ACTH (1-17) (TFA)
CAS No. ——
ACTH (1-17) (TFA) ( α1-17-ACTH TFA )
Catalog No. M29709 CAS No. ——
ACTH (1-17) TFA is a corticotrophin analogue and an effective human melanocortin 1 (MC1) receptor agonist with Ki value of 0.21 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameACTH (1-17) (TFA)
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NoteResearch use only, not for human use.
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Brief DescriptionACTH (1-17) TFA is a corticotrophin analogue and an effective human melanocortin 1 (MC1) receptor agonist with Ki value of 0.21 nM.
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DescriptionACTH (1-17) TFA is a corticotrophin analogue and an effective human melanocortin 1 (MC1) receptor agonist with Ki value of 0.21 nM.(In Vitro):ACTH (1-17) TFA is a potent agonist at the hMC1R. ACTH (1-17) shows high affinity for the hMC1R with a Ki value of 0.21±0.03 nM which is slightly higher than that of 0.13±0.005 nM for alpha-MSH. ACTH (1-17) induces a slight and not significant increase in growth hormone secretion even when micromolar concentrations of the peptide are employed in rat pituitary cultures.(In Vivo):Inhibition of DNA labeling is noted when the ACTH (1-17) is administered at 2 hr after the beginning of the daily dark span when nocturnal animals become active. When administered at this circadian stage, the larger dose in particular is associated with an inhibition of DNA labeling lasting for 24 hr. The inhibitory effect is much shorter when the same dose is injected 4 hr earlier.
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In Vitro——
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In Vivo——
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Synonymsα1-17-ACTH TFA
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PathwayOthers
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TargetOther Targets
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RecptorKi: 0.21 nM (human MC1 receptor)
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Research Area——
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Indication——
Chemical Information
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CAS Number——
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Formula Weight2207.43
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Molecular FormulaC95H145N29O23S.C2HF3O2
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Purity>98% (HPLC)
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Solubility——
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SMILES——
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Chemical NameSequence:Ser-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
Tsatmali M et al. ACTH1-17 is a more potent agonist at the human MC1 receptor than alpha-MSH. Cell Mol Biol (Noisy-le-grand). 1999 Nov;45(7):1029-34.
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