enkephalin-Met, Arg(6)-PheNH2(7)-
Basic information
- CAS
78761-61-2- Standard SMILES
CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1ccccc1)C(N)=O- InChIKey
DIESNRFJUNWWPJ-LJADHVKFSA-N- Molecular formula
- C42H57N11O8S
- Average molar mass
- 876 g/mol
- Monoisotopic mass
- 875.41122899
Overview
heptapeptide enkephalinamide analog
Names & identifiers
- Preferred name
- enkephalin-Met, Arg(6)-PheNH2(7)-
- IUPAC
- (2S)-2-[[(2S)-2-[[(2S)-2-[[2-[[2-[[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]amino]acetyl]amino]acetyl]amino]-3-phenylpropanoyl]amino]-4-methylsulfanylbutanoyl]amino]-N-[(2S)-1-amino-1-oxo-3-phenylpropan-2-yl]-5-(diaminomethylideneamino)pentanamide
- English name
- enkephalin-Met, Arg(6)-PheNH2(7)-
- Molecular formula
- C42H57N11O8S
- Molecular weight
- 876.04
Names & synonyms
Meapaa78761-61-2Yggfmrf amide6-Arg-7-phenh2-met-enkephalinEnkephalin-met, arg(6)-phenh2(7)-Met-enkephalin, arg(6)-phenh2(7)-Methionine-enkephalin, arg(6)-phenh2(7)-Enkephalin-met, arginyl(6)phenylalaninamide(7)-L-Phenylalaninamide, L-tyrosylglycylglycyl-L-phenylalanyl-L-methionyl-L-arginyl-RefChem:136909Met-Enkephalin-Arg-Phe amide(2S)-2-[[(2S)-2-[[(2S)-2-[[2-[[2-[[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]amino]acetyl]amino]acetyl]amino]-3-phenylpropanoyl]amino]-4-methylsulfanylbutanoyl]amino]-N-[(2S)-1-amino-1-oxo-3-phenylpropan-2-yl]-5-(diaminomethylideneamino)pentanamide
Show more names
YGGFMRFMet-Enkephalin-RF amide
Met-Enkephalin-Arg-Phe amide H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2Tyr-Gly-Gly-Phe-Met-Arg-Phe-amideTyr-Gly-Gly-Phe-Met-Arg-Phe-NH2H-YGGFMRF-NH2H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2FM108790
Properties
Computed structural properties
- XLogP
- 0.2
- Topological polar surface area
- 354 Ų
- Hydrogen bond donors
- 11
- Hydrogen bond acceptors
- 11
- Rotatable bonds
- 26
- Heavy atoms
- 62
- Formal charge
- 0
- Complexity
- 1,480
Physicochemical properties
- Density
- 1.38 · 1.38±0.1 g/cm3(Predicted)
- pka
- 9.97 · 9.97±0.15(Predicted)
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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