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74135-04-9

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74135-04-9 Structure

74135-04-9 Structure
IdentificationBack Directory
[Name]

Deproceptin
[CAS]

74135-04-9
[Synonyms]

Aids002088
Aids-002088
Deproceptin
β-Casomorphin-4-amide
B-Casomorphin-4-amide
Tyr-pro-phe-pro amide
β-Casomorphin-4-amide
.beta.-Casomorphin-4-nh2
L-Tyr-L-Pro-L-Phe-L-Pro-NH2
β-Casomorphin (1-4) amide (bovine)，Morphiceptin
β-Casomorphin (1-4) amide (bovine),Morphiceptin
L-Prolinamide, L-tyrosyl-L-prolyl-L-phenylalanyl-
Beta-Casomorphin (1-4) amide (bovine) acetate salt
(2S)-1-[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]-N-[(2S)-1-[(2S)-2-carbamoylpyrrolidin-1-yl]-1-oxo-3-phenyl-propan-2-yl]pyrrolidine-2-carboxamide
[Molecular Formula]

C28H35N5O5
[MDL Number]

MFCD00076328
[MOL File]

74135-04-9.mol
[Molecular Weight]

521.61
Chemical PropertiesBack Directory
[Boiling point ]

919.9±65.0 °C(Predicted)
[density ]

1.327±0.06 g/cm3(Predicted)
[form ]

Solid
[pka]

9.86±0.15(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

Beta-Casomorphin (1-4) Amide (Bovine) Acetate Salt can be used to study opiod and cannabinoid receptors.
[Definition]

ChEBI: Morphiceptin is an oligopeptide.
[in vivo]

Morphiceptin potently inhibits the binding of [3H]dihydromorphine, 125I-labeled FK33824, and [3H]naloxone to rat brain membrane preparations with a 50 percent inhibition concentration (IC50) of about 20 nM[1].

[IC 50]

μ Opioid Receptor/MOR
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