-MSH (α-Melanocyte-Stimulating Hormone) TFA, an endogenous neuropeptide, is an endogenous melanocortin receptor 4 (MC4R) agonist with anti-inflammatory and antipyretic activities. α-MSH TFA is a post-translational derivative of pro-opiomelanocortin (POMC)[1][2]. | ||||||
| Invitro | α-MSH TFA modulates CNS inflammation by acting directly on melanocortin receptors in glial cells. α-MSH TFA modulates NFκB activation. α-MSH TFA inhibits translocation of transcription factor κB to the nucleus[3]. | ||||||
| Name | α-MSH TFA | ||||||
| CAS | 171869-93-5 | ||||||
| Sequence | Ac-Ser-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2 | ||||||
| Shortening | Ac-SYSMEHFRWGKPV-NH2 | ||||||
| Formula | C77H109N21O19S.xC2HF3O2 | ||||||
| Molar Mass | 1778.90 | ||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||
| Storage | Sealed storage, away from moisture
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) |
α-MSH TFA
CAS: 171869-93-5 F: C77H109N21O19S.xC2HF3O2 W: 1778.90
α-MSH (α-Melanocyte-Stimulating Hormone) TFA, an endogenous neuropeptide, is an endogenous melanocortin receptor 4 (MC
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