L-Phenylalaninamide, L-tyrosyl-D-alanylglycyl-N-(2-hydroxyethyl)-Nalpha-methyl-, monoacetate (salt)

Base Information

• Chemical Name: L-Phenylalaninamide, L-tyrosyl-D-alanylglycyl-N-(2-hydroxyethyl)-Nalpha-methyl-, monoacetate (salt)
• CAS No.: 100929-53-1
• Molecular Formula: C28H39N5O8
• Molecular Weight: 573.64
• DSSTox Substance ID: DTXSID70905851
• Mol file: 100929-53-1.mol

Synonyms:2 Ala 4 MePhe 5 Gly Enkephalin;2-Ala-4-MePhe-5-Gly-Enkephalin;Ala(2)-MePhe(4)-Gly-ol(5) Enkephalin;D Ala2 NMe Phe4 Gly ol Enkephalin;D-Ala(2)-MePhe(4)-Gly-ol(5) Enkephalin;D-Ala2-NMe-Phe4-Gly-ol Enkephalin;DAGO;DAGOL;DAMGE;DAMGO;Enkephalin, Ala(2)-MePhe(4)-Gly(5)-;Enkephalin, alanyl(2)-methylphenylalanyl(4)-glycine(5)-;Enkephalin, D-Ala2-NMe-Phe4-Gly-ol;RX 783006;RX-783006;Tyr-Ala-Gly-(NMe)Phe-Gly-ol

Chemical Property of L-Phenylalaninamide, L-tyrosyl-D-alanylglycyl-N-(2-hydroxyethyl)-Nalpha-methyl-, monoacetate (salt)

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Boiling Point: 922.7°Cat760mmHg
• Flash Point: 511.8°C
• PSA: 211.39000
• Density: g/cm³
• LogP: 1.02500
• Storage Temp.: −20°C
• Hydrogen Bond Donor Count: 7
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 13
• Exact Mass: 573.27986322
• Heavy Atom Count: 41
• Complexity: 783

Purity/Quality:

99%, ^*data from raw suppliers

[D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate salt ≥97% (HPLC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC(C(=O)NCC(=O)N(C)C(CC1=CC=CC=C1)C(=O)NCCO)NC(=O)C(CC2=CC=C(C=C2)O)N.CC(=O)O
• Isomeric SMILES: C[C@H](C(=O)NCC(=O)N(C)[C@@H](CC1=CC=CC=C1)C(=O)NCCO)NC(=O)[C@H](CC2=CC=C(C=C2)O)N.CC(=O)O
• Uses: Mu-opioid receptor-specific enkephalin analog [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate salt or DAMGO has been used:for use as a positive control in the assay of G-protein activation with μ-opioid receptor, to assay the inhibition of cAMP inhibition by DAMGO for the determination of the suppression of contraction by opioid receptors to determine whether the peripheral application of DAMGO suppresses the hypertonic saline (HS)-induced masseter nociception in slightly anaesthetized rats

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