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ChemicalBook--->CAS DataBase List--->77465-10-2

77465-10-2

77465-10-2 Structure

77465-10-2 Structure
IdentificationBack Directory
[Name]

ADRENOCORTICOTROPIC HORMONE RAT
[CAS]

77465-10-2
[Synonyms]

ACTH 1-39
CORTICOTROPIN A
ACTH (1-39) (RAT)
ACTH (1-39) (MOUSE, RAT)
α1-39-Corticotropin (rat)
ADRENOCORTICOTROPIC HORMONE RAT
ADRENOCORTICOTROPIC HORMONE (1-39) (RAT)
Adrenocorticotropic Hormone (ACTH) (1-39), rat
SER-TYR-SER-MET-GLU-HIS-PHE-ARG-TRP-GLY-LYS-PRO-VAL-GLY-LYS-LYS-ARG-ARG-PRO-VAL-LYS-VAL-TYR-PRO-ASN-VAL-ALA-GLU-ASN-GLU-SER-ALA-GLU-ALA-PHE-PRO-LEU-GLU-PHE
H-SER-TYR-SER-MET-GLU-HIS-PHE-ARG-TRP-GLY-LYS-PRO-VAL-GLY-LYS-LYS-ARG-ARG-PRO-VAL-LYS-VAL-TYR-PRO-ASN-VAL-ALA-GLU-ASN-GLU-SER-ALA-GLU-ALA-PHE-PRO-LEU-GLU-PHE-OH
SER-TYR-SER-MET-GLU-HIS-PHE-ARG-TRP-GLY-LYS-PRO-VAL-GLY-LYS-LYS-ARG-ARG-PRO-VAL-LYS-VAL-TYR-PRO-ASN-VAL-ALA-GLU-ASN-GLU-SER-ALA-GLU-ALA-PHE-PRO-LEU-GLU-PHE: SYSMEHFRWGKPVGKKRRPVKVYPNVAENESAEAFPLGF
ACTH (1-39) (mouse, rat) trifluoroacetate salt H-Ser-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-Asn-Val-Ala-Glu-Asn-Glu-Ser-Ala-Glu-Ala-Phe-Pro-Leu-Glu-Phe-OH trifluoroacetate salt
[Molecular Formula]

C210H315N57O57S1
[MDL Number]

MFCD00167431
[Molecular Weight]

4582.16
Chemical PropertiesBack Directory
[storage temp. ]

−20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[color ]

White to off-white
[Sequence]

H-Ser-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-Gly-Lys-Lys-Arg-Arg-Pro-Val-Lys-Val-Tyr-Pro-Asn-Val-Ala-Glu-Asn-Glu-Ser-Ala-Glu-Ala-Phe-Pro-Leu-Glu-Phe-OH
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS08
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H351
[Precautionary statements ]

P201-P280-P301+P312-P302+P352+P312-P304+P340+P312-P308+P313
[Hazard Codes ]

Xn
[Risk Statements ]

20/21/22-40
[Safety Statements ]

22-36
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Adrenocorticotropic Hormone (ACTH) (1-39), rat is a potent melanocortin 2 (MC2) receptor agonist.
[in vivo]

The icv injection of ACTH significantly reduces cumulative food intake over the observation period compared with the saline/IgG group. The injection of ACTH Ab into the PVN abolishes the anorexigenic effect of ACTH. Infusion icv of ACTH significantly decreases cumulative food intake in rats that receive α-MSH Ab into the PVN and ACTH icv, and food intake is as low as in the group treated with ACTH icv and IgG into the PVN. Injection of either ACTH Ab or α-MSH Ab into the PVN significantly increase cumulative food intake compared with IgG-treated animals; the combined application of both Ab’s do not increase food intake further[2].

[References]

[1] Lisak RP, et al. Melanocortin receptor agonist ACTH 1-39 protects rat forebrain neurons from apoptotic, excitotoxic and inflammation-related damage. Exp Neurol. 2015 Nov;273:161-7. DOI:10.1016/j.expneurol.2015.08.012
[2] Schulz C, et al. Endogenous ACTH, not only alpha-melanocyte-stimulating hormone, reduces food intake mediated by hypothalamic mechanisms. Am J Physiol Endocrinol Metab. 2010 Feb;298(2):E237-44. DOI:10.1152/ajpendo.00408.2009
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